Familial dilated cardiomyopathy: from clinical presentation to molecular genetics

被引:10
作者
Arbustini, E
Morbini, P
Pilotto, A
Gavazzi, A
Tavazzi, L
机构
[1] Univ Pavia, Policlin San Matteo, IRCCS,Mol Diagnost & Cardiovasc Pathol Dept, Cardiovasc Pathol & Mol Diagnost Lab,Pathol Inst, I-27100 Pavia, Italy
[2] Univ Pavia, Policlin San Matteo, IRCCS, Dept Cardiol, I-27100 Pavia, Italy
关键词
D O I
10.1053/euhj.2000.2173
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:1825 / 1832
页数:8
相关论文
共 51 条
[1]   SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J].
ANDERSON, S ;
BANKIER, AT ;
BARRELL, BG ;
DEBRUIJN, MHL ;
COULSON, AR ;
DROUIN, J ;
EPERON, IC ;
NIERLICH, DP ;
ROE, BA ;
SANGER, F ;
SCHREIER, PH ;
SMITH, AJH ;
STADEN, R ;
YOUNG, IG .
NATURE, 1981, 290 (5806) :457-465
[2]   Prevalence and characteristics of dystrophin defects in adult male patients with dilated cardiomyopathy [J].
Arbustini, E ;
Diegoli, M ;
Morbini, P ;
Dal Bello, B ;
Banchieri, N ;
Pilotto, A ;
Magani, F ;
Grasso, M ;
Narula, J ;
Gavazzi, A ;
Viganò, N ;
Tavazzi, L .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 35 (07) :1760-1768
[3]   Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy [J].
Arbustini, E ;
Diegoli, M ;
Fasani, R ;
Grasso, M ;
Morbini, P ;
Banchieri, N ;
Bellini, O ;
Dal Bello, B ;
Pilotto, A ;
Magrini, G ;
Campana, C ;
Fortina, P ;
Gavazzi, A ;
Narula, J ;
Viganò, M .
AMERICAN JOURNAL OF PATHOLOGY, 1998, 153 (05) :1501-1510
[4]   H-FERRITINS AND L-FERRITINS IN MYOCARDIUM IN IRON OVERLOAD [J].
ARBUSTINI, E ;
GRASSO, M ;
RINDI, G ;
AROSIO, P ;
GAVAZZI, A ;
DIEGOLI, M ;
BRAMERIO, M ;
LEVI, S ;
BAROSI, G .
AMERICAN JOURNAL OF CARDIOLOGY, 1991, 68 (11) :1233-1236
[5]   Coexistence of mitochondrial DNA and β myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure [J].
Arbustini, E ;
Fasani, R ;
Morbini, P ;
Diegoli, M ;
Grasso, M ;
Dal Bello, B ;
Marangoni, E ;
Banfi, P ;
Banchieri, N ;
Bellini, O ;
Comi, G ;
Narula, J ;
Campana, C ;
Gavazzi, A ;
Danesino, C ;
Viganó, M .
HEART, 1998, 80 (06) :548-558
[6]   Restrictive cardiomyopathy, atrioventricular block and mild to subclinical myopathy in patients with desmin-immunoreactive material deposits [J].
Arbustini, E ;
Morbini, P ;
Grasso, M ;
Fasani, R ;
Verga, L ;
Bellini, O ;
Dal Bello, B ;
Campana, C ;
Piccolo, G ;
Febo, O ;
Opasich, C ;
Gavazzi, A ;
Ferrans, VJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1998, 31 (03) :645-653
[7]   Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporter [J].
Bennett, MJ ;
Hale, DE ;
Pollitt, RJ ;
Stanley, CA ;
Variend, S .
CLINICAL CARDIOLOGY, 1996, 19 (03) :243-246
[8]   A 5′ dystrophin duplication mutation causes membrane deficiency of α-dystroglycan in a family with X-linked cardiomyopathy [J].
Bies, RD ;
Maeda, M ;
Roberds, SL ;
Holder, E ;
Bohlmeyer, T ;
Young, JB ;
Campbell, KP .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (12) :3175-3188
[9]   IDENTIFICATION OF A NOVEL X-LINKED GENE RESPONSIBLE FOR EMERY-DREIFUSS MUSCULAR-DYSTROPHY [J].
BIONE, S ;
MAESTRINI, E ;
RIVELLA, S ;
MANCINI, M ;
REGIS, S ;
ROMEO, G ;
TONIOLO, D .
NATURE GENETICS, 1994, 8 (04) :323-327
[10]   Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy [J].
Bonne, G ;
Di Barletta, MR ;
Varnous, S ;
Bécane, HM ;
Hammouda, EH ;
Merlini, L ;
Muntoni, F ;
Greenberg, CR ;
Gary, F ;
Urtizberea, JA ;
Duboc, D ;
Fardeau, M ;
Toniolo, D ;
Schwartz, K .
NATURE GENETICS, 1999, 21 (03) :285-288