Infantile and fetal globoid cell leukodystrophy: Analysis of galactosylceramide and galactosylsphingosine-Reference-Cited by-同舟云学术

Infantile and fetal globoid cell leukodystrophy: Analysis of galactosylceramide and galactosylsphingosine

Published:1988-10 Issue:4 Volume:24 Page:517-522
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Kobayashi Takuro,Goto Ikuo,Yamanaka Tatsuhiro,Suzuki Yoshiyuki,Nakano Takeshi,Suzuki Kunihiko

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference24 articles.

1. Globoid Cell Leucodystrophy (Krabbe's Disease): Deficiency of Galactocerebroside -Galactosidase

2. Hydrolysis of galactosylceramide is catalyzed by two genetically distinct acid beta-galactosidases.

3. Galactosylceramide lipidosis: globoid cell leukodystrophy (Krabbe's disease). In: et al, ed. The metabolic basis of inherited disease. New York: McGraw-Hill, 1983; 857-880

4. Globoid cell leukodystrophy: Additional deficiency of psychosine galactosidase

5. Krabbe disease: a galactosylsphingosine (psychosine) lipidosis.

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