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Kaoru Fujinami

Showing results (81-90 of 148) with videos related to

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Ophthalmology|January 10, 2018
Early Patterns of Macular Degeneration in ABCA4-Associated RetinopathyKamron N Khan, Melissa Kasilian, Omar A R Mahroo, et al.
Ophthalmology. Retina|March 14, 2025
Best Vitelliform Macular Dystrophy Natural History Study Report 2: Fundus Autofluorescence and OCTYannik Laich, Michalis Georgiou, Kaoru Fujinami, et al.
International Journal of Molecular Sciences|February 22, 2020
Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with <i>DRAM2</i>-Associated RetinopathyKazuki Kuniyoshi, Takaaki Hayashi, Shuhei Kameya, et al.
Ophthalmology|January 26, 2024
Best Vitelliform Macular Dystrophy Natural History Study Report 1: Clinical Features and Genetic FindingsYannik Laich, Michalis Georgiou, Kaoru Fujinami, et al.
Molecular Vision|November 2, 2019
Autosomal dominant optic atrophy with <i>OPA1</i> gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohortAkiko Maeda-Katahira, Natsuko Nakamura, Takaaki Hayashi, et al.
Investigative Ophthalmology & Visual Science|November 23, 2013
A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, et al.
Ophthalmology|October 15, 2014
Clinical and molecular characteristics of childhood-onset Stargardt diseaseKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
American Journal of Ophthalmology|September 13, 2022
CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural HistoryMalena Daich Varela, Michalis Georgiou, Yahya Alswaiti, et al.
Ophthalmology|June 18, 2013
The clinical effect of homozygous ABCA4 alleles in 18 patientsKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
Molecular Vision|July 26, 2013
Molecular characteristics of four Japanese cases with KCNV2 retinopathy: report of novel disease-causing variantsKaoru Fujinami, Kazushige Tsunoda, Natsuko Nakamura, et al.
Pageof 15

Showing results (81-90 of 148) with videos related to

Sort By:
Pageof 15
Ophthalmology|January 10, 2018
Early Patterns of Macular Degeneration in ABCA4-Associated RetinopathyKamron N Khan, Melissa Kasilian, Omar A R Mahroo, et al.
Ophthalmology. Retina|March 14, 2025
Best Vitelliform Macular Dystrophy Natural History Study Report 2: Fundus Autofluorescence and OCTYannik Laich, Michalis Georgiou, Kaoru Fujinami, et al.
International Journal of Molecular Sciences|February 22, 2020
Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with <i>DRAM2</i>-Associated RetinopathyKazuki Kuniyoshi, Takaaki Hayashi, Shuhei Kameya, et al.
Ophthalmology|January 26, 2024
Best Vitelliform Macular Dystrophy Natural History Study Report 1: Clinical Features and Genetic FindingsYannik Laich, Michalis Georgiou, Kaoru Fujinami, et al.
Molecular Vision|November 2, 2019
Autosomal dominant optic atrophy with <i>OPA1</i> gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohortAkiko Maeda-Katahira, Natsuko Nakamura, Takaaki Hayashi, et al.
Investigative Ophthalmology & Visual Science|November 23, 2013
A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, et al.
Ophthalmology|October 15, 2014
Clinical and molecular characteristics of childhood-onset Stargardt diseaseKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
American Journal of Ophthalmology|September 13, 2022
CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural HistoryMalena Daich Varela, Michalis Georgiou, Yahya Alswaiti, et al.
Ophthalmology|June 18, 2013
The clinical effect of homozygous ABCA4 alleles in 18 patientsKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
Molecular Vision|July 26, 2013
Molecular characteristics of four Japanese cases with KCNV2 retinopathy: report of novel disease-causing variantsKaoru Fujinami, Kazushige Tsunoda, Natsuko Nakamura, et al.
Pageof 15