Detalhe da pesquisa
1.
Lamin A/C phosphorylation at serine 22 is a conserved heat shock response to regulate nuclear adaptation during stress.
J Cell Sci
; 136(4)2023 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36695453
2.
Endomyocardial biopsy: safety and prognostic utility in paediatric and adult myocarditis in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Long-Term Registry.
Eur Heart J
; 2024 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38594778
3.
Successful palliative resection of giant epimyocardial lymphatic malformation with 14 years of follow-up: a case report.
BMC Cardiovasc Disord
; 23(1): 414, 2023 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37612617
4.
Genotype-phenotype correlation in arrhythmogenic right ventricular cardiomyopathy-risk of arrhythmias and heart failure.
J Med Genet
; 59(9): 858-864, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34400560
5.
Prognostic significance of incidental suspected transthyretin amyloidosis on routine bone scintigraphy.
J Nucl Cardiol
; 29(3): 1021-1029, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33094472
6.
Complications of implantable cardioverter-defibrillator treatment in arrhythmogenic right ventricular cardiomyopathy.
Europace
; 24(2): 306-312, 2022 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34279601
7.
Prognostic Value of 99mTc-HMDP Scintigraphy in Elderly Patients With Chronic Heart Failure.
Heart Lung Circ
; 31(5): 629-637, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35063379
8.
Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients.
BMC Cardiovasc Disord
; 21(1): 126, 2021 03 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33673806
9.
DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy.
BMC Med Genet
; 21(1): 19, 2020 01 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-32005173
10.
Pregnancies, ventricular arrhythmias, and substrate progression in women with arrhythmogenic right ventricular cardiomyopathy in the Nordic ARVC Registry.
Europace
; 22(12): 1873-1879, 2020 12 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-32681178
11.
The Cardiomyopathy Registry of the EURObservational Research Programme of the European Society of Cardiology: baseline data and contemporary management of adult patients with cardiomyopathies.
Eur Heart J
; 39(20): 1784-1793, 2018 05 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29378019
12.
Deleterious assembly of the lamin A/C mutant p.S143P causes ER stress in familial dilated cardiomyopathy.
J Cell Sci
; 129(14): 2732-43, 2016 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27235420
13.
Fibrosis and wall thickness affect ventricular repolarization dynamics in hypertrophic cardiomyopathy.
Ann Noninvasive Electrocardiol
; 23(6): e12582, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29974557
14.
Novel electrocardiographic features in carriers of hypertrophic cardiomyopathy causing sarcomeric mutations.
J Electrocardiol
; 51(6): 983-989, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30497761
15.
Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2.
BMC Med Genet
; 18(1): 86, 2017 08 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28818065
16.
Cardiovascular magnetic resonance of mitral valve length in hypertrophic cardiomyopathy.
J Cardiovasc Magn Reson
; 18(1): 33, 2016 06 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27259862
17.
Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy.
Eur Heart J
; 36(34): 2327-37, 2015 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26084686
18.
Cardiovascular magnetic resonance findings in patients with PRKAG2 gene mutations.
J Cardiovasc Magn Reson
; 17: 89, 2015 Oct 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-26496977
19.
Use of home telemonitoring to support multidisciplinary care of heart failure patients in Finland: randomized controlled trial.
J Med Internet Res
; 16(12): e282, 2014 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-25498992
20.
Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases.
Eur Heart J
; 34(19): 1448-58, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23211230