Thursday, January 18, 2018
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Li, Zhang M.D.

Director, Cardiovascular Outcomes Research
Center for Clinical Cardiology, Lankenau Institute for Medical Research
100 Lancaster Avenue
Wynnewood, PA 19096
Not available


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Academic ranking: Associate Professor, Jefferson Medical College

Dr. Li Zhang completed her medical residency and cardiology training at the 2nd Affiliated Hospital of Xi’an Jiaotong University. She started full-time clinical research in 1994 at LDS Hospital, Salt Lake City, Utah, USA and has become a renowned expert in investigating inherited arrhythmias associated with increased risks of sudden death in young but otherwise healthy individuals. She is a principal investigator and a collaborator in studies of arrhythmogenic right ventricular dysplasia (ARVD) and long QT syndrome (LQTS) sponsored by AHA and NIH, respectively. Dr. Zhang’s primary goal in research is to improve the early diagnosis of lethal heart rhythm disorder for prompt medical intervention and sudden death prevention. She is an author/co-author of > 160 research manuscripts and abstracts with the vast majority of publications in SCI journals.  She has made important contributions in establishing the ongoing registry studies in China for LQTS, ARVD and left ventricular noncompaction. Besides productive research, Dr. Zhang has facilitated various US-China medical exchange programs. For medical education, she and the team which she organized made great success in delivering a series of ISHNE world-wide cardiology symposiums to China in 2007-2012, and CNAHA online education programs As the Chair of CNAHA-GWICC subcommittee, she has actively involved in organizing the CNAHA delegations to participate the annual joint scientific sessions of the Great Wall International Congress of Cardiology and Asian Pacific Heart Congress since 2013.

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张莉在西安交通大学第二附属医院完成了住院医师,住院总医师和心脏科培训。她于1994年开始在美国犹他州盐湖城LDS医院从事专职临床研究,并成为研究青少年健康人群突然死亡风险增加相关遗传性心律失常的知名专家。她和她的合作者分别获得美国心脏学会(AHA)和美国卫生研究院(NIH)科研基金资助研究致心律失常性右室发育不良(ARVD)和长QT综合征(LQTS)。张莉从事心律失常研究的主要目的是提高对致命性心律紊乱早期诊断水平,从而给予及时的医疗干预以预防心律失常导致的猝死。作为第一作者和合作者,她有160多篇研究论文或论文摘要绝大多数在SCI收录的出版物上发表。她对建立中国LQTS和ARVD注册研究作出了重要贡献。在学术研究之外,张莉积极促进各种中美医学交流活动。在医学教育领域,她和她领导的团队在2007-2012年为中国同行呈现出一系列国际动态心电图和无创性心电协会(ISHNE)和国际心血管病研究在线论坛并取得卓越成效 。从2013年起,作为CNAHA-GWICC委员会主席,张莉积极有效地组织了了美国华裔心脏协会代表团参加长城国际心脏病大会及亚太心脏大会的大会年度联合学术会议。
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Selected publication

1. Zareba W, Moss AJ, Schwartz PJ, Vincent GM, Robinson JL, Priori SG, Benhorin J, Locati EH, Towbin JA, Keating MT, Lehmann MH, Hall WJ, Zhang L: For the International LQTS Registry. Influence of Genotype on the Clinical Course of the Long QT Syndrome. New England Journal of Medicine 1998;339(14):960-965.
2. Moss AJ, Robinson JL, Gessman L, Gillespie R, Zareba W, Andrews ML, Hall J, Schwartz PJ, Vincent GM, Benhorin J, Locati EH, Towbin JA, Priori SG, Napolitano C, Zhang L, Medina A, Timothy K: Comparison of Clinical and Genetic Variables of Cardiac Events Associated with Loud Noise Versus Swimming Among Subjects with the Long QT Syndrome. American Journal of Cardiology 1999;84:876-879.
3. Zhang L, Timothy KW, Vincent GM, Lehmann MH, Fox J, Giuli LC, Shen J, Priori SG, Compton SJ, Yanowitz F, Benhorin J, Moss AJ, Schwartz PJ, Robinson JL, Wang Q, Zareba W, Keating MT, Towbin JA, Napolitano C, Medina A: The Spectrum of ST-T Wave Patterns and Repolarization Parameters in Congenital Long QT Syndrome: ECG Findings Identify Genotypes. Circulation 2000;102:2849-2855.
4. Kimbrough J, Moss AJ, Zareba W, Robinson JL, Hall WJ, Benhorin J, Locati EH, Medina A, Napolitano C, Priori S, Schwartz PJ, Timothy K, Towbin JA, Vincent GM, Zhang L: Clinical Implications for Affected Parents and Siblings of LQTS Probands. Circulation 2001;104 (5):557-62.
5. Moss AJ, Zareba W, Kaufman ES, Gartman E, Peterson DR, Benhorin J, Towbin JA, Keating MT, Priori SG, Schwartz PJ, Vincent GM, Robinson JL, Andrews ML, Feng C, Hall WJ, Medina A, Zhang L, Wang Z. Increased Risk of Arrhythmia Events in Long QT Syndrome with Mutations in the Pore Region of the Human Ether-a-go-go Related Gene Potassium Channel. Circulation 2002: 105:7:794-799.
6. Zareba W, Moss AJ, Locati EH, Lehmann MH, Peterson DR, Hall WJ, Schwartz PJ, Vincent GM, Priori SG, Benhorin J, Towbin JA, Robinson JL, Andrews ML, Napolitano C, Timothy K, Zhang L, Medina A, for the International Long QT Syndrome Registry. Modulating Effects of Age and Gender on the Clinical Course of Long QT Syndrome by Genotype. J Am Coll Cardiol 2003;42:103-109
7. Chen S, Zhang L, Bryant RM, Vincent GM, Flippin M, Lee JC, Brown E, Zimmerman F, Rozich R, Szafranski P, Oberti C, SterbaR, Marangi D, Tchou PJ, Chung MK, Wang Q. KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death. Clin Genet 2003;63:273-282.
8. Zhang L, Vincent GM, Baralle M, Baralle FE, Anson B, Benson DW, Whiting B, Timothy KW, Carlquist J. January CT, Keating MT, Splawski I. An Intronic Mutation Causes Long QT Syndrome. J Am Coll Cardiol 2004;44-1283-91.
9. Zhang L, Benson DW, Tristani-Firouzi M, Ptacek LJ, Tawil R, Schwartz PJ, George AL, Horie Minoru, Anderlfinger G, Fu YH, Ackerman MJ Vincent GM. ECG Features in Patients with KCNJ2 Mutations: Characteristic T-U Wave patterns Predict Genotype. Circulation 2005;111:2720-2726.
10. Viskin S, Rosovski U, Sands A, Phil M, Chen E, Kistler PM, Kalman JM, Chavez LR, Torres PI, Cruz F. F. E. S, Centurion O.A. Fujiki A, Maury P, Chen XM, Krahn A, Roithinger F, Zhang L, Vincent GM, Zeltser D. Inaccurate electrocardiographic interpretation of long QT: The majority of physicians cannot recognize a long QT when they see one. Heart Rhythm. 2005 Jun;2(6):569-74.
11. Hobbs JB, Peterson DR, Moss AJ, McNitt S, Zareba W, Goldenberg I, Qi M, Robinson JL, Sauer AJ, Ackerman MJ, Benhorin J, Kaufman ES, Locati EH, Napolitano C, Priori SG, Towbin JA, Vincent GM, Zhang L. Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome. JAMA 2006 Sep 13;296(10):1249-54.
12. Gong Q, Zhang L, Vincent GM, Horne BD, Zhou ZF. Nonsense Mutations in hERG Cause a Decrease in Mutant mRNA Transcripts by Nonsense-mediated mRNA Decay in Human Long QT Syndrome. Circulation 2007,116(1):17-24.
13. Gong Q,  Zhang L, Moss AJ, Vincent GM,  Ackerman MJ, Robinson JC, Jones MA, Tester DJ, and Zhou  ZF. Cryptic splicing caused by a splice site mutation in hERG leads to a large in-frame insertion in long QT syndrome. J Mol Cell Cardiol. 2008;44(3):502-9.
14. Goldenberg I, Moss AJ, Peterson DR, McNitt S, Zareba W, Andrew ML, Robinson JL, Locati EH, Ackerman MJ, Benhorin J, Kaufman ES, Napolitano C, Priori SG, Qi M, Peter J. Schwartz PJ, Towbin JA, Vincent, Zhang L. Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndrome. Circulation 2008;117(17)2184-91.
15. Vincent GM, Schwartz, PJ, Denjoy,I, Swan H, Bithell C, Spazzolini C, Crotti L, Piippo K, Lupoglazoff JM, Villain E,  Priori SG, Napolitano C, Zhang L. High Efficacy of Beta-Blockers in Long QT syndrome Type 1: Contribution of non-compliance and QT prolonging drugs in the occurrence of Beta-blocker “failure”. Circulation 2009, 20;119(2):215-21.
16. Qiu XL, Liu WL, Hu DY, Zhu TG, Li CL, Li L, Zhang L. Novel plakophilin-2 mutations in symptomatic Chinese patients with arrhythmogenic right ventricular dysplasia. Amer J Cardiol 2009,103:1439-1444.
17. Goldenberg I, Horr S, Moss AJ, Lopes CM, Barsheshet A, McNitt S, Zareba W, Andrews ML, Robinson JL, Locati EH, Ackerman MJ, Benhorin J, Kaufman ES, Napolitano C, Platonov PG, Priori SG, Qi M, Schwartz PJ, Shimizu W, Towbin JA, Vincent GM, Wilde AA, Zhang L. Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals. J Am Coll Cardiol 2010;57(1):51-9.10.
18. Zarraga IGE, Zhang L, Stump M, Gong QM, Vincent GM, Zhou ZF. Phenotype-Genotype Correlation in a Large Kindred of Type 2 Long QT Syndrome Caused by a Frameshift Mutation Producing Nonsense-Mediated mRNA Decay. Heart Rhythm Journal 2011;8(8):1200-6.
19. Sun Y, Quan XQ, Fromme S, Cox RH, Zhang P, Zhang L, Guo D, Guo J, Patel C, Kowey PR, Yan GX. A novel mutation in the KCNH2 gene associated with short QT syndrome. J Mol Cell Cardiol. 2011;50(3):433-41.
20. Gao YF, Li CL,Liu WL, Wu R, Qiu XL, Liang RJ, Li L, Zhang L, MD, Hu DY. Genotype-Phenotype Analysis of Three Chinese Families with Jervell and Lange-Nielsen Syndrome. J Cardiovascular Disease Research 2012;3(2):67-75
21. Zhang A, Sun C, Zhang L, Lv Y, Xue X, Cui C, Yan GX. L539fs/47, a Truncated Mutation of hERG, Decreases hERG Ion Channel Currents in HEK 293 Cells. Clin Exp Pharmacol Physiol. 2013 Jan;40(1):28-36.
22. Mathias A, Moss AJ, Lopes CM, Barsheshet A, McNitt S, Zareba W, Robinson JL, Locati EH, Ackerman MJ, Benhorin J, Kaufman ES, Platonov PG, Qi M, Shimizu W, Towbin JA, Michael Vincent G, Wilde AA, Zhang L, Goldenberg I. Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndrome. Heart Rhythm. 2013 May;10(5):720-5.
23. Gao YF, Xue XL, Hu DY, Liu WL; Yuan Y, Sun HM, Li L, Timothy TW, Zhang L, Li CL, Yan GX. Inhibition of Late Sodium Current by Mexiletine: A Novel Pharmotherapeutical Approach in Timothy Syndrome. Circulation-Arrhythmia and Electrophysiology 2013;6:614-622
24. Wang F, Liu JQ, Hong L, Liang L, Graff C, Yang YZ, Christiansen M, Olesen SP, Zhang L, Kanters JK. The Phenotype Characteristics of Type-13 Long QT Syndrome. Heart Rhythm  2013 Oct;10(10):1500-6
25. Khaji A, Zhang L, Kowey PR, Martinez-Lage M, Kocovic D. Mega-Epsilon Waves on 12-Lead ECG— Just Another Case Of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy? J Electrocardiol. 2013 Nov-Dec;46(6):524-7
26. Liu WL, Qiu XL, Hu DY, Zhu TG, Wang CL Beer D, Zhang L. From recurrent syncope to sudden cardiac death-clinical characteristics in a Chinese patient carrying a plakophilin-2 gene mutation. Case Reports in Cardiology vol. 2013, 246891
27. Gottschalk B, Gysel M, Barbosa-Barros R, De Sousa Rocha RP, Pérez-Riera AR, Zhang L, Fontaine G, Baranchuk A. The use of Fontaine Leads in the Diagnosis of Arrhythmogenic Right Ventricular Dysplasia. Ann Noninv Electrocardiol 2014 May;19(3):279-84
28. Gong QM, Stump MR, Deng V, Zhang L, Zhou ZF. Identification of a novel splice site mutation that causes hERG channel isoform switch in long QT syndrome. Circulation: Cardiovascular Genetics 2014 (Accepted)
29. Zhang L, Mmagu O, Liu LW, Li DY, Fan YX, Baranchuk A, Kowey PR. Hypertrophic Cardiomyopathy ?Can the Noninvasive Diagnostic Testing Identify High Risk Patients? World J Cardiol 2014 (in press)
30. Al-Senaidi KS, Wang GL, Zhang L, Beer DA, Al-Farqani AM, Al-Maskaryi SN, Kowey PR, Fan YX. A Severe Type of Long QT Syndrome and Cardiovascular Anomaly in a Homozygous Carrier of a Novel KCNH2 Mutation and Findings in Family Screening. Intel J Cardiol Heart & Vessel 2014 (in press)
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