Detalhe da pesquisa
1.
Electrocardiogram Changes in the Spectrum of TTNtv Dilated Cardiomyopathy: Accuracy and Predictive Value of a New Index for LV-Changes Identification.
Heart Lung Circ
; 30(10): 1487-1495, 2021 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-33994281
2.
Potential Molecular Pathways Related to Pulmonary Artery Aneurysm Development: Lessons to Learn from the Aorta.
Int J Mol Sci
; 21(7)2020 04 04.
Artigo
Inglês
| MEDLINE | ID: mdl-32260370
3.
Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot.
BMC Genet
; 14: 57, 2013 Jun 19.
Artigo
Inglês
| MEDLINE | ID: mdl-23782575
4.
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
Inglês
| MEDLINE | ID: mdl-37562008
5.
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
Inglês
| MEDLINE | ID: mdl-35485241
6.
Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy.
J Am Coll Cardiol
; 80(12): 1115-1126, 2022 09 20.
Artigo
Inglês
| MEDLINE | ID: mdl-36109106
7.
Genotype-phenotype correlations in hypertrophic cardiomyopathy: a multicenter study in Portugal and Spain of the TPM1 p.Arg21Leu variant.
Rev Esp Cardiol (Engl Ed)
; 75(3): 242-250, 2022 Mar.
Artigo
Inglês, Espanhol
| MEDLINE | ID: mdl-33642254
8.
Natural History of MYH7-Related Dilated Cardiomyopathy.
J Am Coll Cardiol
; 80(15): 1447-1461, 2022 10 11.
Artigo
Inglês
| MEDLINE | ID: mdl-36007715
9.
Screening of Fabry Disease in Patients with Chest Pain Without Obstructive Coronary Artery Disease.
J Cardiovasc Transl Res
; 14(5): 948-950, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-33474682
10.
Clinical utility of genetic testing in patients with dilated cardiomyopathy. / Utilidad clínica del estudio genético en pacientes con miocardiopatía dilatada.
Med Clin (Barc)
; 156(10): 485-495, 2021 05 21.
Artigo
Inglês, Espanhol
| MEDLINE | ID: mdl-32826072
11.
Novel Genetic and Molecular Pathways in Pulmonary Arterial Hypertension Associated with Connective Tissue Disease.
Cells
; 10(6)2021 06 13.
Artigo
Inglês
| MEDLINE | ID: mdl-34199176
12.
Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure.
JAMA Cardiol
; 6(8): 891-901, 2021 08 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33978673
13.
Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy.
Eur J Heart Fail
; 23(8): 1276-1286, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-34050592
14.
Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy.
J Am Coll Cardiol
; 78(17): 1682-1699, 2021 10 26.
Artigo
Inglês
| MEDLINE | ID: mdl-34674813
15.
Clinical Risk Prediction in Patients With Left Ventricular Myocardial Noncompaction.
J Am Coll Cardiol
; 78(7): 643-662, 2021 08 17.
Artigo
Inglês
| MEDLINE | ID: mdl-34384546
16.
Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry.
Rev Esp Cardiol (Engl Ed)
; 74(3): 216-224, 2021 Mar.
Artigo
Inglês, Espanhol
| MEDLINE | ID: mdl-32616434
17.
Prognostic implications of pathogenic truncating variants in the TTN gene.
Int J Cardiol
; 316: 180-183, 2020 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32371228
18.
Customized Massive Parallel Sequencing Panel for Diagnosis of Pulmonary Arterial Hypertension.
Genes (Basel)
; 11(10)2020 09 30.
Artigo
Inglês
| MEDLINE | ID: mdl-33007923
19.
The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals.
Eur J Med Genet
; 63(12): 104079, 2020 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-33035702
20.
Clinical heterogeneity of Pulmonary Arterial Hypertension associated with variants in TBX4.
PLoS One
; 15(4): e0232216, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32348326