Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ángeles Yahel Hernández-Vázquez"'
Autor:
Mauricio Bayram-Suverza, Karla Alejandra Torres-Navarro, Ángeles Yahel Hernández-Vázquez, Juan Abel Ramírez-Estudillo
Publikováno v:
Diagnostics, Vol 13, Iss 15, p 2588 (2023)
Microcephaly and chorioretinopathy are genetic disorders that are inherited in an autosomal recessive manner. The most frequent ocular manifestation is the presence of lacunar atrophy in the retina and choroid. The diagnosis of this condition can be
Externí odkaz:
https://doaj.org/article/3c1e9d2755334950932cfd3af240f2be
Publikováno v:
Gaceta Médica de México. 153
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf27f41ed29304d5cd36a2114372c460
https://doi.org/10.24875/gmm.m18000099
https://doi.org/10.24875/gmm.m18000099
Maculopatía intermedia paracentral aguda asociada a asas vasculares prepapilares. Reporte de un caso
Autor:
Abel Ramirez-Estudillo, Sergio Rojas-Juárez, Ángeles Yahel Hernández-Vázquez, Jorge Arturo Sánchez-Ramos, Benito Celis-Suazo, Carla Rocío Pérez-Montaño
Publikováno v:
Revista Mexicana de Oftalmología. 96
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9188c083c9e44da7e62b185fffbffba7
https://doi.org/10.24875/rmo.m21000168
https://doi.org/10.24875/rmo.m21000168
Autor:
Ezequiel Díaz-Benítez, Jorge Arturo Sánchez-Ramos, Carla Rocío Pérez-Montaño, Juan Abel Ramírez-Estudillo, Fernando Zavaleta-Herrera, Sergio Rojas-Juárez, Ángeles Yahel Hernández-Vázquez
Publikováno v:
Revista Mexicana de Oftalmología (English Edition). 93
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f06c500635a15b85f73a4422eab8cb70
https://doi.org/10.24875/rmoe.m19000067
https://doi.org/10.24875/rmoe.m19000067
Autor:
Ángeles Yahel Hernández-Vázquez, Jorge Arturo Sánchez-Ramos, Abel Ramirez-Estudillo, Fernando Del Valle-Nava, Gerardo González-Saldivar
Publikováno v:
Clinical Case Reports
Key Clinical Message Posterior polar annular choroidal dystrophy (PPACD) is an uncommon retinal dystrophy causing nyctalopia. PPACD has been characteristically described as a foveal sparing dystrophy. We report the first case with cystoid macular ede
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::702dd50eeaf9f01355053a2cee3073b4
https://pubmed.ncbi.nlm.nih.gov/30847215
https://pubmed.ncbi.nlm.nih.gov/30847215
Publikováno v:
Gaceta de M�xico. 153
Leber congenital amaurosis is a retinal dystrophy with several forms of presentation due to its genetic variability. Case of a female girl followed up from 4 to 11 years old is presented, with positive clinical data of nyctalopia, myopia and choroid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ef02cf963fccbc913935ddba87e045a
https://doi.org/10.24875/gmm.17002945
https://doi.org/10.24875/gmm.17002945
Autor:
Ezequiel Díaz Benítez, Juan Abel Ramírez Estudillo, Jorge Arturo Sánchez Ramos, Sergio Rojas Juárez, Fernando Zavaleta Herrera, Carla Rocío Pérez Montaño, Ángeles Yahel Hernández Vázquez
Publikováno v:
Revista Mexicana de Oftalmología. 93
Resumen Caso clinico Se trata de un paciente masculino de 19 anos con paresia bilateral del musculo recto externo secundario a un traumatismo craneoencefalico. Durante su tratamiento se produjo una inyeccion intraocular inadvertida de toxina botulini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95daec40609a65a3f715228072f3fa51
https://doi.org/10.1016/j.mexoft.2017.05.004
https://doi.org/10.1016/j.mexoft.2017.05.004