Neuropediatrics

Issue 04 · August 2012

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Issue
173
Boltshauser, Eugen; Neubauer, Bernd; Plecko, Barbara: Message from the Editors-in-Chief

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Editorial
174
Amato, Maria Pia: Cognitive and Psychosocial Issues in Pediatric Multiple Sclerosis: Where We Are and Where We Need To Go FREE ACCESS

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Review Article
176
Blaschek, Astrid; van's Gravesande, Karin Storm; Heinen, Florian; Pritsch, Martin; Mall, Volker; Calabrese, Pasquale: Neuropsychological Aspects of Childhood Multiple Sclerosis: An Overview

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184
Schara, Ulrike; Della Marina, Adela; Abicht, Angela: Congenital Myasthenic Syndromes: Current Diagnostic and Therapeutic Approaches

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Original Article
194
Nur, B.G.; Sahinturk, D.; Coskun, M.; Duman, O.; Yavuzer, U.; Haspolat, S.: Single Nucleotide Polymorphism and Production of IL-1β and IL-10 Cytokines in Febrile Seizures

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Short Communication
201
Libernini, Laura; Lupis, Chiara; Mastrangelo, Mario; Carrozzo, Rosalba; Santorelli, Filippo Maria; Inghilleri, Maurizio; Leuzzi, Vincenzo: Mitochondrial Neurogastrointestinal Encephalomyopathy: Novel Pathogenic Mutations in Thymidine Phosphorylase Gene in Two Italian Brothers

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209
van Baalen, Andreas; Häusler, Martin; Plecko-Startinig, Barbara; Strautmanis, Jurgis; Vlaho, Stefan; Gebhardt, Boris; Rohr, Axel; Abicht, Angela; Kluger, Gerhard; Stephani, Ulrich; Probst, Christian; Vincent, Angela; Bien, Christian G.: Febrile Infection-Related Epilepsy Syndrome without Detectable Autoantibodies and Response to Immunotherapy: A Case Series and Discussion of Epileptogenesis in FIRES

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217
Toto, Maddalena; De Giacomo, Andrea; Petruzzelli, Maria Giuseppina; Dicuonzo, Franca; Santoro, Nicola; Del Vecchio, Giovanni Carlo; Craig, Francesco; Margari, Lucia: Guillain-Barré-Like Syndrome in a Child with Lead Poisoning

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221
Toelle, Sandra; Poretti, Andrea; Scheer, Ianina; Huisman, Thierry; Boltshauser, Eugen: Bannayan–Riley–Ruvalcaba Syndrome with Progressive Spinal Epidural Lipomatosis

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225
Hachiya, Yasuo; Hayashi, Masaharu; Negishi, Takashi; Atsumi, Soh; Kubota, Masaya; Nishihara, Tetsuhiro: A Case of Osteogenesis Imperfecta Type II Caused by a Novel COL1A2 Gene Mutation: Endoscopic Third Ventriculostomy to Prevent Hydrocephalus

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Book Review
229
The Developing Human Brain: Growth and Adversities

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