Neuropediatrics

Issue 03 · June 2001

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Review Article
113
Haas, Dorothea; Kelley, R. I.; Hoffmann, G. F.: Inherited Disorders of Cholesterol Biosynthesis

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Hypothesis
123
Oexle, K.; Kohlschütter, A.: Cause of Progression in Duchenne Muscular Dystrophy: Impaired Differentiation More Probable Than Replicative Aging

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Original Article
130
Toelle, S. P.; Boltshauser, E.: Long-Term Outcome in Children with Congenital Unilateral Facial Nerve Palsy

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136
Bamiou, Doris-Eva; Campbell, Pauline; Liasis, Alki; Page, J.; Sirimanna, T.; Boyd, S.; Vellodi, A.; Harris, C.: Audiometric Abnormalities in Children with Gaucher Disease Type 3

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142
Gücüyener, K.; Özgül, Köksal; Paternotte, Caroline; Erdem, H.; Prud'homme, J. F.; Özgüç, M.; Topaloğlu, H.: Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay in Two Unrelated Turkish Families

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Short Communication
147
Parano, E.; Falcidia, E.; Grillo, A.; Takabayashi, H.; Trifiletti, R. R.; Pavone, P.: Fetal Nucleated Red Blood Cell Counts in Peripheral Blood of Mothers Bearing Down Syndrome Fetus

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150
Gauthier-Villars, Marion; Landrieu, P.; Cormier-Daire, Valérie; Jacquemin, E.; Chrétien, D.; Rötig, Agnès; Rustin, P.; Munnich, A.; de Lonlay, Pascale: Respiratory Chain Deficiency in Alpers Syndrome

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153
Soto-Ares, G.; Vinchon, M.; Delmaire, Ch.; Pruvo, J. P.; Vallee, L.; Dhellemes, P.: Report of Eight Cases of Occipital Dermal Sinus: An Update, and MRI Findings

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159
Staudt, M.; Pieper, T.; Grodd, W.; Winkler, P.; Holthausen, H.; Krägeloh-Mann, I.: Functional MRI in a 6-Year-Old Boy with Unilateral Cortical Malformation: Concordant Representation of Both Hands in the Unaffected Hemisphere

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162
Schwartzman, J. S.; Bernardino, Andrea; Nishimura, Agnes; Gomes, Raquel R.; Zatz, Mayana: Rett Syndrome in a Boy with a 47,XXY Karyotype Confirmed by a Rare Mutation in the MECP2 Gene

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Letter to the Editor
165
Brockmann, K.; Hanefeld, F.: Progressive Elevation of Liver Enzymes in a Child Treated with Sulthiame

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