DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 04 · Volume 43 · August 2012 DOI: 10.1055/s-002-23643

  • 173
    Boltshauser, Eugen; Neubauer, Bernd; Plecko, Barbara:

    Message from the Editors-in-Chief

    • Editorial

  • 174
    Amato, Maria Pia:

    Cognitive and Psychosocial Issues in Pediatric Multiple Sclerosis: Where We Are and Where We Need To Go

    • 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

  • 184
    Schara, Ulrike; Della Marina, Adela; Abicht, Angela:

    Congenital Myasthenic Syndromes: Current Diagnostic and Therapeutic Approaches

    • 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

    • 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

  • 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

  • 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

  • 221
    Toelle, Sandra; Poretti, Andrea; Scheer, Ianina; Huisman, Thierry; Boltshauser, Eugen:

    Bannayan–Riley–Ruvalcaba Syndrome with Progressive Spinal Epidural Lipomatosis

  • 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

    • Book Review

  • 229

    The Developing Human Brain: Growth and Adversities