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Current Eye Research|March 1, 1995
Alteration of glutamine concentration in the vitreous humor in patients with proliferative vitreoretinopathyS Ishikawa, M Nakazawa, A Ishikawa, et al.Current Eye Research|June 1, 1997
Determination of ascorbic acid in human vitreous humor by high-performance liquid chromatography with UV detectionS Takano, S Ishiwata, M Nakazawa, et al.The British Journal of Ophthalmology|February 1, 1995
X linked ocular albinism in Japanese patientsT Shiono, M Tsunoda, Y Chida, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|March 1, 1996
Variable expressivity in a Japanese family with autosomal dominant retinitis pigmentosa closely linked to chromosome 19qM Nakazawa, S Xu, A Gal, et al.Retina (Philadelphia, Pa.)|January 1, 1997
Oguchi disease: phenotypic characteristics of patients with the frequent 1147delA mutation in the arrestin geneM Nakazawa, Y Wada, S Fuchs, et al.Nature Genetics|July 1, 1995
A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in JapaneseS Fuchs, M Nakazawa, M Maw, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1996
Autosomal dominant cone-rod dystrophy associated with mutations in codon 244 (Asn244His) and codon 184 (Tyr184Ser) of the peripherin/RDS geneM Nakazawa, E Kikawa, Y Chida, et al.The British Journal of Ophthalmology|October 1, 1995
Autosomal dominant cone-rod dystrophy with negative electroretinogramN Fujii, T Shiono, Y Wada, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|December 1, 1994
Ocular findings in patients with autosomal dominant retinitis pigmentosa and transversion mutation in codon 244 (Asn244Lys) of the peripherin/RDS geneM Nakazawa, E Kikawa, K Kamio, et al.Retina (Philadelphia, Pa.)|January 1, 1996
Autosomal dominant cone-rod dystrophy associated with a Val200Glu mutation of the peripherin/RDS geneM Nakazawa, N Naoi, Y Wada, et al.Pageof 87