スポンサーリンク
Department Of Ophthalmology Nagoya University Graduate School Of Medicine | 論文
- Analysis of DOK-6 function in downstream signaling of RET in human neuroblastoma cells
- Multicenter Genetic Study of Retinitis Pigmentosa in Japan : I. Genetic Heterogeneity in Typical Retinitis Pigmentosa
- Multicenter Genetic Study of Retinitis Pigmentosa in Japan : II. Prevalence of Autosomal Recessive Retinitis Pigmentosa
- PE-164 Significance of Small Dense Low-density Lipoprotein-Cholesterol Concentrations in Relation to the Severity of Coronary Heart Diseases(Atherosclerosis, clinical-7 (H) PE28,Poster Session (English),The 70th Anniversary Annual Scientific Meeting of th
- Magnetic Resonance Imaging of the Extraocular Muscle Path Before and After Strabismus Surgery for a Large Degree of Cyclotorsion Induced by Macular Translocation Surgery
- Unique Characteristics of Two Types of Retinitis Pigmentosa Patients with Different Rod Sensitivities
- Charles Bonnet Syndrome Associated with First Attack of MS
- Direct application of drugs upon the choroid and ERG changes (Symposium on electroretinography〔議事録〕)
- Structural change of bovine retinal cGMP phosphodiesterase by release of its γ subunit : direct imaging by improved low angle rotary shadowing
- Periciliary structure of developing rat photoreceptor cells. A deep etch replica and freeze substitution study
- High Prevalence of Myopia in Japanese Patients with Multiple Evanescent White Dot Syndrome
- S- and M-cone electroretinograms in rd7 mice with NR2E3 gene mutation
- Selective dysfunction of On- and/or Off-bipolar cell in human diseases
- Amplitude Decrease of Photopic ERG b-Wave at Higher Stimulus Intensities in Humans
- Focal Macular Electroretinography
- Effect of Age On Short-Wavelength Sensitive Cone Electroretinogram and Long- and Middle-Wavelength Sensitive Cone Electroretinogram
- ELECTROPHYSIOLOGICAL FINDINGS IN PATIENTS WITH OGUCHI'S DISEASE
- Body Sway Induced by Depth Linear Vection in Reference to Central and Peripheral Visual Field
- Postural Adjustment Response to Depth Direction Moving Patterns Produced by Virtual Reality Graphics
- Autosomal Dominant Cone-Rod Dystrophy with R838H and R838C Mutations in the GUCY2D Gene in Japanese Patients