Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Cristina Blanco Marchite"'
Publikováno v:
Advances in Ophthalmology Practice and Research, Vol 2, Iss 3, Pp 100076- (2022)
Purpose: To analyse the differences between 30° blue autofluorescence (BAF30), 55° blue autofluorescence (BAF55) and 200° green Ultra-Wide Field autofluorescence (UWF200) imaging to detect retinal displacement (RD) after vitrectomy surgery for rhe
Externí odkaz:
https://doaj.org/article/fa20382b07d044c79d458a8139c0ac28
Autor:
Enrique López-Sánchez, Julio Escribano, Pedro-Pablo Rodríguez-Calvo, Julian Garcia-Feijoo, Luis Fernández-Vega, Cristina Blanco-Marchite, Lydia Álvarez, Miguel Coca-Prados, Mercedes Iñigez-de-Onzoño, Francisco Sánchez-Sánchez, Francisco López-Martínez, Julian Garcia-Sanchez, María-Pilar López-Garrido, Carmen Mendez-Hernandez
Publikováno v:
Investigative ophthalmologyvisual science. 52(11)
To investigate the role of WDR36 and P53 sequence variations in POAG susceptibility.The authors performed a case-control genetic association study in 268 unrelated Spanish patients (POAG1) and 380 control subjects matched for sex, age, and ethnicity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecdedd07ecba637072761706fa39748d
https://pubmed.ncbi.nlm.nih.gov/21931130
https://pubmed.ncbi.nlm.nih.gov/21931130
Autor:
Chaqués-Alepuz, Enrique López-Sánchez, Antonio S. Salinas-Sánchez, Francisco Sánchez-Sánchez, E. Campos-Mollo, María-Pilar López-Garrido, Cristina Blanco-Marchite, Julio Escribano
Publikováno v:
Clinical genetics. 77(1)
Lopez-Garrido M-P, Blanco-Marchite C, Sanchez-Sanchez F, Lopez-Sanchez E, Chaques-Alepuz V, Campos-Mollo E, Salinas-Sanchez AS, Escribano J. Functional analysis of CYP1B1 mutations and association of heterozygous hypomorphic alleles with primary open
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0b8f706bd2620c5d0f0d8cdcbd28dfc
https://pubmed.ncbi.nlm.nih.gov/19793111
https://pubmed.ncbi.nlm.nih.gov/19793111
Autor:
Ezequiel, Campos-Mollo, María-Pilar, López-Garrido, Cristina, Blanco-Marchite, Julián, Garcia-Feijoo, Jesús, Peralta, José, Belmonte-Martínez, Carmen, Ayuso, Julio, Escribano
Publikováno v:
Molecular Vision
Purpose To analyze the contributions of cytochrome P4501B1 (CYP1B1) mutations to primary congenital glaucoma (PCG) in Spanish patients. Methods We analyzed, by polymerase chain reaction (PCR) DNA sequencing, the presence of promoter (−1 to −867)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::de731d4973135df08eb48a85cc2d3897
https://pubmed.ncbi.nlm.nih.gov/19234632
https://pubmed.ncbi.nlm.nih.gov/19234632
Autor:
Cristina, Blanco-Marchite, Francisco, Sánchez-Sánchez, Enrique, López-Sánchez, Julio, Escribano
Publikováno v:
Molecular vision. 13
Mutations in the transforming growth factor beta I (TGFBI) gene cause several types of autosomal-dominant corneal dystrophies. We investigated the role of this gene in two Spanish families affected by lattice type I or granular type I corneal dystrop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3f51e5f8c9c203ccf55d4e110bcaa50b
https://pubmed.ncbi.nlm.nih.gov/17768377
https://pubmed.ncbi.nlm.nih.gov/17768377
Autor:
María-Pilar, López-Garrido, Francisco, Sánchez-Sánchez, Francisco, López-Martínez, José-Daniel, Aroca-Aguilar, Cristina, Blanco-Marchite, Miguel, Coca-Prados, Julio, Escribano
Publikováno v:
Molecular vision. 12
To investigate CYP1B1 gene mutations in Spanish patients with ocular hypertension (OHT) or primary open angle glaucoma (POAG).The two coding exons of CYP1B1 were screened for sequence alterations by direct PCR DNA sequencing in 37 and 82 unrelated Sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::13c61f1734429e33cafc06ca2f0b3104
https://pubmed.ncbi.nlm.nih.gov/16862072
https://pubmed.ncbi.nlm.nih.gov/16862072