Detalhe da pesquisa
1.
Sex Differences in Transthyretin Cardiac Amyloidosis: Unraveling the Complexities in Epidemiology, Pathophysiology, Diagnosis, and Treatment.
Curr Heart Fail Rep
; 2024 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38775878
2.
Epicardial ablation for ventricular tachycardia in Freidreich's ataxia cardiomyopathy.
Europace
; 21(7): 1095, 2019 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30879060
3.
Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives.
J Am Coll Cardiol
; 83(17): 1640-1651, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38658103
4.
Phenotype and clinical outcomes of Glu89Lys hereditary transthyretin amyloidosis: a new endemic variant in Spain.
Amyloid
; 30(2): 199-207, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36343383
5.
Late gadolinium enhancement distribution patterns in non-ischaemic dilated cardiomyopathy: genotype-phenotype correlation.
Eur Heart J Cardiovasc Imaging
; 25(1): 75-85, 2023 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37562008
6.
Combination of late gadolinium enhancement and genotype improves prediction of prognosis in non-ischaemic dilated cardiomyopathy.
Eur J Heart Fail
; 24(7): 1183-1196, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35485241
7.
Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy.
J Am Coll Cardiol
; 80(12): 1115-1126, 2022 09 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36109106
8.
Founder mutation in myosin-binding protein C with an early onset and a high penetrance in males.
Open Heart
; 8(2)2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34588271
9.
Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy.
J Am Coll Cardiol
; 78(17): 1682-1699, 2021 10 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34674813
10.
Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry.
Rev Esp Cardiol (Engl Ed)
; 74(3): 216-224, 2021 Mar.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-32616434
11.
Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis.
J Am Coll Cardiol
; 76(2): 186-197, 2020 07 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-32646569
12.
Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker.
Orphanet J Rare Dis
; 14(1): 170, 2019 07 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31286959
13.
Role of copy number variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practice.
Eur J Hum Genet
; 26(7): 1014-1025, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29511324
14.
The Functional Significance of Paradoxical Low-Gradient Aortic Valve Stenosis: Hemodynamic Findings During Cardiopulmonary Exercise Testing.
JACC Cardiovasc Imaging
; 10(1): 29-39, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27568118
15.
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.
PLoS One
; 12(8): e0181465, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28771489
16.
Permanent atrioventricular block after flecainide testing.
Rev Esp Cardiol (Engl Ed)
; 73(2): 177-178, 2020 Feb.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-31631050
17.
Long-Term LV Characterization Using CMR in Patients With Spontaneous Coronary Artery Dissection.
JACC Cardiovasc Imaging
; 13(6): 1441-1442, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32061560