Publicacións nas que colabora con Marisa Crespo Leiro (20)
2024
-
Diagnosing transthyretin amyloidosis in patients with known genetic cardiomyopathies - opportunities and open questions. Response
Revista Espanola de Cardiologia
-
Diagnosis of transthyretin amyloidosis in patients with established cardiomyopathy
Revista Espanola de Cardiologia, Vol. 77, Núm. 4, pp. 347-349
2023
-
Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 Variants
Circulation: Genomic and Precision Medicine, Vol. 16, Núm. 5, pp. 434-441
2021
-
Clinical utility of genetic testing in patients with dilated cardiomyopathy
Medicina Clinica, Vol. 156, Núm. 10, pp. 485-495
-
Determinants of maximal oxygen uptake in patients with heart failure
ESC Heart Failure, Vol. 8, Núm. 3, pp. 2002-2008
-
Dilated cardiomyopathy and mild limb girdle muscular dystrophy caused by the p.Gly424Ser genetic variant in the fukutin gene
Revista Espanola de Cardiologia, Vol. 74, Núm. 11, pp. 987-989
-
Light chain and transthyretin cardiac amyloidosis: Clinical characteristics, natural history and prognostic factors
Medicina Clinica, Vol. 156, Núm. 8, pp. 369-378
-
Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry
Revista Espanola de Cardiologia, Vol. 74, Núm. 3, pp. 216-224
2020
-
Diagnostic and prognostic value of cardiac imaging in amyloidosis
World Journal of Cardiology, Vol. 12, Núm. 12, pp. 599-614
-
Prognostic implications of pathogenic truncating variants in the TTN gene
International Journal of Cardiology, Vol. 316, pp. 180-183
2019
-
Cambio de paradigma en el diagnóstico y tratamiento de la amiloidosis cardiaca por transtirretina
REC: CardioClinics, Vol. 54, Núm. 1, pp. 9-12
-
Classification of Pulmonary Arterial Hypertension by Genetic and Familial Testing
Revista Espanola de Cardiologia, Vol. 72, Núm. 7, pp. 591-593
-
Paradigm shift in the diagnosis and treatment of transthyretin-related cardiac amyloidosis
REC: CardioClinics, Vol. 54, Núm. 1, pp. 9-12
2018
-
The importance of genotype-phenotype correlation in the clinical management of Marfan syndrome
Orphanet Journal of Rare Diseases, Vol. 13, Núm. 1
2017
-
¿Cómo enfrentarse a una sospecha clínica de amiloidosis cardíaca? Un enfoque práctico para el diagnóstico
Cardiocore, Vol. 52, Núm. 1, pp. 27-34
2016
-
Estado serológico frente a Toxoplasma gondii en receptores de trasplante cardiaco: ¿un factor pronóstico independiente?
Revista Espanola de Cardiologia, Vol. 69, Núm. 12, pp. 1160-1166
2015
-
Atlas of the clinical genetics of human dilated cardiomyopathy
European Heart Journal, Vol. 36, Núm. 18, pp. 1123-1135
2004
-
Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations
American Journal of Cardiology, Vol. 94, Núm. 1, pp. 50-54
2003
-
Radiology and Heart Transplant
Radiologia, Vol. 45, Núm. 6, pp. 249-260
2002
-
Familial dilated cardiomyopathy in patients transplanted for idiopathic dilated cardiomyopathy
Revista Espanola de Cardiologia, Vol. 55, Núm. 7, pp. 725-732