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Yozo Miyake

Showing results (121-130 of 135) with videos related to

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Investigative Ophthalmology & Visual Science|November 15, 2019
Clinical Stages of Occult Macular Dystrophy Based on Optical Coherence Tomographic FindingsNatsuko Nakamura, Kazushige Tsunoda, Yoshinobu Mizuno, 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.
Human Genome Variation|October 25, 2019
Clinical and genetic characteristics of 14 patients from 13 Japanese families with <i>RPGR</i>-associated retinal disorder: report of eight novel variantsGo Mawatari, Kaoru Fujinami, Xiao Liu, et al.
Human Genome Variation|February 13, 2020
Correction to: Clinical and genetic characteristics of 14 patients from 13 Japanese families with <i>RPGR</i>-associated retinal disorder: report of eight novel variantsGo Mawatari, Kaoru Fujinami, Xiao Liu, et al.
Investigative Ophthalmology & Visual Science|January 7, 2022
Visual Field Characteristics in East Asian Patients With Occult Macular Dystrophy (Miyake Disease): EAOMD Report No. 3Seong Joon Ahn, Lizhu Yang, Kazushige Tsunoda, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 22, 2020
Clinical and genetic characteristics of 10 Japanese patients with PROM1-associated retinal disorder: A report of the phenotype spectrum and a literature review in the Japanese populationKaoru Fujinami, Akio Oishi, Lizhu Yang, et al.
Ophthalmology|April 28, 2019
Clinical and Genetic Characteristics of East Asian Patients with Occult Macular Dystrophy (Miyake Disease): East Asia Occult Macular Dystrophy Studies Report Number 1Kaoru Fujinami, Lizhu Yang, Kwangsic Joo, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 3, 2020
RP2-associated retinal disorder in a Japanese cohort: Report of novel variants and a literature review, identifying a genotype-phenotype associationKaoru Fujinami, Xiao Liu, Shinji Ueno, et al.
Investigative Ophthalmology & Visual Science|August 8, 2019
Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic AppearanceShuhei Kameya, Kaoru Fujinami, Shinji Ueno, et al.
Investigative Ophthalmology & Visual Science|September 14, 2016
Novel RP1L1 Variants and Genotype-Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular DystrophyKaoru Fujinami, Shuhei Kameya, Sachiko Kikuchi, et al.
Pageof 14

Showing results (121-130 of 135) with videos related to

Sort By:
Pageof 14
Investigative Ophthalmology & Visual Science|November 15, 2019
Clinical Stages of Occult Macular Dystrophy Based on Optical Coherence Tomographic FindingsNatsuko Nakamura, Kazushige Tsunoda, Yoshinobu Mizuno, 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.
Human Genome Variation|October 25, 2019
Clinical and genetic characteristics of 14 patients from 13 Japanese families with <i>RPGR</i>-associated retinal disorder: report of eight novel variantsGo Mawatari, Kaoru Fujinami, Xiao Liu, et al.
Human Genome Variation|February 13, 2020
Correction to: Clinical and genetic characteristics of 14 patients from 13 Japanese families with <i>RPGR</i>-associated retinal disorder: report of eight novel variantsGo Mawatari, Kaoru Fujinami, Xiao Liu, et al.
Investigative Ophthalmology & Visual Science|January 7, 2022
Visual Field Characteristics in East Asian Patients With Occult Macular Dystrophy (Miyake Disease): EAOMD Report No. 3Seong Joon Ahn, Lizhu Yang, Kazushige Tsunoda, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 22, 2020
Clinical and genetic characteristics of 10 Japanese patients with PROM1-associated retinal disorder: A report of the phenotype spectrum and a literature review in the Japanese populationKaoru Fujinami, Akio Oishi, Lizhu Yang, et al.
Ophthalmology|April 28, 2019
Clinical and Genetic Characteristics of East Asian Patients with Occult Macular Dystrophy (Miyake Disease): East Asia Occult Macular Dystrophy Studies Report Number 1Kaoru Fujinami, Lizhu Yang, Kwangsic Joo, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 3, 2020
RP2-associated retinal disorder in a Japanese cohort: Report of novel variants and a literature review, identifying a genotype-phenotype associationKaoru Fujinami, Xiao Liu, Shinji Ueno, et al.
Investigative Ophthalmology & Visual Science|August 8, 2019
Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic AppearanceShuhei Kameya, Kaoru Fujinami, Shinji Ueno, et al.
Investigative Ophthalmology & Visual Science|September 14, 2016
Novel RP1L1 Variants and Genotype-Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular DystrophyKaoru Fujinami, Shuhei Kameya, Sachiko Kikuchi, et al.
Pageof 14