DOI: 10.1055/s-00000041

Neuropediatrics

Issue 04 · Volume 32 · August 2001 DOI: 10.1055/s-002-1178

Original Article

169
Kojo, M.; Wada, M.; Akiyoshi, K.; Inutsuka, M.; Izumi, T.: Reduction of Carotid Artery Blood Flow in Pediatric Patients with Syncope: Evaluation with Head-Up Tilt Test
176
Kristjánsdóttir, R.; Uvebrant, P.; Lekman, A.; Månsson, J.-E.: Cerebrospinal Fluid Markers in Children with Cerebral White Matter Abnormalities
183
Okhuijsen-Kroes, E. J.; Trijbels, J. M. F.; Sengers, R. C. A.; Mariman, E.; van den Heuvel, L. P.; Wendel, U.; Koch, G.; Smeitink, J. A. M.: Infantile Presentation of the mtDNA A3243G tRNALeu (UUR) Mutation
191
Häusler, M. G.; Jaeken, J.; Mönch, E.; Ramaekers, V. Th.: Phenotypic Heterogeneity and Adverse Effects of Serine Treatment in 3-Phosphoglycerate Dehydrogenase Deficiency: Report on Two Siblings
196
Goebel, H. H.; Halbig, L. E.; Goldfarb, L.; Schober, R.; Albani, M.; Neuen-Jacob, E.; Voit, T.: Reducing Body Myopathy with Cytoplasmic Bodies and Rigid Spine Syndrome: A Mixed Congenital Myopathy
206
Schroten, H.; Spors, Birgit; Hucke, C.; Stins, Monique; Kim, K. S.; Adam, R.; Däubener, W.: Potential Role of Human Brain Microvascular Endothelial Cells in the Pathogenesis of Brain Abscess: Inhibition of Staphylococcus aureus by Activation of Indoleamine 2,3-Dioxygenase

Short Communication

211
Waubant, E.; Hietpas, J.; Stewart, T.; Dyme, Z.; Herbert, J.; Lacy, J.; Miller, C.; Rensel, M.; Schwid, S.; Goodkin, D.: Interferon Beta-1a in Children with Multiple Sclerosis is Well Tolerated
214
Anlar, B.; Alikaşifoglu, M.; Köse, G.; Güven, A.; Gürer, Y.; Yakut, A.: Tumor Necrosis Factor-Alpha Gene Polymorphisms in Children with Multiple Sclerosis
217
Xiang, F.; Stenbom, Y.; Anvret, Maria; Hagberg, B.: Closely Related Swedish Rett Syndrome Females - None with MECP2 Mutation Revealed

Letter to the Editor

219
Klusmann, Anne; Engelbrecht, V.; Unsöld, R.; Hassler, W.; Gärtner, Jutta: Retrobulbar Abscess in a Neonate
221
Klinge, L.; Scott, R. C.; de Sousa, C.: Neonatal Subdural and Extradural Haemorrhage in Prader-Willi Syndrome