DOI: 10.1055/s-00000041

Neuropediatrics

Issue 03 · Volume 47 · June 2016 DOI: 10.1055/s-006-31717

Editorial Comment

137
Dale, Russell C.: Treatment Choices in Optic Neuritis: Corticosteroids, Intravenous Immunoglobulin, Plasma Exchange, or Other?

Review Article

139
Tibussek, Daniel; Klepper, Jörg; Korinthenberg, Rudolf; Kurlemann, Gerhard; Rating, Dietz; Wohlrab, Gabriele; Wolff, Markus; Schmitt, Bernhard: Treatment of Infantile Spasms: Report of the Interdisciplinary Guideline Committee Coordinated by the German-Speaking Society for Neuropediatrics

Original Article

151
Mansour, Lobna A.; Girgis, Marian Y.; Abdulhay, Mohamed; ElEinein, Ehab I. Abou; ElHawary, Rabab; Hanna, Mariam Onsy F.: Polymorphisms of Immunoglobulin G Fc Receptors in Pediatric Guillain–Barré Syndrome
157
Özdemir, Rahmi; Güzel, Orkide; Küçük, Mehmet; Karadeniz, Cem; Yılmaz, Ünsal; Calik, Tansel; Meşe, Timur: The Impact of 3:1 Ketogenic Diet on Cardiac Repolarization Changes in Children with Refractory Seizures: A Prospective Follow-Up Study
162
Sätilä, Heli; Beilmann, Anneli; Olsén, Päivi; Helander, Heli; Eskelinen, Mari; Huhtala, Heini: Does Botulinum Toxin A Treatment Enhance the Walking Pattern in Idiopathic Toe-Walking?
169
Pisani, Francesco; Pavlidis, Elena; Cattani, Luca; Ferrari, Gianluigi; Raheli, Riccardo; Spagnoli, Carlotta: Optimizing Detection Rate and Characterization of Subtle Paroxysmal Neonatal Abnormal Facial Movements with Multi-Camera Video-Electroencephalogram Recordings

Short Communication

175
Jacquet, Coralie; Garnier, Arnaud; Cheuret, Emmanuel: Plasma Exchange and Immunoadsorption in Pediatric Inflammatory Optic Neuropathy Resistant to Corticosteroid Therapy: Four French Cases
179
Sorlin, Arthur; Briand, Gilbert; Cheillan, David; Wiedemann, Arnaud; Montaut-Verient, Bettina; Schmitt, Emmanuelle; Feillet, François: Effect of l-Arginine in One Patient with Peroxisome Biogenesis Disorder due to PEX12 Deficiency
182
Dehmel, Maria; Brenner, Sebastian; Suttorp, Meinolf; Hahn, Gabriele; Schützle, Heike; Dinger, Jürgen; Di Donato, Nataliya; Mackenroth, Luisa; von der Hagen, Maja: Novel Mutation in the DKC1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome As a Rare Differential Diagnosis in Pontocerebellar Hypoplasia, Primary Microcephaly, and Progressive Bone Marrow Failure
187
Grande-Martín, Alberto; Pardal-Fernández, José Manuel; Carrascosa-Romero, María Carmen; De Cabo, Carlos: Tonic Seizure Status Epilepticus Triggered by Valproate in a Child with Doose Syndrome
190
Vaassen, Pia; Rosenbaum, Thorsten: Nevus Anemicus As an Additional Diagnostic Marker of Neurofibromatosis Type 1 in Childhood
194
Johannsen, Jessika; Nickel, Miriam; Schulz, Angela; Denecke, Jonas: Considering Valproate as a Risk Factor for Rapid Exacerbation of Complex Movement Disorder in Progressed Stages of Late-Infantile CLN2 Disease
197
Koenigstein, Karsten; Gramsch, Carolin; Kolodziej, Malgorzata; Neubauer, Bernd A.; Weber, Axel; Lechner, Sarah; Hahn, Andreas: Chudley–McCullough Syndrome: Variable Clinical Picture in Twins with a Novel GPSM2 Mutation

Videos & Images in Neuropediatrics

202
Spors, Hartwig; Merz, Christoph; Dießel, Johanna; Dutzmann, Christina Maria; Neubauer, Bernd A.; Hahn, Andreas: Sulcal Artery Syndrome in a 10-Year-Old Boy