Ackerman MJ - Search Results

1

Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?

Roberts JD, Krahn AD, Ackerman MJ, Rohatgi RK, Moss AJ, Nazer B, Tadros R, Gerull B, Sanatani S, Wijeyeratne YD, Baruteau AE, Muir AR, Pang B, Cadrin-Tourigny J, Talajic M, Rivard L, Tester DJ, Liu T, Whitman IR, Wojciak J, Conacher S, Gula LJ, Leong-Sit P, Manlucu J, Green MS, Hamilton R, Healey JS, Lopes CM, Behr ER, Wilde AA, Gollob MH, Scheinman MM. Roberts JD, et al. Among authors: ackerman mj. Circ Arrhythm Electrophysiol. 2017 Aug;10(8):e005282. doi: 10.1161/CIRCEP.117.005282. Circ Arrhythm Electrophysiol. 2017. PMID: 28794082

2

Molecular diagnosis of the inherited long-QT syndrome in a woman who died after near-drowning.

Ackerman MJ, Tester DJ, Porter CJ, Edwards WD. Ackerman MJ, et al. N Engl J Med. 1999 Oct 7;341(15):1121-5. doi: 10.1056/NEJM199910073411504. N Engl J Med. 1999. PMID: 10511610 Free article. No abstract available.

3

Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome.

Ackerman MJ, Tester DJ, Porter CJ. Ackerman MJ, et al. Mayo Clin Proc. 1999 Nov;74(11):1088-94. doi: 10.4065/74.11.1088. Mayo Clin Proc. 1999. PMID: 10560595

4

Molecular autopsy of sudden unexplained death in the young.

Ackerman MJ, Tester DJ, Driscoll DJ. Ackerman MJ, et al. Am J Forensic Med Pathol. 2001 Jun;22(2):105-11. doi: 10.1097/00000433-200106000-00001. Am J Forensic Med Pathol. 2001. PMID: 11394742

5

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

Ackerman MJ, Siu BL, Sturner WQ, Tester DJ, Valdivia CR, Makielski JC, Towbin JA. Ackerman MJ, et al. JAMA. 2001 Nov 14;286(18):2264-9. doi: 10.1001/jama.286.18.2264. JAMA. 2001. PMID: 11710892

6

Epinephrine-induced QT interval prolongation: a gene-specific paradoxical response in congenital long QT syndrome.

Ackerman MJ, Khositseth A, Tester DJ, Hejlik JB, Shen WK, Porter CB. Ackerman MJ, et al. Mayo Clin Proc. 2002 May;77(5):413-21. doi: 10.4065/77.5.413. Mayo Clin Proc. 2002. PMID: 12004990 Clinical Trial.

7

A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine.

Valdivia CR, Ackerman MJ, Tester DJ, Wada T, McCormack J, Ye B, Makielski JC. Valdivia CR, et al. Among authors: ackerman mj. Cardiovasc Res. 2002 Aug 1;55(2):279-89. doi: 10.1016/s0008-6363(02)00445-5. Cardiovasc Res. 2002. PMID: 12123767

8

Catecholamine-provoked microvoltage T wave alternans in genotyped long QT syndrome.

Nemec J, Ackerman MJ, Tester DJ, Hejlik J, Shen WK. Nemec J, et al. Among authors: ackerman mj. Pacing Clin Electrophysiol. 2003 Aug;26(8):1660-7. doi: 10.1046/j.1460-9592.2003.t01-1-00249.x. Pacing Clin Electrophysiol. 2003. PMID: 12877697

9

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels.

Makielski JC, Ye B, Valdivia CR, Pagel MD, Pu J, Tester DJ, Ackerman MJ. Makielski JC, et al. Among authors: ackerman mj. Circ Res. 2003 Oct 31;93(9):821-8. doi: 10.1161/01.RES.0000096652.14509.96. Epub 2003 Sep 18. Circ Res. 2003. PMID: 14500339

10

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome.

Ackerman MJ, Tester DJ, Jones GS, Will ML, Burrow CR, Curran ME. Ackerman MJ, et al. Mayo Clin Proc. 2003 Dec;78(12):1479-87. doi: 10.4065/78.12.1479. Mayo Clin Proc. 2003. PMID: 14661677

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