Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Rita Quintas‐Rey"'
Autor:
Héctor Fernández-Susavila, Cristina Mora, Marta Aramburu-Núñez, Rita Quintas-Rey, Susana Arias, Manuel Collado, Esteban López-Arias, Tomás Sobrino, José Castillo, Patrizia Dell'Era, Francisco Campos
Publikováno v:
Stem Cell Research, Vol 28, Iss , Pp 16-20 (2018)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common form of hereditary stroke disorder. It is caused by mutations in NOTCH3 that lead to progressive degeneration of the smooth muscle
Externí odkaz:
https://doaj.org/article/dceba6faaaca488f98d03ab000beae18
Autor:
Mario Pérez‐Sayáns, Cintia M. Chamorro‐Petronacci, Susana B. Bravo, María E. Padín‐Iruegas, Esteban Guitián‐Fernández, Francisco Barros‐Angueira, Rita Quintas‐Rey, Abel García‐García
Publikováno v:
Oral Diseases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5775184ff2cbf9d73d98bbfe62e8a80d
https://doi.org/10.1111/odi.14572
https://doi.org/10.1111/odi.14572
Autor:
Rita Quintas-Rey, Tomás Sobrino, Cristina Mora, Manuel Collado, Patrizia Dell'Era, Esteban López-Arias, Susana Arias, Héctor Fernández-Susavila, Marta Aramburu-Núñez, José Castillo, Francisco Campos
Publikováno v:
Stem Cell Research, Vol 28, Iss, Pp 16-20 (2018)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common form of hereditary stroke disorder. It is caused by mutations in NOTCH3 that lead to progressive degeneration of the smooth muscle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7d4a132cbd26dc0bf47150c09930ae7
https://doi.org/10.1016/j.scr.2018.01.023
https://doi.org/10.1016/j.scr.2018.01.023