Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tomotsugu Yura"'
Autor:
Tomotsugu Yura
Publikováno v:
Acta Ophthalmologica Scandinavica. 76:90-95
PURPOSE: To assess the relationship between the prevalence of lattice degeneration and the types of axial elongation. METHODS: Nine hundred seventy eyes of 542 highly myopic patients with axial length of 26.00-31.99 mm were evaluated by using A-scan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::609745c806e1a00f71dfa88eae2b4b98
https://doi.org/10.1034/j.1600-0420.1998.760117.x
https://doi.org/10.1034/j.1600-0420.1998.760117.x
Autor:
Osamu Tamura, Takehiko Sakuma, Takakazu Honda, Yasushi Isashiki, Muneyasu Takeda, Atsushi Kanai, Kazuyuki Yoshida, Yoshihito Honda, Mizuo Matsui, Wakabayashi K, Nobue Kubota, Kawano S, Miyo Matsumura, Kiyoshi Akeo, Keiko Fujiki, Masayuki Horiguchi, Emiko Adachi, Tomotsugu Yura, Masanobu Uyama, Tsuyoshi Kimura, Yozo Miyake, Hisayuki Ueno, Takashi Tokoro, Mutsuko Hayakawa, Kan Koizumi, Norio Ohba, Nobuto Ishizaka, Kanji Choshi, H Sakaue, Takashi Nakagawa, Michio Watanabe, Nobuko Tagami, Naomi Shimowake, Mitsuko Yuzawa, Yoshihisa Oguchi, Tatsuro Ishibashi, Makoto Tamai
Publikováno v:
Japanese Journal of Ophthalmology. 41:1-6
A nationwide, multicenter study of typical retinitis pigmentosa (RP) was carried out in collaboration with 18 hospitals throughout Japan to obtain current information for genetic counseling. We analyzed the genetic heterogeneity of RP based on the pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d1b4d294a778e7ce4337bf0a9cfec8b
https://doi.org/10.1016/s0021-5155(96)00018-4
https://doi.org/10.1016/s0021-5155(96)00018-4
Autor:
Keiko Fujiki, Muneyasu Takeda, Takashi Nakagawa, Michio Watanabe, Takashi Tokoro, H Sakaue, Kazuyuki Yoshida, Masayuki Horiguchi, Tsuyoshi Kimura, Mutsuko Hayakawa, Nobuto Ishizaka, Takakazu Honda, Miyo Matsumura, Kanji Choshi, Wakabayashi K, Nobue Kubota, Mizuo Matsui, Kiyoshi Akeo, Yozo Miyake, Kan Koizumi, Tatsuro Ishibashi, Mitsuko Yuzawa, Yoshihisa Oguchi, Emiko Adachi, Yoshihito Honda, Osamu Tamura, Makoto Tamai, Norio Ohba, Takehiko Sakuma, Masanobu Uyama, Yasushi Isashiki, Atsushi Kanai, Nobuko Tagami, Naomi Shimowake, Kawano S, Tomotsugu Yura, Hisayuki Ueno
Publikováno v:
Japanese journal of ophthalmology. 41(1)
Retinitis pigmentosa (RP) is a group of genetically heterogeneous diseases with autosomal recessive (AR), autosomal dominant, and X-linked modes of inheritance. Autosomal recessive retinitis pigmentosa (ARRP) is the most common form in Japan. A genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d16f62d78d2b69fb642e2dd2837a74
https://pubmed.ncbi.nlm.nih.gov/9147181
https://pubmed.ncbi.nlm.nih.gov/9147181