Works by Yoshihiro Hotta

Results: 67

Genotype-Phenotype Correlations in RP1 -Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN.

Published in:

Journal of Clinical Medicine, 2021, v. 10, n. 11, p. 2265, doi. 10.3390/jcm10112265

By:

Mizobuchi, Kei;
Hayashi, Takaaki;
Oishi, Noriko;
Kubota, Daiki;
Kameya, Shuhei;
Higasa, Koichiro;
Futami, Takuma;
Kondo, Hiroyuki;
Hosono, Katsuhiro;
Kurata, Kentaro;
Hotta, Yoshihiro;
Yoshitake, Kazutoshi;
Iwata, Takeshi;
Matsuura, Tomokazu;
Nakano, Tadashi

Publication type:

Article

Multimodal therapy with surgery and adjuvant nivolumab for late-onset multiple liver metastases of choroidal malignant melanoma: a case report.

Published in:

Surgical Case Reports, 2020, v. 6, n. 1, p. 1, doi. 10.1186/s40792-020-00948-0

By:

Muraki, Ryuta;
Morita, Yoshifumi;
Ida, Shinya;
Kitajima, Ryo;
Furuhashi, Satoru;
Kiuchi, Ryota;
Takeda, Makoto;
Kikuchi, Hirotoshi;
Hiramatsu, Yoshihiro;
Sakaguchi, Takanori;
Kasuya, Akira;
Hotta, Yoshihiro;
Takeuchi, Hiroya

Publication type:

Article

Multicenter open-label randomized phase II study of second-line panitumumab and irinotecan with or without fluoropyrimidines in patients with KRAS wild-type metastatic colorectal cancer (PACIFIC study).

Published in:

2019

By:

Nagata, Naoki;
Maeda, Hiromichi;
Ishibashi, Keiichiro;
Hirata, Keiji;
Makiyama, Akitaka;
Iwamoto, Shigeyoshi;
Takemoto, Hiroyoshi;
Imasato, Mitsunobu;
Yoshida, Yoichiro;
Munemoto, Yoshinori;
Tanaka, Chihiro;
Morita, Yoshitaka;
Hotta, Yoshihiro;
Toyofuku, Atsushi;
Nagasaka, Takeshi;
Morita, Satoshi;
Sakamoto, Junichi;
Mishima, Hideyuki

Publication type:

journal article

Early onset flecked retinal dystrophy associated with new compound heterozygous RPE65 variants.

Published in:

Molecular Vision, 2018, v. 24, p. 286

By:

Satoshi Katagiri;
Katsuhiro Hosono;
Takaaki Hayashi;
Kentaro Kurata;
Kei Mizobuchi;
Tomokazu Matsuura;
Kazutoshi Yoshitake;
Takeshi Iwata;
Tadashi Nakano;
Yoshihiro Hotta

Publication type:

Article

Interaction between optineurin and the b ZIP transcription factor NRL.

Published in:

Cell Biology International, 2014, v. 38, n. 1, p. 16, doi. 10.1002/cbin.10174

By:

Wang, Chunxia;
Hosono, Katsuhiro;
Ohtsubo, Masafumi;
Ohishi, Kentaro;
Gao, Jie;
Nakanishi, Nobuo;
Hikoya, Akiko;
Sato, Miho;
Hotta, Yoshihiro;
Minoshima, Shinsei

Publication type:

Article

The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 9, p. 521, doi. 10.1038/jhg.2014.65

By:

Zhao, Yang;
Hosono, Katsuhiro;
Suto, Kimiko;
Ishigami, Chie;
Arai, Yuuki;
Hikoya, Akiko;
Hirami, Yasuhiko;
Ohtsubo, Masafumi;
Ueno, Shinji;
Terasaki, Hiroko;
Sato, Miho;
Nakanishi, Hiroshi;
Endo, Shiori;
Mizuta, Kunihiro;
Mineta, Hiroyuki;
Kondo, Mineo;
Takahashi, Masayo;
Minoshima, Shinsei;
Hotta, Yoshihiro

Publication type:

Article

Novel USH2A mutations in Japanese Usher syndrome type 2 patients: marked differences in the mutation spectrum between the Japanese and other populations.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 7, p. 484, doi. 10.1038/jhg.2011.45

By:

Nakanishi, Hiroshi;
Ohtsubo, Masafumi;
Iwasaki, Satoshi;
Hotta, Yoshihiro;
Usami, Shin-ichi;
Mizuta, Kunihiro;
Mineta, Hiroyuki;
Minoshima, Shinsei

Publication type:

Article

Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 12, p. 796, doi. 10.1038/jhg.2010.115

By:

Nakanishi, Hiroshi;
Ohtsubo, Masafumi;
Iwasaki, Satoshi;
Hotta, Yoshihiro;
Takizawa, Yoshinori;
Hosono, Katsuhiro;
Mizuta, Kunihiro;
Mineta, Hiroyuki;
Minoshima, Shinsei

Publication type:

Article

Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genes.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 701, doi. 10.1038/jhg.2010.83

By:

Nakanishi, Hiroshi;
Ohtsubo, Masafumi;
Iwasaki, Satoshi;
Hotta, Yoshihiro;
Mizuta, Kunihiro;
Mineta, Hiroyuki;
Minoshima, Shinsei

Publication type:

Article

Three novel mutations of the PAX6 gene in Japanese aniridia patients.

Published in:

Journal of Human Genetics, 2007, v. 52, n. 7, p. 571, doi. 10.1007/s10038-007-0153-2

By:

Kawano, Toshio;
Chunxia Wang;
Hotta, Yoshihiro;
Sato, Miho;
Iwata-Amano, Emi;
Hikoya, Akiko;
Fujita, Naoya;
Koyama, Norihisa;
Shirai, Shoichiro;
Azuma, Noriyuki;
Ohtsubo, Masafumi;
Shimizu, Nobuyoshi;
Minoshima, Shinsei

Publication type:

Article

Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 4, p. 242, doi. 10.1007/s100380050081

By:

Matsumoto, M.;
Hayasaka, Seiji;
Hotta, Yoshihiro;
Fujiki, Keiko;
Fujimaki, Takuro;
Takeda, Misako;
Ishida, Nobuo;
Endo, Shin-ichiro;
Kanai, Atsushi

Publication type:

Article

De novo heterozygous variants in KIF5B cause kyphomelic dysplasia.

Published in:

Clinical Genetics, 2022, v. 102, n. 1, p. 3, doi. 10.1111/cge.14133

By:

Itai, Toshiyuki;
Wang, Zheng;
Nishimura, Gen;
Ohashi, Hirofumi;
Guo, Long;
Wakano, Yasuhiro;
Sugiura, Takahiro;
Hayakawa, Hiromi;
Okada, Mayumi;
Saisu, Takashi;
Kitta, Ayana;
Doi, Hiroshi;
Kurosawa, Kenji;
Hotta, Yoshihiro;
Hosono, Katsuhiro;
Sato, Miho;
Shimizu, Kenji;
Takikawa, Kazuharu;
Watanabe, Seiji;
Ikeda, Naho

Publication type:

Article

Characteristics and surgical outcomes of consecutive exotropia of different etiologies.

Published in:

Japanese Journal of Ophthalmology, 2015, v. 59, n. 5, p. 335, doi. 10.1007/s10384-015-0395-z

By:

Sawada, Mayu;
Hikoya, Akiko;
Negishi, Takashi;
Hotta, Yoshihiro;
Sato, Miho

Publication type:

Article

Central corneal thickness in Japanese children.

Published in:

Japanese Journal of Ophthalmology, 2009, v. 53, n. 1, p. 7, doi. 10.1007/s10384-008-0619-6

By:

Akiko Hikoya;
Kinnichi Tsuzuki;
Yuka Koide;
Ryo Asaoka;
Yoshihiro Hotta

Publication type:

Article

Coenzyme Q10 in the eye isomerizes by sunlight irradiation.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-16343-8

By:

Mamun, Md. Al;
Nabi, Md. Mahamodun;
Sato, Tomohito;
Aramaki, Shuhei;
Takanashi, Yusuke;
Sakamoto, Takumi;
Hizume, Kaito;
Mori, Chikako;
Yasue, Maiha;
Ozaki, Masataka;
Islam, Ariful;
Kahyo, Tomoaki;
Horikawa, Makoto;
Takahashi, Yutaka;
Okazaki, Shigetoshi;
Ohishi, Kentaro;
Nagashima, Yu;
Seno, Keiji;
Hotta, Yoshihiro;
Setou, Mitsutoshi

Publication type:

Article

Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3 -Congenital Disorders of Glycosylation and RP1 -Related Retinitis Pigmentosa.

Published in:

Genes, 2022, v. 13, n. 2, p. 359, doi. 10.3390/genes13020359

By:

Tachibana, Nobutaka;
Hosono, Katsuhiro;
Nomura, Shuhei;
Arai, Shinji;
Torii, Kaoruko;
Kurata, Kentaro;
Sato, Miho;
Shimakawa, Shuichi;
Azuma, Noriyuki;
Ogata, Tsutomu;
Wada, Yoshinao;
Okamoto, Nobuhiko;
Saitsu, Hirotomo;
Nishina, Sachiko;
Hotta, Yoshihiro

Publication type:

Article

Evaluation of Surgical Strategy Based on the Intraoperative Superior Oblique Tendon Traction Test.

Published in:

PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0168245

By:

Komori, Miwa;
Suzuki, Hiroko;
Hikoya, Akiko;
Sawada, Mayu;
Hotta, Yoshihiro;
Sato, Miho

Publication type:

Article

The Structural Abnormalities Are Deeply Involved in the Cause of RPGRIP1 -Related Retinal Dystrophy in Japanese Patients.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 18, p. 13678, doi. 10.3390/ijms241813678

By:

Torii, Kaoruko;
Nishina, Sachiko;
Morikawa, Hazuki;
Mizobuchi, Kei;
Takayama, Masakazu;
Tachibana, Nobutaka;
Kurata, Kentaro;
Hikoya, Akiko;
Sato, Miho;
Nakano, Tadashi;
Fukami, Maki;
Azuma, Noriyuki;
Hayashi, Takaaki;
Saitsu, Hirotomo;
Hotta, Yoshihiro

Publication type:

Article

X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers.

Published in:

International Journal of Molecular Sciences, 2019, v. 20, n. 6, p. 1518, doi. 10.3390/ijms20061518

By:

Kurata, Kentaro;
Hosono, Katsuhiro;
Miyamichi, Daisuke;
Sato, Miho;
Hotta, Yoshihiro;
Hayashi, Takaaki;
Mizobuchi, Kei;
Katagiri, Satoshi;
Nakano, Tadashi;
Nishina, Sachiko;
Azuma, Noriyuki

Publication type:

Article

A family with neuronal intranuclear inclusion disease with focal segmental glomerulosclerosis.

Published in:

Journal of Neurology, 2024, v. 271, n. 9, p. 6227, doi. 10.1007/s00415-024-12593-w

By:

Watanabe, Kazuki;
Bunai, Tomoyasu;
Sakamoto, Masamune;
Ishigaki, Sayaka;
Iwakura, Takamasa;
Ohashi, Naro;
Wakatsuki, Rie;
Takenouchi, Akiyuki;
Iwaizumi, Moriya;
Hotta, Yoshihiro;
Saida, Ken;
Koshimizu, Eriko;
Miyatake, Satoko;
Saitsu, Hirotomo;
Matsumoto, Naomichi;
Nakamura, Tomohiko

Publication type:

Article

A case of siblings with juvenile retinitis pigmentosa associated with NEK1 gene variants.

Published in:

Ophthalmic Genetics, 2023, v. 44, n. 5, p. 480, doi. 10.1080/13816810.2022.2141788

By:

Hikoya, Akiko;
Hosono, Katsuhiro;
Ono, Kaoru;
Arai, Shinji;
Tachibana, Nobutaka;
Kurata, Kentaro;
Torii, Kaoruko;
Sato, Miho;
Saitsu, Hirotomo;
Ogata, Tsutomu;
Hotta, Yoshihiro

Publication type:

Article

A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation.

Published in:

Ophthalmic Genetics, 2020, v. 41, n. 2, p. 175, doi. 10.1080/13816810.2020.1744019

By:

Hosono, Katsuhiro;
Kawase, Kazuhide;
Kurata, Kentaro;
Niimi, Yusuke;
Saitsu, Hirotomo;
Minoshima, Shinsei;
Ohnishi, Hidenori;
Yamamoto, Takahiro;
Hikoya, Akiko;
Tachibana, Nobutaka;
Fukao, Toshiyuki;
Yamamoto, Tetsuya;
Hotta, Yoshihiro

Publication type:

Article

Clinical Phenotype in Ten Unrelated Japanese Patients with Mutations in the EYS Gene.

Published in:

Ophthalmic Genetics, 2014, v. 35, n. 1, p. 25, doi. 10.3109/13816810.2013.768673

By:

Suto, Kimiko;
Hosono, Katsuhiro;
Takahashi, Masayo;
Hirami, Yasuhiko;
Arai, Yuki;
Nagase, Yasunori;
Ueno, Shinji;
Terasaki, Hiroko;
Minoshima, Shinsei;
Kondo, Mineo;
Hotta, Yoshihiro

Publication type:

Article

Clinical features of a Japanese case with Bothnia dystrophy.

Published in:

Ophthalmic Genetics, 2012, v. 33, n. 2, p. 83, doi. 10.3109/13816810.2011.634877

By:

Nojima, Kazutoshi;
Hosono, Katsuhiro;
Zhao, Yang;
Toshiba, Takaaki;
Hikoya, Akiko;
Asai, Tatsuhiko;
Kato, Masaru;
Kondo, Mineo;
Minoshima, Shinsei;
Hotta, Yoshihiro

Publication type:

Article

Novel RDH5 Mutation in Family with Mother Having Fundus Albipunctatus and Three Children with Retinitis Pigmentosa.

Published in:

Ophthalmic Genetics, 2008, v. 29, n. 1, p. 29, doi. 10.1080/13816810701663535

By:

Wang, Chunxia;
Nakanishi, Nobuo;
Ohishi, Kentaro;
Hikoya, Akiko;
Koide, Kenro;
Sato, Miho;
Nakamura, Makoto;
Hotta, Yoshihiro;
Minoshima, Shinsei

Publication type:

Article

Secondary mutations of mitochondrial DNA in Japanese patients withLeber's hereditary optic neuropathy.

Published in:

Ophthalmic Genetics, 1999, v. 20, n. 3, p. 153, doi. 10.1076/opge.20.3.153.2281

By:

Matsumoto, Masayuki;
Hayasaka, Seiji;
Kadoi, Chiharu;
Hotta, Yoshihiro;
Fujiki, Keiko;
Fujimaki, Takuro;
Takeda, Misako;
Ishida, Nobuo;
Endo, Shinichiro;
Kanai, Atsushi

Publication type:

Article

Analysis of phosducin as a candidate gene for retinopathies.

Published in:

Ophthalmic Genetics, 1996, v. 17, n. 1, p. 3, doi. 10.3109/13816819609057863

By:

Ara-iwata, Fumino;
Jacobson, Samuel G.;
Gass, J. Donald M.;
Hotta, Yoshihiro;
Fujiki, Keiko;
Hayakawa, Mutsuko;
Inana, George

Publication type:

Article

PRESENCE AND QUANTIFICATION OF NEUROPEPTIDE Y IN PULMONARY EDEMA FLUIDS IN RATS.

Published in:

Experimental Lung Research, 2000, v. 26, n. 3, p. 137, doi. 10.1080/019021400269835

By:

Hamdy, Ossama;
Nishiwaki, Kimitoshi;
Yajima, Michio;
Murakami, Hidetsugu O.;
Maekawa, Hiroshi;
Moy, Robert T.;
Shimada, Yasuhiro;
Hotta, Yoshihiro;
Ishikawa, Naohisa

Publication type:

Article

Novel biallelic splice-site BBS1 variants in Bardet–Biedle syndrome: a case report of the first Japanese patient.

Published in:

Documenta Ophthalmologica, 2020, v. 141, n. 1, p. 77, doi. 10.1007/s10633-020-09752-5

By:

Katagiri, Satoshi;
Hosono, Katsuhiro;
Hayashi, Takaaki;
Murai, Noriyuki;
Wake, Eiichi;
Miyata, Ichiro;
Mizobuchi, Kei;
Kurata, Kentaro;
Matsuura, Tomokazu;
Nakano, Tadashi;
Hotta, Yoshihiro

Publication type:

Article

Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy.

Published in:

Documenta Ophthalmologica, 2020, v. 140, n. 2, p. 147, doi. 10.1007/s10633-019-09727-1

By:

Hayashi, Takaaki;
Hosono, Katsuhiro;
Kurata, Kentaro;
Katagiri, Satoshi;
Mizobuchi, Kei;
Ueno, Shinji;
Kondo, Mineo;
Nakano, Tadashi;
Hotta, Yoshihiro

Publication type:

Article

Clinical and genetic findings of a Japanese patient with RP1-related autosomal recessive retinitis pigmentosa.

Published in:

Documenta Ophthalmologica, 2018, v. 137, n. 1, p. 47, doi. 10.1007/s10633-018-9649-7

By:

Kurata, Kentaro;
Hosono, Katsuhiro;
Hotta, Yoshihiro

Publication type:

Article

Kessler Psychological Distress (K6) Questionnaire Scores Can Predict Autistic Traits and the Current and Prospective Suicidal Ideation in Medical University Students: A Prospective Study.

Published in:

SAGE Open, 2021, v. 11, n. 1, p. 1, doi. 10.1177/2158244021994590

By:

Naito, Yumi;
Enomoto, Noriyuki;
Kameno, Yosuke;
Yamasue, Hidenori;
Suda, Takafumi;
Hotta, Yoshihiro

Publication type:

Article

Multicenter study on the frequency of three primary mutations ofmitochondrial DNA in Japanese pedigrees with Leber's hereditary optic neuropathy:comparison with American and British counterparts.

Published in:

Neuro-Ophthalmology, 1999, v. 22, n. 3, p. 187, doi. 10.1076/noph.22.3.187.3724

By:

Yamada, Keiko;
Oguchi, Yoshihisa;
Hotta, Yoshihiro;
Nakamura, Makoto;
Isashiki, Yasushi;
Mashima, Yukihiko

Publication type:

Article

The effect of levocabastine hydrochloride on human Tenon’s capsule fibroblasts: Inhibition of proliferation, suppression of DNA synthesis and induction of apoptosis.

Published in:

Cutaneous & Ocular Toxicology, 2009, v. 28, n. 2, p. 83, doi. 10.1080/15569520902937901

By:

Asaoka, Ryo;
Nakagamil, Tetsushi;
Zhu, Haogang;
Liu, Yan;
Hotta, Yoshihiro

Publication type:

Article

Novel mutations in the myocilin gene in Japanese glaucoma patients.

Published in:

Human Mutation, 2000, v. 16, n. 3, p. 270, doi. 10.1002/1098-1004(200009)16:3<270::AID-HUMU13>3.0.CO;2-M

By:

Kubota, Ryo;
Mashima, Yukihiko;
Ohtake, Yuichiro;
Tanino, Tomihiko;
Kimura, Tairo;
Hotta, Yoshihiro;
Kanai, Atsushi;
Tokuoka, Satoru;
Azuma, Ikuo;
Tanihara, Hidenobu;
Inatani, Masaru;
Inoue, Yoichi;
Kudoh, Jun;
Oguchi, Yoshihisa;
Shimizu, Nobuyoshi

Publication type:

Article

Low frequency of oncogenic mutations in the core promoter region of the RB1 gene.

Published in:

Human Mutation, 1999, v. 13, n. 5, p. 410, doi. 10.1002/(SICI)1098-1004(1999)13:5<410::AID-HUMU10>3.0.CO;2-1

By:

Fujita, Tsuyoshi;
Ohtani-Fujita, Naoko;
Sakai, Toshiyuki;
Rapaport, Joyce M.;
Dryja, Thaddeus P.;
Kato, Mitsuo V.;
Ishizaki, Kanji;
Sasaki, Masao S.;
Hotta, Yoshihiro;
Maeda, Koshi;
Kinoshita, Shigeru;
Ohnishi, Yoshitaka;
Minoda, Kensei

Publication type:

Article

Ocular genetics in the Japanese population.

Published in:

Japanese Journal of Ophthalmology, 2024, v. 68, n. 5, p. 401, doi. 10.1007/s10384-024-01109-8

By:

Hotta, Yoshihiro;
Torii, Kaoruko;
Takayama, Masakazu

Publication type:

Article

Specification of variant interpretation guidelines for inherited retinal dystrophy in Japan.

Published in:

Japanese Journal of Ophthalmology, 2024, v. 68, n. 4, p. 389, doi. 10.1007/s10384-024-01063-5

By:

Fujinami, Kaoru;
Nishiguchi, Koji M;
Oishi, Akio;
Akiyama, Masato;
Ikeda, Yasuhiro;
Hotta, Yoshihiro;
Kondo, Hiroyuki;
Maeda, Akiko;
Miyake, Masahiro;
Kondo, Mineo;
Sakamoto, Taiji

Publication type:

Article

Intraocular pressure changes at different gaze positions after superior rectus muscle-lateral rectus muscle loop myopexy in highly myopic strabismus.

Published in:

Japanese Journal of Ophthalmology, 2024, v. 68, n. 1, p. 26, doi. 10.1007/s10384-023-01032-4

By:

Arai, Shinji;
Suzuki, Hiroko;
Hayashi, Shion;
Inagaki, Risako;
Haseoka, Takashi;
Hikoya, Akiko;
Komori, Miwa;
Shimizu, Tamami;
Hotta, Yoshihiro;
Sato, Miho

Publication type:

Article

Steroid-induced ocular hypertensive response in pediatric patients with acute lymphoblastic leukemia.

Published in:

Japanese Journal of Ophthalmology, 2023, v. 67, n. 4, p. 396, doi. 10.1007/s10384-023-01005-7

By:

Sawada, Mayu;
Takachi, Takayuki;
Watanabe, Kenichiro;
Tsuchiya, Yoko;
Nishimura, Kasumi;
Hotta, Yoshihiro;
Sato, Miho

Publication type:

Article

Intraocular pressure at different gaze positions in patients with highly myopic strabismus.

Published in:

Japanese Journal of Ophthalmology, 2022, v. 66, n. 6, p. 572, doi. 10.1007/s10384-022-00939-8

By:

Arai, Shinji;
Suzuki, Hiroko;
Hayashi, Shion;
Inagaki, Risako;
Haseoka, Takashi;
Hikoya, Akiko;
Komori, Miwa;
Shimizu, Tamami;
Muhammad, Nazmul Haque;
Hotta, Yoshihiro;
Sato, Miho

Publication type:

Article

Exophthalmos associated with chronic progressive external ophthalmoplegia.

Published in:

Japanese Journal of Ophthalmology, 2022, v. 66, n. 3, p. 314, doi. 10.1007/s10384-022-00920-5

By:

Takeda, Yu;
Suzuki, Hiroko;
Hosono, Katsuhiro;
Hikoya, Akiko;
Komori, Miwa;
Inagaki, Risako;
Haseoka, Takashi;
Arai, Shinji;
Takagi, Yuri;
Hotta, Yoshihiro;
Sato, Miho

Publication type:

Article

Clinical findings of acute acquired comitant esotropia in young patients.

Published in:

Japanese Journal of Ophthalmology, 2022, v. 66, n. 1, p. 87, doi. 10.1007/s10384-021-00879-9

By:

Iimori, Hirohito;
Suzuki, Hiroko;
Komori, Miwa;
Hikoya, Akiko;
Hotta, Yoshihiro;
Sato, Miho

Publication type:

Article

Regional differences in genes and variants causing retinitis pigmentosa in Japan.

Published in:

Japanese Journal of Ophthalmology, 2021, v. 65, n. 3, p. 338, doi. 10.1007/s10384-021-00824-w

By:

Koyanagi, Yoshito;
Akiyama, Masato;
Nishiguchi, Koji M;
Momozawa, Yukihide;
Kamatani, Yoichiro;
Takata, Sadaaki;
Inai, Chihiro;
Iwasaki, Yusuke;
Kumano, Mikako;
Murakami, Yusuke;
Komori, Shiori;
Gao, Dan;
Kurata, Kentaro;
Hosono, Katsuhiro;
Ueno, Shinji;
Hotta, Yoshihiro;
Murakami, Akira;
Terasaki, Hiroko;
Wada, Yuko;
Nakazawa, Toru

Publication type:

Article

Usefulness of handheld electroretinogram system for diagnosing blue-cone monochromatism in children.

Published in:

Japanese Journal of Ophthalmology, 2021, v. 65, n. 1, p. 23, doi. 10.1007/s10384-020-00782-9

By:

Haseoka, Takashi;
Inagaki, Risako;
Kurata, Kentaro;
Arai, Shinji;
Takagi, Yuri;
Suzuki, Hiroko;
Hikoya, Akiko;
Nishimura, Kasumi;
Hotta, Yoshihiro;
Sato, Miho

Publication type:

Article

Changes in conjunctival-scleral thickness after strabismus surgery measured with anterior segment optical coherence tomography.

Published in:

Japanese Journal of Ophthalmology, 2018, v. 62, n. 5, p. 554, doi. 10.1007/s10384-018-0609-2

By:

Suzuki, Hiroko;
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Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-29891-9

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