Detalhe da pesquisa
1.
[A Novel and Fast P Wave Detection Algorithm in ECG Signals].
Zhongguo Yi Liao Qi Xie Za Zhi
; 41(1): 13-6, 2017 Jan.
Artigo
em Zh
| MEDLINE | ID: mdl-29792645
2.
Identification and characterization of a transient outward K+ current in human induced pluripotent stem cell-derived cardiomyocytes.
J Mol Cell Cardiol
; 60: 36-46, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23542310
3.
DiBAC4(3) hits a "sweet spot" for the activation of arterial large-conductance Ca²âº-activated potassium channels independently of the ß1-subunit.
Am J Physiol Heart Circ Physiol
; 304(11): H1471-82, 2013 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23542916
4.
Some new inequalities of Jordan type for sine.
ScientificWorldJournal
; 2013: 834159, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24307882
5.
Therapeutic Targeting of Cancer: Epigenetic Homeostasis.
Front Oncol
; 11: 747022, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34765551
6.
Lidocaine-induced Brugada syndrome phenotype linked to a novel double mutation in the cardiac sodium channel.
Circ Res
; 103(4): 396-404, 2008 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18599870
7.
Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndrome.
Pacing Clin Electrophysiol
; 33(3): 274-85, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20025708
8.
Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death.
Circulation
; 115(4): 442-9, 2007 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-17224476
9.
Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation.
Heart Rhythm
; 5(3): 427-35, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18313602
10.
A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndrome.
J Cardiovasc Electrophysiol
; 18(9): 972-7, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17655673
11.
Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction.
Heart Rhythm
; 4(8): 1072-80, 2007 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-17675083
12.
High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia.
Heart Rhythm
; 12(7): 1584-94, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25998140
13.
ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.
Int J Cardiol
; 171(3): 431-42, 2014 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24439875
14.
Maximum diastolic potential of human induced pluripotent stem cell-derived cardiomyocytes depends critically on I(Kr).
PLoS One
; 7(7): e40288, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22815737
15.
Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8.
Heart Rhythm
; 9(4): 548-55, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22056721
16.
A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype.
Circ Cardiovasc Genet
; 2(3): 270-8, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20031595
17.
Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome.
Circ Arrhythm Electrophysiol
; 1(3): 209-18, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19122847