Bone Marrow Transplantation in the Treatment of Lysosomal Storage Diseases-Reference-Cited by-同舟云学术

Bone Marrow Transplantation in the Treatment of Lysosomal Storage Diseases

Published:1990 Issue: Volume: Page:659-670
ISSN:
Container-title:Inborn Metabolic Diseases
language:
Short-container-title:

Author:

Hoogerbrugge P. M.,Vossen J. M. J. J.

Publisher

Springer Berlin Heidelberg

Link

http://link.springer.com/content/pdf/10.1007/978-3-662-02613-7_52

Reference57 articles.

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2. Bekkum DW van, Löwenberg B (1985) Bone marrow transplantation: biological mechanisms and clinical practice. Dekker, New York

3. Barranger JA, Ginns EI (1989) Glycosylceramide lipidoses: Gaucher disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) (1983) The metabolic basis of inherited disease, 6th edn. McGraw-Hill, New York, pp 1699–1720

4. Olsen I, Muir H, Smith R et al. (1983) Direct enzyme transfer from lymphocytes is specific. Nature 306: 75–77

5. Jolly RD, Thompson KG, Murphy CE et al. (1976) Enzyme replacement therapy: an experiment of nature in a chimeric mannosidosis calf. Pediatr Res 10: 219–224

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3. α-L-iduronidase mutations (Q70X and P533R) associate with a severe Hurler phenotype;Human Mutation;1992

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5. From a Historical Outline of Transplants to the Concept of Biological Ego;Pediatric Hematology and Oncology;1992-01