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1.
The expression of Ubc9 and the intensity of SERCA2a-SUMOylation were reduced in diet-induced obese rats and partially restored by trimetazidine.
J Cardiovasc Pharmacol
; 65(1): 47-53, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-25329748
2.
[Safety and feasibility of carotid artery stenting in patients with coexisting carotid and coronary artery disease].
Zhonghua Xin Xue Guan Bing Za Zhi
; 41(7): 577-82, 2013 Jul.
Artículo
en Zh
| MEDLINE | ID: mdl-24284185
3.
[Clinical analysis of simultaneous bilateral carotid stenting for treating patients with bilateral atherosclerotic carotid stenosis].
Zhonghua Xin Xue Guan Bing Za Zhi
; 40(4): 278-82, 2012 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-22801303
4.
[Readthrough of nonsense mutation W822X in the SCN5A gene can effectively restore expression of cardiac Na+ channels W822X].
Zhonghua Xin Xue Guan Bing Za Zhi
; 39(3): 238-41, 2011 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-21609529
5.
Cross-sectional study of retroperitoneal hematoma after invasive intervention in a Chinese population: Prevalence, characteristics, management and outcomes.
Exp Ther Med
; 20(4): 2975-2984, 2020 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-32855663
6.
Invasive versus conservative strategy in consecutive patients aged 80 years or older with non-ST-segment elevation myocardial infarction: a retrospective study in China.
J Geriatr Cardiol
; 16(10): 741-748, 2019 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-31700513
7.
Gender differences in treatment strategies among patients ≥80 years old with non-ST-segment elevation myocardial infarction.
J Thorac Dis
; 11(12): 5258-5265, 2019 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-32030243
8.
[The Val606Met mutation of human beta myosin heavy chain in a Chinese familial hypertrophic cardiomyopathy family].
Zhonghua Xin Xue Guan Bing Za Zhi
; 36(4): 313-6, 2008 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-19100006
9.
Modulation of KCNQ1 current by atrial fibrillation-associated KCNE4 (145E/D) gene polymorphism.
Chin Med J (Engl)
; 120(2): 150-4, 2007 Jan 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-17335661
10.
[Electrocardiogram analysis in high risk population of unexplained sudden death in Yunnan province].
Zhonghua Xin Xue Guan Bing Za Zhi
; 35(12): 1155-8, 2007 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-18341823
11.
[Observation of functional remodeling of Ca2+-activated Cl- channel in pacing-induced canine failing heart].
Zhonghua Xin Xue Guan Bing Za Zhi
; 34(9): 797-800, 2006 Sep.
Artículo
en Zh
| MEDLINE | ID: mdl-17217686
12.
[Electrophysiological characterization of long QT syndrome associated mutations V630A and N633S].
Zhonghua Xin Xue Guan Bing Za Zhi
; 34(6): 523-7, 2006 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-16842670
13.
[The association of single nucleotide polymorphism of slow delayed rectifier K+ channel genes with atrial fibrillation in Han nationality Chinese].
Zhonghua Xin Xue Guan Bing Za Zhi
; 33(11): 987-91, 2005 Nov.
Artículo
en Zh
| MEDLINE | ID: mdl-16563243
14.
[Hypertrophic cardiomyopathy with right aortic arch, right descending aorta, and Kommerell's diverticulum: a case report].
Zhonghua Xin Xue Guan Bing Za Zhi
; 37(8): 755-6, 2009 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-20021935
15.
A retrospective study of an invasive versus conservative strategy in patients aged ≥80 years with acute ST-segment elevation myocardial infarction.
J Int Med Res
; 47(9): 4431-4441, 2019 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-31347422
16.
Clinical and angiographic correlates of left ventricular dysfunction in patients with three vessel coronary disease.
Chin Med J (Engl)
; 125(23): 4221-5, 2012 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-23217390
17.
Novel compound heterozygous mutations T2C and 1149insT in the KCNQ1 gene cause Jervell and Lange-Nielsen syndrome.
Int J Mol Med
; 28(1): 41-6, 2011 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-21380488
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