Kaoru Fujinami

Tokyo, Japan

Last Updated: 09/26/2026

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Found 145 publications

Initial Site of Macular Involvement in Central Retinal Dystrophies Revealed by Fundus Autofluorescence and Optical Coherence Tomography.

Initial Site of Macular Involvement in Central Retinal Dystrophies Revealed by Fundus Autofluorescence and Optical Coherence Tomography.

Journal: Investigative ophthalmology & visual science

Published: May 19, 2026

MERTK-associated retinal dystrophy: clinical course and imaging.

MERTK-associated retinal dystrophy: clinical course and imaging.

Journal: Ophthalmic genetics

Published: May 04, 2026

ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological Findings.

ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological Findings.

Journal: Investigative ophthalmology & visual science

Published: April 14, 2026

Clinical endpoints special session, ISCEV 2025, Utrecht.

Clinical endpoints special session, ISCEV 2025, Utrecht.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: December 23, 2025

Longitudinal evaluation of peripheral photoreceptor atrophy in fundus albipunctatus.

Longitudinal evaluation of peripheral photoreceptor atrophy in fundus albipunctatus.

Journal: Japanese journal of ophthalmology

Published: October 06, 2025

Genetic and Phenotypic Characterization of a Large Cohort of Patients with BBS1-Retinopathy.

Genetic and Phenotypic Characterization of a Large Cohort of Patients with BBS1-Retinopathy.

Journal: Ophthalmology science

Published: September 20, 2025

Fundus Autofluorescence as a Sensitive Biomarker of Disease Progression in Bietti Crystalline Dystrophy.

Fundus Autofluorescence as a Sensitive Biomarker of Disease Progression in Bietti Crystalline Dystrophy.

Journal: Ophthalmology science

Published: August 24, 2025

Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations.

Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations.

Journal: medRxiv : the preprint server for health sciences

Published: July 09, 2025

Autosomal dominant pigmented paravenous retinochoroidal atrophy associated with pathogenic variant in HK1 gene.

Autosomal dominant pigmented paravenous retinochoroidal atrophy associated with pathogenic variant in HK1 gene.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: June 23, 2025

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic retinal degeneration.

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic retinal degeneration.

Journal: Research square

Published: June 05, 2025

SNRNP200- Associated Retinopathy: In-Depth Clinical Phenotyping and Genetic Characterization.

SNRNP200- Associated Retinopathy: In-Depth Clinical Phenotyping and Genetic Characterization.

Journal: American journal of ophthalmology

Published: May 31, 2025

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity.

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity.

Journal: NPJ genomic medicine

Published: April 22, 2025

Showing 1-12 of 145

Last Updated: 09/26/2026