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pro vyhledávání: '"Verena Terrado"'
Autor:
Victoria Campuzano, Maria Segura-Puimedon, Verena Terrado, Carolina Sánchez-Rodríguez, Mathilde Coustets, Mauricio Menacho-Márquez, Julián Nevado, Xosé R Bustelo, Uta Francke, Luis A Pérez-Jurado
Publikováno v:
PLoS Genetics, Vol 8, Iss 2, p e1002458 (2012)
A hallmark feature of Williams-Beuren Syndrome (WBS) is a generalized arteriopathy due to elastin deficiency, presenting as stenoses of medium and large arteries and leading to hypertension and other cardiovascular complications. Deletion of a functi
Externí odkaz:
https://doaj.org/article/4199344e2bde496e817d2ba41ec1da8f
Autor:
Uta Francke, Xosé R. Bustelo, Mauricio Menacho-Márquez, Victoria Campuzano, Mathilde Coustets, Carolina Sánchez-Rodríguez, Verena Terrado, Luis A. Pérez-Jurado, Maria Segura-Puimedon, Julián Nevado
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
PLoS Genetics, Vol 8, Iss 2, p e1002458 (2012)
PLoS Genetics
Digital.CSIC. Repositorio Institucional del CSIC
instname
PLoS Genetics, Vol 8, Iss 2, p e1002458 (2012)
PLoS Genetics
Digital.CSIC. Repositorio Institucional del CSIC
This is an open-access article distributed under the terms of the Creative Commons Attribution License.-- et al.
A hallmark feature of Williams-Beuren Syndrome (WBS) is a generalized arteriopathy due to elastin deficiency, presenting as stenoses
A hallmark feature of Williams-Beuren Syndrome (WBS) is a generalized arteriopathy due to elastin deficiency, presenting as stenoses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ae94d3802fdd44a16156f34b157c92e
http://hdl.handle.net/10230/23439
http://hdl.handle.net/10230/23439
Autor:
Serra-Juhé, Clara1,2, Rodríguez-Santiago, Benjamín3, Cuscó, Ivon1,2, Vendrell, Teresa4, Camats, Núria5, Torán, Núria5, Pérez-Jurado, Luis A.1,2 luis.perez@upf.edu
Publikováno v:
PLoS ONE. Oct2012, Vol. 7 Issue 10, Special section p1-9. 9p.
Autor:
Lucena, Jaume1, Pezzi, Susana1, Aso, Ester2, Valero, Maria C.3, Carreiro, Candelas4, Dubus, Pierre5, Sampaio, Adriana6, Segura, Maria1,7, Barthelemy, Isabel4, Zindel, Marc Y.1,7, Sousa, Nuno6, Barbero, José L.8, Maldonado, Rafael2, Pérez-Jurado, Luis A.1,7,9 luis.perez@upf.edu, Campuzano, Victoria1,7 victoria.campuzano@upf.edu
Publikováno v:
BMC Medical Genetics. 2010, Vol. 11, p61-70. 10p.
Autor:
Segura-Puimedon, Maria, Sahún, Ignasi, Velot, Emilie, Dubus, Pierre, Borralleras, Cristina, Rodrigues, Ana J., Valero, María C., Valverde, Olga, Sousa, Nuno, Herault, Yann, Dierssen, Mara, Pérez-Jurado, Luis A., Campuzano, Victoria
Publikováno v:
Human Molecular Genetics; Dec2014, Vol. 23 Issue 24, p6481-6494, 14p