Yoshihiro Hotta
Hotta, Yoshihiro, 1967-
堀田, 典裕, 1967-
홋타 요시히로 1967-
堀田, 典裕
VIAF ID: 251579045 (Personal)
Permalink: http://viaf.org/viaf/251579045
Preferred Forms
- 100 1 _ ‡a Hotta, Yoshihiro ‡d 1967-
- 100 1 _ ‡a Hotta, Yoshihiro, ‡d 1967-
- 100 0 _ ‡a Yoshihiro Hotta
- 100 1 _ ‡a 堀田, 典裕
- 100 1 _ ‡a 堀田, 典裕, ‡d 1967-
- 100 1 _ ‡a 홋타 요시히로 ‡d 1967-
4xx's: Alternate Name Forms (16)
Works
Title | Sources |
---|---|
Analysis of IKBKG/NEMO gene in five Japanese cases of incontinentia pigmenti with retinopathy: fine genomic assay of a rare male case with mosaicism | |
Ascorbic acid concentration in rabbit vitreous measured by microdialysis with HPLC-electrochemical detection before and after vitreous surgery. | |
A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation | |
Case of Japanese patient with x-linked ocular albinism associated with GPR143 gene mutation. | |
Diagnosis of Leber's optic neuropathy by means of polymerase chain reaction amplification. | |
Different mutation of the XLRS1 gene causes juvenile retinoschisis with retinal white flecks | |
Enhanced S-cone syndrome with subfoveal neovascularization. | |
Evaluation of Surgical Strategy Based on the Intraoperative Superior Oblique Tendon Traction Test | |
A hemizygous A to CC base change of the CHM gene causing choroideremia associated with pinealoma. | |
Homozygotic patient with betaig-h3 gene mutation in granular dystrophy. | |
Jidōsha to kenchiku : Mōtarizēshon jidai no kankyō dezain | |
Long-Term Clinical Course in a Patient with Complete Congenital Stationary Night Blindness. | |
Long-term follow-up of two sisters with Leber's Hereditary Optic Neuropathy. | |
Long-term observation of a Japanese mucolipidosis IV patient with a novel homozygous p.F313del variant of MCOLN1 | |
Low frequency of oncogenic mutations in the core promoter region of the RB1 gene | |
Missense mutations in the PAX6 gene in aniridia | |
Molecular genetics of ornithine aminotransferase defect in gyrate atrophy | |
Novel biallelic splice-site BBS1 variants in Bardet-Biedle syndrome: a case report of the first Japanese patient | |
Novel GUCY2D Gene Mutations in Japanese Male Twins with Leber Congenital Amaurosis. | |
Novel HPS6 mutations identified by whole-exome sequencing in two Japanese sisters with suspected ocular albinism | |
Novel mutations in the OPA1 gene and associated clinical features in Japanese patients with optic atrophy | |
Novel OPN1LW/OPN1MW deletion mutations in 2 Japanese families with blue cone monochromacy. | |
Novel RDH5 mutation in family with mother having fundus albipunctatus and three children with retinitis pigmentosa. | |
Paraoxonase 1 gene polymorphisms influence clinical features of open-angle glaucoma | |
Q118X mutation of M1S1 gene caused gelatinous drop-like corneal dystrophy: the P501T of BIGH3 gene found in a family with gelatinous drop-like corneal dystrophy | |
Sanrin toshi : Kurotani ryotaro no shiso to sono tenkai. | |
Six different mutations of TGFBI (betaig-h3, keratoepithelin) gene found in Japanese corneal dystrophies | |
Toyota kōdō to furukawa toshokan : Nagoya daigaku no kifu tatemono | |
Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population | |
Visual function in retinitis pigmentosa related to a codon 15 rhodopsin gene mutation | |
Visual impairment and REP-1 gene mutations in Japanese choroideremia patients | |
Visual Outcomes in Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations. | |
X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers | |
Yoshida hatsusaburō no chōkanzu o yomu : Egakareta kindai nihon no fūkei | |
「モータウン」のデザイン | |
豊田講堂と古川図書館 : 名古屋大学の寄付建物 | |
吉田初三郎の鳥瞰図を読む : 描かれた近代日本の風景 | |
〈山林都市〉 : 黒谷了太郎の思想とその展開 | |
自動車と建築 : モータリゼーション時代の環境デザイン | |
近代名古屋における郊外住宅地開発に関する史的研究 | |
都市創作 |