Long QT syndrome: A double hit hurts more

被引：5

作者：

Wilde, Arthur A. M. ^{[1
]}

机构：

[1] Univ Amsterdam, Acad Med Ctr, Dept Cardiol, Heart Failure Res Ctr, NL-1105 AZ Amsterdam, Netherlands

来源：

HEART RHYTHM | 2010年 / 7卷 / 10期

关键词：

INHERITED ARRHYTHMIA SYNDROMES; MUTATIONS; COMPOUND; HETEROZYGOSITY; CARDIOMYOPATHY; PHENOTYPE;

D O I：

10.1016/j.hrthm.2010.06.027

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1419 / 1420

页数：2

共 16 条

[1] Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients Results From a Multicenter Study [J].

Bhuiyan, Zahurul A. ;

Jongbloed, Jan D. H. ;

van der Smagt, Jasper ;

Lombardi, Paola M. ;

Wiesfeld, Ans C. P. ;

Nelen, Marcel ;

Schouten, Meyke ;

Jongbloed, Roselie ;

Cox, Moniek G. P. J. ;

van Wolferen, Marleen ;

Rodriguez, Luz M. ;

van Gelder, Isabelle C. ;

Bikker, Hennie ;

Suurmeijer, Albert J. H. ;

van den Berg, Maarten P. ;

Mannens, Marcel M. A. M. ;

Hauer, Richard N. W. ;

Wilde, Arthur A. M. ;

van Tintelen, J. Peter .

CIRCULATION-CARDIOVASCULAR GENETICS, 2009, 2 (05) :418-U22

[2] NOS1AP Is a Genetic Modifier of the Long-QT Syndrome [J].

Crotti, Lia ;

Monti, Maria Cristina ;

Insolia, Roberto ;

Peljto, Anna ;

Goosen, Althea ;

Brink, Paul A. ;

Greenberg, David A. ;

Schwartz, Peter J. ;

George, Alfred L., Jr. .

CIRCULATION, 2009, 120 (17) :1657-1663

[3] GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES) [J].

FRASER, GR ;

FROGGATT, P ;

MURPHY, T .

ANNALS OF HUMAN GENETICS, 1964, 28 (02) :133-157

[4] Familial disease with a risk of sudden death: A longitudinal study of the psychological consequences of predictive testing for long QT syndrome [J].

Hendriks, Karin S. W. H. ;

Hendriks, Margriet M. W. B. ;

Birnie, Erwin ;

Grosfed, Frans J. M. ;

Wilde, Arthur A. M. ;

van den Bout, Jan ;

Smets, Ellen M. A. ;

van Tinteten, J. Peter ;

ten Kroode, Herman F. J. ;

van Langen, Irene M. .

HEART RHYTHM, 2008, 5 (05) :719-724

[5] Active Cascade Screening in Primary Inherited Arrhythmia Syndromes [J].

Hofman, Nynke ;

Tan, Hanno L. ;

Alders, Marielle ;

van Langen, Irene M. ;

Wilde, Arthur A. M. .

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2010, 55 (23) :2570-2576

[6] Long QT syndrome with compound mutations is associated with a more severe phenotype: A Japanese multicenter study [J].

Itoh, Hideki ;

Shimizu, Wataru ;

Hayashi, Kenshi ;

Yamagata, Kenichiro ;

Sakaguchi, Tomoko ;

Ohno, Seiko ;

Makiyama, Takeru ;

Akao, Masaharu ;

Ai, Tomohiko ;

Noda, Takashi ;

Miyazaki, Aya ;

Miyamoto, Yoshihiro ;

Yamagishi, Masakazu ;

Kamakura, Shiro ;

Horie, Minoru .

HEART RHYTHM, 2010, 7 (10) :1411-1418

[7] Genetic Testing for Long-QT Syndrome Distinguishing Pathogenic Mutations From Benign Variants [J].

Kapa, Suraj ;

Tester, David J. ;

Salisbury, Benjamin A. ;

Harris-Kerr, Carole ;

Pungliya, Manish S. ;

Alders, Marielle ;

Wilde, Arthur A. M. ;

Ackerman, Michael J. .

CIRCULATION, 2009, 120 (18) :1752-U31

[8] Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias [J].

Mohammad-Panah, R ;

Demolombe, S ;

Neyroud, N ;

Guicheney, P ;

Kyndt, F ;

van den Hoff, M ;

Baró, I ;

Escande, D .

AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (04) :1015-1023

[9] Long-QT syndrome [J].

Roden, Dan M. .

NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (02) :169-176

[10] The primary arrhythmia syndromes:: Same mutation, different manifestations.: Are we starting to understand why? [J].

Scicluna, Brendon P. ;

Wilde, Arthur W. ;

Bezzina, Connie R. .

JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2008, 19 (04) :445-452

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