Amin AS - Search Results

1

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome.

Adler A, Novelli V, Amin AS, Abiusi E, Care M, Nannenberg EA, Feilotter H, Amenta S, Mazza D, Bikker H, Sturm AC, Garcia J, Ackerman MJ, Hershberger RE, Perez MV, Zareba W, Ware JS, Wilde AAM, Gollob MH. Adler A, et al. Among authors: amin as. Circulation. 2020 Feb 11;141(6):418-428. doi: 10.1161/CIRCULATIONAHA.119.043132. Epub 2020 Jan 27. Circulation. 2020. PMID: 31983240 Free PMC article.

2

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. Acta Physiol Scand. 2005 Dec;185(4):291-301. doi: 10.1111/j.1365-201X.2005.01496.x. Acta Physiol Scand. 2005. PMID: 16266370

3

Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.

Bhuiyan ZA, Momenah TS, Gong Q, Amin AS, Ghamdi SA, Carvalho JS, Homfray T, Mannens MM, Zhou Z, Wilde AA. Bhuiyan ZA, et al. Among authors: amin as. Heart Rhythm. 2008 Apr;5(4):553-61. doi: 10.1016/j.hrthm.2008.01.020. Epub 2008 Jan 29. Heart Rhythm. 2008. PMID: 18362022 Free PMC article.

4

Fever-induced QTc prolongation and ventricular arrhythmias in individuals with type 2 congenital long QT syndrome.

Amin AS, Herfst LJ, Delisle BP, Klemens CA, Rook MB, Bezzina CR, Underkofler HA, Holzem KM, Ruijter JM, Tan HL, January CT, Wilde AA. Amin AS, et al. J Clin Invest. 2008 Jul;118(7):2552-61. doi: 10.1172/JCI35337. J Clin Invest. 2008. PMID: 18551196 Free PMC article.

5

An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome.

Bhuiyan ZA, Momenah TS, Amin AS, Al-Khadra AS, Alders M, Wilde AA, Mannens MM. Bhuiyan ZA, et al. Among authors: amin as. Prog Biophys Mol Biol. 2008 Oct-Nov;98(2-3):319-27. doi: 10.1016/j.pbiomolbio.2008.10.004. Epub 2008 Nov 5. Prog Biophys Mol Biol. 2008. PMID: 19027783 Free article.

6

Genetically determined differences in sodium current characteristics modulate conduction disease severity in mice with cardiac sodium channelopathy.

Remme CA, Scicluna BP, Verkerk AO, Amin AS, van Brunschot S, Beekman L, Deneer VH, Chevalier C, Oyama F, Miyazaki H, Nukina N, Wilders R, Escande D, Houlgatte R, Wilde AA, Tan HL, Veldkamp MW, de Bakker JM, Bezzina CR. Remme CA, et al. Among authors: amin as. Circ Res. 2009 Jun 5;104(11):1283-92. doi: 10.1161/CIRCRESAHA.109.194423. Epub 2009 Apr 30. Circ Res. 2009. PMID: 19407241

7

Exercise-induced ECG changes in Brugada syndrome.

Amin AS, de Groot EA, Ruijter JM, Wilde AA, Tan HL. Amin AS, et al. Circ Arrhythm Electrophysiol. 2009 Oct;2(5):531-9. doi: 10.1161/CIRCEP.109.862441. Epub 2009 Aug 24. Circ Arrhythm Electrophysiol. 2009. PMID: 19843921

8

Cardiac ion channels in health and disease.

Amin AS, Tan HL, Wilde AA. Amin AS, et al. Heart Rhythm. 2010 Jan;7(1):117-26. doi: 10.1016/j.hrthm.2009.08.005. Epub 2009 Aug 5. Heart Rhythm. 2010. PMID: 19875343 Review.

9

Fever-triggered ventricular arrhythmias in Brugada syndrome and type 2 long-QT syndrome.

Amin AS, Klemens CA, Verkerk AO, Meregalli PG, Asghari-Roodsari A, de Bakker JM, January CT, Wilde AA, Tan HL. Amin AS, et al. Neth Heart J. 2010 Mar;18(3):165-9. doi: 10.1007/BF03091755. Neth Heart J. 2010. PMID: 20390067 Free PMC article.

10

Facilitatory and inhibitory effects of SCN5A mutations on atrial fibrillation in Brugada syndrome.

Amin AS, Boink GJ, Atrafi F, Spanjaart AM, Asghari-Roodsari A, Molenaar RJ, Ruijter JM, Wilde AA, Tan HL. Amin AS, et al. Europace. 2011 Jul;13(7):968-75. doi: 10.1093/europace/eur011. Epub 2011 Jan 26. Europace. 2011. PMID: 21273195

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