Author:
Consiglio Antonella,Quattrini Angelo,Martino Sabata,Bensadoun Jean Charles,Dolcetta Diego,Trojani Alessandra,Benaglia Giuliana,Marchesini Sergio,Cestari Vincenzo,Oliverio Alberto,Bordignon Claudio,Naldini Luigi
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Reference45 articles.
1. Kolodney, E.H. & Fluharty A.L. Metachromatic Leukodistrophy and multiple sulfatase deficiency: Sulfatide lipidosis. in The Metabolic and Molecular Bases of Inherited Disease 6th edn. (eds. Scriver, C.R., Beaudet, A.L, Sly W.S. & Valle, D.) 2693–7391 (McGraw-Hill, New York, 1995).
2. Neufeld, E.F. Lysosomal disease. Annu. Rev. Biochem 60, 257–280 (1991).
3. Kapaun, P. et al. A slow progression of juvenile metachromatic leukodystrophy 6 years after bone marrow transplantation. J. Child Neurol. 14, 222–228 (1999).
4. Krivit, W., Peters, C. & Shapiro, E.G. Bone marrow transplantation as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartylglucosaminuria, Hurler, Maroteaux-Lamy, and Sly syndromes, and Gaucher disease type III. Curr. Opin. Neurol. 12, 167–176 (1999).
5. Ohashi, T., Eto, Y., Learish, R. & Barranger, J.A. Correction of enzyme deficiency in metachromatic leukodystrophy fibroblasts by retroviral-mediated transfer of the human arylsulphatase A gene. J. Inherit. Metab. Dis. 16, 881–885 (1993).
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