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Department Of Ophthalmology Hamamatsu University School Of Medicine | 論文
- CLINICAL FEATURES OF JAPANESE LEBER'S HEREDITARY OPTIC NEUROPATHY WITH 11778 MUTATION OF MITOCHONDRIAL DNA
- Mast Cells in Pterygium : Number and Phenotype
- Protective effects of dimethyl amiloride, a Na^+/H^+ exchange inhibitor against ischemia-reperfusion injury of rabbit hearts : ^P-NMR study on ion dynamics and energy metabolism.
- 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
- Plus/Minus Screening of Rabbit Corneal Endothelial cDNA Library
- Analysis of Peripherin/RDS Gene for Japanese Retinal Dystrophies
- FREQUENCIES OF POLYMORPHISMS IN THE RHODOPSIN GENE OF JAPANESE RETINITIS PIGMENTOSA AND NORMAL INDIVIDUALS
- Expression of Stem Cell Factor in Pterygium
- Magnetic Resonance Imaging of the Extraocular Muscle Path Before and After Strabismus Surgery for a Large Degree of Cyclotorsion Induced by Macular Translocation Surgery
- 1/f Resistance Fluctuation of a Carbon Fiber : General Physics
- Voluntary Nystagmus Associated With Accommodation Spasms
- Studies on Cardiac Ingredients of Plants. XIII : Chemical Modification of Gitoxin to Cardiotonic Compounds without Vascular Contractile Effect
- Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778
- The Herth Hope Index (HHI) and related factors in the Japanese general urban population
- POSTERIOR TENOTOMY OF THE SUPERIOR OBLIQUE AT THE SCLERAL INSERTION FOR A-PATTERN DEVIATIONS
- 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
- Development of Stereoscopic Acuity : Longitudinal Study Using a Computer-based Random-dot Stereo Test