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Abbasi, A.
Identification of Novel MCPH Genes: A Study of Consanguineous Families of Pakistani Descent
Abela, L.
A Novel Plasma Biomarker for Snyder Robinson Syndrome (X-Linked Spermine Synthase Deficiency)
Abicht, A.
Infantile Manifestation of a Mitochondriopathy due to a Homozygous Mutation in DARS2 Gene
Adler, C.
Hemispheric Dissociation between Ipsilateral Motor and Contralateral Somatosensory Representation of the Paretic Hand: Deterioration of Hand Function after Hemispherotomy in a Case of Hemispheric Polymicrogyria
Ahting, U.
Case Report: Patient with POLG Mutation with the Clinical Picture of a Myocerebrohepatopathy Syndrome
Aktas-Koptagel, M.
Spinal Hemorrhage: An Interdisciplinary Emergency
Albers, L.
Health-Related Quality of Life of Children with Vertigo: Retrospective Study at the German Center for Vertigo and Balance Disorders
Albrecht, U.
Headache and Focal Status Epilepticus as Initial Symptom of POLG Mutation
Althaus, J.
Predictive Value of Cerebrospinal Fluid Flow Cytometry in Pediatric Multiple Sclerosis
Ketogenic Diet in Childhood Pharmacoresistant Epilepsy
Alves-Pinto, A.
Cerebral Blood Circulation in Premature Infants by Means of Mathematical Modeling
André, M.
Acute Hemiparesis Revealing Neuroborreliosis in a 3-Year-Old Boy
Arroyo, M. Riaño
Muscle Contractures in Children with Spastic Cerebral Palsy
Assmann, B.
Diagnostic Pitfalls in Tuberculous Meningitis
Aznar Lain, G.
Neurogenic Thoracic Outlet Syndrome: A Rare Differential Diagnosis of upper Extremity Paresthesia in a Pediatric Patient
Bach, C.
German Version and Standardization of the Bayley Scales of Infant and Toddler Development, 3rd Edition: First Results on Clinical Validity and Criteria Validity of the Cognitive Scale and Language Scale
Bachmann, M.
Headache and Focal Status Epilepticus as Initial Symptom of POLG Mutation
Bachmann-Holzinger, I.
Feasibility and Usefulness of Rapid 2 Channel EEG Monitoring for Acute CNS Disorders in the Pediatric Emergency Ward
Baethmann, M.
Heterozygous Mutation in the KCNMA1 Gene with “Loss of Function” Phenotype in a Patient with Generalized Epilepsy
Bajer-Kornek, B.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Bak-Göcke, U.
Opsoclonus Myoclonus Syndrome: A Case Report
Ballabio, A.
LYSOPLEX: An Efficient Toolkit to Detect Sequence Variations in Genes Involved in the Lysosomal-Autophagic Pathway and Neurodegenerative Diseases
Bast, T.
Quinidine: A Targeted Drug Treatment for Patients with the Syndrome of Malignant Migrating Partial Seizures in Infancy and KCNT1 Mutation
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Modified Atkins Diet, an Alternative Treatment of Glucose Transporter Type 1 Deficiency Syndrome
Battke, F.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases
Baumann, M.
Headache and Focal Status Epilepticus as Initial Symptom of POLG Mutation
Baumgartner Sigl, S.
Headache and Focal Status Epilepticus as Initial Symptom of POLG Mutation
Beaud, N.
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Bechtel, N.
Attention Problems in Children with Epilepsy. How is the Long-Term Outcome?
ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient
Beck-Wödl, S.
GM2-Activator Deficiency Mimics Tay–Sachs Disease
Beer, S.
Inclusion and Augmentative and Alternative Communication as Most Important Participation Issue
AAC as an Approach toward Language Development
Behre, S.
Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses
Bendszus, M.
Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses
Bengesser, K.
Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases
Berger, T.
ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient
Bergmann, C.
Ciliopathies with Hepatic Involvement the Broad Phenotypical Spectrum of TMEM67 Mutations
Berner, R.
Novel Mutation in the DCK1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome as a Rare Differential Diagnosis in Primary Microcephaly, Cerebellar Hypoplasia, and Severe Developmental Delay with Progressive Bone Marrow Failure
Berweck, S.
Retrospective Analysis of Tetrahydrocannabinol Based on 31 Neurologically Critically Ill Children
Hemispheric Dissociation between Ipsilateral Motor and Contralateral Somatosensory Representation of the Paretic Hand: Deterioration of Hand Function after Hemispherotomy in a Case of Hemispheric Polymicrogyria
Betzler, C.
Retrospective Analysis of Tetrahydrocannabinol Based on 31 Neurologically Critically Ill Children
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Bieri, O.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Bischof, C.
The Abusive Head Trauma: Case Report and Neurological Follow-Up
Biskup, S.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Somatic PIK3CA Mosaic as a Cause of Hemimegalencephaly and Congenital Infiltrating Lipomatosis of the Face
Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases
Heterozygous Mutation in the KCNMA1 Gene with “Loss of Function” Phenotype in a Patient with Generalized Epilepsy
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Blankenburg, M.
MERS: Mild Encephalopathy/Encephalitis with Reversible Lesions in the Splenium Another Three Cases
Manganese Storage Disease as a Rare Cause of Dystonia with Bilateral Changes in Basal Ganglia and Polycythemia
Longitudinally Extensive Transverse Myelitis in Four Children
Blaschek, A.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Blassnig-Ezeh, A.
Spinal Cord Monitoring in Patients with SMA Type III: A Case Report
Bley, A.
Optic Atrophy in an Iron Storage Disorder Reducing Tissue Iron Load in a Child with MPAN Disease
Hypomyelination without Hypogonadotropic Hypogonadism and Hypodontia as a Variant of 4H Syndrome
Hematopoietic Stem Cell Transplantation for Late-Onset Krabbe Disease
Blumberg, J.
Fast fMRI Sequence Allows for Analysis of BOLD Responses to Single Interictal Epileptic Spikes
Blumenstein, T.
Cerebral Blood Circulation in Premature Infants by Means of Mathematical Modeling
Boelen, M.
A Comparison of Language Lateralization as Assessed using Functional MRI using Scanner-Generated versus Externally Calculated Statistical Parameter Maps
Böhm, R.
Stress And The Cortisol Diurnal Profile — Is Only “High” Critical?
Böhringer, J.
Intrafamilial Variability of Natural Disease Course in Metachromatic Leukodystrophy
GM2-Activator Deficiency Mimics Tay–Sachs Disease
Boltshauser, E.
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Corpus Callosum Anomalies in Joubert Syndrome: Low Prevalence and Weak Phenotype–Genotype Correlation
Cerebellar Hypoplasia and Dysmorphia in Neurofibromatosis Type 1
Oral-Facial-Digital Syndrome Type VI: is C5orf42 Really the Major Gene?
Cerebellar Cysts in Children: A Pattern-Recognition Approach
Brain Stem Disconnection: Two Additional Patients and Expansion of the Phenotype
Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
Video-Documented Long-Term Follow-Up of a 10 Years' Old Girl with Severe Dyskinesia and Paroxysmal Choreoathetosis: A Variant Ataxia-Telangiectasia (A-T)
Bonati, U.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Borck, G.
Pontocerebellar Hypoplasia Type 9: A New Subtype
Borell, S.
Immunomodulatory Treatment of a Patient with Cross-Reactive Immunologic Material Negative Infantile Pompe Disease and Hypertrophic Cardiomyopathy
Severe Neonatal Apnea Episodes Associated with a Nondystrophic Congenital Myotonia Caused by a Mutation in the Gene SCN4A
Borggräfe, I.
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Borusiak, P.
Never Trust a Normal MRI
EBV Encephalitis in Acute Infectious Mononucleosis
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Botkin, N.
Cerebral Blood Circulation in Premature Infants by Means of Mathematical Modeling
Bouikidis, A.
Growth and Endocrinological Evaluation in Autosomal Recessive Proximal Spinal Muscular Atrophies Type I–III
X-Linked Myotubular Myopathy Clinical Improvement by Use of Pyridostigmine in an Infant
Brackmann, F.
Leigh-Like Course of Progressive Encephalopathy Associated with ECHS1-Mutation— A Case Report
Rare Variant of GM2 Gangliosidosis due to Activator Protein Deficiency: A Case Report
Braulke, T.
LYSOPLEX: An Efficient Toolkit to Detect Sequence Variations in Genes Involved in the Lysosomal-Autophagic Pathway and Neurodegenerative Diseases
Brecht, I.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Brenner, S.
Novel Mutation in the DCK1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome as a Rare Differential Diagnosis in Primary Microcephaly, Cerebellar Hypoplasia, and Severe Developmental Delay with Progressive Bone Marrow Failure
Brockmann, K.
Novel Mutation in the Inverted Formin 2 Gene in a Family with Hereditary Motor and Sensory Neuropathy, and Nephropathy
Bromberg, J.
Cerebellar Hypoplasia and Dysmorphia in Neurofibromatosis Type 1
Brunner-Krainz, M.
Neuralgic Amyotrophy: A Rare Disease in Adolescence
Bubl, B.
Impact of Advanced MRI Imaging in Acute Stroke-Like Episodes
Budde, J.
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Buhk, J.
Brain Stem Disconnection: Two Additional Patients and Expansion of the Phenotype
Bürger, F.
Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses
Buschmann, A.
German Version and Standardization of the Bayley Scales of Infant and Toddler Development, 3rd Edition: First Results on Clinical Validity and Criteria Validity of the Cognitive Scale and Language Scale
Bussmann, C.
Genetically Misdiagnosed Duchenne: Confirmation of a Becker Muscle Dystrophy with Proof of an In-Frame Mutation with Deletion of Three Additional Exons on mRNA Level Based on Experimental cDNA Analysis
Buttmann, M.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Buyse, G.
Idebenone Reduces Loss of Respiratory Function in Duchenne Muscular Dystrophy: Outcome of a Phase III Double Blind, Randomized, Placebo-Controlled Trial
Cagnoli, S.
Never Trust a Normal MRI
EBV Encephalitis in Acute Infectious Mononucleosis
Capone Mori, A.
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Chen, W.
Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
Identification of Novel MCPH Genes: A Study of Consanguineous Families of Pakistani Descent
Classen, G.
Case Report of a Patient with partial Trisomy 13q21.1qter
Clusmann, H.
Spinal Hemorrhage: An Interdisciplinary Emergency
Company, M.
Explorative Saccade Training for Children with Homonymous Hemianopia: Case Report and Presentation of a Planned Study
Coppola, A.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Courage, C.
Video-Documented Long-Term Follow-Up of a 10 Years' Old Girl with Severe Dyskinesia and Paroxysmal Choreoathetosis: A Variant Ataxia-Telangiectasia (A-T)
Cremer, M.
Immediate Effects of Phototherapy on Sleep of Very Preterm Neonates: An Observational Study
Cross, H.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Crowther, L.
A Novel Plasma Biomarker for Snyder Robinson Syndrome (X-Linked Spermine Synthase Deficiency)
Damm, M.
MERS: Mild Encephalopathy/Encephalitis with Reversible Lesions in the Splenium Another Three Cases
Daseking, M.
Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search
Datta, A.
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
The Impact of Infectious Diseases on Sleeping Behavior in Preterm Infants
Impact of Advanced MRI Imaging in Acute Stroke-Like Episodes
Internetwork Connectivity Alterations in Children with Benign Epilepsy with Centrotemporal Spikes
Immediate Effects of Phototherapy on Sleep of Very Preterm Neonates: An Observational Study
Debus, O.
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Dehmel, M.
Novel Mutation in the DCK1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome as a Rare Differential Diagnosis in Primary Microcephaly, Cerebellar Hypoplasia, and Severe Developmental Delay with Progressive Bone Marrow Failure
Deißler, A.
Health-Related Quality of Life of Children with Vertigo: Retrospective Study at the German Center for Vertigo and Balance Disorders
Dekomien, G.
Rare Variant of GM2 Gangliosidosis due to Activator Protein Deficiency: A Case Report
Delgado, J.
Longitudinal Functional Reorganization after Pediatric Stroke: A Descriptive Case Study
Delgado, J. Rodríguez
Muscle Contractures in Children with Spastic Cerebral Palsy
Della Marina, A.
Growth and Endocrinological Evaluation in Autosomal Recessive Proximal Spinal Muscular Atrophies Type I–III
X-Linked Myotubular Myopathy Clinical Improvement by Use of Pyridostigmine in an Infant
Denecke, J.
ASAH1 Mutation in a Boy with Non-5q SMA and Progressive Myoclonic Epilepsy
Brain Stem Disconnection: Two Additional Patients and Expansion of the Phenotype
Hematopoietic Stem Cell Transplantation for Late-Onset Krabbe Disease
Deuster, S.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Deutz, U.
Spinal Hemorrhage: An Interdisciplinary Emergency
DiDonato, N.
Novel Mutation in the DCK1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome as a Rare Differential Diagnosis in Primary Microcephaly, Cerebellar Hypoplasia, and Severe Developmental Delay with Progressive Bone Marrow Failure
Diessel, J.
Sulcal Artery Syndrome in a 10-Year-Old Boy
Dietel, T.
Quinidine: A Targeted Drug Treatment for Patients with the Syndrome of Malignant Migrating Partial Seizures in Infancy and KCNT1 Mutation
Di Fruscio, G.
LYSOPLEX: An Efficient Toolkit to Detect Sequence Variations in Genes Involved in the Lysosomal-Autophagic Pathway and Neurodegenerative Diseases
Dikow, N.
Postnatal Microcephaly, Dyskinesia, and Agenesis of the Corpus Callosum as Indication of FOXG1-Related Disorders: A Case Report
Dimova, P.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Dittrich, S.
Connatal Nutritional Deficiency of Vitamin B12 in a Newborn with Early Neurologic Symptoms
Döcker, M.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Doherty, D.
Brain Stem Disconnection: Two Additional Patients and Expansion of the Phenotype
Döring, C.
Manganese Storage Disease as a Rare Cause of Dystonia with Bilateral Changes in Basal Ganglia and Polycythemia
Dotzler, E.
Retrospective Analysis of Tetrahydrocannabinol Based on 31 Neurologically Critically Ill Children
Dougherty, G.
Subcellular Analysis of the Motor Protein Apparatus in Ependymal Cilia
Dreher, T.
The Objective Measurement of Diadochokinesis in Children with Bilateral Spastic Cerebral Palsy
Dutzmann, C.
Sulcal Artery Syndrome in a 10-Year-Old Boy
Eckenweiler, M.
Severe Neonatal Apnea Episodes Associated with a Nondystrophic Congenital Myotonia Caused by a Mutation in the Gene SCN4A
Ehl, S.
Immunomodulatory Treatment of a Patient with Cross-Reactive Immunologic Material Negative Infantile Pompe Disease and Hypertrophic Cardiomyopathy
Eitel, H.
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Elfring, G.
Design of a Confirmatory Phase 3, Multicenter, Randomized, Double Blind, Placebo-Controlled Study (ACT DMD) of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy
Elpers, C.
Predictive Value of Cerebrospinal Fluid Flow Cytometry in Pediatric Multiple Sclerosis
Ketogenic Diet in Childhood Pharmacoresistant Epilepsy
Erlewein, R.
Offering Interdisciplinary Evaluation and Crisis Intervention in View of Neuropediatric, Psychiatric, and Special Needs Aspects for Mentally Disabled Children showing Behavioral Problems as their Cardinal Symptom
Erne, B.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Everts, R.
Longitudinal Functional Reorganization after Pediatric Stroke: A Descriptive Case Study
Fehr, S.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Fellinger, J.
The Developmental Coordination Disorder Questionnaire—German Version—in a Pediatric Outpatient Clinic for Communication Disorders
Ferrarini, A.
High Prevalence of Pathologic Copy Number Variations Detected by Array Comparative Genomic Hybridization in Children with Autism Spectrum Disorders: The Experience of Southern Switzerland
Fiedler, B.
Predictive Value of Cerebrospinal Fluid Flow Cytometry in Pediatric Multiple Sclerosis
Ketogenic Diet in Childhood Pharmacoresistant Epilepsy
Fischalek, A.
ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient
Fischer, D.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Fischmann, A.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Fleck, T.
Immunomodulatory Treatment of a Patient with Cross-Reactive Immunologic Material Negative Infantile Pompe Disease and Hypertrophic Cardiomyopathy
Flümann, S.
Life-Threatening Complication of Spastic Cerebral Palsy: Atlantoaxial Instability
Fluss, J.
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Corpus Callosum Anomalies in Joubert Syndrome: Low Prevalence and Weak Phenotype–Genotype Correlation
Fogarasi, A.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Förster, K.
Association between Analgosedation of Premature Infants Using Fentanyl with Neurodevelopmental Outcome at the Corrected Age of 24 Months
Franck, P.
Immunomodulatory Treatment of a Patient with Cross-Reactive Immunologic Material Negative Infantile Pompe Disease and Hypertrophic Cardiomyopathy
Frank, S.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Freisinger, P.
Case Report: Patient with POLG Mutation with the Clinical Picture of a Myocerebrohepatopathy Syndrome
Freudenberg, L.
Concepts of Pediatric Palliative Care in Medical Complex Children with Neurodegenerative Disease: Concurrent Care is an Option
Fritsch, J.
Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability
Fröhler, S.
Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
Identification of Novel MCPH Genes: A Study of Consanguineous Families of Pakistani Descent
Fuchs, H.
Immunomodulatory Treatment of a Patient with Cross-Reactive Immunologic Material Negative Infantile Pompe Disease and Hypertrophic Cardiomyopathy
Gärtner, J.
Bone Marrow Transplantation in a Mouse Model for Rett Syndrome
Gattinger, N.
Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability
Gburek-Augustat, J.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Geis, T.
Genotype and Phenotype in 34 Families with Genetically Confirmed Walker-Warburg Syndrome or Muscle Eye Brain Disease
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Gleich, B.
Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability
Gleixner, E.
Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases
Glöckle, N.
Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases
Gloor, M.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Göpel, W.
Very Low Birth Weight Infants in Germany: How many Therapies Do They Get until Preschool Age?
Graness, I.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Grange, D.
Brain Stem Disconnection: Two Additional Patients and Expansion of the Phenotype
Granström, S.
Executive Dysfunction in Neurofibromatosis Type 1: Comparison to Idiopathic ADHD
Grau, T.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases
Greulich, N.
Becker Muscular Dystrophy in a 2-Year-Old Boy caused by a Novel Missense Mutation p.Arg145Pro in the Dystrophin Gene
Gröschel, S.
Intrafamilial Variability of Natural Disease Course in Metachromatic Leukodystrophy
Groß, C.
Predictive Value of Cerebrospinal Fluid Flow Cytometry in Pediatric Multiple Sclerosis
Groß, M.
Cerebral Palsy and Breathing: More than Prophylaxis of Pneumonia
Grosse, R.
Optic Atrophy in an Iron Storage Disorder Reducing Tissue Iron Load in a Child with MPAN Disease
Große-Opphoff, J.
Never Trust a Normal MRI
Grosser, K.
Olfactory Function in Head Trauma Patients a Link to Frontal Brain Damage?
Gruber-Sedlmayr, U.
Neuralgic Amyotrophy: A Rare Disease in Adolescence
Grunt, S.
Pontocerebellar Hypoplasia Type 9: A New Subtype
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Longitudinal Functional Reorganization after Pediatric Stroke: A Descriptive Case Study
Muscle Contractures in Children with Spastic Cerebral Palsy
LPIN1 Mutations are an Important Cause of Rhabdomyolysis
Guerrini, R.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Gusek-Schneider, G.
Rare Variant of GM2 Gangliosidosis due to Activator Protein Deficiency: A Case Report
Guzman, R.
Arrested Hydrocephalus in Children: Report of Five Consecutive Cases and Comprehensive Review of the Literature
Haak, T.
Leigh-Like Course of Progressive Encephalopathy Associated with ECHS1-Mutation— A Case Report
Haas-Lude, K.
Clinical and Imaging Findings and Postoperative Esthetic Results in Patients with Single or Bilateral Coronal Synostosis
Haberlandt, E.
Headache and Focal Status Epilepticus as Initial Symptom of POLG Mutation
Hachmann, W.
Life-Threatening Complication of Spastic Cerebral Palsy: Atlantoaxial Instability
Hafner, P.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Hahn, A.
Somatic PIK3CA Mosaic as a Cause of Hemimegalencephaly and Congenital Infiltrating Lipomatosis of the Face
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Sulcal Artery Syndrome in a 10-Year-Old Boy
Hahn, G.
Novel Mutation in the DCK1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome as a Rare Differential Diagnosis in Primary Microcephaly, Cerebellar Hypoplasia, and Severe Developmental Delay with Progressive Bone Marrow Failure
Hamelmann, E.
Case Report of a Patient with partial Trisomy 13q21.1qter
Hartenstein, S.
Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
Hartig, M.
Optic Atrophy in an Iron Storage Disorder Reducing Tissue Iron Load in a Child with MPAN Disease
Hasselmann, O.
Crosstalk between Doctors, Ethicists, and Economist for the Good of Neuropediatrics
Hauffa, B.
Growth and Endocrinological Evaluation in Autosomal Recessive Proximal Spinal Muscular Atrophies Type I–III
Haug, V.
Connatal Nutritional Deficiency of Vitamin B12 in a Newborn with Early Neurologic Symptoms
Häusler, M.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Spinal Hemorrhage: An Interdisciplinary Emergency
Häußler, M.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Hehr, U.
Mutation Spectrum and Infantile Manifestation in Hereditary Spastic Paraplegia
Genotype and Phenotype in 34 Families with Genetically Confirmed Walker-Warburg Syndrome or Muscle Eye Brain Disease
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Heimgärtner, M.
Executive Dysfunction in Neurofibromatosis Type 1: Comparison to Idiopathic ADHD
Heinemeyer, J.
ASAH1 Mutation in a Boy with Non-5q SMA and Progressive Myoclonic Epilepsy
Heinen, F.
Clinical Neurophysiology in Dizzy Children: Which Tests do I Need?
Health-Related Quality of Life of Children with Vertigo: Retrospective Study at the German Center for Vertigo and Balance Disorders
Heininger, U.
Acute Hemiparesis Revealing Neuroborreliosis in a 3-Year-Old Boy
Hellenbroich, Y.
Case Report: Patient with POLG Mutation with the Clinical Picture of a Myocerebrohepatopathy Syndrome
Heller, C.
Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases
Helmke, F.
Rolandic Epilepsy: Retrospective Analysis of Neuropsychological and Clinical Data
Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search
Hennig, J.
Fast fMRI Sequence Allows for Analysis of BOLD Responses to Single Interictal Epileptic Spikes
Herberhold, T.
Retrospective Analysis of Tetrahydrocannabinol Based on 31 Neurologically Critically Ill Children
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Herbst, S.
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Herkenrath, P.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Hernandez Castellano, M.
Neurogenic Thoracic Outlet Syndrome: A Rare Differential Diagnosis of upper Extremity Paresthesia in a Pediatric Patient
Herting, E.
Very Low Birth Weight Infants in Germany: How many Therapies Do They Get until Preschool Age?
Heußinger, N.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Becker Muscular Dystrophy in a 2-Year-Old Boy caused by a Novel Missense Mutation p.Arg145Pro in the Dystrophin Gene
Heyer, C.
Infantile Manifestation of a Mitochondriopathy due to a Homozygous Mutation in DARS2 Gene
Hilgendorff, A.
Association between Analgosedation of Premature Infants Using Fentanyl with Neurodevelopmental Outcome at the Corrected Age of 24 Months
Hilker, C.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Hinderhofer, K.
Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses
Genetically Misdiagnosed Duchenne: Confirmation of a Becker Muscle Dystrophy with Proof of an In-Frame Mutation with Deletion of Three Additional Exons on mRNA Level Based on Experimental cDNA Analysis
Hjalgrim, H.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Hoffjan, S.
Infantile Manifestation of a Mitochondriopathy due to a Homozygous Mutation in DARS2 Gene
Hoffmann, G.
Diagnostic Pitfalls in Tuberculous Meningitis
Juvenile Scleroderma with Isolated CNS Manifestations: Difficulties in Diagnosis and Possible Treatment Plans
Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses
Bohring-Opitz Syndrome: Mutation in the ASXL1 Gene as a Rare Cause of Mental Retardation with Failure to Thrive and Characteristic Phenotype
Genetically Misdiagnosed Duchenne: Confirmation of a Becker Muscle Dystrophy with Proof of an In-Frame Mutation with Deletion of Three Additional Exons on mRNA Level Based on Experimental cDNA Analysis
Hoffmann, J.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Somatic PIK3CA Mosaic as a Cause of Hemimegalencephaly and Congenital Infiltrating Lipomatosis of the Face
Hofmann, R.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Hofstetter, P.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Hörtnagel, K.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Video-Documented Long-Term Follow-Up of a 10 Years' Old Girl with Severe Dyskinesia and Paroxysmal Choreoathetosis: A Variant Ataxia-Telangiectasia (A-T)
Hubacher, M.
Internetwork Connectivity Alterations in Children with Benign Epilepsy with Centrotemporal Spikes
Huisman, T.
Corpus Callosum Anomalies in Joubert Syndrome: Low Prevalence and Weak Phenotype–Genotype Correlation
Cerebellar Cysts in Children: A Pattern-Recognition Approach
Hummel, T.
The Depth of the Olfactory Sulcus in Normosmic Children and Adolescents
Olfactory Function in Head Trauma Patients a Link to Frontal Brain Damage?
Huppke, P.
Bone Marrow Transplantation in a Mouse Model for Rett Syndrome
Hurni, Y.
Arrested Hydrocephalus in Children: Report of Five Consecutive Cases and Comprehensive Review of the Literature
Husain, M.
Design of a Confirmatory Phase 3, Multicenter, Randomized, Double Blind, Placebo-Controlled Study (ACT DMD) of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy
Idris, N.
Never Trust a Normal MRI
EBV Encephalitis in Acute Infectious Mononucleosis
Illing, G.
Modified Atkins Diet, an Alternative Treatment of Glucose Transporter Type 1 Deficiency Syndrome
Imahorn, P.
Feasibility and Usefulness of Rapid 2 Channel EEG Monitoring for Acute CNS Disorders in the Pediatric Emergency Ward
Ivanov, I.
Explorative Saccade Training for Children with Homonymous Hemianopia: Case Report and Presentation of a Planned Study
Jacobs, J.
Fast fMRI Sequence Allows for Analysis of BOLD Responses to Single Interictal Epileptic Spikes
Jahn, K.
Clinical Neurophysiology in Dizzy Children: Which Tests do I Need?
Health-Related Quality of Life of Children with Vertigo: Retrospective Study at the German Center for Vertigo and Balance Disorders
Jelesch, E.
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Jenke, A.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
EBV Encephalitis in Acute Infectious Mononucleosis
Johannsen, J.
ASAH1 Mutation in a Boy with Non-5q SMA and Progressive Myoclonic Epilepsy
Jost, K.
The Impact of Infectious Diseases on Sleeping Behavior in Preterm Infants
Immediate Effects of Phototherapy on Sleep of Very Preterm Neonates: An Observational Study
Jünemann, S.
Old Drug, New Mutation in Neonatal Epileptic Encephalopathies
Jung, N.
Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability
Junghanss, T.
Diagnostic Pitfalls in Tuberculous Meningitis
Jüngling, J.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Kaindl, A.
Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
Identification of Novel MCPH Genes: A Study of Consanguineous Families of Pakistani Descent
Kaiser, O.
X-Linked Myotubular Myopathy Clinical Improvement by Use of Pyridostigmine in an Infant
Kalache, K.
Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
Kalb, A.
Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability
Karall, D.
Headache and Focal Status Epilepticus as Initial Symptom of POLG Mutation
Karch, S.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Postnatal Microcephaly, Dyskinesia, and Agenesis of the Corpus Callosum as Indication of FOXG1-Related Disorders: A Case Report
Kästner, B.
Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses
Kehrer, C.
Intrafamilial Variability of Natural Disease Course in Metachromatic Leukodystrophy
GM2-Activator Deficiency Mimics Tay–Sachs Disease
Keimer, R.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Keller, E.
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Kiefer, C.
Longitudinal Functional Reorganization after Pediatric Stroke: A Descriptive Case Study
Kilian, D.
The DEM-CHILD Neuronal Ceroid Lipofuscinoses Patient Database: A Tool for the Evaluation of Therapies in Neuronal Ceroid Lipofuscinoses
Kirschner, J.
Immunomodulatory Treatment of a Patient with Cross-Reactive Immunologic Material Negative Infantile Pompe Disease and Hypertrophic Cardiomyopathy
Severe Neonatal Apnea Episodes Associated with a Nondystrophic Congenital Myotonia Caused by a Mutation in the Gene SCN4A
Klein, A.
Cerebellar Cysts in Children: A Pattern-Recognition Approach
Klein, C.
Manganese Storage Disease as a Rare Cause of Dystonia with Bilateral Changes in Basal Ganglia and Polycythemia
Klepper, J.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Becker Muscular Dystrophy in a 2-Year-Old Boy caused by a Novel Missense Mutation p.Arg145Pro in the Dystrophin Gene
Klotz, M.
The Objective Measurement of Diadochokinesis in Children with Bilateral Spastic Cerebral Palsy
Kluger, G.
Retrospective Analysis of Tetrahydrocannabinol Based on 31 Neurologically Critically Ill Children
Quinidine: A Targeted Drug Treatment for Patients with the Syndrome of Malignant Migrating Partial Seizures in Infancy and KCNT1 Mutation
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Koch, J.
Corpus Callosum Anomalies in Joubert Syndrome: Low Prevalence and Weak Phenotype–Genotype Correlation
Koch, K.
Zoster Neuropathy: Rare Diagnosis in Atypical Facial Pain not Responding to Treatment
Koch, M.
ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient
Koehler, K.
Case Report of a Patient with partial Trisomy 13q21.1qter
Kohl, Z.
Mutation Spectrum and Infantile Manifestation in Hereditary Spastic Paraplegia
Köhler, C.
Infantile Manifestation of a Mitochondriopathy due to a Homozygous Mutation in DARS2 Gene
Rolandic Epilepsy: Retrospective Analysis of Neuropsychological and Clinical Data
Therapeutic Options in Treatment of Juvenile Huntington Disease: Difference to Adult Patients
Kohlschütter, A.
The DEM-CHILD Neuronal Ceroid Lipofuscinoses Patient Database: A Tool for the Evaluation of Therapies in Neuronal Ceroid Lipofuscinoses
Optic Atrophy in an Iron Storage Disorder Reducing Tissue Iron Load in a Child with MPAN Disease
Infantile Manifestation of a Mitochondriopathy due to a Homozygous Mutation in DARS2 Gene
Hypomyelination without Hypogonadotropic Hypogonadism and Hypodontia as a Variant of 4H Syndrome
Hematopoietic Stem Cell Transplantation for Late-Onset Krabbe Disease
Late Talkers in Late Infantile CLN2 Disease: Red Flag for an Early Diagnosis
Kölfen, W.
Life-Threatening Complication of Spastic Cerebral Palsy: Atlantoaxial Instability
König, J.
Nephronophthisis Registry
Ciliopathies with Hepatic Involvement the Broad Phenotypical Spectrum of TMEM67 Mutations
Kontopantelis, E.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Konzett, K.
Spinal Cord Monitoring in Patients with SMA Type III: A Case Report
Körbl, K.
Fast fMRI Sequence Allows for Analysis of BOLD Responses to Single Interictal Epileptic Spikes
Korinthenberg, R.
Immunomodulatory Treatment of a Patient with Cross-Reactive Immunologic Material Negative Infantile Pompe Disease and Hypertrophic Cardiomyopathy
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Severe Neonatal Apnea Episodes Associated with a Nondystrophic Congenital Myotonia Caused by a Mutation in the Gene SCN4A
Becker Muscular Dystrophy in a 2-Year-Old Boy caused by a Novel Missense Mutation p.Arg145Pro in the Dystrophin Gene
Kornfeld, S.
Longitudinal Functional Reorganization after Pediatric Stroke: A Descriptive Case Study
Krägeloh-Mann, I.
Intrafamilial Variability of Natural Disease Course in Metachromatic Leukodystrophy
Clinical and Imaging Findings and Postoperative Esthetic Results in Patients with Single or Bilateral Coronal Synostosis
GM2-Activator Deficiency Mimics Tay–Sachs Disease
Rare Variant of GM2 Gangliosidosis due to Activator Protein Deficiency: A Case Report
Krämer, N.
Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
Identification of Novel MCPH Genes: A Study of Consanguineous Families of Pakistani Descent
Krautwurst, B.
The Objective Measurement of Diadochokinesis in Children with Bilateral Spastic Cerebral Palsy
Krimmel, M.
Clinical and Imaging Findings and Postoperative Esthetic Results in Patients with Single or Bilateral Coronal Synostosis
Krumm, A.
Explorative Saccade Training for Children with Homonymous Hemianopia: Case Report and Presentation of a Planned Study
Kubicki, R.
Severe Neonatal Apnea Episodes Associated with a Nondystrophic Congenital Myotonia Caused by a Mutation in the Gene SCN4A
Kudernatsch, M.
Hemispheric Dissociation between Ipsilateral Motor and Contralateral Somatosensory Representation of the Paretic Hand: Deterioration of Hand Function after Hemispherotomy in a Case of Hemispheric Polymicrogyria
Künzle, C.
Developmental Profile of 3-Year-Old Girl with Atypical Rett Syndrome with Detection of a Currently Unpublished Mutation in the MECP2 Gen
Video-Documented Long-Term Follow-Up of a 10 Years' Old Girl with Severe Dyskinesia and Paroxysmal Choreoathetosis: A Variant Ataxia-Telangiectasia (A-T)
Küpper, H.
Hemispheric Dissociation between Ipsilateral Motor and Contralateral Somatosensory Representation of the Paretic Hand: Deterioration of Hand Function after Hemispherotomy in a Case of Hemispheric Polymicrogyria
Kurlemann, G.
Ciliopathies with Hepatic Involvement the Broad Phenotypical Spectrum of TMEM67 Mutations
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Predictive Value of Cerebrospinal Fluid Flow Cytometry in Pediatric Multiple Sclerosis
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Küster, A.
Explorative Saccade Training for Children with Homonymous Hemianopia: Case Report and Presentation of a Planned Study
Kustermann, W.
Rare Variant of GM2 Gangliosidosis due to Activator Protein Deficiency: A Case Report
Laine, M.
The DEM-CHILD Neuronal Ceroid Lipofuscinoses Patient Database: A Tool for the Evaluation of Therapies in Neuronal Ceroid Lipofuscinoses
Lampe, R.
Cerebral Blood Circulation in Premature Infants by Means of Mathematical Modeling
Lang-Dullenkopf, A.
Developmental Profile of 3-Year-Old Girl with Atypical Rett Syndrome with Detection of a Currently Unpublished Mutation in the MECP2 Gen
Langhagen, T.
Clinical Neurophysiology in Dizzy Children: Which Tests do I Need?
Health-Related Quality of Life of Children with Vertigo: Retrospective Study at the German Center for Vertigo and Balance Disorders
Lassay, L.
Spinal Hemorrhage: An Interdisciplinary Emergency
Lava, S.
High Prevalence of Pathologic Copy Number Variations Detected by Array Comparative Genomic Hybridization in Children with Autism Spectrum Disorders: The Experience of Southern Switzerland
Ledergerber, K.
The Impact of Infectious Diseases on Sleeping Behavior in Preterm Infants
Leis, T.
Rare Variant of GM2 Gangliosidosis due to Activator Protein Deficiency: A Case Report
Leitz, S.
Quinidine: A Targeted Drug Treatment for Patients with the Syndrome of Malignant Migrating Partial Seizures in Infancy and KCNT1 Mutation
Leiz, S.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Heterozygous Mutation in the KCNMA1 Gene with “Loss of Function” Phenotype in a Patient with Generalized Epilepsy
Lemberg, K.
ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient
Lemke, J.
Pontocerebellar Hypoplasia Type 9: A New Subtype
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Video-Documented Long-Term Follow-Up of a 10 Years' Old Girl with Severe Dyskinesia and Paroxysmal Choreoathetosis: A Variant Ataxia-Telangiectasia (A-T)
Lerche, H.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
LeVan, P.
Fast fMRI Sequence Allows for Analysis of BOLD Responses to Single Interictal Epileptic Spikes
Lidzba, K.
Executive Dysfunction in Neurofibromatosis Type 1: Comparison to Idiopathic ADHD
A Comparison of Language Lateralization as Assessed using Functional MRI using Scanner-Generated versus Externally Calculated Statistical Parameter Maps
Limburg, K.
Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability
Linder-Lucht, M.
Neurogenic Thoracic Outlet Syndrome: A Rare Differential Diagnosis of upper Extremity Paresthesia in a Pediatric Patient
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Löbel, U.
Optic Atrophy in an Iron Storage Disorder Reducing Tissue Iron Load in a Child with MPAN Disease
Hypomyelination without Hypogonadotropic Hypogonadism and Hypodontia as a Variant of 4H Syndrome
Hematopoietic Stem Cell Transplantation for Late-Onset Krabbe Disease
Loddenkemper, T.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Loges, N.
Subcellular Analysis of the Motor Protein Apparatus in Ependymal Cilia
Lotte, J.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Lücke, T.
Infantile Manifestation of a Mitochondriopathy due to a Homozygous Mutation in DARS2 Gene
Rolandic Epilepsy: Retrospective Analysis of Neuropsychological and Clinical Data
Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search
Therapeutic Options in Treatment of Juvenile Huntington Disease: Difference to Adult Patients
Luntz, S.
Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses
Lustenberger, A.
Pontocerebellar Hypoplasia Type 9: A New Subtype
Lütschg, J.
Spinal Cord Monitoring in Patients with SMA Type III: A Case Report
Lutz, N.
Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses
Lutz, S.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Growth and Endocrinological Evaluation in Autosomal Recessive Proximal Spinal Muscular Atrophies Type I–III
X-Linked Myotubular Myopathy Clinical Improvement by Use of Pyridostigmine in an Infant
Mackenroth, L.
Novel Mutation in the DCK1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome as a Rare Differential Diagnosis in Primary Microcephaly, Cerebellar Hypoplasia, and Severe Developmental Delay with Progressive Bone Marrow Failure
Maier, M.
The Objective Measurement of Diadochokinesis in Children with Bilateral Spastic Cerebral Palsy
Maier, O.
Developmental Profile of 3-Year-Old Girl with Atypical Rett Syndrome with Detection of a Currently Unpublished Mutation in the MECP2 Gen
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Video-Documented Long-Term Follow-Up of a 10 Years' Old Girl with Severe Dyskinesia and Paroxysmal Choreoathetosis: A Variant Ataxia-Telangiectasia (A-T)
Makowski, C.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Mall, V.
Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability
Mancini, F.
Corpus Callosum Anomalies in Joubert Syndrome: Low Prevalence and Weak Phenotype–Genotype Correlation
Oral-Facial-Digital Syndrome Type VI: is C5orf42 Really the Major Gene?
Marquard, K.
Manganese Storage Disease as a Rare Cause of Dystonia with Bilateral Changes in Basal Ganglia and Polycythemia
Longitudinally Extensive Transverse Myelitis in Four Children
Marsch, B.
ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient
Matheisl, D.
Connatal Nutritional Deficiency of Vitamin B12 in a Newborn with Early Neurologic Symptoms
Mattner, S.
The Objective Measurement of Diadochokinesis in Children with Bilateral Spastic Cerebral Palsy
Mautner, V.
Executive Dysfunction in Neurofibromatosis Type 1: Comparison to Idiopathic ADHD
Mayer, K.
Somatic PIK3CA Mosaic as a Cause of Hemimegalencephaly and Congenital Infiltrating Lipomatosis of the Face
Mechtl, R.
Inclusion and Augmentative and Alternative Communication as Most Important Participation Issue
Meier, S.
Feasibility and Usefulness of Rapid 2 Channel EEG Monitoring for Acute CNS Disorders in the Pediatric Emergency Ward
Meier, T.
Idebenone Reduces Loss of Respiratory Function in Duchenne Muscular Dystrophy: Outcome of a Phase III Double Blind, Randomized, Placebo-Controlled Trial
Meisner, T.
Opsoclonus Myoclonus Syndrome: A Case Report
Mercati, D.
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Merkenschlager, A.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Merschhemke, P.
Stress And The Cortisol Diurnal Profile — Is Only “High” Critical?
Meuth, S.
Predictive Value of Cerebrospinal Fluid Flow Cytometry in Pediatric Multiple Sclerosis
Meyer, S.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Micalizzi, A.
Corpus Callosum Anomalies in Joubert Syndrome: Low Prevalence and Weak Phenotype–Genotype Correlation
Oral-Facial-Digital Syndrome Type VI: is C5orf42 Really the Major Gene?
Miccinilli, E.
Oral-Facial-Digital Syndrome Type VI: is C5orf42 Really the Major Gene?
Michl, E.
Inclusion and Augmentative and Alternative Communication as Most Important Participation Issue
Miller, D.
Brain Stem Disconnection: Two Additional Patients and Expansion of the Phenotype
Mohr, J.
Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases
Morris-Rosendahl, D.
Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
Muchart Lopez, J.
Neurogenic Thoracic Outlet Syndrome: A Rare Differential Diagnosis of upper Extremity Paresthesia in a Pediatric Patient
Mühe, C.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Mull, M.
Spinal Hemorrhage: An Interdisciplinary Emergency
Müller, A.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Müller, C.
Becker Muscular Dystrophy in a 2-Year-Old Boy caused by a Novel Missense Mutation p.Arg145Pro in the Dystrophin Gene
Münter, S.
Case Report of a Patient with partial Trisomy 13q21.1qter
Mur Sierra, A.
Neurogenic Thoracic Outlet Syndrome: A Rare Differential Diagnosis of upper Extremity Paresthesia in a Pediatric Patient
Nägele, T.
Clinical and Imaging Findings and Postoperative Esthetic Results in Patients with Single or Bilateral Coronal Synostosis
Neubauer, B.
Somatic PIK3CA Mosaic as a Cause of Hemimegalencephaly and Congenital Infiltrating Lipomatosis of the Face
Sulcal Artery Syndrome in a 10-Year-Old Boy
Neumann, H.
Rolandic Epilepsy: Retrospective Analysis of Neuropsychological and Clinical Data
Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search
Nickel, M.
The DEM-CHILD Neuronal Ceroid Lipofuscinoses Patient Database: A Tool for the Evaluation of Therapies in Neuronal Ceroid Lipofuscinoses
Optic Atrophy in an Iron Storage Disorder Reducing Tissue Iron Load in a Child with MPAN Disease
Hypomyelination without Hypogonadotropic Hypogonadism and Hypodontia as a Variant of 4H Syndrome
Hematopoietic Stem Cell Transplantation for Late-Onset Krabbe Disease
Late Talkers in Late Infantile CLN2 Disease: Red Flag for an Early Diagnosis
Nicolai, J.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Niedermaier, S.
Association between Analgosedation of Premature Infants Using Fentanyl with Neurodevelopmental Outcome at the Corrected Age of 24 Months
Nigro, V.
LYSOPLEX: An Efficient Toolkit to Detect Sequence Variations in Genes Involved in the Lysosomal-Autophagic Pathway and Neurodegenerative Diseases
Niklasch, M.
The Objective Measurement of Diadochokinesis in Children with Bilateral Spastic Cerebral Palsy
Nolte-Buchholtz, S.
Concepts of Pediatric Palliative Care in Medical Complex Children with Neurodegenerative Disease: Concurrent Care is an Option
Noßwitz, U.
ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient
Och, U.
Ketogenic Diet in Childhood Pharmacoresistant Epilepsy
Ohlenbusch, A.
Hematopoietic Stem Cell Transplantation for Late-Onset Krabbe Disease
Olbrich, H.
Subcellular Analysis of the Motor Protein Apparatus in Ependymal Cilia
Omran, H.
Subcellular Analysis of the Motor Protein Apparatus in Ependymal Cilia
Nephronophthisis Registry
Ciliopathies with Hepatic Involvement the Broad Phenotypical Spectrum of TMEM67 Mutations
Ketogenic Diet in Childhood Pharmacoresistant Epilepsy
Ong, T.
Design of a Confirmatory Phase 3, Multicenter, Randomized, Double Blind, Placebo-Controlled Study (ACT DMD) of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy
Oser, N.
Internetwork Connectivity Alterations in Children with Benign Epilepsy with Centrotemporal Spikes
Papuc, M.
A Novel Plasma Biomarker for Snyder Robinson Syndrome (X-Linked Spermine Synthase Deficiency)
Pascal, J.
A Novel Plasma Biomarker for Snyder Robinson Syndrome (X-Linked Spermine Synthase Deficiency)
Pascher, B.
Hemispheric Dissociation between Ipsilateral Motor and Contralateral Somatosensory Representation of the Paretic Hand: Deterioration of Hand Function after Hemispherotomy in a Case of Hemispheric Polymicrogyria
Paulussen, M.
ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient
Pellacani, S.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Pellanda, G.
High Prevalence of Pathologic Copy Number Variations Detected by Array Comparative Genomic Hybridization in Children with Autism Spectrum Disorders: The Experience of Southern Switzerland
Peltz, S.
Design of a Confirmatory Phase 3, Multicenter, Randomized, Double Blind, Placebo-Controlled Study (ACT DMD) of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy
Pennekamp, P.
Subcellular Analysis of the Motor Protein Apparatus in Ependymal Cilia
Penner, I.
Internetwork Connectivity Alterations in Children with Benign Epilepsy with Centrotemporal Spikes
Perret-Hoigné, E.
LPIN1 Mutations are an Important Cause of Rhabdomyolysis
Petermann, F.
Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search
Philip, S.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Phillipi, H.
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Picker-Minh, S.
Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
Identification of Novel MCPH Genes: A Study of Consanguineous Families of Pakistani Descent
Pieper, T.
Hemispheric Dissociation between Ipsilateral Motor and Contralateral Somatosensory Representation of the Paretic Hand: Deterioration of Hand Function after Hemispherotomy in a Case of Hemispheric Polymicrogyria
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Piepkorn, M.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Pietz, J.
Postnatal Microcephaly, Dyskinesia, and Agenesis of the Corpus Callosum as Indication of FOXG1-Related Disorders: A Case Report
German Version and Standardization of the Bayley Scales of Infant and Toddler Development, 3rd Edition: First Results on Clinical Validity and Criteria Validity of the Cognitive Scale and Language Scale
Piroth, W.
Never Trust a Normal MRI
Plecko, B.
A Novel Plasma Biomarker for Snyder Robinson Syndrome (X-Linked Spermine Synthase Deficiency)
Poloni, C.
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Poretti, A.
Corpus Callosum Anomalies in Joubert Syndrome: Low Prevalence and Weak Phenotype–Genotype Correlation
Cerebellar Hypoplasia and Dysmorphia in Neurofibromatosis Type 1
Oral-Facial-Digital Syndrome Type VI: is C5orf42 Really the Major Gene?
Cerebellar Cysts in Children: A Pattern-Recognition Approach
Cerebellar Cysts in Children: A Pattern-Recognition Approach
Brain Stem Disconnection: Two Additional Patients and Expansion of the Phenotype
Brain Stem Disconnection: Two Additional Patients and Expansion of the Phenotype
Poschmann, S.
Heterozygous Mutation in the KCNMA1 Gene with “Loss of Function” Phenotype in a Patient with Generalized Epilepsy
Prehl, I.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Pringsheim, M.
Retrospective Analysis of Tetrahydrocannabinol Based on 31 Neurologically Critically Ill Children
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Prokisch, H.
Leigh-Like Course of Progressive Encephalopathy Associated with ECHS1-Mutation— A Case Report
Proquitté, H.
Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
Puk, O.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Pulido, R. Poma
Muscle Contractures in Children with Spastic Cerebral Palsy
Quasthoff, S.
Neuralgic Amyotrophy: A Rare Disease in Adolescence
Raile, V.
Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
Ramelli, G.
High Prevalence of Pathologic Copy Number Variations Detected by Array Comparative Genomic Hybridization in Children with Autism Spectrum Disorders: The Experience of Southern Switzerland
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Arrested Hydrocephalus in Children: Report of Five Consecutive Cases and Comprehensive Review of the Literature
Rating, D.
Quinidine: A Targeted Drug Treatment for Patients with the Syndrome of Malignant Migrating Partial Seizures in Infancy and KCNT1 Mutation
Rauch, A.
A Novel Plasma Biomarker for Snyder Robinson Syndrome (X-Linked Spermine Synthase Deficiency)
Rautenstrauss, B.
Novel Mutation in the Inverted Formin 2 Gene in a Family with Hereditary Motor and Sensory Neuropathy, and Nephropathy
Reha, A.
Design of a Confirmatory Phase 3, Multicenter, Randomized, Double Blind, Placebo-Controlled Study (ACT DMD) of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy
Rehm, D.
Acute Hemiparesis Revealing Neuroborreliosis in a 3-Year-Old Boy
Reich, B.
Somatic PIK3CA Mosaic as a Cause of Hemimegalencephaly and Congenital Infiltrating Lipomatosis of the Face
Reichardt, H.
Bone Marrow Transplantation in a Mouse Model for Rett Syndrome
Reichardt, S.
Bone Marrow Transplantation in a Mouse Model for Rett Syndrome
Reicherter, K.
Developmental Profile of 3-Year-Old Girl with Atypical Rett Syndrome with Detection of a Currently Unpublished Mutation in the MECP2 Gen
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Reihle, C.
MERS: Mild Encephalopathy/Encephalitis with Reversible Lesions in the Splenium Another Three Cases
Manganese Storage Disease as a Rare Cause of Dystonia with Bilateral Changes in Basal Ganglia and Polycythemia
Longitudinally Extensive Transverse Myelitis in Four Children
Rettig, O.
The Objective Measurement of Diadochokinesis in Children with Bilateral Spastic Cerebral Palsy
Reuner, G.
Juvenile Scleroderma with Isolated CNS Manifestations: Difficulties in Diagnosis and Possible Treatment Plans
German Version and Standardization of the Bayley Scales of Infant and Toddler Development, 3rd Edition: First Results on Clinical Validity and Criteria Validity of the Cognitive Scale and Language Scale
Reutlinger, C.
Cerebral Palsy and Breathing: More than Prophylaxis of Pneumonia
Opsoclonus Myoclonus Syndrome: A Case Report
Ries, M.
Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses
Riesch, E.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Rieß, A.
Genotype and Phenotype in 34 Families with Genetically Confirmed Walker-Warburg Syndrome or Muscle Eye Brain Disease
Rödl, T.
Genotype and Phenotype in 34 Families with Genetically Confirmed Walker-Warburg Syndrome or Muscle Eye Brain Disease
Rolfs, A.
Manganese Storage Disease as a Rare Cause of Dystonia with Bilateral Changes in Basal Ganglia and Polycythemia
Romani, M.
Corpus Callosum Anomalies in Joubert Syndrome: Low Prevalence and Weak Phenotype–Genotype Correlation
Oral-Facial-Digital Syndrome Type VI: is C5orf42 Really the Major Gene?
Rosenbaum, T.
Nevus Anemicus as Indication of Neurofibromatosis Type 1 in Childhood
Rosenkranz, J.
German Version and Standardization of the Bayley Scales of Infant and Toddler Development, 3rd Edition: First Results on Clinical Validity and Criteria Validity of the Cognitive Scale and Language Scale
Ross, S.
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Rossegg, U.
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Rostasy, K.
ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Headache and Focal Status Epilepticus as Initial Symptom of POLG Mutation
Röthlisberger, B.
Old Drug, New Mutation in Neonatal Epileptic Encephalopathies
Ruf, S.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Russ, A.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Rutz, E.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Saft, C.
Therapeutic Options in Treatment of Juvenile Huntington Disease: Difference to Adult Patients
Sánchez, I. Fernández
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Sauter, T.
Longitudinally Extensive Transverse Myelitis in Four Children
Schallner, J.
Concepts of Pediatric Palliative Care in Medical Complex Children with Neurodegenerative Disease: Concurrent Care is an Option
Schara, U.
Genotype and Phenotype in 34 Families with Genetically Confirmed Walker-Warburg Syndrome or Muscle Eye Brain Disease
Growth and Endocrinological Evaluation in Autosomal Recessive Proximal Spinal Muscular Atrophies Type I–III
X-Linked Myotubular Myopathy Clinical Improvement by Use of Pyridostigmine in an Infant
Scheer, I.
Cerebellar Hypoplasia and Dysmorphia in Neurofibromatosis Type 1
Somatic PIK3CA Mosaic as a Cause of Hemimegalencephaly and Congenital Infiltrating Lipomatosis of the Face
Cerebellar Cysts in Children: A Pattern-Recognition Approach
Schiffmann, H.
Brain Stem Disconnection: Two Additional Patients and Expansion of the Phenotype
Schimmel, M.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Schimpfößl, M.
Retrospective Analysis of Tetrahydrocannabinol Based on 31 Neurologically Critically Ill Children
Schirmer, S.
Mutation Spectrum and Infantile Manifestation in Hereditary Spastic Paraplegia
Schlachter, K.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Schmiedel, G.
Longitudinally Extensive Transverse Myelitis in Four Children
Schmitt, B.
A Novel Plasma Biomarker for Snyder Robinson Syndrome (X-Linked Spermine Synthase Deficiency)
Schmitt-Mechelke, T.
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Feasibility and Usefulness of Rapid 2 Channel EEG Monitoring for Acute CNS Disorders in the Pediatric Emergency Ward
Old Drug, New Mutation in Neonatal Epileptic Encephalopathies
Schneider, J.
Arrested Hydrocephalus in Children: Report of Five Consecutive Cases and Comprehensive Review of the Literature
Impact of Advanced MRI Imaging in Acute Stroke-Like Episodes
Internetwork Connectivity Alterations in Children with Benign Epilepsy with Centrotemporal Spikes
Acute Hemiparesis Revealing Neuroborreliosis in a 3-Year-Old Boy
Schober, H.
Spinal Cord Monitoring in Patients with SMA Type III: A Case Report
Scholl-Bürgi, S.
Headache and Focal Status Epilepticus as Initial Symptom of POLG Mutation
Schöls, L.
Intrafamilial Variability of Natural Disease Course in Metachromatic Leukodystrophy
Schriever, V.
Olfactory Function in Head Trauma Patients a Link to Frontal Brain Damage?
Schröder, S.
Cerebral Palsy and Breathing: More than Prophylaxis of Pneumonia
Health-Related Quality of Life of Children with Vertigo: Retrospective Study at the German Center for Vertigo and Balance Disorders
Schroth, M.
Manganese Storage Disease as a Rare Cause of Dystonia with Bilateral Changes in Basal Ganglia and Polycythemia
Schuhmann, M.
Clinical and Imaging Findings and Postoperative Esthetic Results in Patients with Single or Bilateral Coronal Synostosis
Schuler, E.
Juvenile Scleroderma with Isolated CNS Manifestations: Difficulties in Diagnosis and Possible Treatment Plans
Bohring-Opitz Syndrome: Mutation in the ASXL1 Gene as a Rare Cause of Mental Retardation with Failure to Thrive and Characteristic Phenotype
Schulte-Mattler, U.
Mutation Spectrum and Infantile Manifestation in Hereditary Spastic Paraplegia
Schulz, A.
The DEM-CHILD Neuronal Ceroid Lipofuscinoses Patient Database: A Tool for the Evaluation of Therapies in Neuronal Ceroid Lipofuscinoses
Optic Atrophy in an Iron Storage Disorder Reducing Tissue Iron Load in a Child with MPAN Disease
LYSOPLEX: An Efficient Toolkit to Detect Sequence Variations in Genes Involved in the Lysosomal-Autophagic Pathway and Neurodegenerative Diseases
Late Talkers in Late Infantile CLN2 Disease: Red Flag for an Early Diagnosis
Schulze, A.
Association between Analgosedation of Premature Infants Using Fentanyl with Neurodevelopmental Outcome at the Corrected Age of 24 Months
Schulze-Bonhage, A.
Fast fMRI Sequence Allows for Analysis of BOLD Responses to Single Interictal Epileptic Spikes
Schulzke, S.
The Impact of Infectious Diseases on Sleeping Behavior in Preterm Infants
Immediate Effects of Phototherapy on Sleep of Very Preterm Neonates: An Observational Study
Schützle, H.
Novel Mutation in the DCK1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome as a Rare Differential Diagnosis in Primary Microcephaly, Cerebellar Hypoplasia, and Severe Developmental Delay with Progressive Bone Marrow Failure
Schwartz, O.
Subcellular Analysis of the Motor Protein Apparatus in Ependymal Cilia
Schwerin-Nagel, A.
Neuralgic Amyotrophy: A Rare Disease in Adolescence
Seifert-Held, T.
Neuralgic Amyotrophy: A Rare Disease in Adolescence
Seitz, A.
Postnatal Microcephaly, Dyskinesia, and Agenesis of the Corpus Callosum as Indication of FOXG1-Related Disorders: A Case Report
Selzer, L.
Rolandic Epilepsy: Retrospective Analysis of Neuropsychological and Clinical Data
Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search
Seute, T.
Cerebellar Hypoplasia and Dysmorphia in Neurofibromatosis Type 1
Severin, C.
Longitudinally Extensive Transverse Myelitis in Four Children
Shamdeen, G.
Genotype and Phenotype in 34 Families with Genetically Confirmed Walker-Warburg Syndrome or Muscle Eye Brain Disease
Siebner, H.
Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability
Siebold, D.
Baby-CIMT as Part of a Rehabprogram for Unilateral CP Especially for Very Young Infants
Simma, B.
Spinal Cord Monitoring in Patients with SMA Type III: A Case Report
Simmons, L.
A Novel Plasma Biomarker for Snyder Robinson Syndrome (X-Linked Spermine Synthase Deficiency)
Simonati, A.
The DEM-CHILD Neuronal Ceroid Lipofuscinoses Patient Database: A Tool for the Evaluation of Therapies in Neuronal Ceroid Lipofuscinoses
Singh, Y.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Sinha, K.
Never Trust a Normal MRI
Sinnreich, M.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Smitka, M.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
The Depth of the Olfactory Sulcus in Normosmic Children and Adolescents
Olfactory Function in Head Trauma Patients a Link to Frontal Brain Damage?
Sommerburg, O.
Diagnostic Pitfalls in Tuberculous Meningitis
Speckmann, C.
Immunomodulatory Treatment of a Patient with Cross-Reactive Immunologic Material Negative Infantile Pompe Disease and Hypertrophic Cardiomyopathy
Spiegel, R.
Design of a Confirmatory Phase 3, Multicenter, Randomized, Double Blind, Placebo-Controlled Study (ACT DMD) of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy
Spiegler, J.
Very Low Birth Weight Infants in Germany: How many Therapies Do They Get until Preschool Age?
Case Report: Patient with POLG Mutation with the Clinical Picture of a Myocerebrohepatopathy Syndrome
Opsoclonus Myoclonus Syndrome: A Case Report
Stahl, A.
Therapeutic Options in Treatment of Juvenile Huntington Disease: Difference to Adult Patients
Staudt, M.
Explorative Saccade Training for Children with Homonymous Hemianopia: Case Report and Presentation of a Planned Study
Retrospective Analysis of Tetrahydrocannabinol Based on 31 Neurologically Critically Ill Children
A Comparison of Language Lateralization as Assessed using Functional MRI using Scanner-Generated versus Externally Calculated Statistical Parameter Maps
Hemispheric Dissociation between Ipsilateral Motor and Contralateral Somatosensory Representation of the Paretic Hand: Deterioration of Hand Function after Hemispherotomy in a Case of Hemispheric Polymicrogyria
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Steindl, K.
A Novel Plasma Biomarker for Snyder Robinson Syndrome (X-Linked Spermine Synthase Deficiency)
Steiner, B.
Old Drug, New Mutation in Neonatal Epileptic Encephalopathies
Steinlin, M.
Pontocerebellar Hypoplasia Type 9: A New Subtype
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Longitudinal Functional Reorganization after Pediatric Stroke: A Descriptive Case Study
Oral-Facial-Digital Syndrome Type VI: is C5orf42 Really the Major Gene?
LPIN1 Mutations are an Important Cause of Rhabdomyolysis
Steinmetz, C.
Connatal Nutritional Deficiency of Vitamin B12 in a Newborn with Early Neurologic Symptoms
Stettner, G.
Novel Mutation in the Inverted Formin 2 Gene in a Family with Hereditary Motor and Sensory Neuropathy, and Nephropathy
Stöbe, P.
Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Storch, K.
Acute Necrotizing Encephalopathy: Two Cases and the Detection of a New RANBP2 Mutation
Striano, P.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Stroedter, L.
Neuralgic Amyotrophy: A Rare Disease in Adolescence
Studer, M.
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Sukhudyan, B.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Suttorp, M.
Novel Mutation in the DCK1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome as a Rare Differential Diagnosis in Primary Microcephaly, Cerebellar Hypoplasia, and Severe Developmental Delay with Progressive Bone Marrow Failure
Tacke, U.
Impact of Advanced MRI Imaging in Acute Stroke-Like Episodes
Acute Hemiparesis Revealing Neuroborreliosis in a 3-Year-Old Boy
Teuscher, M.
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Thiede, A.
The Developmental Coordination Disorder Questionnaire—German Version—in a Pediatric Outpatient Clinic for Communication Disorders
Thiels, C.
Infantile Manifestation of a Mitochondriopathy due to a Homozygous Mutation in DARS2 Gene
Rolandic Epilepsy: Retrospective Analysis of Neuropsychological and Clinical Data
Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search
Therapeutic Options in Treatment of Juvenile Huntington Disease: Difference to Adult Patients
Thomas, E.
Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin
Till, H.
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Toelle, S.
Cerebellar Hypoplasia and Dysmorphia in Neurofibromatosis Type 1
Cerebellar Cysts in Children: A Pattern-Recognition Approach
Trauzettel-Klosinski, S.
Explorative Saccade Training for Children with Homonymous Hemianopia: Case Report and Presentation of a Planned Study
Trippe, H.
Genotype and Phenotype in 34 Families with Genetically Confirmed Walker-Warburg Syndrome or Muscle Eye Brain Disease
Growth and Endocrinological Evaluation in Autosomal Recessive Proximal Spinal Muscular Atrophies Type I–III
X-Linked Myotubular Myopathy Clinical Improvement by Use of Pyridostigmine in an Infant
Trollmann, R.
Leigh-Like Course of Progressive Encephalopathy Associated with ECHS1-Mutation— A Case Report
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Rare Variant of GM2 Gangliosidosis due to Activator Protein Deficiency: A Case Report
Turova, V.
Cerebral Blood Circulation in Premature Infants by Means of Mathematical Modeling
Vaassen, P.
Nevus Anemicus as Indication of Neurofibromatosis Type 1 in Childhood
Valente, E.
Corpus Callosum Anomalies in Joubert Syndrome: Low Prevalence and Weak Phenotype–Genotype Correlation
Oral-Facial-Digital Syndrome Type VI: is C5orf42 Really the Major Gene?
van Rappard, D.
Intrafamilial Variability of Natural Disease Course in Metachromatic Leukodystrophy
Vermeulen, J.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Viellieber, M.
Quinidine: A Targeted Drug Treatment for Patients with the Syndrome of Malignant Migrating Partial Seizures in Infancy and KCNT1 Mutation
Vollrath, G.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
von der Hagen, M.
Novel Mutation in the DCK1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome as a Rare Differential Diagnosis in Primary Microcephaly, Cerebellar Hypoplasia, and Severe Developmental Delay with Progressive Bone Marrow Failure
Concepts of Pediatric Palliative Care in Medical Complex Children with Neurodegenerative Disease: Concurrent Care is an Option
von Kalle, T.
MERS: Mild Encephalopathy/Encephalitis with Reversible Lesions in the Splenium Another Three Cases
Manganese Storage Disease as a Rare Cause of Dystonia with Bilateral Changes in Basal Ganglia and Polycythemia
Longitudinally Extensive Transverse Myelitis in Four Children
von Kries, R.
Health-Related Quality of Life of Children with Vertigo: Retrospective Study at the German Center for Vertigo and Balance Disorders
von Stülpnagel-Steinbeis, C.
Retrospective Analysis of Tetrahydrocannabinol Based on 31 Neurologically Critically Ill Children
Vosschulte, P.
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
Waibel, J.
Intrafamilial Variability of Natural Disease Course in Metachromatic Leukodystrophy
Wallmeier, J.
Subcellular Analysis of the Motor Protein Apparatus in Ependymal Cilia
Weber, P.
Attention Problems in Children with Epilepsy. How is the Long-Term Outcome?
The Impact of Infectious Diseases on Sleeping Behavior in Preterm Infants
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Cerebellar Hypoplasia and Dysmorphia in Neurofibromatosis Type 1
Impact of Advanced MRI Imaging in Acute Stroke-Like Episodes
Internetwork Connectivity Alterations in Children with Benign Epilepsy with Centrotemporal Spikes
Immediate Effects of Phototherapy on Sleep of Very Preterm Neonates: An Observational Study
Wegener, J.
Bone Marrow Transplantation in a Mouse Model for Rett Syndrome
Weigt-Usinger, K.
Rolandic Epilepsy: Retrospective Analysis of Neuropsychological and Clinical Data
Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search
Weisbrod, T.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Weissert, R.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Weisstanner, C.
Longitudinal Functional Reorganization after Pediatric Stroke: A Descriptive Case Study
Wenner, K.
Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study
Wieczorek, D.
Genotype and Phenotype in 34 Families with Genetically Confirmed Walker-Warburg Syndrome or Muscle Eye Brain Disease
Wiemer-Kruel, A.
Modified Atkins Diet, an Alternative Treatment of Glucose Transporter Type 1 Deficiency Syndrome
Wiesel, T.
ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient
Wiesmann, C.
Design of a Confirmatory Phase 3, Multicenter, Randomized, Double Blind, Placebo-Controlled Study (ACT DMD) of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy
Wiest, R.
Longitudinal Functional Reorganization after Pediatric Stroke: A Descriptive Case Study
Wilhelm, C.
Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases
Wilichowski, E.
Novel Mutation in the Inverted Formin 2 Gene in a Family with Hereditary Motor and Sensory Neuropathy, and Nephropathy
Wilke, M.
A Comparison of Language Lateralization as Assessed using Functional MRI using Scanner-Generated versus Externally Calculated Statistical Parameter Maps
Wilken, B.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Wilkens, B.
Cerebral Palsy and Breathing: More than Prophylaxis of Pneumonia
Will, B.
Clinical and Imaging Findings and Postoperative Esthetic Results in Patients with Single or Bilateral Coronal Synostosis
William, R.
The DEM-CHILD Neuronal Ceroid Lipofuscinoses Patient Database: A Tool for the Evaluation of Therapies in Neuronal Ceroid Lipofuscinoses
Winkler, P.
Hemispheric Dissociation between Ipsilateral Motor and Contralateral Somatosensory Representation of the Paretic Hand: Deterioration of Hand Function after Hemispherotomy in a Case of Hemispheric Polymicrogyria
Focal Cortical Dysplasia in a Family with KCNQ3 Mutation
Wittmann, W.
Mutation Spectrum and Infantile Manifestation in Hereditary Spastic Paraplegia
Wolf, N.
Intrafamilial Variability of Natural Disease Course in Metachromatic Leukodystrophy
Oral-Facial-Digital Syndrome Type VI: is C5orf42 Really the Major Gene?
Hypomyelination without Hypogonadotropic Hypogonadism and Hypodontia as a Variant of 4H Syndrome
Wolf, P.
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
Wolf, S.
The Objective Measurement of Diadochokinesis in Children with Bilateral Spastic Cerebral Palsy
Wolff, M.
Quinidine: A Targeted Drug Treatment for Patients with the Syndrome of Malignant Migrating Partial Seizures in Infancy and KCNT1 Mutation
Wörle, H.
MERS: Mild Encephalopathy/Encephalitis with Reversible Lesions in the Splenium Another Three Cases
Manganese Storage Disease as a Rare Cause of Dystonia with Bilateral Changes in Basal Ganglia and Polycythemia
Ziegler, A.
Diagnostic Pitfalls in Tuberculous Meningitis
Juvenile Scleroderma with Isolated CNS Manifestations: Difficulties in Diagnosis and Possible Treatment Plans
Bohring-Opitz Syndrome: Mutation in the ASXL1 Gene as a Rare Cause of Mental Retardation with Failure to Thrive and Characteristic Phenotype
Genetically Misdiagnosed Duchenne: Confirmation of a Becker Muscle Dystrophy with Proof of an In-Frame Mutation with Deletion of Three Additional Exons on mRNA Level Based on Experimental cDNA Analysis
Zielonka, M.
Diagnostic Pitfalls in Tuberculous Meningitis
Zsoter, A.
A Comparison of Language Lateralization as Assessed using Functional MRI using Scanner-Generated versus Externally Calculated Statistical Parameter Maps
Hemispheric Dissociation between Ipsilateral Motor and Contralateral Somatosensory Representation of the Paretic Hand: Deterioration of Hand Function after Hemispherotomy in a Case of Hemispheric Polymicrogyria