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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