Neuropediatrics

Issue 05 · October 1995

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

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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

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243
Groenendaal, F.; van der Grond, J.; Witkamp, T. D.; de Vries, Linda S.: Proton Magnetic Resonance Spectroscopic Imaging in Neonatal Stroke

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249
Denišlič, M.; Meh, D.: Botulinum Toxin in the Treatment of Cerebral Palsy

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253
Uldall, P.; Alving, J.; Gram, L.; Høgenhaven, H.: Vigabatrin in Childhood Epilepsy: A 5-Year Follow-Up Study

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257
Goertzen, M.; Baltzer, A.; Voit, T.: Clinical Results of Early Orthopaedic Management in Duchenne Muscular Dystrophy

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260
Hauser, E.; Hoger, H.; Bittner, R.; Widhalm, K.; Herkner, K.; Lubec, G.: Oxyradical Damage and Mitochondrial Enzyme Activities in the mdx Mouse

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263
Koskinen, T.; Pihko, H.; Voutilainen, R.: Primary Hypogonadism in Females with Infantile Onset Spinocerebellar Ataxia

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Short communications
267
Winter, Esther; Prendergast, M.: Cured of Acute Lymphoblastic Leukaemia But Lost for Words

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270
Fujimoto, S.; Yokochi, K.; Nakano, M.; Wada, Y.: Progressive Encephalopathy with Edema, Hypsarrhythmia, and Optic Atrophy (PEHO Syndrome) in Two Japanese Siblings

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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

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276
O'Meara, M.; Wise, G.: Painful Torticollis with Tongue Atrophy - A Different Neck-Tongue Syndrome

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281
Zifko, U.; Hartmann, M.; Girsch, W.; Zoder, Gerlinde; Rokitansky, A.; Grisold, W.; Lischka, A.: Diaphragmatic Paresis in Newborns Due to Phrenic Nerve Injury

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