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Yozo Miyake

Showing results (111-120 of 135) with videos related to

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Scientific Reports|August 6, 2016
Electroretinographic evaluations of retinal function before, just after, and after intravitreal injectionsKazuma Yagura, Kei Shinoda, Soiti Matsumoto, et al.
Japanese Journal of Ophthalmology|February 10, 2004
A case of sectorial benign flecked retinaTakako Tsuchiya, Masaru Kato, Natsuyo Tomita, et al.
Nippon Ganka Gakkai Zasshi|September 26, 2013
[Long-term observation over ten years of four cases of cone dystrophy with supernormal rod electroretinogram]Natsuko Nakamura, Kazushige Tsunoda, Kaoru Fujinami, et al.
Retina (Philadelphia, Pa.)|April 3, 2012
Clinical characteristics of occult macular dystrophy in family with mutation of RP1l1 geneKazushige Tsunoda, Tomoaki Usui, Tetsuhisa Hatase, et al.
Molecular Vision|March 20, 2010
TRPM1 mutations are associated with the complete form of congenital stationary night blindnessMakoto Nakamura, Rikako Sanuki, Tetsuhiro R Yasuma, et al.
Molecular Vision|May 19, 2012
A new mutation in the RP1L1 gene in a patient with occult macular dystrophy associated with a depolarizing pattern of focal macular electroretinogramsTakenori Kabuto, Hisatomo Takahashi, Yoko Goto-Fukuura, et al.
The American Journal of Pathology|March 29, 2008
Retinal dysfunction and progressive retinal cell death in SOD1-deficient miceKouhei Hashizume, Manabu Hirasawa, Yutaka Imamura, et al.
American Journal of Human Genetics|September 10, 2010
Dominant mutations in RP1L1 are responsible for occult macular dystrophyMasakazu Akahori, Kazushige Tsunoda, Yozo Miyake, et al.
Molecular Vision|March 17, 2006
Complement factor H polymorphisms in Japanese population with age-related macular degenerationHaru Okamoto, Shinsuke Umeda, Minoru Obazawa, et al.
Investigative Ophthalmology & Visual Science|August 31, 2002
ABCA4 gene mutations in Japanese patients with Stargardt disease and retinitis pigmentosaTakehiro Fukui, Shuji Yamamoto, Kaoru Nakano, et al.
Pageof 14

Showing results (111-120 of 135) with videos related to

Sort By:
Pageof 14
Scientific Reports|August 6, 2016
Electroretinographic evaluations of retinal function before, just after, and after intravitreal injectionsKazuma Yagura, Kei Shinoda, Soiti Matsumoto, et al.
Japanese Journal of Ophthalmology|February 10, 2004
A case of sectorial benign flecked retinaTakako Tsuchiya, Masaru Kato, Natsuyo Tomita, et al.
Nippon Ganka Gakkai Zasshi|September 26, 2013
[Long-term observation over ten years of four cases of cone dystrophy with supernormal rod electroretinogram]Natsuko Nakamura, Kazushige Tsunoda, Kaoru Fujinami, et al.
Retina (Philadelphia, Pa.)|April 3, 2012
Clinical characteristics of occult macular dystrophy in family with mutation of RP1l1 geneKazushige Tsunoda, Tomoaki Usui, Tetsuhisa Hatase, et al.
Molecular Vision|March 20, 2010
TRPM1 mutations are associated with the complete form of congenital stationary night blindnessMakoto Nakamura, Rikako Sanuki, Tetsuhiro R Yasuma, et al.
Molecular Vision|May 19, 2012
A new mutation in the RP1L1 gene in a patient with occult macular dystrophy associated with a depolarizing pattern of focal macular electroretinogramsTakenori Kabuto, Hisatomo Takahashi, Yoko Goto-Fukuura, et al.
The American Journal of Pathology|March 29, 2008
Retinal dysfunction and progressive retinal cell death in SOD1-deficient miceKouhei Hashizume, Manabu Hirasawa, Yutaka Imamura, et al.
American Journal of Human Genetics|September 10, 2010
Dominant mutations in RP1L1 are responsible for occult macular dystrophyMasakazu Akahori, Kazushige Tsunoda, Yozo Miyake, et al.
Molecular Vision|March 17, 2006
Complement factor H polymorphisms in Japanese population with age-related macular degenerationHaru Okamoto, Shinsuke Umeda, Minoru Obazawa, et al.
Investigative Ophthalmology & Visual Science|August 31, 2002
ABCA4 gene mutations in Japanese patients with Stargardt disease and retinitis pigmentosaTakehiro Fukui, Shuji Yamamoto, Kaoru Nakano, et al.
Pageof 14