Detalhe da pesquisa
1.
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
2.
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
3.
Is blockade of the Renin-Angiotensin system able to reverse the structural and functional remodeling of the left ventricle in severe aortic stenosis?
J Cardiovasc Pharmacol
; 65(3): 233-40, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25469804
4.
Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy.
J Cardiovasc Magn Reson
; 13: 30, 2011 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-21689390
5.
Outcome of aortic valve replacement with bioprostheses in the elderly.
J Heart Valve Dis
; 18(5): 514-23, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20099692
6.
Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy.
ESC Heart Fail
; 6(2): 436-445, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30775854
7.
Early familial dilated cardiomyopathy: identification with determination of disease state parameter from cine MR image data.
Radiology
; 249(1): 88-96, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18796670
8.
Electrocardiographic ventricular repolarization during cardiovascular autonomic function testing in patients with arrhythmogenic right ventricular cardiomyopathy.
Scand Cardiovasc J
; 42(6): 375-82, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18615356
9.
Clinical disease presentation and ECG characteristics of LMNA mutation carriers.
Open Heart
; 4(1): e000474, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28123761
10.
Increased ventilatory response to exercise in symptomatic and asymptomatic LMNA mutation carriers: a follow-up study.
Clin Physiol Funct Imaging
; 37(1): 8-16, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27966284
11.
Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathy.
Eur J Heart Fail
; 7(1): 103-8, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15642540
12.
Serum tryptase levels in acute coronary syndromes.
Int J Cardiol
; 104(2): 138-43, 2005 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-16168805
13.
A novel mutation, Arg71Thr, in the delta-sarcoglycan gene is associated with dilated cardiomyopathy.
J Mol Med (Berl)
; 81(12): 795-800, 2003 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-14564412
14.
The need for comprehensive cardiac and neurologic assessment of lamin A/C mutation carriers.
Radiology
; 251(1): 305-6; author reply 306, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19332860
15.
Magnetocardiographic indices of left ventricular hypertrophy.
J Hypertens
; 20(11): 2285-92, 2002 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-12409968
16.
Prognostic usefulness of plasma monocyte/macrophage and T-lymphocyte activation markers in patients with acute coronary syndromes.
Am J Cardiol
; 94(8): 993-6, 2004 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-15476610
17.
Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy.
Eur J Heart Fail
; 6(7): 861-8, 2004 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-15556047
18.
A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy.
Ann Med
; 46(6): 424-9, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24888384
19.
Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population.
Ann Med
; 45(1): 85-90, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22462493
20.
Serum lipidomics meets cardiac magnetic resonance imaging: profiling of subjects at risk of dilated cardiomyopathy.
PLoS One
; 6(1): e15744, 2011 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-21283746