1. Genetic variants as determinants of outcome in lamin A/C-related cardiac disease. (14th October 2021) Authors: Garcia Hernandez, S; Ortiz-Genga, M; Ochoa, J P; Lamounier, A; Fernandez, X; Cardenas, I; Garcia-Giustiniani, D; Brogger, M N; Fernandez, G; Valverde, M; Monserrat, L; McKenna, W J Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Marfan syndrome: genetic variant determinants of cardiovascular outcomes. (14th October 2021) Authors: Brogger, M N; Fernandez Ferro, G; Cardenas Reyes, I; Ochoa, J P; Garcia Hernandez, S; Fernandez, X; Garcia Giustiniani, D; Lamounier, A; Valverde, M; De La Higuera Romero, L; Ortiz Genga, M; Monserrat, L; McKenna, W J Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Narrowing Beta-myosin hot spots in its association with hypertrophic cardiomyopathy. (3rd October 2022) Authors: Garcia Hernandez, S; De La Higuera Romero, L; Fernandez, X; Valverde Gomez, M; Cazon Varela, L; Peteiro Deben, R; Rebolo, P; Sanluis Verdes, A; Cardenas, I; Ortiz-Genga, M; Amor Salamanca, A; Perez Barbeito, M; Gomez Diaz, I; Sanchez Flores, M; Ochoa, J P Journal: European heart journal Issue: Volume 43(2022)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Narrowing of the neonatal region in the FBN1 gene. (14th October 2021) Authors: Brogger, M N; Fernandez Ferro, G; Cardenas Reyes, I; Ochoa, J P; Garcia Hernandez, S; Valverde, M; Fernandez, X; Garcia Giustiniani, D; Lamounier, A; De La Higuera Romero, L; Ortiz Genga, M; Monserrat, L; McKenna, W J Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Natural history of MYH7-related dilated cardiomyopathy. (3rd October 2022) Authors: Frutos Seminario, F; Ochoa, J P; Navarro-Penalver, M; Baas, A; Bjerre, J V; Zorio, E; Mendez, I; Lorca, R; Verdonschot, J A J; Garcia-Granja, P E; Bilinska, Z; Fatkin, D; Fuentes-Canamero, M E; Garcia-Pinilla, J M; Garcia-Pavia, P Journal: European heart journal Issue: Volume 43(2022)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. P3169Clinical characteristics and natural history of dilated cardiomyopathy due to BAG3 mutations. (28th August 2018) Authors: Dominguez Rodriguez, F; Cuenca, S; Bilinska, Z; Toro, R; Charron, P; Barriales-Villa, R; Asselbergs, F; Akhtar, M; Morris Hey, T; Rangel-Sousa, D; Limeres, J M; Garcia-Pinilla, J M; Ochoa, J P; Elliott, P; Garcia-Pavia, P Journal: European heart journal Issue: Volume 39(2018)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Specific actin (ACTC1) missense variants are associated with different overlapping clinical phenotypes and outcomes. (14th October 2021) Authors: Valverde, M; Garcia Hernandez, S; Brogger, M N; Fernandez, G; Cardenas, I; Garcia-Gustiniani, D; Fernandez, X; Lamounier, A; Ochoa, J P; Ortiz-Genga, M; Monserrat, L; McKenna, W Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗