Hotta Y | Department Of Ophthalmology Juntendo University School Of Medicine

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著作論文

Multicenter Genetic Study of Retinitis Pigmentosa in Japan : II. Prevalence of Autosomal Recessive Retinitis Pigmentosa
OPA1 Gene Mutations in Japanese Patients with Bilateral Optic Atrophy Unassociated with Mitochondrial DNA Mutations at nt 11778, 3460, and 14484
MISSENSE MUTATION OF RHODOPSIN GENE CODON 15 FOUND IN JAPANESE AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA
Long-term Follow-up of Two Sisters with Leber's Hereditary Optic Neuropathy
Analysis of Peripherin/RDS Gene for Japanese Retinal Dystrophies
FREQUENCIES OF POLYMORPHISMS IN THE RHODOPSIN GENE OF JAPANESE RETINITIS PIGMENTOSA AND NORMAL INDIVIDUALS
Effects of Scutellariae Radix Extract and its Components (Baicalein, Baicalin, and Wogonin) on the Experimental Elevation of Aqueous Flare in Pigmented Rabbits
Studies on Cardiac Ingredients of Plants. XIII : Chemical Modification of Gitoxin to Cardiotonic Compounds without Vascular Contractile Effect
Ophthalmomyiasis Caused by Larvae of Boettcherisca Peregrina
Heterozygous 17-bp deletion in the forkhead transcription factor gene, FOXL2, in a Japanese family with blepharophimosis-ptosis-epicanthus inversus syndrome
Peripherin/RDS Gene Mutation (Pro210Leu) and Polymorphisms in Japanese Patients with Retinal Dystrophies
Rhodopsin Gene Codon 106 Mutation (Gly-to-Arg) in a Japanese Family with Autosomal Dominant Retinitis Pigmentosa
Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778
Effects of Topical Instillation of Traditional Herbal Medicines, Herbal Extracts, and Their Components on Prostaglandin E_2-induced Aqueous Flare Elevation in Pigmented Rabbits
Arg124Cys Mutation of the βig-h3 Gene in a Japanese Family With Lattice Corneal Dystrophy Type I
Central Corneal Thickness in Japanese Children
DNA Analysis for Diagnosis of X-Linked Juvenile Retinoschisis When Clinical Examination Is Difficult in a Young Child
CLONING AND HIGH EXPRESSION OF RABBIT FKBP25 IN CORNEA
Cystoid Macular Edema Associated with Latanoprost Use in a Pseudophakic Eye with a History of Surgical Complications
Effects of astaxanthin on accommodation, critical flicker fusion, and pattern visual evoked potential in visual display terminal workers
Effect of Topical Betaxolol on Acute Rise of Aqueous Flare Induced by Prostaglandin E_2 in Pigmented Rabbits
Effect of Berberine on Barrier Function in a Human Retinal Pigment Epithelial Cell Line
Effect of N-Acetylcysteine on Lipopolysaccharide-Induced Uveitis in Rats
Case of a Japanese Patient with X-linked Ocular Albinism Associated with the GPR143 Gene Mutation
Novel USH2A mutations in Japanese Usher syndrome type 2 patients : marked differences in the mutation spectrum between the Japanese and other populations
Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1
Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genes

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