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