Tan HL - Search Results

1

Gene therapy to create biological pacemakers.

Boink GJ, Seppen J, de Bakker JM, Tan HL. Boink GJ, et al. Among authors: tan hl. Med Biol Eng Comput. 2007 Feb;45(2):167-76. doi: 10.1007/s11517-006-0112-7. Epub 2006 Oct 18. Med Biol Eng Comput. 2007. PMID: 17048028 Review.

2

T wave alternans after sotalol: evidence for increased sensitivity to sotalol after conversion from atrial fibrillation to sinus rhythm.

Tan HL, Wilde AA. Tan HL, et al. Heart. 1998 Sep;80(3):303-6. doi: 10.1136/hrt.80.3.303. Heart. 1998. PMID: 9875096 Free PMC article.

3

A sodium-channel mutation causes isolated cardiac conduction disease.

Tan HL, Bink-Boelkens MT, Bezzina CR, Viswanathan PC, Beaufort-Krol GC, van Tintelen PJ, van den Berg MP, Wilde AA, Balser JR. Tan HL, et al. Nature. 2001 Feb 22;409(6823):1043-7. doi: 10.1038/35059090. Nature. 2001. PMID: 11234013

4

Genetic control of sodium channel function.

Tan HL, Bezzina CR, Smits JP, Verkerk AO, Wilde AA. Tan HL, et al. Cardiovasc Res. 2003 Mar 15;57(4):961-73. doi: 10.1016/s0008-6363(02)00714-9. Cardiovasc Res. 2003. PMID: 12650874 Review.

5

Ca2+-activated Cl- current reduces transmural electrical heterogeneity within the rabbit left ventricle.

Verkerk AO, Tan HL, Ravesloot JH. Verkerk AO, et al. Among authors: tan hl. Acta Physiol Scand. 2004 Mar;180(3):239-47. doi: 10.1111/j.0001-6772.2003.01252.x. Acta Physiol Scand. 2004. PMID: 14962005

6

Family and population strategies for screening and counselling of inherited cardiac arrhythmias.

van Langen IM, Hofman N, Tan HL, Wilde AA. van Langen IM, et al. Among authors: tan hl. Ann Med. 2004;36 Suppl 1:116-24. doi: 10.1080/17431380410032526. Ann Med. 2004. PMID: 15176433

7

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families.

Smits JP, Koopmann TT, Wilders R, Veldkamp MW, Opthof T, Bhuiyan ZA, Mannens MM, Balser JR, Tan HL, Bezzina CR, Wilde AA. Smits JP, et al. Among authors: tan hl. J Mol Cell Cardiol. 2005 Jun;38(6):969-81. doi: 10.1016/j.yjmcc.2005.02.024. Epub 2005 Apr 1. J Mol Cell Cardiol. 2005. PMID: 15910881

8

Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives.

Tan HL, Hofman N, van Langen IM, van der Wal AC, Wilde AA. Tan HL, et al. Circulation. 2005 Jul 12;112(2):207-13. doi: 10.1161/CIRCULATIONAHA.104.522581. Epub 2005 Jul 5. Circulation. 2005. PMID: 15998675

9

Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome.

Verkerk AO, Wilders R, Schulze-Bahr E, Beekman L, Bhuiyan ZA, Bertrand J, Eckardt L, Lin D, Borggrefe M, Breithardt G, Mannens MM, Tan HL, Wilde AA, Bezzina CR. Verkerk AO, et al. Among authors: tan hl. Cardiovasc Res. 2005 Dec 1;68(3):441-53. doi: 10.1016/j.cardiores.2005.06.027. Epub 2005 Jul 25. Cardiovasc Res. 2005. PMID: 16043162

10

Novel Brugada syndrome-causing mutation in ion-conducting pore of cardiac Na+ channel does not affect ion selectivity properties.

Amin AS, Verkerk AO, Bhuiyan ZA, Wilde AA, Tan HL. Amin AS, et al. Among authors: tan hl. Acta Physiol Scand. 2005 Dec;185(4):291-301. doi: 10.1111/j.1365-201X.2005.01496.x. Acta Physiol Scand. 2005. PMID: 16266370

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