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R Koike

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Human Genetics|September 1, 1997

Adult onset globoid cell leukodystrophy (Krabbe disease): analysis of galactosylceramidase cDNA from four Japanese patientsH Furuya, Y Kukita, S Nagano, et al.

Neurology|November 18, 2009

Pathologic and immunologic profiles of a limited form of neuromyelitis optica with myelitisK Yanagawa, I Kawachi, Y Toyoshima, et al.

Nature Genetics|October 5, 2001

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily geneH Date, O Onodera, H Tanaka, et al.

American Journal of Human Genetics|March 1, 1997

Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27H Matsumine, M Saito, S Shimoda-Matsubayashi, et al.

Pageof 13

Search research articles

Showing results (121-130 of 124) with videos related to

Sort By:

Pageof 13

You have reached the last page of results.This site can display upto 124 results.

Human Genetics|September 1, 1997

Adult onset globoid cell leukodystrophy (Krabbe disease): analysis of galactosylceramidase cDNA from four Japanese patientsH Furuya, Y Kukita, S Nagano, et al.

Neurology|November 18, 2009

Pathologic and immunologic profiles of a limited form of neuromyelitis optica with myelitisK Yanagawa, I Kawachi, Y Toyoshima, et al.

Nature Genetics|October 5, 2001

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily geneH Date, O Onodera, H Tanaka, et al.

American Journal of Human Genetics|March 1, 1997

Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27H Matsumine, M Saito, S Shimoda-Matsubayashi, et al.

Pageof 13