Xusto
Fernández Fernández
Universidade da Coruña
La Coruña, EspañaPublicacións en colaboración con investigadores/as de Universidade da Coruña (13)
2022
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Genotype-phenotype correlations in hypertrophic cardiomyopathy: a multicenter study in Portugal and Spain of the TPM1 p.Arg21Leu variant
Revista Espanola de Cardiologia, Vol. 75, Núm. 3, pp. 242-250
2021
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Clinical utility of genetic testing in patients with dilated cardiomyopathy
Medicina Clinica, Vol. 156, Núm. 10, pp. 485-495
2020
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Prognostic implications of pathogenic truncating variants in the TTN gene
International Journal of Cardiology, Vol. 316, pp. 180-183
2016
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Prognostic role of stress echocardiography in hypertrophic cardiomyopathy: The International Stress Echo Registry
International Journal of Cardiology, Vol. 219, pp. 331-338
2015
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Exercise echocardiography and cardiac magnetic resonance imaging to predict outcome in patients with hypertrophic cardiomyopathy
European Heart Journal Cardiovascular Imaging, Vol. 16, Núm. 4, pp. 423-432
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Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain
Heart, Vol. 101, Núm. 13, pp. 1047-1053
2011
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Cardiotrophin-1 plasma levels are associated with the severity of hypertrophy in hypertrophic cardiomyopathy
European Heart Journal, Vol. 32, Núm. 2, pp. 177-183
2010
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Disease: Cardiomyopathy, hypertrophic
Human Genetics
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Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy
BMC Medical Genetics, Vol. 11, Núm. 1
2009
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Mutación en homocigosis en el gen MYBPC3 asociada a fenotipos severos y alto riesgo de muerte súbita en una familia con miocardiopatía hipertrófica
Revista Espanola de Cardiologia, Vol. 62, Núm. 5, pp. 572-575
2008
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Sudden death in a patient with lamin A/C gene mutation and near normal left ventricular systolic function
International Journal of Cardiology, Vol. 126, Núm. 1, pp. 136-137
2007
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Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects
European Heart Journal, Vol. 28, Núm. 16, pp. 1953-1961
2005
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Mutaciones en el fosfolamban en pacientes con miocardiopatía hipertrófica y miocardiopatiía dilatada idiopática
Investigacion Cardiovascular, Vol. 8, Núm. 2, pp. 125-134