DOI: 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 31 · April 2000 DOI: 10.1055/s-002-401

Editorial

  • 57
    Grünewald, Stephanie; Matthijs, Gert:

    Congenital Disorders of Glycosylation (CDG): A Rapidly Expanding Group of Neurometabolic Disorders

    • Rapid Publication

  • 60
    Hanefeld, F.; Körner, C.; Holzbach-Eberle, Ulrike; von Figura, K.:

    Congenital Disorder of Glycosylation-Ic: Case Report and Genetic Defect

    • Original Article

  • 63
    Chu, D.; Huttenlocher, P. R.; Levin, D. N.; Towle, V. L.:

    Reorganization of the Hand Somatosensory Cortex Following Perinatal Unilateral Brain Injury

  • 70
    Maegaki, Yoshihiro; Akaboshi, Shinjiro; Inagaki, Masumi; Takeshita, Kenzo:

    Unilateral Involuntary Movement Associated with Streptococcal Infection: Neurophysiological Investigation

  • 82
    Urlesberger, B.; Pichler, G.; Gradnitzer, Eva; Reiterer, F.; Zobel, G.; Müller, W.:

    Changes in Cerebral Blood Volume and Cerebral Oxygenation during Periodic Breathing in Term Infants

  • 82
    Waltz, S.; Stephani, U.:

    Inheritance of Photosensitivity

  • 86
    Springer, S.; Erlewein, Rita; Naegele, T.; Becker, Ingrid; Auer, Dorothee; Grodd, W.; Krägeloh-Mann, Ingeborg:

    Alexander Disease - Classification Revisited and Isolation of a Neonatal Form

  • 93
    Zanssen, S.; Molnar, M.; Buse, G.; Schröder, M. J.:

    Novel Cluster of tRNA Leu (UUR) Mutations in a Sporadic Case of Infantile Myopathy Restricted to Muscle Tissue

    • Short Communication

  • 97
    Drost, G.; Verrips, A.; Thijssen, M. H. O.; Gabreëls, M. F. J.:

    Cerebellar Involvement as a Rare Complication of Pneumococcal Meningitis

  • 104
    Bührer, C.; van Landeghem, F.; Brück, W.; Felderhoff-Müser, Ursula; Vorgerd, M.; Obladen, M.:

    Fetal-Onset Severe Skeletal Muscle Glycogenosis Associated with Phosphorylase-b Kinase Deficiency

    • Letter to the Editor

  • 107
    Al-Matar, M.; Jaimes, J.; Malleson, P.:

    Chorea as the Presenting Clinical Feature of Primary Antiphospholipid Syndrome in Childhood

  • 108
    Kiechl-Kohlendorfer, U.; Ellemunter, H.; Kiechl, S.:

    Sydenham Chorea or Primary Antiphospholipid Syndrome?

  • 109
    Dan, B.; Boyd, S. G.; Christiaens, Florence; Courtens, Winnie; Van Maldergem, L.; Kahn, A.:

    Atypical Features in Angelman Syndrome Due to Imprinting Defect or Uniparental Disomy of Chromosome 15