These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

99 related articles for article (PubMed ID: 10563488)

  • 1. Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene.
    Andersen PS; Havndrup O; Bundgaard H; Larsen LA; Vuust J; Kjeldsen K; Christiansen M
    Clin Genet; 1999 Sep; 56(3):244-6. PubMed ID: 10563488
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. [Analysis of genotype-phenotype correlation for a novel MYH7-D554Y mutation identified in an ethnic Han Chinese pedigree affected with hypertrophic cardiomyopathy].
    Yang Q; Wang B; Wang J; Sun C; Ma Z; Zuo L; Zhang Y; Liu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Oct; 35(5):667-671. PubMed ID: 30298491
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation.
    Overeem S; Schelhaas HJ; Blijham PJ; Grootscholten MI; ter Laak HJ; Timmermans J; van den Wijngaard A; Zwarts MJ
    Neuromuscul Disord; 2007 Jun; 17(6):490-3. PubMed ID: 17383184
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gene symbol: MYH7. Disease: cardiomyopathy, hypertrophic.
    Capek PC
    Hum Genet; 2005 Dec; 118(3-4):537. PubMed ID: 16521248
    [No Abstract]   [Full Text] [Related]  

  • 7. [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]  

  • 8. Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathy.
    Richard P; Charron P; Leclercq C; Ledeuil C; Carrier L; Dubourg O; Desnos M; Bouhour JB; Schwartz K; Daubert JC; Komajda M; Hainque B
    J Mol Cell Cardiol; 2000 Aug; 32(8):1575-83. PubMed ID: 10900182
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel cardiac beta-myosin heavy chain gene missense mutations (R869C and R870C) that cause familial hypertrophic cardiomyopathy.
    Anan R; Shono H; Tei C
    Hum Mutat; 2000 Jun; 15(6):584. PubMed ID: 10862102
    [No Abstract]   [Full Text] [Related]  

  • 10.
    Dias GM; Lamounier Júnior A; Seifert M; Barájas-Martinez H; Barr D; Sternick EB; Medina-Acosta E; Campos de Carvalho AC; Cruz Filho FES
    Circ Genom Precis Med; 2021 Oct; 14(5):e003476. PubMed ID: 34555931
    [No Abstract]   [Full Text] [Related]  

  • 11. A new mutation affecting the converter region of the beta-myosin heavy chain related to hypertrophic cardiomyopathy with poor prognosis.
    Nuche J; Salguero-Bodes R; Valverde-Gómez M; Delgado JF; Arribas-Ynsaurriaga F; Palomino-Doza J
    Rev Esp Cardiol (Engl Ed); 2020 Feb; 73(2):180-183. PubMed ID: 31416728
    [No Abstract]   [Full Text] [Related]  

  • 12. A previously undescribed de novo insertion-deletion mutation in the beta myosin heavy chain gene in a kindred with familial hypertrophic cardiomyopathy.
    Cuda G; Perrotti N; Perticone F; Mattioli PL
    Heart; 1996 Nov; 76(5):451-2. PubMed ID: 8944596
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation.
    Gruver EJ; Fatkin D; Dodds GA; Kisslo J; Maron BJ; Seidman JG; Seidman CE
    Am J Cardiol; 1999 Jun; 83(12A):13H-18H. PubMed ID: 10750581
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of mutations in symptomatic patients with hypertrophic cardiomyopathy in Taiwan.
    Chiou KR; Chu CT; Charng MJ
    J Cardiol; 2015 Mar; 65(3):250-6. PubMed ID: 25086479
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.
    Perrot A; Schmidt-Traub H; Hoffmann B; Prager M; Bit-Avragim N; Rudenko RI; Usupbaeva DA; Kabaeva Z; Imanov B; Mirrakhimov MM; Dietz R; Wycisk A; Tendera M; Gessner R; Osterziel KJ
    J Mol Med (Berl); 2005 Jun; 83(6):468-77. PubMed ID: 15856146
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype-phenotype correlation of R870H mutation in hypertrophic cardiomyopathy.
    Tanjore RR; Sikindlapuram AD; Calambur N; Thakkar B; Kerkar PG; Nallari P
    Clin Genet; 2006 May; 69(5):434-6. PubMed ID: 16650083
    [No Abstract]   [Full Text] [Related]  

  • 17. Cranial, axial and proximal myopathy and hypertrophic cardiomyopathy caused by a mutation in the globular head region of the MYH7 gene.
    Díaz-Manera J; Alejaldre A; Llauger J; Mirabet S; Rojas-García R; Ramos-Fransi A; Gallardo E; Illa I
    Eur J Neurol; 2014 Jun; 21(6):e51-2. PubMed ID: 24805292
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy.
    Jääskeläinen P; Heliö T; Aalto-Setälä K; Kaartinen M; Ilveskoski E; Hämäläinen L; Melin J; Kärkkäinen S; Peuhkurinen K; Nieminen MS; Laakso M; ; Kuusisto J
    Ann Med; 2014 Sep; 46(6):424-9. PubMed ID: 24888384
    [TBL] [Abstract][Full Text] [Related]  

  • 20. First description of germline mosaicism in familial hypertrophic cardiomyopathy.
    Forissier JF; Richard P; Briault S; Ledeuil C; Dubourg O; Charbonnier B; Carrier L; Moraine C; Bonne G; Komajda M; Schwartz K; Hainque B
    J Med Genet; 2000 Feb; 37(2):132-4. PubMed ID: 10662815
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.