Detalhe da pesquisa
1.
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies.
Genet Med
; 23(5): 856-864, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33500567
2.
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center.
Genet Med
; 21(2): 284-292, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29875424
3.
Investigation on the high recurrence of the ATTRv-causing transthyretin variant Val142Ile in central Italy.
Eur J Hum Genet
; 31(5): 541-547, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36380086
4.
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.
medRxiv
; 2023 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36778260
5.
Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing?
J Am Heart Assoc
; 9(8): e015473, 2020 04 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32306808
6.
Prevalence of cardiac amyloidosis among adult patients referred to tertiary centres with an initial diagnosis of hypertrophic cardiomyopathy.
Int J Cardiol
; 300: 191-195, 2020 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31371117