Zobrazeno 1 - 4
of 4
pro vyhledávání: '"F. David Carmona"'
Autor:
Miriam Cerván-Martín, Lara Bossini-Castillo, Andrea Guzmán-Jimenez, Rocío Rivera-Egea, Nicolás Garrido, Saturnino Luján, Gema Romeu, Samuel Santos-Ribeiro, IVIRMA Group, Lisbon Clinical Group, José A. Castilla, M. Carmen Gonzalvo, Ana Clavero, F. Javier Vicente, Vicente Maldonado, Sara González-Muñoz, Inmaculada Rodríguez-Martín, Miguel Burgos, Rafael Jiménez, Maria Graça Pinto, Isabel Pereira, Joaquim Nunes, Josvany Sánchez-Curbelo, Olga López-Rodrigo, Iris Pereira-Caetano, Patricia Isabel Marques, Filipa Carvalho, Alberto Barros, Lluís Bassas, Susana Seixas, João Gonçalves, Sara Larriba, Alexandra M. Lopes, F. David Carmona, Rogelio J. Palomino-Morales
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 6, p 932 (2022)
We aimed to analyze the role of the common genetic variants located in the PIN1 locus, a relevant prolyl isomerase required to control the proliferation of spermatogonial stem cells and the integrity of the blood–testis barrier, in the genetic risk
Externí odkaz:
https://doaj.org/article/7a24ea05e5c342a682a99a88c7c0494e
Autor:
Sofía Aguilar-Lacasaña, Inmaculada López-Flores, Beatriz González-Alzaga, María José Giménez-Asensio, F. David Carmona, Antonio F. Hernández, María Felicidad López Gallego, Desirée Romero-Molina, Marina Lacasaña
Publikováno v:
Nutrients, Vol 13, Iss 3, p 831 (2021)
Identification of causal factors that influence fetal growth and anthropometry at birth is of great importance as they provide information about increased risk of disease throughout life. The association between maternal genetic polymorphism MTHFR(67
Externí odkaz:
https://doaj.org/article/dd3f9127185b4932a7f780a7dc5fdf6b
Autor:
Miriam Cerván-Martín, Lara Bossini-Castillo, Rocío Rivera-Egea, Nicolás Garrido, Saturnino Luján, Gema Romeu, Samuel Santos-Ribeiro, IVIRMA Group, Lisbon Clinical Group, José A. Castilla, M. Carmen Gonzalvo, Ana Clavero, F. Javier Vicente, Andrea Guzmán-Jiménez, Cláudia Costa, Inés Llinares-Burguet, Chiranan Khantham, Miguel Burgos, Francisco J. Barrionuevo, Rafael Jiménez, Josvany Sánchez-Curbelo, Olga López-Rodrigo, M. Fernanda Peraza, Iris Pereira-Caetano, Patricia I. Marques, Filipa Carvalho, Alberto Barros, Lluís Bassas, Susana Seixas, João Gonçalves, Sara Larriba, Alexandra M. Lopes, Rogelio J. Palomino-Morales, F. David Carmona
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 1, p 22 (2020)
Infertility is a growing concern in developed societies. Two extreme phenotypes of male infertility are non-obstructive azoospermia (NOA) and severe oligospermia (SO), which are characterized by severe spermatogenic failure (SpF). We designed a genet
Externí odkaz:
https://doaj.org/article/fd7d40a1efd048c4a5f1825a040635eb
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 2, p 300 (2020)
Nonobstructive azoospermia (NOA) represents the most severe expression of male infertility, involving around 1% of the male population and 10% of infertile men. This condition is characterised by the inability of the testis to produce sperm cells, an
Externí odkaz:
https://doaj.org/article/b87135c578b4497791a16bab7dfac63b