DOI: 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 49 · April 2018 DOI: 10.1055/s-008-39401

Review Article

  • 083
    Alfadhel, Majid; Tabarki, Brahim:

    SLC19A3 Gene Defects Sorting the Phenotype and Acronyms: Review

  • 093
    Ramantani, Georgia; Reuner, Gitta:

    Cognitive Development in Pediatric Epilepsy Surgery

  • 104
    Juliá-Palacios, N.; Boronat, S.; Delgado, I.; Felipe, A.; Macaya, A.:

    Pediatric Klüver–Bucy Syndrome: Report of Two Cases and Review of the Literature

    • Original Article

  • 112
    Cayami, Ferdy K.; Bugiani, Marianna; Pouwels, Petra J.W.; Bernard, Geneviève; van der Knaap, Marjo S.; Wolf, Nicole I.:

    4H Leukodystrophy: Lessons from 3T Imaging

  • 118
    Green, Lydia; Berry, Ian R.; Childs, Anne-Marie; McCullagh, Helen; Jose, Sandhya; Warren, Dan; Craven, Ian; Camm, Nick; Prescott, Katrina; van der Knaap, Marjo S.; Sheridan, Eamonn; Livingston, John H.:

    Whole Exon Deletion in the GFAP Gene Is a Novel Molecular Mechanism Causing Alexander Disease

  • 123
    Pranzatelli, Michael R.; Tate, Elizabeth D.; Alber, Michael; Awadalla, Maha; Blumkin, Lubov; Lina, Elena S.; Leiz, Steffen; Móser, Judit:

    Rituximab, IVIg, and Tetracosactide (ACTH1–24) Combination Immunotherapy (“RITE-CI”) for Pediatric Opsoclonus-Myoclonus Syndrome: Immunomarkers and Clinical Observations

    Supplementary Material (PDF)
  • 135
    Kanemura, Hideaki; Sano, Fumikazu; Ohyama, Tetsuo; Sugita, Kanji; Aihara, Masao:

    Effect of Levetiracetam Monotherapy in Nonlesional Focal Childhood Epilepsy

  • 142
    Haaga, Manja; Trauzettel-Klosinski, Susanne; Krumm, Anna; Küster, Stephan; Ivanov, Iliya; Cordey, Angelika; Gehrlich, Claudia; Staudt, Martin:

    Homonymous Hemianopia in Children and Adolescents: An MRI Study

    • Short Communication

  • 150
    Varvagiannis, K.; Hanquinet, S.; Billieux, M. H.; De Luca, R.; Rimensberger, P.; Lidgren, M.; Guipponi, M.; Makrythanasis, P.; Blouin, J. L.; Antonarakis, S. E.; Steinfeld, R.; Kern, I.; Poretti, A.; Fluss, J.; Fokstuen, S.:

    Congenital Neuronal Ceroid Lipofuscinosis with a Novel CTSD Gene Mutation: A Rare Cause of Neonatal-Onset Neurodegenerative Disorder

  • 154
    Srinivasaraghavan, Rangan; Parameswaran, Narayanan; Mathis, Deborah; Bürer, Celine; Plecko, Barbara:

    Antiquitin Deficiency with Adolescent Onset Epilepsy: Molecular Diagnosis in a Mother of Affected Offsprings

    • Images in Neuropediatrics

  • 158
    De Pieri, Carlo; Bravar, Giulia; Dolcemascolo, Valentina; Dallorto, Anna; De Colle, Maria Cristina; Cogo, Paola Elisa:

    Hoofbeats, Zebras, and a Child with Vomiting

    • Book Review

  • 160
    Boltshauser, Eugen:

    Pediatric Spinal Deformities

  • 161
    Neubauer, Bernd A.:

    Rett Syndrome

    • Erratum

  • e1
    Neubauer, Bernd A.:

    Erratum: Rett Syndrome