Pediatric myocardial disease

被引:35
作者
Towbin, JA
机构
[1] Texas Childrens Hosp, Baylor Coll Med, Dept Pediat Cardiol Mol & Human Genet, Heart Failure Program, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Baylor Coll Med, Phoebe Willingham muzzy Pediat Mol Cardiol Lab, Houston, TX 77030 USA
关键词
D O I
10.1016/S0031-3955(05)70119-X
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Cardiomyopathies are diseases of the heart muscles. This article reviews the causes, clinical presentation, diagnosis, management, and long-term outcomes of dilated and hypertrophic cardiomyopathy.
引用
收藏
页码:289 / +
页数:25
相关论文
共 102 条
[1]   THE PREVALENCE OF HYPERTROPHIC CARDIOMYOPATHY IN MEN - AN ECHOCARDIOGRAPHIC POPULATION SCREENING STUDY WITH A REVIEW OF DEATH RECORDS [J].
AGNARSSON, UT ;
HARDARSON, T ;
HALLGRIMSSON, J ;
SIGFUSSON, N .
JOURNAL OF INTERNAL MEDICINE, 1992, 232 (06) :499-506
[2]  
Aretz H T, 1987, Am J Cardiovasc Pathol, V1, P3
[3]   A novel X-linked gene, G4.5. is responsible for Barth syndrome [J].
Bione, S ;
DAdamo, P ;
Maestrini, E ;
Gedeon, AK ;
Bolhuis, PA ;
Toniolo, D .
NATURE GENETICS, 1996, 12 (04) :385-389
[4]   Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth Syndrome [J].
Bleyl, SB ;
Mumford, BR ;
Thompson, V ;
Carey, JC ;
Pysher, TJ ;
Chin, TK ;
Ward, K .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) :868-872
[5]  
BOLHUIS PA, 1991, AM J HUM GENET, V48, P481
[6]   CARDIAC MYOSIN BINDING PROTEIN-C GENE SPLICE ACCEPTOR SITE MUTATION IS ASSOCIATED WITH FAMILIAL HYPERTROPHIC CARDIOMYOPATHY [J].
BONNE, G ;
CARRIER, L ;
BERCOVICI, J ;
CRUAUD, C ;
RICHARD, P ;
HAINQUE, B ;
GAUTEL, M ;
LABEIT, S ;
JAMES, M ;
BECKMANN, J ;
WEISSENBACH, J ;
VOSBERG, HP ;
FISZMAN, M ;
KOMAJDA, M ;
SCHWARTZ, K .
NATURE GENETICS, 1995, 11 (04) :438-440
[7]   VERAPAMIL-INDUCED IMPROVEMENT IN LEFT-VENTRICULAR DIASTOLIC FILLING AND INCREASED EXERCISE TOLERANCE IN PATIENTS WITH HYPERTROPHIC CARDIOMYOPATHY - SHORT-TERM AND LONG-TERM EFFECTS [J].
BONOW, RO ;
DILSIZIAN, V ;
ROSING, DR ;
MARON, BJ ;
BACHARACH, SL ;
GREEN, MV .
CIRCULATION, 1985, 72 (04) :853-864
[8]  
Bowles Karla R., 1998, Pediatric Research, V43, p18A
[9]   Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 1Oq21-23 [J].
Bowles, KR ;
Gajarski, R ;
Porter, P ;
Goytia, V ;
Bachinski, L ;
Roberts, R ;
Pignatelli, R ;
Towbin, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (06) :1355-1360
[10]  
BRIGDEN W, 1957, LANCET, V2, P1179