DOI: 10.1055/s-00000041

Neuropediatrics

Issue 03 · Volume 32 · June 2001 DOI: 10.1055/s-002-1121

Review Article

  • 113
    Haas, Dorothea; Kelley, R. I.; Hoffmann, G. F.:

    Inherited Disorders of Cholesterol Biosynthesis

  • Hypothesis

  • 123
  • Original Article

  • 130
  • 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

  • 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

  • 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

  • 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

  • 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

  • 159
  • 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

  • Letter to the Editor

  • 165