Ackerman MJ - Search Results

1

Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter Registry.

Yamagata K, Horie M, Aiba T, Ogawa S, Aizawa Y, Ohe T, Yamagishi M, Makita N, Sakurada H, Tanaka T, Shimizu A, Hagiwara N, Kishi R, Nakano Y, Takagi M, Makiyama T, Ohno S, Fukuda K, Watanabe H, Morita H, Hayashi K, Kusano K, Kamakura S, Yasuda S, Ogawa H, Miyamoto Y, Kapplinger JD, Ackerman MJ, Shimizu W. Yamagata K, et al. Among authors: ackerman mj. Circulation. 2017 Jun 6;135(23):2255-2270. doi: 10.1161/CIRCULATIONAHA.117.027983. Epub 2017 Mar 24. Circulation. 2017. PMID: 28341781

2

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

3

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

4

Sex-selective QT prolongation during rapid eye movement sleep.

Lanfranchi PA, Shamsuzzaman AS, Ackerman MJ, Kara T, Jurak P, Wolk R, Somers VK. Lanfranchi PA, et al. Among authors: ackerman mj. Circulation. 2002 Sep 17;106(12):1488-92. doi: 10.1161/01.cir.0000030183.10934.95. Circulation. 2002. PMID: 12234953

5

Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy.

Van Driest SL, Ackerman MJ, Ommen SR, Shakur R, Will ML, Nishimura RA, Tajik AJ, Gersh BJ. Van Driest SL, et al. Among authors: ackerman mj. Circulation. 2002 Dec 10;106(24):3085-90. doi: 10.1161/01.cir.0000042675.59901.14. Circulation. 2002. PMID: 12473556

6

Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy.

Van Driest SL, Ellsworth EG, Ommen SR, Tajik AJ, Gersh BJ, Ackerman MJ. Van Driest SL, et al. Among authors: ackerman mj. Circulation. 2003 Jul 29;108(4):445-51. doi: 10.1161/01.CIR.0000080896.52003.DF. Epub 2003 Jul 14. Circulation. 2003. PMID: 12860912

7

Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes.

Choi G, Kopplin LJ, Tester DJ, Will ML, Haglund CM, Ackerman MJ. Choi G, et al. Among authors: ackerman mj. Circulation. 2004 Oct 12;110(15):2119-24. doi: 10.1161/01.CIR.0000144471.98080.CA. Epub 2004 Oct 4. Circulation. 2004. PMID: 15466642

8

Beta-blocker therapy failures in symptomatic probands with genotyped long-QT syndrome.

Chatrath R, Bell CM, Ackerman MJ. Chatrath R, et al. Among authors: ackerman mj. Pediatr Cardiol. 2004 Sep-Oct;25(5):459-65. doi: 10.1007/s00246-003-0567-3. Epub 2004 Jul 30. Pediatr Cardiol. 2004. PMID: 15534720

9

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.

Tester DJ, Will ML, Haglund CM, Ackerman MJ. Tester DJ, et al. Among authors: ackerman mj. Heart Rhythm. 2005 May;2(5):507-17. doi: 10.1016/j.hrthm.2005.01.020. Heart Rhythm. 2005. PMID: 15840476

10

Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.

Zhang L, Benson DW, Tristani-Firouzi M, Ptacek LJ, Tawil R, Schwartz PJ, George AL, Horie M, Andelfinger G, Snow GL, Fu YH, Ackerman MJ, Vincent GM. Zhang L, et al. Among authors: ackerman mj. Circulation. 2005 May 31;111(21):2720-6. doi: 10.1161/CIRCULATIONAHA.104.472498. Epub 2005 May 23. Circulation. 2005. PMID: 15911703

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