Detalhe da pesquisa
1.
Effect of Mavacamten in Women Compared With Men With Obstructive Hypertrophic Cardiomyopathy: Insights From EXPLORER-HCM.
Circulation
; 149(7): 498-509, 2024 02 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37961906
2.
Left Ventricular Systolic Dysfunction in Patients Diagnosed With Hypertrophic Cardiomyopathy During Childhood: Insights From the SHaRe Registry.
Circulation
; 148(5): 394-404, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37226762
3.
Dilated cardiomyopathy: causes, mechanisms, and current and future treatment approaches.
Lancet
; 402(10406): 998-1011, 2023 09 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37716772
4.
Discordant clinical features of identical hypertrophic cardiomyopathy twins.
Proc Natl Acad Sci U S A
; 118(10)2021 03 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33658374
5.
LMNA Cardiomyopathy: Important Considerations for the Heart Failure Clinician.
J Card Fail
; 29(12): 1657-1666, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37659618
6.
Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.
Circulation
; 144(20): 1600-1611, 2021 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34587765
7.
The Road Not Yet Traveled: Distinction in Critical Care Cardiology through the Advanced Heart Failure and Transplant Cardiology Training Pathway.
J Card Fail
; 28(2): 339-342, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35148880
8.
Cascade testing for inherited cardiac conditions: Risk perception and screening after a negative genetic test result.
J Genet Couns
; 31(6): 1273-1281, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35763674
9.
Understanding the genetics of adult-onset dilated cardiomyopathy: what a clinician needs to know.
Eur Heart J
; 42(24): 2384-2396, 2021 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34153989
10.
Worldwide differences in primary prevention implantable cardioverter defibrillator utilization and outcomes in hypertrophic cardiomyopathy.
Eur Heart J
; 42(38): 3932-3944, 2021 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34491319
11.
Desmoplakin Cardiomyopathy, a Fibrotic and Inflammatory Form of Cardiomyopathy Distinct From Typical Dilated or Arrhythmogenic Right Ventricular Cardiomyopathy.
Circulation
; 141(23): 1872-1884, 2020 06 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32372669
12.
Hypertrophic Cardiomyopathy With Left Ventricular Systolic Dysfunction: Insights From the SHaRe Registry.
Circulation
; 141(17): 1371-1383, 2020 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32228044
13.
Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): a randomised, double-blind, placebo-controlled, phase 3 trial.
Lancet
; 396(10253): 759-769, 2020 09 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32871100
14.
Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation.
Genet Med
; 23(7): 1281-1287, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33782553
15.
Feasibility of somatostatin receptor-targeted imaging for detection of myocardial inflammation: A pilot study.
J Nucl Cardiol
; 28(3): 1089-1099, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31197742
16.
Sex Differences in Hypertrophic Cardiomyopathy: Interaction With Genetics and Environment.
Curr Heart Fail Rep
; 18(5): 264-273, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34478112
17.
Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies.
Circulation
; 140(4): 293-302, 2019 07 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-31155932
18.
Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants.
Am Heart J
; 225: 108-119, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32480058
19.
Second Hits in Dilated Cardiomyopathy.
Curr Cardiol Rep
; 22(2): 8, 2020 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-31980956
20.
Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights from the Sarcomeric Human Cardiomyopathy Registry (SHaRe).
Circulation
; 138(14): 1387-1398, 2018 10 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30297972