Juvenile metachromatic leukodystrophy 10 years post transplant compared with a non-transplanted cohort

Author:

Krägeloh-Mann I,Groeschel S,Kehrer C,Opherk K,Nägele T,Handgretinger R,Müller I

Publisher

Springer Science and Business Media LLC

Subject

Transplantation,Hematology

Reference29 articles.

1. Heim P, Claussen M, Hoffmann B, Conzelmann E, Gaertner J, Harzer K et al. Leukodystrophy incidence in Germany. Am J Med Genet 1997; 71: 475–478.

2. Poorthuis BJ, Wevers RA, Kleijer WJ, Groeber JE, de Jong JG, van Weely S et al. The frequency of lysosomal storage diseases in The Netherlands. Hum Genet 1999; 105: 151–156.

3. von Figura K, Gieselmann V, Jacken J . Metachromatic leukodystrophy. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The Metabolic and Molecular Bases of Inherited Disease, 8th edn. McGraw-Hill: New York, 2001, pp 3695–3724.

4. Moser H, Lees M . Sulfatide lipidosis: metachromatic leukodystrophy. In: Stanbury JB, Wyngaarden JB, Fredrickson DS (eds) The Metabolic Basis of Inherited Disease. McGraw-Hill: New York, 1965, pp 539–559.

5. Kehrer C, Blumenstock G, Gieselmann V, Krägeloh-Mann I . The natural course of gross motor deterioration in Metachromatic Leukodystrophy. Dev Med Child Neurol 2011; 53: 850–855.

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