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Biochimica Et Biophysica Acta|July 31, 1985

Galactosylceramide- and lactosylceramide-loading studies in cultured fibroblasts from normal individuals and patients with globoid cell leukodystrophy (Krabbe's disease) and GM1-gangliosidosisT Kobayashi, N Shinnoh, I Goto, et al.

Neurology|February 20, 1999

Adrenoleukodystrophy protein enhances association of very long-chain acyl-coenzyme A synthetase with the peroxisomeT Yamada, T Taniwaki, N Shinnoh, et al.

Biochemical and Biophysical Research Communications|May 25, 1995

Adrenoleukodystrophy: the restoration of peroxisomal beta-oxidation by transfection of normal cDNAN Shinnoh, T Yamada, T Yoshimura, et al.

Neurology|December 31, 1997

Adult-onset Krabbe disease with homozygous T1853C mutation in the galactocerebrosidase gene. Unusual MRI findings of corticospinal tract demyelinationJ I Satoh, H Tokumoto, K Kurohara, et al.

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Showing results (21-30 of 24) with videos related to

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You have reached the last page of results.This site can display upto 24 results.

Biochimica Et Biophysica Acta|July 31, 1985

Galactosylceramide- and lactosylceramide-loading studies in cultured fibroblasts from normal individuals and patients with globoid cell leukodystrophy (Krabbe's disease) and GM1-gangliosidosisT Kobayashi, N Shinnoh, I Goto, et al.

Neurology|February 20, 1999

Adrenoleukodystrophy protein enhances association of very long-chain acyl-coenzyme A synthetase with the peroxisomeT Yamada, T Taniwaki, N Shinnoh, et al.

Biochemical and Biophysical Research Communications|May 25, 1995

Adrenoleukodystrophy: the restoration of peroxisomal beta-oxidation by transfection of normal cDNAN Shinnoh, T Yamada, T Yoshimura, et al.

Neurology|December 31, 1997

Adult-onset Krabbe disease with homozygous T1853C mutation in the galactocerebrosidase gene. Unusual MRI findings of corticospinal tract demyelinationJ I Satoh, H Tokumoto, K Kurohara, et al.

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