DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 04 · Volume 46 · August 2015 DOI: 10.1055/s-005-29701

Editorial

  • 233
    Plecko, Barbara:

    Honorary Award of the German-Speaking Child Neurology Society — Gesellschaft für Neuropädiatrie — 2015

    • Review Article

  • 234
    de Vries, Linda S.; Benders, Manon J. N. L.; Groenendaal, Floris:

    Progress in Neonatal Neurology with a Focus on Neuroimaging in the Preterm Infant

    • Original Article

  • 242
    Ilea, Aranka; Cristea, Alexandru; Dudescu, Cristian M.; Hurubeanu, Lucia; Vâjâean, Cosmin; Albu, Silviu; Câmpian, Radu S.:

    Lip Forces and Chewing Efficiency in Children with Peripheral Facial Paralysis

  • 248
    Tabea Aurich (-Schuler); Warken, Birgit; Graser, Judith V.; Ulrich, Thilo; Borggraefe, Ingo; Heinen, Florian; Meyer-Heim, Andreas; van Hedel, Hubertus J. A.; Schroeder, A. Sebastian:

    Practical Recommendations for Robot-Assisted Treadmill Therapy (Lokomat) in Children with Cerebral Palsy: Indications, Goal Setting, and Clinical Implementation within the WHO-ICF Framework

    Supplementary material (PDF)
  • 261
    Mazzotta, Silvia; Pavlidis, Elena; Cordori, Cecilia; Spagnoli, Carlotta; Pini, Luigi Alberto; Pisani, Francesco:

    Children's Headache: Drawings in the Diagnostic Work Up

    Supplementary material Tables 1, 2, and 3 (PDF)
  • 269
    Metsähonkala, Liisa; Gaily, Eija; Valanne, Leena; Blomstedt, Göran:

    Etiology and Long-Term Outcomes of Late-Onset Infantile Spasms

    • Short Communications

  • 277
    Sonam, Kothari; Bindu, P. S.; Taly, Arun B.; Govindaraju, Chikkanna; Gayathri, Narayanappa; Arvinda, Hanumanthapura R.; Nagappa, Madhu; Sinha, Sanjib; Khan, Nahid Akthar; Govindaraj, Periyasamy; Thangaraj, Kumarasamy:

    Clinical and Neuroimaging Features in Two Children with Mutations in the Mitochondrial ND5 Gene

    • Short Communication

  • 282
    Vill, Katharina; Kuhn, Marius; Gläser, Dieter; Walter, Maggie C.; Müller-Felber, Wolfgang:

    Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 Gene

    Supplementary material 1 (DOC) Supplementary material 2 (PDF)
  • 287
    von Stülpnagel, Celina; Funke, Claudia; Haberl, Caroline; Hörtnagel, Konstanze; Jüngling, Jerome; Weber, Yvonne G.; Staudt, Martin; Kluger, Gerhard:

    SYNGAP1 Mutation in Focal and Generalized Epilepsy: A Literature Overview and A Case Report with Special Aspects of the EEG

    Supplementary material figure (PDF) Supplementary material Table (DOC)
  • 292
    Elpers, Christiane; Gross, Catharina C.; Fiedler, Barbara; Meuth, Sven G.; Kurlemann, Gerhard:

    A Case Report on Juvenile Neuromyelitis Optica: Early Onset, Long Remission Period, and Atypical Treatment Response

    • Book Review

  • 296

    Paediatric Neurological Disorders with Cerebellar Involvement: Diagnosis and Management – Mariani Foundation Paediaric Neurology Volume 27