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The Japanese Journal of Human Genetics|March 1, 1997
Genotypes of aldehyde dehydrogenase and alcohol dehydrogenase polymorphisms in patients with Leber's hereditary optic neuropathyY Isashiki, Y Tabata, K Kamimura, et al.Nippon Ganka Gakkai Zasshi|September 1, 1994
[Antibodies to human T-cell lymphotropic virus type 1 in the aqueous humor of HTLV-I associated uveitis]K Nakao, Y Isashiki, M Uto, et al.Chinese Medical Journal|January 5, 2002
Diagnostic potential of mitochondrial DNA assessment in patients with optic neuropathyX Feng, W Pu, D Gao, et al.Human Genetics|October 6, 1998
A novel splice site mutation in the tissue inhibitor of the metalloproteinases-3 gene in Sorsby's fundus dystrophy with unusual clinical featuresY Tabata, Y Isashiki, K Kamimura, et al.The Japanese Journal of Human Genetics|March 1, 1996
A novel AvaI polymorphism within exon 5 of the rhodopsin geneY Isashiki, X M Feng, N Ohba, et al.American Journal of Ophthalmology|December 22, 2000
Genetic association of manganese superoxide dismutase with exudative age-related macular degenerationK Kimura, Y Isashiki, S Sonoda, et al.Japanese Journal of Ophthalmology|January 1, 1989
Pigmentary retinal degeneration in patients with HTLV-I-associated myelopathyK Nakao, N Ohba, M Isashiki, et al.American Journal of Ophthalmology|October 8, 1999
A novel truncating mutation of cytochrome P4501B1 (CYP1B1) gene in primary infantile glaucomaT Kakiuchi, Y Isashiki, K Nakao, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 24, 2000
A novel PAX6 gene mutation (P118R) in a family with congenital nystagmus associated with a variant form of aniridiaS Sonoda, Y Isashiki, Y Tabata, et al.American Journal of Ophthalmology|March 10, 2001
Cytochrome P450 1B1 gene mutations in Japanese patients with primary congenital glaucoma(1)T Kakiuchi-Matsumoto, Y Isashiki, N Ohba, et al.Pageof 15