Zobrazeno 1 - 10
of 916
pro vyhledávání: '"Ripoll, Vera"'
Publikováno v:
Medicina Clínica Práctica, Vol 7, Iss 4, Pp 100450- (2024)
Externí odkaz:
https://doaj.org/article/ac0349074bf7423f9f6c08b11d775ce7
Autor:
Ochoa, Juan Pablo, Espinosa, Maria Ángeles, Gayan-Ordas, Jara, Fernández-Valledor, Andrea, Gallego-Delgado, María, Tirón, Coloma, Lozano-Ibañez, Adrián, García-Pinilla, José Manuel, Rodríguez-Palomares, José F., Larrañaga-Moreira, José María, Llamas-Gómez, Helena, Ripoll-Vera, Tomas, Braza-Boïls, Aitana, Vilches, Silvia, Méndez, Irene, Bascompte-Claret, Ramón, García-Álvarez, Ana, Villacorta, Eduardo, Fernandez-Lozano, Ignacio, Lara-Pezzi, Enrique, Garcia-Pavia, Pablo
Publikováno v:
In JACC: Clinical Electrophysiology October 2024 10(10):2250-2260
Autor:
García-Izquierdo, Eusebio, Scrocco, Chiara, Palacios-Rubio, Julián, Assaf, Amira, Ripoll-Vera, Tomás, Hernandez-Betancor, Iván, Ramos-Ruiz, Pablo, Melero-Pita, Antonio, Segura-Domínguez, Melodie, Jiménez-Sánchez, Diego, Castro-Urda, Victor, Toquero-Ramos, Jorge, Yap, Sing-Chien, Behr, Elijah R., Fernández-Lozano, Ignacio
Publikováno v:
In Heart Rhythm August 2024 21(8):1317-1324
Autor:
Viana Tejedor, Ana, Ripoll-Vera, Tomás, Bravo Amaro, María Sol, Ariza-Solé, Albert, Sandín Rollán, Miriam, Vivas Balcones, David, Romero Rodríguez, Nieves, Fernández Olmo, María Rosa
Publikováno v:
In REC: CardioClinics July-September 2024 59(3):201-211
Autor:
Aina Gayà-Barroso, Juan González-Moreno, Adrián Rodríguez, Tomás Ripoll-Vera, Inés Losada-López, Margarita Gili, Milena Paneque, Sara Pérez-Martínez, Eugenia Cisneros-Barroso
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Background Hereditary transthyretin amyloidosis (ATTRv) is a rare genetic disease that negatively affects patients' quality of life through the involvement of various organs and tissues. Despite a large amount of research on medical and psyc
Externí odkaz:
https://doaj.org/article/7ecaeaeaa59e4f45be8fb91e15e07268
Autor:
E. Cisneros-Barroso, F. Gorram, M. A. Ribot-Sansó, F. Alarcon, G. Nuel, J. González-Moreno, A. Rodríguez, J. Hernandez-Rodriguez, E. Amengual-Cladera, I. Martínez-López, T. Ripoll-Vera, I. Losada-López, D. Heine-Suñer, V. Plante-Bordeneuve
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-7 (2023)
Abstract Background Variant transthyretin amyloidosis (A-ATTRv) is an autosomal dominant disease caused by a range of TTR gene variants which entail great phenotypical heterogeneity and penetrance. In Majorca, the A-ATTRv caused by the V30M gene vari
Externí odkaz:
https://doaj.org/article/3501c5edd17945e8bf02f9ed4ad5383c
Autor:
Rocío Blanco, Yolanda Rico-Ramírez, Álvaro Hermida-Ameijeiras, Israa Mahmoud Sanad Abdullah, Kolja Lau, Jorge Alvarez-Rubio, Elena Fortuny, Amparo Martínez-Monzonís, Albina Nowak, Peter Nordbeck, Carlos Veras-Burgos, Jaume Pons-Llinares, Emiliano Rossi, Fiama Caimi-Martínez, Teresa Bosch-Rovira, Marta Alamar-Cervera, Virginia Ruiz-Pizarro, Laura Torres-Juan, Damian Heine-Suñer, Tomás Ripoll-Vera
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 8, p 4299 (2024)
The p.Arg301Gln variant in the α -galactosidase A gene (GLA) has been poorly described in the literature. The few reports show controversial information, with both classical and nonclassical Anderson–Fabry Disease (AFD) presentation patterns. The
Externí odkaz:
https://doaj.org/article/2f0e8a45e1a5487b9b0ecaab22b81f0c
Autor:
Rosario Sánchez, Tomás Ripoll-Vera, Manuel López-Mendoza, Joaquín de Juan-Ribera, Juan Ramón Gimeno, Álvaro Hermida, María Aurora Ruz-Zafra, José Vicente Torregrosa, Antonia Mora, José Manuel García-Pinilla, Elena Fortuny, Ana Aguinaga-Barrilero, Roser Torra
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Fabry disease (FD) is an X-linked condition caused by variants in the GLA gene. Since females have two X chromosomes, they were historically thought to be carriers. Although increased knowledge has shown that females often develop
Externí odkaz:
https://doaj.org/article/97d9b7378eee421696d9ada54b59aa94
Autor:
Jiménez-Jáimez, Juan, Villacorta, Eduardo, Zorio-Grima, Esther, Ripoll-Vera, Tomás, Macías-Ruiz, Rosa, Bermúdez-Jiménez, Francisco, Limeres-Freire, Javier
Publikováno v:
In REC: CardioClinics January 2023 58 Supplement 1:S68-S73
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.