GM1 gangliosidosis in adults: Clinical and molecular analysis of 16 Japanese patients-Reference-Cited by-同舟云学术

GM1 gangliosidosis in adults: Clinical and molecular analysis of 16 Japanese patients

Published:1992-03 Issue:3 Volume:31 Page:328-332
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Yoshida Kunihiro,Oshima Akihiro,Sakuraba Hitoshi,Nakano Takeshi,Yanagisawa Nobuo,Inui Koji,Okada Shintaro,Uyama Ei-ichiro,Namba Reiko,Kondo Kiyohiko,Iwasaki Shin-ichi,Takamiya Kiyoshi,Suzuki Yoshiyuki

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference22 articles.

1. ?-Galactosidase deficiency (GM1 gangliosidosis, galactosialidosis, and Morquio syndrome type B); ganglioside sialidase deficiency (mucolipidosis IV). In: eds. The metabolic basis of inherited disease, ed 6. New York: McGraw-Hill, 1989: 1797-1806

2. ?-Galactosidase deficiency in juvenile and adult patients

3. β-galactosidase deficiency: Prolonged survival in three patients following early central nervous system deterioration

4. Adult Gmi gangliosidosis: Clinical and biochemical studies on two patients and comparison to other patients called variant or adult Gm1 gangliosidosis

5. Adult GM1-gangliosidosis: Clinical patterns and rectal biopsy

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