Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Vitor K. L. Takahashi"'
Autor:
Vitor K. L. Takahashi, Christine L. Xu, Júlia T. Takiuti, Mary Ben L. Apatoff, Jimmy K. Duong, Vinit B. Mahajan, Stephen H. Tsang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Background To evaluate and compare the progression of ciliopathy and non-ciliopathy autosomal recessive Retinitis Pigmentosa patients (arRP) by measuring the constriction of hyperautofluorescent rings in fundus autofluorescence (FAF) images
Externí odkaz:
https://doaj.org/article/d8d7f428d28a4c898d76ce6a94f0c1c6
Autor:
Vitor K. L. Takahashi, Ruben Jauregui, Júlia T. Takiuti, Stephen H. Tsang, Jose Ronaldo Lima de Carvalho, Xuan Cui, Karen Sophia Park
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-7 (2019)
Scientific Reports
Scientific Reports
We analyze disease progression in retinitis pigmentosa (RP) according to mode of inheritance by quantifying the progressive decrease of the ellipsoid zone (EZ) line width on spectral domain optical coherence tomography (SD-OCT) and of the dimensions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57ba3619321f80906dae480472af11a3
http://link.springer.com/article/10.1038/s41598-019-47251-z
http://link.springer.com/article/10.1038/s41598-019-47251-z
Autor:
Luiz H. Lima, Stephen H. Tsang, Ruben Jauregui, Vitor K. L. Takahashi, Jimmy Duong, Júlia T. Takiuti, Christine L. Xu
Publikováno v:
Graefes Arch Clin Exp Ophthalmol
OBJECTIVE: To evaluate and compare the B-scan OCT loss of ellipsoid zone, OCT en face thickness map constriction, and hyperautofluorescent ring constriction in RP patients. METHODS: Retrospective case series study. Forty-eight eyes of 24 RP patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7ffaf49165491b294fcfdd90bd9bdf9
https://doi.org/10.1007/s00417-019-04265-7
https://doi.org/10.1007/s00417-019-04265-7
Publikováno v:
Expert Review of Ophthalmology. 13:321-327
Introduction: Retinal degenerative disorders affect patients of all age groups and cause devastating, irreversible vision loss. To date there is no effective treatment capable of restoring retinal ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13e9e532de519011c6991d639c758881
https://doi.org/10.1080/17469899.2018.1555034
https://doi.org/10.1080/17469899.2018.1555034
Publikováno v:
American Journal of Ophthalmology. 195:176-180
Purpose To determine rate of bone spicule pigmentation appearance in patients with retinitis pigmentosa (RP). Design Retrospective, observational case series. Participants A total of 240 patients were analyzed for this study. Methods A retrospective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7356793889e218b828f33cbf0483aa1
https://doi.org/10.1016/j.ajo.2018.07.036
https://doi.org/10.1016/j.ajo.2018.07.036
Publikováno v:
Ophthalmic Genet
Autoimmune retinopathy (AIR) is a rare inflammatory condition characterized by progressive visual loss, abnormalities in visual fields and electroretinographic exams, along with presence of circulating anti-retinal antibodies. There are two main form
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23016dfb4c24f40f9cf4de20b9f95951
https://europepmc.org/articles/PMC6774818/
https://europepmc.org/articles/PMC6774818/
Publikováno v:
Ophthalmic genetics. 39(5)
To evaluate the progression of retinitis pigmentosa (RP) caused by mutations in either PDE6A or PDE6B by measuring the progressive constriction of the hyperautofluorescent ring and shortening of the ellipsoid zone (EZ)-line width.Fundus autofluoresce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::989d38cad97ced8bafc93674e2e0eab8
https://pubmed.ncbi.nlm.nih.gov/30153077
https://pubmed.ncbi.nlm.nih.gov/30153077
Autor:
Jose R. L. Carvalho-Jr, Stephen H. Tsang, Júlia T. Takiuti, Vinit B. Mahajan, Christine L. Xu, Jimmy Duong, Vitor K. L. Takahashi
Publikováno v:
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. 257(4)
To evaluate the progression of retinitis pigmentosa (RP) due to mutations in rhodopsin (RHO) by measuring the short-wavelength autofluorescence (SW-AF) increased autofluorescence ring and ellipsoid zone (EZ)-line width. Fundus autofluorescence (FAF)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2df112bfed6f42f4fe6776208d623bb
https://pubmed.ncbi.nlm.nih.gov/30635721
https://pubmed.ncbi.nlm.nih.gov/30635721
Publikováno v:
Ophthalmic genetics. 39(5)
Hereditary diseases of the retina represent a group of diseases with several heterogeneous mutations that have the common end result of progressive photoreceptor death leading to blindness. Retinal degenerations encompass multifactorial diseases such
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1181497b4b3cba687df27c73cf3b79da
https://pubmed.ncbi.nlm.nih.gov/30040511
https://pubmed.ncbi.nlm.nih.gov/30040511
Autor:
Vinit B. Mahajan, Júlia T. Takiuti, Stephen H. Tsang, Vitor K. L. Takahashi, Ruben Jauregui, Alexander G. Bassuk, Galaxy Y. Cho
Publikováno v:
Asia-Pacific journal of ophthalmology (Philadelphia, Pa.). 7(3)
Inherited retinal diseases (IRDs) are a major cause of incurable familial blindness in the Western world. In the pediatric population, IRDs are a major contributor to the 19 million children worldwide with visual impairment. Unfortunately, the road t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91c6f1fb93899c3612dce7be4de7802e
https://pubmed.ncbi.nlm.nih.gov/29536675
https://pubmed.ncbi.nlm.nih.gov/29536675