256 related articles for article (PubMed ID: 9829907)
1. Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.
Tesson F; Richard P; Charron P; Mathieu B; Cruaud C; Carrier L; Dubourg O; Lautié N; Desnos M; Millaire A; Isnard R; Hagege AA; Bouhour JB; Bennaceur M; Hainque B; Guicheney P; Schwartz K; Komajda M
Hum Mutat; 1998; 12(6):385-92. PubMed ID: 9829907
[TBL] [Abstract][Full Text] [Related]
2. Prognostic significance of beta-myosin heavy chain mutations is reflective of their hypertrophic expressivity in patients with hypertrophic cardiomyopathy.
Abchee A; Marian AJ
J Investig Med; 1997 Apr; 45(4):191-6. PubMed ID: 9154300
[TBL] [Abstract][Full Text] [Related]
3. Familial hypertrophic cardiomyopathy: the same mutation, different prognosis. Comparison of two families with a long follow-up.
Brito D; Richard P; Isnard R; Pipa J; Komajda M; Madeira H
Rev Port Cardiol; 2003 Dec; 22(12):1445-61. PubMed ID: 15008060
[TBL] [Abstract][Full Text] [Related]
4. Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy.
Richard P; Isnard R; Carrier L; Dubourg O; Donatien Y; Mathieu B; Bonne G; Gary F; Charron P; Hagege M; Komajda M; Schwartz K; Hainque B
J Med Genet; 1999 Jul; 36(7):542-5. PubMed ID: 10424815
[TBL] [Abstract][Full Text] [Related]
5. Beta-myosin heavy chain gene mutations and hypertrophic cardiomyopathy in Austrian children.
Greber-Platzer S; Marx M; Fleischmann C; Suppan C; Dobner M; Wimmer M
J Mol Cell Cardiol; 2001 Jan; 33(1):141-8. PubMed ID: 11133230
[TBL] [Abstract][Full Text] [Related]
6. A novel deletion mutation in the beta-myosin heavy chain gene found in Japanese patients with hypertrophic cardiomyopathy.
Nakajima-Taniguchi C; Matsui H; Eguchi N; Nagata S; Kishimoto T; Yamauchi-Takihara K
J Mol Cell Cardiol; 1995 Dec; 27(12):2607-12. PubMed ID: 8825881
[TBL] [Abstract][Full Text] [Related]
7. Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy.
Van Driest SL; Jaeger MA; Ommen SR; Will ML; Gersh BJ; Tajik AJ; Ackerman MJ
J Am Coll Cardiol; 2004 Aug; 44(3):602-10. PubMed ID: 15358028
[TBL] [Abstract][Full Text] [Related]
8. Missense mutation of the beta-cardiac myosin heavy-chain gene in hypertrophic cardiomyopathy.
Arai S; Matsuoka R; Hirayama K; Sakurai H; Tamura M; Ozawa T; Kimura M; Imamura S; Furutani Y; Joh-o K
Am J Med Genet; 1995 Sep; 58(3):267-76. PubMed ID: 8533830
[TBL] [Abstract][Full Text] [Related]
9. Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy.
Kabaeva ZT; Perrot A; Wolter B; Dietz R; Cardim N; Correia JM; Schulte HD; Aldashev AA; Mirrakhimov MM; Osterziel KJ
Eur J Hum Genet; 2002 Nov; 10(11):741-8. PubMed ID: 12404107
[TBL] [Abstract][Full Text] [Related]
10. [Mutation analysis of beta myosin heavy chain gene in hypertrophic cardiomyopathy families].
Fan XP; Yang ZW; Feng XL; Yang FH; Xiao B; Liang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug; 28(4):387-92. PubMed ID: 21811976
[TBL] [Abstract][Full Text] [Related]
11. Malignant hypertrophic cardiomyopathy caused by the Arg723Gly mutation in beta-myosin heavy chain gene.
Enjuto M; Francino A; Navarro-López F; Viles D; Paré JC; Ballesta AM
J Mol Cell Cardiol; 2000 Dec; 32(12):2307-13. PubMed ID: 11113006
[TBL] [Abstract][Full Text] [Related]
12. [Hypertrophic cardiomyopathy: infrequent mutation of the cardiac beta-myosin heavy-chain gene].
Mora R; Merino JL; Peinado R; Olias F; García-Guereta L; del Cerro MJ; Tarín MN; Molano J
Rev Esp Cardiol; 2006 Aug; 59(8):846-9. PubMed ID: 16938236
[TBL] [Abstract][Full Text] [Related]
13. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.
Watkins H; Rosenzweig A; Hwang DS; Levi T; McKenna W; Seidman CE; Seidman JG
N Engl J Med; 1992 Apr; 326(17):1108-14. PubMed ID: 1552912
[TBL] [Abstract][Full Text] [Related]
14. Identification of an Arg403Gln beta myosin heavy chain gene mutation in a Portuguese family with hypertrophic cardiomyopathy.
Gonçalves LM; Vieira M; Faro C; Ventura M; Pires E; Providência LA
Rev Port Cardiol; 2000 Apr; 19(4):431-43. PubMed ID: 10874840
[TBL] [Abstract][Full Text] [Related]
15. Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy.
Niimura H; Bachinski LL; Sangwatanaroj S; Watkins H; Chudley AE; McKenna W; Kristinsson A; Roberts R; Sole M; Maron BJ; Seidman JG; Seidman CE
N Engl J Med; 1998 Apr; 338(18):1248-57. PubMed ID: 9562578
[TBL] [Abstract][Full Text] [Related]
16. Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.
Dausse E; Komajda M; Fetler L; Dubourg O; Dufour C; Carrier L; Wisnewsky C; Bercovici J; Hengstenberg C; al-Mahdawi S
J Clin Invest; 1993 Dec; 92(6):2807-13. PubMed ID: 8254035
[TBL] [Abstract][Full Text] [Related]
17. Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain.
Bundgaard H; Havndrup O; Andersen PS; Larsen LA; Brandt NJ; Vuust J; Kjeldsen K; Christiansen M
J Mol Cell Cardiol; 1999 Apr; 31(4):745-50. PubMed ID: 10329202
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel missense mutation in the cardiac beta-myosin heavy chain gene in a Chinese patient with sporadic hypertrophic cardiomyopathy.
Kuang SQ; Yu JD; Lu L; He LM; Gong LS; Chen SJ; Chen Z
J Mol Cell Cardiol; 1996 Sep; 28(9):1879-83. PubMed ID: 8899546
[TBL] [Abstract][Full Text] [Related]
19. Identification of a novel Ala797Thr mutation in exon 21 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy.
Moolman JC; Brink PA; Corfield VA
Hum Mutat; 1995; 6(2):197-8. PubMed ID: 7581410
[No Abstract] [Full Text] [Related]
20. A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.
Girolami F; Olivotto I; Passerini I; Zachara E; Nistri S; Re F; Fantini S; Baldini K; Torricelli F; Cecchi F
J Cardiovasc Med (Hagerstown); 2006 Aug; 7(8):601-7. PubMed ID: 16858239
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
