DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 06 · Volume 25 · Dezember 1994 DOI: 10.1055/s-002-12394

Editorial

283
Voit, Thomas: Editorial

Original article

284
Uvebrant, P.; Bauzienè, Ruta: Intractable Epilepsy in Children. The Efficacy of Lamotrigine Treatment, Including Non-Seizure-Related Benefits
290
Korte, W.; Otremba, H.; Lutz, S.; Flury, R.; Schmid, L.; Weissert, M.: Childhood Stroke at Three Years of Age with Transient Protein C Deficiency, Familial Antiphospholipid Antibodies and F. XII Deficiency - A Family Study
295
Kuenzle, Ch.; Weissert, M.; Roulet, E.; Bode, H.; Schefer, S.; Huisman, Th.; Landau, K.; Boltshauser, E.: Follow-Up of Optic Pathway Gliomas in Children with Neurofibromatosis Type 1
301
Eken, P.; Jansen, G. H.; Groenendaal, F.; Rademaker, K. J.; de Vries, L. S.: Intracranial Lesions in the Fullterm Infant with Hypoxic Ischaemic Encephalopathy: Ultrasound and Autopsy Correlation
308
Vuopala, Katri; Leisti, J.; Herva, Riitta: Lethal Arthrogryposis in Finland - A Clinico-Pathological Study of 83 Cases During Thirteen Years
316
Darin, N.; Bergström, T.; Fast, A.; Kyllerman, M.: Clinical, Serological and PCR Evidence of Cytomegalovirus Infection in the Central Nervous System in Infancy and Childhood

Short communication

323
Anvret, M.; Zhang, Z. P.; Hagberg, B.: Rett Syndrome: The bcl-2 Gene - A Mediator of Neurotrophic Mechanisms?
325
Miyazaki, M.; Hashimoto, T.; Omura, H.; Satomura, S.; Bando, N.; Yoshimoto, T.; Tayama, M.; Kuroda, Y.: Infantile Spasms with Predominantly Unilateral Cerebral Abnormalities

Letter to the editor

331
Hanefeld, F. A.; Ernst, B. P.; Wilichowski, E.; Christen, H.-J.: Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutations in Childhood Multiple Sclerosis*
332
Voit, T.; Fardeau, M.; Tomé, F. M. S.: Prenatal Detection of Merosin Expression in Human Placenta
334
Nieto Barrera, M.; Rufo Campos, M.; Silieström Ribed, M. L.: Partial Hydranencephaly in a Child Coincidental with Intrauterine Exposure to Sodium Valproate