DOI: 10.1055/s-00000041

Neuropediatrics

Issue 05 · Volume 26 · October 1995 DOI: 10.1055/s-002-6625

Rapid communications

235
Stibler, Helena; Stephani, U.; Kutsch, Ulrike: Carbohydrate-Deficient Glycoprotein Syndrome - A Fourth Subtype

Original articles

238
Merinero, B.; Pérez-Cerdá, C.; Font, L. M.; Garcia, M. J.; Aparicio, M.; Lorenzo, G.; Pardo, M. Martinez; Garzo, C.; Martinez-Bermejo, A.; Castroviejo, I. Pascual; Christensen, E.; Ugarte, M.: Variable Clinical and Biochemical Presentation of Seven Spanish Cases with Glutaryl-CoA-Dehydrogenase Deficiency
243
Groenendaal, F.; van der Grond, J.; Witkamp, T. D.; de Vries, Linda S.: Proton Magnetic Resonance Spectroscopic Imaging in Neonatal Stroke
249
Denišlič, M.; Meh, D.: Botulinum Toxin in the Treatment of Cerebral Palsy
253
Uldall, P.; Alving, J.; Gram, L.; Høgenhaven, H.: Vigabatrin in Childhood Epilepsy: A 5-Year Follow-Up Study
257
Goertzen, M.; Baltzer, A.; Voit, T.: Clinical Results of Early Orthopaedic Management in Duchenne Muscular Dystrophy
260
Hauser, E.; Hoger, H.; Bittner, R.; Widhalm, K.; Herkner, K.; Lubec, G.: Oxyradical Damage and Mitochondrial Enzyme Activities in the mdx Mouse
263
Koskinen, T.; Pihko, H.; Voutilainen, R.: Primary Hypogonadism in Females with Infantile Onset Spinocerebellar Ataxia

Short communications

267
Winter, Esther; Prendergast, M.: Cured of Acute Lymphoblastic Leukaemia But Lost for Words
270
Fujimoto, S.; Yokochi, K.; Nakano, M.; Wada, Y.: Progressive Encephalopathy with Edema, Hypsarrhythmia, and Optic Atrophy (PEHO Syndrome) in Two Japanese Siblings
273
Dunac, A.; van Bogaert, P.; David, P.; Avni, E. F.; Paduart, O.; Szliwowski, H. B.; van Regemorter, N.: Mid-Portion Agenesis of Corpus Callosum in a Presumed Baller-Gerold Syndrome
276
O'Meara, M.; Wise, G.: Painful Torticollis with Tongue Atrophy - A Different Neck-Tongue Syndrome
281
Zifko, U.; Hartmann, M.; Girsch, W.; Zoder, Gerlinde; Rokitansky, A.; Grisold, W.; Lischka, A.: Diaphragmatic Paresis in Newborns Due to Phrenic Nerve Injury