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Japanese Journal of Ophthalmology|July 19, 2021
Visual outcome of aquaporin-4 antibody-positive optic neuritis with maintenance therapySatoshi Ueki, Tetsuhisa Hatase, Megumi Kiyokawa, 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.
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|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.
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.
Annals of Neurology|February 3, 2016
Clinicopathological features in anterior visual pathway in neuromyelitis opticaMariko Hokari, Akiko Yokoseki, Musashi Arakawa, et al.
Human Mutation|October 26, 2022
Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencingAkiko Suga, Kazutoshi Yoshitake, Naoko Minematsu, et al.
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