Detalhe da pesquisa
1.
A novel AGK splicing mutation in a patient with Sengers syndrome and left ventricular non-compaction cardiomyopathy.
Pediatr Res
; 94(2): 683-690, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36759750
2.
Genotype-phenotype analysis of F-helix mutations at the kinase domain of TGFBR2, including a type 2 Marfan syndrome familial study.
Mol Vis
; 18: 55-63, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22259224
3.
Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family.
Front Pediatr
; 10: 887214, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35685915
4.
Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family.
Front Pediatr
; 10: 961964, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35844754
5.
Clinical characteristics, target organ damage and associate risk factors of resistant hypertension determined by ambulatory blood pressure monitoring in patients aged ≥ 80 years.
J Geriatr Cardiol
; 14(5): 308-314, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28630606
6.
Establishing a predictive model for aspirin resistance in elderly Chinese patients with chronic cardiovascular disease.
J Geriatr Cardiol
; 13(5): 458-64, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27594876
7.
Coenzyme Q10 treatment of cardiovascular disorders of ageing including heart failure, hypertension and endothelial dysfunction.
Clin Chim Acta
; 450: 83-9, 2015 Oct 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-26254995
8.
Molecular genetics of Liddle's syndrome.
Clin Chim Acta
; 436: 202-6, 2014 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-24882431
9.
Influence of omega-3 polyunsaturated fatty acid-supplementation on platelet aggregation in humans: a meta-analysis of randomized controlled trials.
Atherosclerosis
; 226(2): 328-34, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23153623
10.
The association of an adenine insertion variant in the 5'UTR of the endothelin-1 gene with hypertension and orthostatic hypotension.
Arch Med Sci
; 8(2): 219-26, 2012 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22661993
11.
Plasma concentrations of interleukin-6, C-reactive protein, tumor necrosis factor-α and matrix metalloproteinase-9 in aortic dissection.
Clin Chim Acta
; 413(1-2): 198-202, 2012 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22001516
12.
Genetic diagnosis of Liddle's syndrome by mutation analysis of SCNN1B and SCNN1G in a Chinese family.
Chin Med J (Engl)
; 125(8): 1401-4, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22613642
13.
Molecular analysis for diagnosis of Marfan syndrome and Marfan-associated disorders.
Chin Med J (Engl)
; 124(6): 930-4, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21518605
14.
Recent molecular biological progress in Marfan syndrome and Marfan-associated disorders.
Ageing Res Rev
; 9(3): 363-8, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19772952
15.
Identification of a novel lethal fibrillin-1 gene mutation in a Chinese Marfan family and correlation of 3' fibrillin-1 gene mutations with phenotype.
Chin Med J (Engl)
; 123(20): 2874-8, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21034599
16.
Febuxostat, a nonpurine selective inhibitor of xanthine oxidase: a promising medical therapy for chronic heart failure?
Chin Med J (Engl)
; 123(17): 2471-4, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21034568