Search Results - "Gimeno, J.R"

Genetics of hypertrophic cardiomyopathy: A review of current state by Sabater‐Molina, M., Pérez‐Sánchez, I., Hernández del Rincón, J.P., Gimeno, J.R.

“…Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disease. HCM is a highly complex and heterogeneous disease regarding not only the…”
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Mutation in JPH2 cause dilated cardiomyopathy by Sabater-Molina, M., Navarro, M., García-Molina Sáez, E., Garrido, I., Pascual-Figal, D., González Carrillo, J., Gimeno Blanes, J.R.

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High prevalence of familial and genetic disease in children with cardiomyopathies: baseline paediatric data from the ESC EORP Cardiomyopathy and Myocarditis registry by Kaski, J.P, Maggioni, A.G, Charron, P, Elliott, P.M, Gimeno, J.R, Laroche, C, Tavazzi, L, Tendera, M, Caforio, A

“…Abstract Background Previous studies on paediatric cardiomyopathies have provided useful information on their epidemiology and clinical presentation but have…”
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Long term outcomes in left ventricular non-compaction by Casas, G, Oristrell, G, Limeres, J, Gutierrez Garcia-Moreno, L, Barriales, R, Garcia-Pavia, P, Zorio, E, Gimeno, J.R, Villacorta, E, Jimenez-Jaimez, J, Ripoll, T, Bayes, A, Diez, C, Ferreira, I, Rodriguez-Palomares, J.F

“…Abstract Background Left ventricular non-compaction (LVNC) is a highly heterogeneous entity with a wide phenotypic expression. Risk factors have not been well…”
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P4521Comparative prevalence and diagnostic yield of family screening in inherited cardiac diseases. 10K single centre registry by Lopez Cuenca, D., Olmo, M.C., Castro, F., Hernandez Del Rincon, J.P., Pastor, F., Munoz Esparza, C., Navarro Penalver, M., Santos, J.J., Pastor, A., Nicolas, E., Sabater, M., Perez Nicolas, I., Gimeno, J.R.

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Prevalence of fabry disease in a cohortof 479 unrelated patients with hypertrophic cardiomyopathy by Monserrat, L, Gimeno-Blanes, J.R, Marin-Ortuño, F, González-Cabrero, J, Hermida-Prieto, M, Garcia-Honrubia, A, Perez, I, Fernández, X, de la Morena, G, Paya, E, Yagüe, J, Egido, J

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Pregnancy related complications in women with hypertrophic cardiomyopathy by Thaman, R, Varnava, A, Hamid, M S, Firoozi, S, Sachdev, B, Condon, M, Gimeno, J R, Murphy, R, Elliott, P M, McKenna, W J

“…Objectives: To determine whether pregnancy is well tolerated in hypertrophic cardiomyopathy. Setting: Referral clinic. Design: The study cohort comprised 127…”
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Baseline features and management in adult and pediatric clinically suspected and biopsy-proven myocarditis in the cardiomyopathy and myocarditis long-term EORP registry by Caforio, A, Kaski, J.P, Gimeno Blanes, J.R, Elliott, P.J, Tavazzi, L, Tendera, M, Laroche, C, Gale, C.P, Charron, P.J, Maggioni, A.P

“…Abstract Background The Myocarditis section of the EORP Cardiomyopathy and Myocarditis Long-term Registry is a prospective, observational, multinational…”
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P716Prevalence of left ventricular hypertrabeculation and non-compaction in a CMR series by Gonzalez Carrillo, J., Gimeno-Blanes, J.R., Rodriguez-Sanchez, D., Saura-Espin, D., Sarabia-Tirado, F., Oliva-Sandoval, M.J., Espinosa-Garcia, M.D., Garcia-Navarro, M., De La Morena-Valenzuela, G.

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442 Implantable cardioverter defibrillator therapy in hypertrophic cardiomyopathy. Experience in three Spanish referral centers by Martinez Martinez, J.G., Paya, E., Gimeno, J.R., Monserrat, L., Marin, F., Garc a-Alberola, A., Vald s, M., Castro-Beiras, A.

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Manifestaciones oftalmológicas en la Enfermedad de Fabry: A propósito de 4 casos con actividad deficiente de a-Galactosidasa A by Rodríguez-González-Herrero, M.E., Marín-Sánchez, J.M., Gimeno, J.R., Molero-Izquierdo, C., De-Casas-Fernández, A., Rodríguez-González-Herrero, B., San-Román, I., Lozano, J., De-La-Morena, G., Llovet-Osuna, F.

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Manifestaciones oftalmológicas en la Enfermedad de Fabry: A propósito de 4 casos con actividad deficiente de a-Galactosidasa A by Rodríguez-González-Herrero, M.E., Marín-Sánchez, J.M., Gimeno, J.R., Molero-Izquierdo, C., De-Casas-Fernández, A., Rodríguez-González-Herrero, B., San-Román, I., Lozano, J., De-La-Morena, G., Llovet-Osuna, F.

“…Caso clínico: La enfermedad de Fabry es una enfermedad producida por una alteración en el catabolismo de los glucoesfingolípidos. Se muestran las alteraciones…”
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Progressive left ventricular remodeling in patients with hypertrophic cardiomyopathy and severe left ventricular hypertrophy by Thaman, R., Gimeno, J.R., Reith, S.

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Non-sustained ventricular tachycardia in hypertrophic cardiomyopathy: an independent marker of sudden death risk in young patients by Monserrat, L, Elliott, P.M, Gimeno, J.R, Sharma, S, Penas-Lado, M, McKenna, W.J

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