DOI: 10.1055/s-00000041

Neuropädiatrie

Issue 01 · Volume 2 · August 1970 DOI: 10.1055/s-002-13217

Survey

  • 3
    Spranger, J. W.; Wiedemann, H.-R.:

    The Genetic Mucolipidoses

    • Original article

  • 17
    Rosen, M. G.; Scibetta, J. J.:

    The Human Fetal Electroencephalogram. 2. Characterizing the EEG During Labor

  • 27
    Martin, D.:

    Die Intravenöse Anwendung von Nitrazepam (Mogadan) in der Epilepsiebehandlung

    The intravenous application of Nitrazepam (Mogadan) in the treatment of epilepsy.
  • 38
    Mizuno, Teiichi; Segawa, M.; Kurumada, T.; Maruyama, H.; Onisawa, J.:

    Clinical and Therapeutic Aspects of the Lesch-Nyhan Syndrome in Japanese Children

  • 53
    Hagberg, Bengt; Öckerman, Per Arne:

    Metachromatic Leucodystrophy – Assay of arylsulfatase activities in the urine

  • 59
    Doose, Hermann; Gerken, Hartmut; Leonhardt, Raimund; Völzke, Edelgard; Völz, Christa:

    Centrencephalic Myoclonic-Astatic Petit Mal1– Clinical and genetic investigations

  • 79
    Peltzman, P.; Ostwald, P. F.; Yeager, C. L.; Manchester, D.:

    Sensory-Vocal Studies of a Twin Pair with Cephalic Union

    • Case report

  • 98
    Schenck, K.; Solcher, H.:

    Diffuse Glioblastose im Kindesalter – Klinische und pathologisch-anatomische Studie

    Diffuse Glioblastose im Kindesalter.
  • 107
    Minauf, M.; Jellinger, K.:

    Zentrale Pontine Myelinolyse bei Einem Kind mit Protrahiertem Posttraumatischen Koma

    Central pontine myelinolysis in a child with protacted posttraxmatic coma.
  • 112
    Gordon, Neil; Marsden, Basil:

    Spinal Cord Injury at Birth

    • Letter to the editor

  • 119
    Gordon, Neil:

    Reactions to Triple Immunisation

  • 121
    Menkes, John H.; Holtzman, Neil A.:

    Phenylalaninemia or Classical Phenylketonuria

    • Correction

  • 124

    Neuropädiatrie Vol. 1, No. 4, p. 428–433