Case of acute zonal occult outer retinopathy with abnormal pattern visual evoked potentials

Por Chai, Yuzhu, Yamazaki, Hiroko, Fujinami, Kaoru, Tsunoda, Kazushige, Yamamoto, Shuichi
Publicado em 2011

Evaluation of cone function by a handheld non-mydriatic flicker electroretinogram device

Por Nakamura, Natsuko, Fujinami, Kaoru, Mizuno, Yoshinobu, Noda, Toru, Tsunoda, Kazushige
Publicado no Clin Ophthalmol (2016)

Pattern-reversal visual-evoked potential in patients with occult macular dystrophy

Por Hanazono, Gen, Ohde, Hisao, Shinoda, Kei, Tsunoda, Kazushige, Tsubota, Kazuo, Miyake, Yozo
Publicado em 2010

Two siblings with late-onset cone–rod dystrophy and no visible macular degeneration

Por Sakuramoto, Hiroyuki, Kuniyoshi, Kazuki, Tsunoda, Kazushige, Akahori, Masakazu, Iwata, Takeshi, Shimomura, Yoshikazu
Publicado em 2013

Clinical course of focal choroidal excavation in Vogt–Koyanagi–Harada disease

Por Nishikawa, Yuko, Fujinami, Kaoru, Watanabe, Ken, Noda, Toru, Tsunoda, Kazushige, Akiyama, Kunihiko
Publicado no Clin Ophthalmol (2014)

Transient macular dysfunction determined by focal macular electroretinogram

Por Terauchi, Naoki, Fujinami, Kaoru, Shinoda, Kei, Tsunoda, Kazushige, Hanazono, Gen, Miyake, Yozo, Inomata, Koichi
Publicado em 2007

ABCA4 Gene Screening by Next-Generation Sequencing in a British Cohort

Por Fujinami, Kaoru, Zernant, Jana, Chana, Ravinder K., Wright, Genevieve A., Tsunoda, Kazushige, Ozawa, Yoko, Tsubota, Kazuo, Webster, Andrew R., Moore, Anthony T., Allikmets, Rando, Michaelides, Michel
Publicado em 2013

Dominant Mutations in RP1L1 Are Responsible for Occult Macular Dystrophy

Por Akahori, Masakazu, Tsunoda, Kazushige, Miyake, Yozo, Fukuda, Yoko, Ishiura, Hiroyuki, Tsuji, Shoji, Usui, Tomoaki, Hatase, Tetsuhisa, Nakamura, Makoto, Ohde, Hisao, Itabashi, Takeshi, Okamoto, Haru, Takada, Yuichiro, Iwata, Takeshi
Publicado em 2010

Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease

Por Fujinami, Kaoru, Zernant, Jana, Chana, Ravinder K., Wright, Genevieve A., Tsunoda, Kazushige, Ozawa, Yoko, Tsubota, Kazuo, Robson, Anthony G., Holder, Graham E., Allikmets, Rando, Michaelides, Michel, Moore, Anthony T.
Publicado no Ophthalmology (2014)

Molecular characteristics of four Japanese cases with KCNV2 retinopathy: Report of novel disease-causing variants

Por Fujinami, Kaoru, Tsunoda, Kazushige, Nakamura, Natsuko, Kato, Yu, Noda, Toru, Shinoda, Kei, Tomita, Kaoru, Hatase, Tetsuhisa, Usui, Tomoaki, Akahori, Masakazu, Itabashi, Takeshi, Iwata, Takeshi, Ozawa, Yoko, Tsubota, Kazuo, Miyake, Yozo
Publicado em 2013

Whole Exome Analysis Identifies Frequent CNGA1 Mutations in Japanese Population with Autosomal Recessive Retinitis Pigmentosa

Por Katagiri, Satoshi, Akahori, Masakazu, Sergeev, Yuri, Yoshitake, Kazutoshi, Ikeo, Kazuho, Furuno, Masaaki, Hayashi, Takaaki, Kondo, Mineo, Ueno, Shinji, Tsunoda, Kazushige, Shinoda, Kei, Kuniyoshi, Kazuki, Tsurusaki, Yohinori, Matsumoto, Naomichi, Tsuneoka, Hiroshi, Iwata, Takeshi
Publicado em 2014