Ganglioside Storage Diseases-Reference-Cited by-同舟云学术

Ganglioside Storage Diseases

Published:1972 Issue: Volume: Page:39-98
ISSN:
Container-title:Advances in Human Genetics
language:
Short-container-title:

Author:

O’Brien John S.

Publisher

Springer US

Link

http://link.springer.com/content/pdf/10.1007/978-1-4757-4429-3_2

Reference82 articles.

1. Aronson, S. M., “Epidemiology” in Tay-Sachs Disease (B. W. Volk, ed.), Grune & Stratton, New York (1964), p. 118.

2. Aronson, S. M., G. Perle, A. Saifer, and B. W. Volk, Biochemical identification of the carrier state in Tay-Sachs disease, Proc. Soc. Exp. Biol. Med. III: 664 (1962).

3. Attal, C., E. Farkas-Bargeton, G. W. F. Edgar, Girard F Pham-Huu-Trung, and P. Mozziconacci, Idiote amaurotique infantile avec surcharge viscerale, Annales de Ped. 14: 457 (1967).

4. Bernheimer, H., and F. Seitelberger, Ober das Verhalten der Ganglioside im Gehirn bei 2 Fällen von Spätinfantiler Amaurotischer Idiotie, Wein. klin. wschr. 80: 163 (1968).

5. Brady, R. O., J. S. O’Brien, R. M. Bradley, and A. E. Gal, Sphingolipid hydrolases in brain tissue of patients with generalized gangliosidosis, Biochem. Biophys. Acta 210: 193 (1970).

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