Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jose Verdu-Diaz"'
Autor:
Marcio M Andrade-Campos, Esther Valero-Tena, Jose Verdu-Diaz, Jordi Diaz-Manera, Isidro Arevalo-Vargas, Irene Serrano-Gonzalo, Mercedes Roca-Espiau, Pilar Giraldo
Publikováno v:
Blood. 140:2605-2606
Autor:
Esther Valero-Tena, Mercedes Roca-Espiau, Jose Verdu-Diaz, Jordi Diaz-Manera, Marcio Andrade-Campos, Pilar Giraldo
Publikováno v:
SSRN Electronic Journal.
Autor:
Patricia Piñol-Jurado, José Verdú-Díaz, Esther Fernández-Simón, Cristina Domínguez-González, Aurelio Hernández-Lain, Conor Lawless, Amy Vincent, Alejandro González-Chamorro, Elisa Villalobos, Alexandra Monceau, Zoe Laidler, Priyanka Mehra, James Clark, Andrew Filby, David McDonald, Paul Rushton, Andrew Bowey, Jorge Alonso Pérez, Giorgio Tasca, Chiara Marini-Bettolo, Michela Guglieri, Volker Straub, Xavier Suárez-Calvet, Jordi Díaz-Manera
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract Becker muscular dystrophy (BMD) is characterised by fiber loss and expansion of fibrotic and adipose tissue. Several cells interact locally in what is known as the degenerative niche. We analysed muscle biopsies of controls and BMD patients
Externí odkaz:
https://doaj.org/article/61a0d77c3dfe43de98fb8cb832575a27
Autor:
Xavier Suárez-Calvet, Esther Fernández-Simón, Daniel Natera, Cristina Jou, Patricia Pinol-Jurado, Elisa Villalobos, Carlos Ortez, Alexandra Monceau, Marianela Schiava, Anna Codina, José Verdu-Díaz, James Clark, Zoe Laidler, Priyanka Mehra, Rasya Gokul-Nath, Jorge Alonso-Perez, Chiara Marini-Bettolo, Giorgio Tasca, Volker Straub, Michela Guglieri, Andrés Nascimento, Jordi Diaz-Manera
Publikováno v:
Cell Death and Disease, Vol 14, Iss 9, Pp 1-15 (2023)
Abstract Duchenne muscular dystrophy is a genetic disease produced by mutations in the dystrophin gene characterized by early onset muscle weakness leading to severe and irreversible disability. The cellular and molecular consequences of the lack of
Externí odkaz:
https://doaj.org/article/63d64f9d3e584ca18f038365d5b380e0
Autor:
Esther Valero-Tena, Mercedes Roca-Espiau, Jose Verdú-Díaz, Jordi Diaz-Manera, Marcio Andrade-Campos, Pilar Giraldo
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Gaucher disease (GD) is a genetic lysosomal disorder characterized by high bone marrow (BM) involvement and skeletal complications. The pathophysiology of these complications is not fully elucidated. Magnetic resonance imaging (MRI) is the gold stand
Externí odkaz:
https://doaj.org/article/5fc0534642184290b209e553bb13ca7b