DOI : 10.1055/s-00000041

Neuropediatrics

Issue S 01 · Volume 46 · April 2015 DOI: 10.1055/s-005-28977


Abstracts of the 41st Annual Meeting of the Society of Neuropediatrics
Basel, 23–26 April 2015

Prof. Dr. Peter Weber
Abstracts (HTML) List of Authors
PS01-01
Krumm, A.; Staudt, M.; Company, M.; Ivanov, I.; Küster, A.; Trauzettel-Klosinski, S.: Explorative Saccade Training for Children with Homonymous Hemianopia: Case Report and Presentation of a Planned Study
PS01-02
Beer, S.; Mechtl, R.; Michl, E.: Inclusion and Augmentative and Alternative Communication as Most Important Participation Issue
PS01-03
Flümann, S.; Hachmann, W.; Kölfen, W.: Life-Threatening Complication of Spastic Cerebral Palsy: Atlantoaxial Instability
PS01-08
Spiegler, J.; Göpel, W.; Herting, E.: Very Low Birth Weight Infants in Germany: How many Therapies Do They Get until Preschool Age?
PS01-09
Niedermaier, S.; Förster, K.; Schulze, A.; Hilgendorff, A.: Association between Analgosedation of Premature Infants Using Fentanyl with Neurodevelopmental Outcome at the Corrected Age of 24 Months
PS01-10
Böhm, R.; Merschhemke, P.: Stress And The Cortisol Diurnal Profile — Is Only “High” Critical?
PS01-11
Bechtel, N.; Weber, P.: Attention Problems in Children with Epilepsy. How is the Long-Term Outcome?
PS01-12
Cagnoli, S.; Idris, N.; Piroth, W.; Große-Opphoff, J.; Borusiak, P.; Sinha, K.: Never Trust a Normal MRI
PS01-13
Koch, K.: Zoster Neuropathy: Rare Diagnosis in Atypical Facial Pain not Responding to Treatment
PS01-14
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
PS01-15
Karch, S.; Dikow, N.; Seitz, A.; Pietz, J.: Postnatal Microcephaly, Dyskinesia, and Agenesis of the Corpus Callosum as Indication of FOXG1-Related Disorders: A Case Report
PS01-16
Picker-Minh, S.; Hartenstein, S.; Proquitté, H.; Fröhler, S.; Raile, V.; Krämer, N.; Kalache, K.; Morris-Rosendahl, D.; Boltshauser, E.; Chen, W.; Kaindl, A.: Pontine Tegmental Cap Dysplasia in an Extremely Low Birth Weight Preterm Infant
PS01-17
Ziegler, A.; Schuler, E.; Hoffmann, G.: Bohring-Opitz Syndrome: Mutation in the ASXL1 Gene as a Rare Cause of Mental Retardation with Failure to Thrive and Characteristic Phenotype
PS01-18
Thiels, C.; Saft, C.; Köhler, C.; Stahl, A.; Lücke, T.: Therapeutic Options in Treatment of Juvenile Huntington Disease: Difference to Adult Patients
PS01-19
Spiegler, J.; Hellenbroich, Y.; Ahting, U.; Freisinger, P.: Case Report: Patient with POLG Mutation with the Clinical Picture of a Myocerebrohepatopathy Syndrome
PS01-20
Nickel, M.; Kohlschütter, A.; Schulz, A.: Late Talkers in Late Infantile CLN2 Disease: Red Flag for an Early Diagnosis
PS01-21
Kustermann, W.; Brackmann, F.; Gusek-Schneider, G.; Krägeloh-Mann, I.; Dekomien, G.; Leis, T.; Trollmann, R.: Rare Variant of GM2 Gangliosidosis due to Activator Protein Deficiency: A Case Report
PS01-22
Bley, A.; Löbel, U.; Nickel, M.; Ohlenbusch, A.; Denecke, J.; Kohlschütter, A.: Hematopoietic Stem Cell Transplantation for Late-Onset Krabbe Disease
PS01-23
Bley, A.; Nickel, M.; Wolf, N.; Löbel, U.; Kohlschütter, A.: Hypomyelination without Hypogonadotropic Hypogonadism and Hypodontia as a Variant of 4H Syndrome
PS01-24
Kehrer, C.; Böhringer, J.; Beck-Wödl, S.; Krägeloh-Mann, I.: GM2-Activator Deficiency Mimics Tay–Sachs Disease
PS01-25
Deutz, U.; Clusmann, H.; Mull, M.; Lassay, L.; Aktas-Koptagel, M.; Häusler, M.: Spinal Hemorrhage: An Interdisciplinary Emergency
PS01-26
Beer, S.: AAC as an Approach toward Language Development
PS01-27
Poretti, A.; Poretti, A.; Toelle, S.; Klein, A.; Scheer, I.; Huisman, T.; Boltshauser, E.: Cerebellar Cysts in Children: A Pattern-Recognition Approach
PS01-28
Poretti, A.; Poretti, A.; Denecke, J.; Miller, D.; Schiffmann, H.; Buhk, J.; Grange, D.; Doherty, D.; Boltshauser, E.: Brain Stem Disconnection: Two Additional Patients and Expansion of the Phenotype
PS01-29
Bischof, C.: The Abusive Head Trauma: Case Report and Neurological Follow-Up
PS01-30
Hasselmann, O.: Crosstalk between Doctors, Ethicists, and Economist for the Good of Neuropediatrics
PS01-31
Deißler, A.; Albers, L.; von Kries, R.; Langhagen, T.; Heinen, F.; Jahn, K.; Schröder, S.: Health-Related Quality of Life of Children with Vertigo: Retrospective Study at the German Center for Vertigo and Balance Disorders
PS01-32
Kästner, B.; Behre, S.; Lutz, N.; Bürger, F.; Luntz, S.; Hinderhofer, K.; Bendszus, M.; Hoffmann, G.; Ries, M.: Neurological Multicenter Clinical Research in Vulnerable Populations: Variability in Institutional Review Boards' Responses
PS01-33
Vaassen, P.; Rosenbaum, T.: Nevus Anemicus as Indication of Neurofibromatosis Type 1 in Childhood
PS01-34
Jung, N.; Gleich, B.; Kalb, A.; Limburg, K.; Gattinger, N.; Fritsch, J.; Siebner, H.; Mall, V.: Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability
PS01-35
Dehmel, M.; von der Hagen, M.; Schützle, H.; Berner, R.; Suttorp, M.; Hahn, G.; DiDonato, N.; Mackenroth, L.; 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
PS01-36
Schwartz, O.; Loges, N.; Wallmeier, J.; Dougherty, G.; Pennekamp, P.; Olbrich, H.; Omran, H.: Subcellular Analysis of the Motor Protein Apparatus in Ependymal Cilia
PS01-37
Omran, H.; König, J.: Nephronophthisis Registry
PS01-38
Omran, H.; Kurlemann, G.; Bergmann, C.; König, J.: Ciliopathies with Hepatic Involvement the Broad Phenotypical Spectrum of TMEM67 Mutations
PS01-39
Döring, C.; Reihle, C.; Schroth, M.; Wörle, H.; Marquard, K.; von Kalle, T.; Rolfs, A.; Klein, C.; Blankenburg, M.: Manganese Storage Disease as a Rare Cause of Dystonia with Bilateral Changes in Basal Ganglia and Polycythemia
PS01-40
Schimpfößl, M.; Berweck, S.; Betzler, C.; Dotzler, E.; Herberhold, T.; Pringsheim, M.; Staudt, M.; von Stülpnagel-Steinbeis, C.; Kluger, G.: Retrospective Analysis of Tetrahydrocannabinol Based on 31 Neurologically Critically Ill Children
PS01-41
Schmitt-Mechelke, T.; Bachmann-Holzinger, I.; Imahorn, P.; Meier, S.: Feasibility and Usefulness of Rapid 2 Channel EEG Monitoring for Acute CNS Disorders in the Pediatric Emergency Ward
PS01-42
Haas-Lude, K.; Krimmel, M.; Will, B.; Schuhmann, M.; Nägele, T.; Krägeloh-Mann, I.: Clinical and Imaging Findings and Postoperative Esthetic Results in Patients with Single or Bilateral Coronal Synostosis
PS01-43
Hurni, Y.; Guzman, R.; Schneider, J.; Ramelli, G.: Arrested Hydrocephalus in Children: Report of Five Consecutive Cases and Comprehensive Review of the Literature
PS01-44
Linder-Lucht, M.; Aznar Lain, G.; Hernandez Castellano, M.; Muchart Lopez, J.; Mur Sierra, A.: Neurogenic Thoracic Outlet Syndrome: A Rare Differential Diagnosis of upper Extremity Paresthesia in a Pediatric Patient
PS01-45
Ledergerber, K.; Jost, K.; Schulzke, S.; Weber, P.; Datta, A.: The Impact of Infectious Diseases on Sleeping Behavior in Preterm Infants
PS01-46
Bechtel, N.; Noßwitz, U.; Koch, M.; Fischalek, A.; Marsch, B.; Lemberg, K.; Wiesel, T.; Berger, T.; Paulussen, M.; Rostasy, K.: ADEM-Like Presentation as the Main Manifestation of X-Linked Lymphoproliferative Disease in a 4-Year-Old Male Patient
PS01-47
Jahn, K.; Langhagen, T.; Heinen, F.: Clinical Neurophysiology in Dizzy Children: Which Tests do I Need?