DOI: 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 33 · April 2002 DOI: 10.1055/s-002-2019

Original Article

  • 57
    Boltshauser, E.; Barth, P. G.; Troost, D.; Martin, E.; Stallmach, T.:

    “Vanishing White Matter” and Ovarian Dysgenesis in an Infant with Cerebro-Oculo-Facio-Skeletal Phenotype

  • 63
    Huppke, P.; Held, M.; Hanefeld, F.; Engel, W.; Laccone, F.:

    Influence of Mutation Type and Location on Phenotype in 123 Patients with Rett Syndrome

  • 69
    Kyllerman, M.; Brandberg, G.; Wiklund, L.-M.; Månsson, J.-E.:

    Dysarthria, Progressive Parkinsonian Features and Symmetric Necrosis of Putamen in a Family with Painful Lipomas (Dercum Disease Variant)

  • 73
    Einspieler, C.; Cioni, G.; Paolicelli, P. B.; Bos, A. F.; Dressler, A.; Ferrari, F.; Roversi, M. F.; Prechtl, H. F. R.:

    The Early Markers for Later Dyskinetic Cerebral Palsy are Different from Those for Spastic Cerebral Palsy

  • 79
    Moroni, I.; Bugiani, M.; Bizzi, A.; Castelli, G.; Lamantea, E.; Uziel, G.:

    Cerebral White Matter Involvement in Children with Mitochondrial Encephalopathies

    • Short Communication

  • 86
    v Maydell, B.; Kopp, M.; v Komorowski, G.; Joe, A.; Juengling, F. D.; Korinthenberg, R.:

    Hashimoto Encephalopathy - is it Underdiagnosed in Pediatric Patients?

  • 90
    Gencik, M.; Hammans, C.; Strehl, H.; Wagner, N.; Epplen, J. T.:

    Chorea Huntington: A Rare Case with Childhood Onset

  • 93
    Martens-Le Bouar, H.; Korinthenberg, R.:

    Polyradiculoneuritis with Myelitis: A Rare Differential Diagnosis of Guillain-Barré Syndrome

  • 97
    Ramenghi, L. A.; Gill, B. J.; Tanner, S. F.; Martinez, D.; Arthur, R.; Levene, M. I.:

    Cerebral Venous Thrombosis, Intraventricular Haemorrhage and White Matter Lesions in a Preterm Newborn with Factor V (Leiden) Mutation

  • 100
    Vanhatalo, S.; Somer, M.; Barth, P. G.:

    Dutch Patients with Progressive Encephalopathy with Edema, Hypsarrhythmia, and Optic Atrophy (PEHO) Syndrome

  • 105
    Huppke, P.; Bohlander, S.; Krämer, N.; Laccone, F.; Hanefeld, F.:

    Altered Methylation Pattern of the G6 PD Promoter in Rett Syndrome

  • 109
    Mongini, T.; Doriguzzi, C.; Bosone, I.; Chiadò-Piat, L.; Hoffman, E. P.; Palmucci, L.:

    Alpha-Sarcoglycan Deficiency Featuring Exercise Intolerance and Myoglobinuria