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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