Search Results - "Garcia Pavia, P"

Retraction: Bmi1 limits dilated cardiomyopathy and heart failure by inhibiting cardiac senescence by Gonzalez-Valdes, I, Hidalgo, I, Bujarrabal, A, Lara-Pezzi, E, Padron-Barthe, L, Garcia-Pavia, P, Gómez-Del Arco, Pablo, Redondo, J M, Ruiz-Cabello, J M, Jimenez-Borreguero, L J, Enriquez, J A, de la Pompa, J L, Hidalgo, A, Gonzalez, S

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Bmi1 limits dilated cardiomyopathy and heart failure by inhibiting cardiac senescence by Gonzalez-Valdes, I., Hidalgo, I., Bujarrabal, A., Lara-Pezzi, E., Padron-Barthe, L., Garcia-Pavia, P., Gómez-del Arco, Pablo, Redondo, J.M., Ruiz-Cabello, J.M., Jimenez-Borreguero, L.J., Enriquez, J.A., de la Pompa, J.L., Hidalgo, A., Gonzalez, S.

“…Dilated cardiomyopathy (DCM) is the most frequent cause of heart failure and the leading indication for heart transplantation. Here we show that epigenetic…”
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The Role of Loss-of-Function Mutations on Death and Development of Rejection in HTX/LTX Patients by van Setten, J, de Jonge, N, Holmes, M.V, Khush, K.K, Sweitzer, N.K, Garcia-Pavia, P, Rossano, J.W, Dries, D.L, Potena, L, Zuckermann, A, Christie, J.D, Wilkes, D.S, Lederer, D, Meyer, K.C, Glanville, A.R, Corris, P, Fisher, A, Palmer, S.M, Belperio, J.A, de Weger, R.A, Otten, H.G, van de Graaf, E.A, Keating, B, Asselbergs, F.W

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Genetic testing of candidate genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia by Campuzano, O, Alcalde, M, Berne, P, Castro, V, Guzzo, G, Iglesias, A, Alonso-Pulpon, L, Garcia-Pavia, P, Brugada, J, Brugada, R

“…Abstract Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a rare cardiac genetic disease characterized by the presence of structural…”
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564 Desmosomal Protein Gene Mutations in Patients with Idiopathic Dilated Cardiomyopathy Undergoing Cardiac Transplantation: A Clinicopathological Study by Garcia-Pavia, P, Segovia, J, Syrris, P, Salas, C, Mirelis, J.G, Gomez-Bueno, M, Vilches, C, Cobo-Marcos, M, Garcia-Cosio Carmena, M.D, Avellana, P, Bornstein, B, Elliott, P.M, Alonso Pulpón, L.A

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392 Genetic Basis of Heart Transplanted Hypertrophic Cardiomyopathy by Garcia-Pavia, P, Segovia, J, Vazquez, M.E, Salas, C, Avellana, P, Gomez-Bueno, M, Gallardo, E, Garcia-Cosio Carmena, M.D, Cobo-Marcos, M, Vilches, C, Garesse, R, Molano, J, Bornstein, B, Alonso Pulpón, L.A

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261: A Novel Primary Graft Failure Risk Score in Heart Transplantation by Segovia, J, Barcelo, J.M, Gomez-Bueno, M, Cobo, M, Garcia-Pavia, P, Mirelis, J, Sufrate, E, Alonso-Pulpon, L

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575: Prognostic Value of Right Ventricular Dysfunction and Pulmonary Artery Hypertension Parameters for Risk Stratification of Patients with Heart Failure by Barcelo, J.M, Segovia, J, Gomez-Bueno, M, Garcia-Pavia, P, Cobo, M, Sufrate, E, Mirelis, J, Alonso-Pulpon, L

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68: Historical Trends of Primary Graft Failure after Heart Transplantation by Gomez-Bueno, M, Barcelo, J.M, Segovia, J, Cobo, M, Mirelis, J, Sufrate, E, Garcia-Pavia, P, Alonso-Pulpon, L

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500: Influence of Reinnervation after Heart Transplantation on Coronary Allograft Vasculopathy and Cardiovascular Death by Segovia, J, Barcelo, J.M, Gomez-Bueno, M, Gallego-Page, J.C, Cobo, M, Mirelis, J, Garcia-Pavia, P, Alonso-Pulpon, L

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340: Coronary Atherosclerosis in Explanted Hearts with Presumed Idiopathic Dilated Cardiomyopathy by Barcelo, J.M, Salas, C, Segovia, J, Gomez-Bueno, M, Garcia-Pavia, P, Cobo, M, Mirelis, J, Alonso-Pulpon, L

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Atrial fibrillation as a prognostic factor for all-cause mortality in patients with transthyretin amyloid cardiomyopathy by Witteles, R, Sultan, M B, Gundapaneni, B, Garcia-Pavia, P

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Single-nucleus RNA sequencing of TMEM43 induced arrhythmogenic cardiomyopathy reveals altered cell compositions and transcriptional states in mice by Lalaguna, L, Lopez-Olaneta, M, Villalba-Orero, M, Garcia-Pavia, P, Lara-Pezzi, E

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Characterization of a new arrhythmogenic cardiomyopathy mouse model due to filamin c haploinsufficiency by Canas, R, Serrano, R, Rubio, B, Ochoa, J P, De La Pompa, J L, Garcia-Pavia, P, Lara-Pezzi, E

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Patients with transthyretin amyloid cardiomyopathy may have preserved, mildly reduced, or reduced ejection fraction by Garcia-Pavia, P, Fine, N, Weissman, N.J, Castano, A, Gundapaneni, B, Sultan, M.B, Shah, S.J

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Tafamidis treatment for transthyretin amyloid cardiomyopathy: results from an open-label, early-access, long-term study extension in an all-comers population by Crespo-Leiro, M G, Hanna, M, Damy, T, Delgado, D, Ebede, B, Angeli, F S, Maurer, M S, Garcia-Pavia, P, Drachman, B M

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Therapeutic potential of wild type TMEM43 overexpression in a mouse model of arrhythmogenic cardiomyopathy type 5 by Lalaguna, L, Lopez-Olaneta, M, Villalba-Orero, M, Rey-Martin, A, Garcia-Pavia, P, Lara-Pezzi, E

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Transthyretin amyloid cardiomyopathy among patients with hypertrophic cardiomyopathy: clinical, cardiac imaging, and electrocardiographic findings from the TTRACK study by Garcia-Pavia, P, Damy, T, Barriales-Villa, R, Piriou, N, Cappelli, F, Munteanu, C, Bahus, C, Keohane, D, Mallaina, P, Elliott, P

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Differential impact of comorbidities and sex on pathophysiological pathways leading to heart failure with preserved ejection fraction by Lara-Pezzi, E, Villalba-Orero, M, Lopez-Olaneta, M, Campos-Olmo, B, Jimenez-Carretero, D, Sanchez-Cabo, F, Camafeita, E, Vazquez, J, Garcia-Pavia, P, Pascual-Figal, D

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Clinical red flags associated with transthyretin amyloid cardiomyopathy in patients with left ventricular hypertrophy: results of the TTRACK study by Damy, T, Garcia-Pavia, P, Piriou, N, Cappelli, F, Barriales-Villa, R, Munteanu, C, Bahus, C, Keohane, D, Mallaina, P, Elliott, P

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