Detalhe da pesquisa
1.
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases.
Europace
; 24(8): 1307-1367, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35373836
2.
Channelopathies - emerging trends in the management of inherited arrhythmias.
Indian Pacing Electrophysiol J
; 15(1): 43-54, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25852242
3.
Mutation location effect on severity of phenotype during exercise testing in type 1 long-QT syndrome: impact of transmembrane and C-loop location.
J Cardiovasc Electrophysiol
; 24(9): 1015-20, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23691991
4.
Derivation and validation of a simple exercise-based algorithm for prediction of genetic testing in relatives of LQTS probands.
Circulation
; 124(20): 2187-94, 2011 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22042885
5.
Continued exploration of biphenylsulfonamide scaffold as a platform for aggrecanase-1 inhibition.
Bioorg Med Chem Lett
; 21(22): 6800-3, 2011 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21982494
6.
Contemporary indications and therapeutic implications for digoxin use.
Am J Ther
; 18(4): 280-7, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20224322
7.
Tenascin-C induces inflammatory mediators and matrix degradation in osteoarthritic cartilage.
BMC Musculoskelet Disord
; 12: 164, 2011 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21762512
8.
A robust multiplexed assay to quantify C1-inhibitor, C1q, and C4 proteins for in vitro diagnosis of hereditary angioedema from dried blood spot.
J Pharm Biomed Anal
; 195: 113844, 2021 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-33388640
9.
The role of the epinephrine test in the diagnosis and management of children suspected of having congenital long QT syndrome.
Pediatr Cardiol
; 31(4): 462-8, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19957170
10.
Considerations for prenatal counselling of patients with cardiac rhabdomyomas based on their cardiac and neurologic outcomes.
Cardiol Young
; 20(1): 18-24, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20092673
11.
Prevalence of cardiovascular health risk behaviors in college-going women in a major metropolis in India.
Indian Heart J
; 72(5): 451-453, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33189212
12.
A multicentre retrospective study on quality and outcomes of cardiac rehabilitation programs in India.
Indian Heart J
; 72(1): 55-57, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32423562
13.
Parallel comparison of three methodologies for measuring functional C1-inhibitor in Hereditary angioedema patients.
Int Immunopharmacol
; 81: 106348, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32143147
14.
A first of its kind quantitative functional C1-esterase inhibitor lateral flow assay for hereditary angioedema point-of-care diagnostic testing.
Int Immunopharmacol
; 83: 106526, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32361670
15.
A novel functional C1 inhibitor activity assay in dried blood spot for diagnosis of Hereditary angioedema.
Clin Chim Acta
; 504: 155-162, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32059947
16.
Fibrosterol sulfates from the Philippine sponge Lissodendoryx (Acanthodoryx) fibrosa: sterol dimers that inhibit PKCzeta.
J Org Chem
; 74(16): 5902-8, 2009 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-20560563
17.
3,4-Disubstituted benzofuran P1' MMP-13 inhibitors: optimization of selectivity and reduction of protein binding.
Bioorg Med Chem Lett
; 19(16): 4546-50, 2009 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19625186
18.
Implantable cardioverter defibrillator as a bridge to recovery in an infant with cardiac rhabdomyoma.
Eur J Pediatr
; 168(7): 863-6, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18815808
19.
Immortalized mouse articular cartilage cell lines retain chondrocyte phenotype and respond to both anabolic factor BMP-2 and pro-inflammatory factor IL-1.
J Cell Physiol
; 215(1): 68-76, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17960567
20.
Loss-of-function sodium channel mutations in infancy: a pattern unfolds.
Circulation
; 125(1): 6-8, 2012 Jan 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-22090165