Familial hypertrophic cardiomyopathy: Prognosis depends rather on mutation than gene

被引:0
|
作者
Langlard, JM
Burban, M
Richard, P
Halnque, B
Dubourg, O
Desnos, M
Charron, P
Komajda, N
Schwartz, K
Bouhour, JB
机构
[1] Laennec Hosp, Nantes, France
[2] Hosp Pitie Salpetriere, Paris, France
[3] Hop Ambroise Pare, Boulogne, France
[4] Boucicaut Hosp, Paris, France
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
4317
引用
收藏
页码:818 / 818
页数:1
相关论文
共 50 条
  • [1] FILAMIN C GENE MUTATION IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY
    Shadman, Shahrad
    Gasimli-Gamache, Leyla
    Luther, Sarah
    Shirani, Jamshid
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2024, 83 (13) : 2827 - 2827
  • [2] Genetic modifiers in familial hypertrophic cardiomyopathy caused by a sarcomeric protein gene mutation
    Semsarian, C
    Glewat, M
    Duffy, C
    Moskowitz, I
    Schoen, FJ
    Seidman, JG
    Seldman, CE
    CIRCULATION, 2000, 102 (18) : 33 - 33
  • [3] The development of familial hypertrophic cardiomyopathy: from mutation to bedside
    Brouwer, Wessel P.
    van Dijk, Sabine J.
    Stienen, Ger J. M.
    van Rossum, Albert C.
    van der Velden, Jolanda
    Germans, Tjeerd
    EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2011, 41 (05) : 568 - 578
  • [5] A rapid protocol for cardiac troponin T gene mutation detection in familial hypertrophic cardiomyopathy
    Gerull, B
    Osterziel, KJ
    Witt, C
    Dietz, R
    Thierfelder, L
    HUMAN MUTATION, 1998, 11 (02) : 179 - 182
  • [6] Is genotype clinically useful in predicting prognosis in hypertrophic cardiomyopathy? Mutation Type Is Not Clinically Useful in Predicting Prognosis in Hypertrophic Cardiomyopathy
    Landstrom, Andrew P.
    Ackerman, Michael J.
    CIRCULATION, 2010, 122 (23) : 2441 - 2449
  • [7] Phenotype comparison of familial hypertrophic cardiomyopathy with β-myosin heavy chain gene mutation with or without mitochondrial DNA mutation
    Arai, S
    Joh-O, K
    Furutani, M
    Hayashi, J
    Imamura, S
    Nishikawa, T
    Nagao, H
    Takao, A
    Momma, K
    Matsuoka, R
    CIRCULATION, 1999, 100 (18) : 817 - 817
  • [8] Sudden cardiac death in familial hypertrophic cardiomyopathy is associated with a novel mutation in the troponin I gene
    Mogensen, J
    Klausen, IC
    Egeblad, H
    Baandrup, U
    CIRCULATION, 1999, 100 (18) : 618 - 618
  • [9] A mouse model of familial hypertrophic cardiomyopathy caused by a α-tropomyosin mutation
    Prabhakar, R
    Petrashevskaya, N
    Schwartz, A
    Aronow, B
    Boivin, GP
    Molkentin, JD
    Wieczorek, DF
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 2003, 251 (1-2) : 33 - 42
  • [10] A mouse model for α-tropomyosin mutation that causes familial hypertrophic cardiomyopathy
    Prabhakar, R
    Boivin, GP
    Grupp, I
    Artega, G
    Aronow, B
    Solaro, RJ
    Wieczorek, DF
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2001, 33 (06) : A96 - A96