DOI: 10.1055/s-00000041

Neuropediatrics

Issue 04 · Volume 30 · August 1999 DOI: 10.1055/s-002-5716

Review Articles

  • 167
    Bornemann, A.; Maier, F.; Kuschel, R.:

    Satellite Cells as Players and Targets in Normal and Diseased Muscle

    • Original articles

  • 176
    Udar, N. S.; Xu, S.; Bay, J.-O.; Dandekar, S. S.; Patel, N.; Chen, X.; Liang, T. Y.; Uhrhammer, N.; Klisak, I.; Shizuya, H.; Yang, H.; Samara, G.; Nelissen, J.; Sawicki, M.; Concannon, P.; Gatti, R. A.:

    Physical Map of the Region Surrounding the Ataxia-Telangiectasia Gene on Human Chromosome 11q22-23

  • 181
    Kivitie-Kallio, S.; Larsen, A.; Kajasto, K.; Norio, R.:

    Neurological and Psychological Findings in Patients with Cohen Syndrome: A Study of 18 Patients Aged 11 Months to 57 Years

  • 190
    Korinthenberg, R.:

    Chronic Inflammatory Demyelinating Polyradiculoneuropathy in Children and Their Response to Treatment

  • 197
    Gurbindo, D.; Resino, S.; Sánchez-Ramón, S.; León, J. A.; Muñoz-Fernández, M. A.:

    Correlation of Viral Load and CD8 T-Lymphocytes with Development of Neurological Manifestations in Vertically HIV-1-Infected Infants. A Prospective Longitudinal Study

    • Short communications

  • 205
    Rossi, L. N.; Triulzi, F.; Parazzini, C.; Maninetti, M. M.:

    Spontaneous Improvement of Optic Pathway Lesions in Children with Neurofibromatosis Type 1

  • 210
    Hager, A.; Staudt, M.; Klare, B.; Gräfin von Einsiedel, H.; Krägeloh-Mann, I.:

    Hemolytic-Uremic Syndrome with Involvement of Basal Ganglia and Cerebellum

  • 214
    Echenne, B.; Ducros, A.; Rivier, F.; Joutel, A.; Humbertclaude, V.; Roubertie, A.; Azaïs, M.; Bousser, M. G.; Tournier-Lasserve, E.:

    Recurrent Episodes of Coma: An Unusual Phenotype of Familial Hemiplegic Migraine with Linkage to Chromosome 1

  • 218
    Christophe, C.; Azzi, N.; Bouché, B.; Dan, B.; Levivier, M.; Ferster, A.:

    Magnetic Resonance Imaging and Angiography in Cerebral Fungal Vasculitis