185 related articles for article (PubMed ID: 25422285)
1. A novel MYH7 mutation in a family with cardiomyopathy presenting with restrictive physiology and varying degrees of left ventricle hypertrophy.
Yu BL; Xiang R; Hu D; Peng DQ
Eur Heart J; 2015 Jan; 36(3):178. PubMed ID: 25422285
[No Abstract] [Full Text] [Related]
2. Whole Exome Sequencing Identified a 13 Base Pair
Fan LL; Guo S; Jin JY; He ZJ; Zhao SP; Xiang R; Zhao W
Ann Clin Lab Sci; 2019 Nov; 49(6):838-840. PubMed ID: 31882438
[No Abstract] [Full Text] [Related]
3. A de novo mutation of the beta cardiac myosin heavy chain gene in an infantile restrictive cardiomyopathy.
Karam S; Raboisson MJ; Ducreux C; Chalabreysse L; Millat G; Bozio A; Bouvagnet P
Congenit Heart Dis; 2008; 3(2):138-43. PubMed ID: 18380764
[TBL] [Abstract][Full Text] [Related]
4. Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.
Selvi Rani D; Nallari P; Dhandapany PS; Rani J; Meraj K; Ganesan M; Narasimhan C; Thangaraj K
DNA Cell Biol; 2015 May; 34(5):350-9. PubMed ID: 25607779
[TBL] [Abstract][Full Text] [Related]
5. Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies.
Hoedemaekers YM; Caliskan K; Majoor-Krakauer D; van de Laar I; Michels M; Witsenburg M; ten Cate FJ; Simoons ML; Dooijes D
Eur Heart J; 2007 Nov; 28(22):2732-7. PubMed ID: 17947214
[TBL] [Abstract][Full Text] [Related]
6. Sudden death in an infant with angina, restrictive cardiomyopathy, and coronary artery bridging: an unusual phenotype for a β-myosin heavy chain (MYH7) sarcomeric protein mutation.
Greenway SC; Wilson GJ; Wilson J; George K; Kantor PF
Circ Heart Fail; 2012 Nov; 5(6):e92-3. PubMed ID: 23170025
[No Abstract] [Full Text] [Related]
7. A p.R870H mutation in the beta-cardiac myosin heavy chain 7 gene causes familial hypertrophic cardiomyopathy in several members of an Indian family.
Bashyam MD; Savithri GR; Gopikrishna M; Narasimhan C
Can J Cardiol; 2007 Aug; 23(10):788-90. PubMed ID: 17703256
[TBL] [Abstract][Full Text] [Related]
8. Exome sequencing identifies a novel MYH7 p.G407C mutation responsible for familial hypertrophic cardiomyopathy.
Guo Q; Xu Y; Wang X; Guo Y; Xu R; Sun K; Chen S
DNA Cell Biol; 2014 Oct; 33(10):699-704. PubMed ID: 24963656
[TBL] [Abstract][Full Text] [Related]
9. Gene symbol: MYH7.
Iascone MR; Marchetti D; Ferrazzi P
Hum Genet; 2007 Feb; 120(6):915. PubMed ID: 17438618
[No Abstract] [Full Text] [Related]
10. A new missense mutation, p.Arg719Leu, of the beta-myosin heavy chain gene in a patient with familial hypertrophic cardiomyopathy.
Gawor M; Bilińska ZT; Franaszczyk M; Michalak E; Rafał P; Grzybowski J
Minerva Cardioangiol; 2017 Feb; 65(1):96-102. PubMed ID: 27910300
[No Abstract] [Full Text] [Related]
11. [The Val606Met mutation of human beta myosin heavy chain in a Chinese familial hypertrophic cardiomyopathy family].
Yuan JS; Qiao SB; Wang SX; Teng SY; You SJ; Yang WX; Gao RL; Chen JL; Yang YJ
Zhonghua Xin Xue Guan Bing Za Zhi; 2008 Apr; 36(4):313-6. PubMed ID: 19100006
[TBL] [Abstract][Full Text] [Related]
12. Intrauterine Treatment of a Fetus with Familial Hypertrophic Cardiomyopathy Secondary to MYH7 Mutation.
Hill MG; Sekhon MK; Reed KL; Anderson CF; Borjon ND; Tardiff JC; Barber BJ
Pediatr Cardiol; 2015 Dec; 36(8):1774-7. PubMed ID: 26337809
[TBL] [Abstract][Full Text] [Related]
13. Mutations in MYH7 reduce the force generating capacity of sarcomeres in human familial hypertrophic cardiomyopathy.
Witjas-Paalberends ER; Piroddi N; Stam K; van Dijk SJ; Oliviera VS; Ferrara C; Scellini B; Hazebroek M; ten Cate FJ; van Slegtenhorst M; dos Remedios C; Niessen HW; Tesi C; Stienen GJ; Heymans S; Michels M; Poggesi C; van der Velden J
Cardiovasc Res; 2013 Aug; 99(3):432-41. PubMed ID: 23674513
[TBL] [Abstract][Full Text] [Related]
14. Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.
Dellefave LM; Pytel P; Mewborn S; Mora B; Guris DL; Fedson S; Waggoner D; Moskowitz I; McNally EM
Circ Cardiovasc Genet; 2009 Oct; 2(5):442-9. PubMed ID: 20031619
[TBL] [Abstract][Full Text] [Related]
15. Gene symbol: MYH7.
Iascone MR; Marchetti D; Ferrazzi P
Hum Genet; 2007 Feb; 120(6):916. PubMed ID: 17438619
[No Abstract] [Full Text] [Related]
16. Lack of Phenotypic Differences by Cardiovascular Magnetic Resonance Imaging in MYH7 (β-Myosin Heavy Chain)- Versus MYBPC3 (Myosin-Binding Protein C)-Related Hypertrophic Cardiomyopathy.
Weissler-Snir A; Hindieh W; Gruner C; Fourey D; Appelbaum E; Rowin E; Care M; Lesser JR; Haas TS; Udelson JE; Manning WJ; Olivotto I; Tomberli B; Maron BJ; Maron MS; Crean AM; Rakowski H; Chan RH
Circ Cardiovasc Imaging; 2017 Feb; 10(2):. PubMed ID: 28193612
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy.
Wang B; Wang J; Wang LF; Yang F; Xu L; Li WX; He Y; Zuo L; Yang QL; Shao H; Hu D; Liu LW
Mol Med Rep; 2019 Dec; 20(6):5229-5238. PubMed ID: 31638223
[TBL] [Abstract][Full Text] [Related]
19. Ventricular fibrillation in MYH7-related hypertrophic cardiomyopathy before onset of ventricular hypertrophy.
Christiaans I; Lekanne dit Deprez RH; van Langen IM; Wilde AA
Heart Rhythm; 2009 Sep; 6(9):1366-9. PubMed ID: 19539541
[No Abstract] [Full Text] [Related]
20. Asn391Thr Mutation of β-Myosin Heavy Chain in a Hypertrophic Cardiomyopathy Family.
Feng X; He T; Wang JG; Zhao P
Int Heart J; 2018 May; 59(3):596-600. PubMed ID: 29743414
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
