Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sachiko Kuroiwa"'
Autor:
Nagahisa Yoshimura, Hitomi Hiratani, Marion Monet, Sachiko Kuroiwa, Sachiko Toyoda, Shohei Chida, Fumihiko Matsuda, Atsushi Otani, Victor Renault, Norimoto Gotoh, Michiko Mandai, Ryo Yamada
Publikováno v:
Human Genetics. 120:139-143
Age-related macular degeneration (ARMD) is the leading cause of blindness in the elderly population not only Western but also Asian industrial countries. In Caucasian, a polymorphism of the complement factor H gene (CFH), the C allele of rs1061170 (Y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73310268dead1bb29972f90a45ec67ba
https://doi.org/10.1007/s00439-006-0187-0
https://doi.org/10.1007/s00439-006-0187-0
Autor:
Norimoto Gotoh, Satoko Arai, Nagahisa Yoshimura, Sachiko Kuroiwa, Noriko Yoshida, Takanobu Kikuchi, Jun Arai
Publikováno v:
American Journal of Ophthalmology. 138:567-573
Purpose To study the genotypes, allelic frequencies, and polymorphisms of apolipoprotein E (Apo E) in unrelated Japanese patients with polypoidal choroidal vasculopathy (PCV) or exudative age-related macular degeneration (AMD) and control subjects wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::540c21da7f2da34243982b82751a96ad
https://doi.org/10.1016/j.ajo.2004.05.025
https://doi.org/10.1016/j.ajo.2004.05.025
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 240:354-361
To report characteristics of polypoidal choroidal vasculopathy (PCV) of large vascular networks that expand across the retinal vascular arcade.Among 60 consecutive eyes diagnosed as having PCV by fluorescein and indocyanine green (ICG) angiography, 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8c8b0a3c0b8c0ea9de940ef72eb3bef
https://doi.org/10.1007/s00417-002-0459-x
https://doi.org/10.1007/s00417-002-0459-x
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 239:66-68
Background: Heterozygous mutations of the bestrophin gene are associated with Best macular dystrophy (BMD). The bestrophin gene is specifically expressed in the retinal pigment epithelium. BMD is a hereditary form of macular degeneration that may dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffd78e52a1b8fe74ef5cf94db46fba20
https://doi.org/10.1007/pl00007900
https://doi.org/10.1007/pl00007900
Publikováno v:
Clinicalexperimental ophthalmology. 32(3)
The histopathological features are reported of surgically excised specimens from five patients with polypoidal choroidal vasculopathy, which had been diagnosed by indocyanine green angiography. On stereomicroscopy, four of the five cases demonstrated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e174788e5613c9426c7836ba225239ce
https://pubmed.ncbi.nlm.nih.gov/15180844
https://pubmed.ncbi.nlm.nih.gov/15180844
Publikováno v:
Retina (Philadelphia, Pa.). 23(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1b6c493333f9b18e17e05c7c62d3d36
https://pubmed.ncbi.nlm.nih.gov/12824852
https://pubmed.ncbi.nlm.nih.gov/12824852
Autor:
Hiroto, Shibuki, Naomichi, Katai, Sachiko, Kuroiwa, Toru, Kurokawa, Jun, Arai, Kunio, Matsumoto, Toshikazu, Nakamura, Nagahisa, Yoshimura
Publikováno v:
Investigative ophthalmologyvisual science. 43(2)
To investigate the expression and possible neuroprotective effects of hepatocyte growth factor (HGF) in a rat model of retinal ischemia-reperfusion injury.Retinal ischemia was induced in adult male Sprague-Dawley rats by raising the intraocular press
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4d048c6280054cb5801e7c1ef2e3b2f8
https://pubmed.ncbi.nlm.nih.gov/11818401
https://pubmed.ncbi.nlm.nih.gov/11818401
Publikováno v:
American journal of ophthalmology. 130(5)
PURPOSE: To report a novel compound heterozygous mutation in the 11-cis retinol dehydrogenase (RDH5) gene in a patient with fundus albipunctatus. METHOD: We examined the RDH5 gene genotype in members of a Japanese family. Clinical examination showed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdccfd3b3749f3954a8bb3866c2a3669
https://pubmed.ncbi.nlm.nih.gov/11078852
https://pubmed.ncbi.nlm.nih.gov/11078852
Publikováno v:
The British journal of ophthalmology. 83(5)
AIM To determine whether mutations in the Stargardt’s disease gene, ATP binding cassette transporter retina (ABCR) affect the occurrence of age related macular degeneration (AMD) in Japanese non-familial patients. METHODS 80 unrelated Japanese pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c99c468fe61d79e1036ab3e274361153
https://pubmed.ncbi.nlm.nih.gov/10216065
https://pubmed.ncbi.nlm.nih.gov/10216065
Publikováno v:
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. 235(7)
• Background: Cytopathological examinations have been used in the diagnosis of intraocular lymphoma. However, sometimes it is not easy to detect malignant cells in the biopsy specimens. We applied a method that identified monoclonal proliferation o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffec3a7cfea2c1c20640afa31c4542a2
https://pubmed.ncbi.nlm.nih.gov/9248839
https://pubmed.ncbi.nlm.nih.gov/9248839