199 related articles for article (PubMed ID: 30235249)
61. Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy.
Friedrich FW; Wilding BR; Reischmann S; Crocini C; Lang P; Charron P; Müller OJ; McGrath MJ; Vollert I; Hansen A; Linke WA; Hengstenberg C; Bonne G; Morner S; Wichter T; Madeira H; Arbustini E; Eschenhagen T; Mitchell CA; Isnard R; Carrier L
Hum Mol Genet; 2012 Jul; 21(14):3237-54. PubMed ID: 22523091
[TBL] [Abstract][Full Text] [Related]
62. Clinical and genetic diagnosis of familial hypertrophic cardiomyopathy: Results in pediatric cardiology.
Cardoso B; Gomes I; Loureiro P; Trigo C; Ferreira Pinto F
Rev Port Cardiol; 2017 Mar; 36(3):155-165. PubMed ID: 28214152
[TBL] [Abstract][Full Text] [Related]
63. A Novel Missense Mutation p.Gly162Glu of the Gene MYL2 Involved in Hypertrophic Cardiomyopathy: A Pedigree Analysis of a Proband.
Renaudin P; Janin A; Millat G; Chevalier P
Mol Diagn Ther; 2018 Apr; 22(2):219-223. PubMed ID: 29549657
[TBL] [Abstract][Full Text] [Related]
64. Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure.
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; Viganò M
Heart; 1998 Dec; 80(6):548-58. PubMed ID: 10065021
[TBL] [Abstract][Full Text] [Related]
65. Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin.
Bos JM; Poley RN; Ny M; Tester DJ; Xu X; Vatta M; Towbin JA; Gersh BJ; Ommen SR; Ackerman MJ
Mol Genet Metab; 2006 May; 88(1):78-85. PubMed ID: 16352453
[TBL] [Abstract][Full Text] [Related]
66. Morphological and functional abnormalities pattern in hypertrophy-free HCM mutation carriers detected with echocardiography.
Peyrou J; Réant P; Reynaud A; Cornolle C; Dijos M; Rooryck-Thambo C; Landelle M; Montaudon M; Laurent F; Roudaut R; Lafitte S
Int J Cardiovasc Imaging; 2016 Sep; 32(9):1379-1389. PubMed ID: 27324645
[TBL] [Abstract][Full Text] [Related]
67. Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy.
Olson TM; Doan TP; Kishimoto NY; Whitby FG; Ackerman MJ; Fananapazir L
J Mol Cell Cardiol; 2000 Sep; 32(9):1687-94. PubMed ID: 10966831
[TBL] [Abstract][Full Text] [Related]
68. Development of left ventricular hypertrophy in adults in hypertrophic cardiomyopathy caused by cardiac myosin-binding protein C gene mutations.
Maron BJ; Niimura H; Casey SA; Soper MK; Wright GB; Seidman JG; Seidman CE
J Am Coll Cardiol; 2001 Aug; 38(2):315-21. PubMed ID: 11499718
[TBL] [Abstract][Full Text] [Related]
69. Myosin-binding Protein C Compound Heterozygous Variant Effect on the Phenotypic Expression of Hypertrophic Cardiomyopathy.
Rafael JF; Cruz FEDS; Carvalho ACC; Gottlieb I; Cazelli JG; Siciliano AP; Dias GM
Arq Bras Cardiol; 2017 Apr; 108(4):354-360. PubMed ID: 28538763
[TBL] [Abstract][Full Text] [Related]
70. Advances in medical treatment of hypertrophic cardiomyopathy.
Hamada M; Ikeda S; Shigematsu Y
J Cardiol; 2014 Jul; 64(1):1-10. PubMed ID: 24735741
[TBL] [Abstract][Full Text] [Related]
71. A case of compound mutations in the MYBPC3 gene associated with biventricular hypertrophy and neonatal death.
Marziliano N; Merlini PA; Vignati G; Orsini F; Motta V; Bandiera L; Intrieri M; Veronese S
Neonatology; 2012; 102(4):254-8. PubMed ID: 22907696
[TBL] [Abstract][Full Text] [Related]
72. Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.
Blair E; Redwood C; de Jesus Oliveira M; Moolman-Smook JC; Brink P; Corfield VA; Ostman-Smith I; Watkins H
Circ Res; 2002 Feb; 90(3):263-9. PubMed ID: 11861413
[TBL] [Abstract][Full Text] [Related]
73. Early changes in apical rotation in genotype positive children with hypertrophic cardiomyopathy mutations without hypertrophic changes on two-dimensional imaging.
Forsey J; Benson L; Rozenblyum E; Friedberg MK; Mertens L
J Am Soc Echocardiogr; 2014 Feb; 27(2):215-21. PubMed ID: 24325958
[TBL] [Abstract][Full Text] [Related]
74. Compound heterozygosity deteriorates phenotypes of hypertrophic cardiomyopathy with founder MYBPC3 mutation: evidence from patients and zebrafish models.
Hodatsu A; Konno T; Hayashi K; Funada A; Fujita T; Nagata Y; Fujino N; Kawashiri MA; Yamagishi M
Am J Physiol Heart Circ Physiol; 2014 Dec; 307(11):H1594-604. PubMed ID: 25281569
[TBL] [Abstract][Full Text] [Related]
75. A missense mutation in the beta myosin heavy chain gene is a predictor of premature sudden death in patients with hypertrophic cardiomyopathy.
Marian AJ; Kelly D; Mares A; Fitzgibbons J; Caira T; Qun-Tao ; Hill R; Perryman MB; Roberts R
J Sports Med Phys Fitness; 1994 Mar; 34(1):1-10. PubMed ID: 7934006
[TBL] [Abstract][Full Text] [Related]
76. Ribosomal protein S6 kinase beta-1 gene variants cause hypertrophic cardiomyopathy.
Jain PK; Jayappa S; Sairam T; Mittal A; Paul S; Rao VJ; Chittora H; Kashyap DK; Palakodeti D; Thangaraj K; Shenthar J; Koranchery R; Rajendran R; Alireza H; Mohanan KS; Rathinavel A; Dhandapany PS
J Med Genet; 2022 Oct; 59(10):984-992. PubMed ID: 34916228
[TBL] [Abstract][Full Text] [Related]
77. Altered myocardial lipid regulation in junctophilin-2-associated familial cardiomyopathies.
Lahiri SK; Jin F; Zhou Y; Quick AP; Kramm CF; Wang MC; Wehrens XH
Life Sci Alliance; 2024 May; 7(5):. PubMed ID: 38438248
[TBL] [Abstract][Full Text] [Related]
78. A double heterozygous variant in
Suzuki T; Saito K; Yoshikawa T; Hirono K; Hata Y; Nishida N; Yasuda K; Nagashima M
J Cardiol Cases; 2022 Apr; 25(4):213-217. PubMed ID: 35911064
[TBL] [Abstract][Full Text] [Related]
79. Protein Thermodynamic Destabilization in the Assessment of Pathogenicity of a Variant of Uncertain Significance in Cardiac Myosin Binding Protein C.
Pricolo MR; Herrero-Galán E; Mazzaccara C; Losi MA; Alegre-Cebollada J; Frisso G
J Cardiovasc Transl Res; 2020 Oct; 13(5):867-877. PubMed ID: 32034629
[TBL] [Abstract][Full Text] [Related]
80. Case Report: Two New Cases of Autosomal-Recessive Hypertrophic Cardiomyopathy Associated With
Andreeva S; Chumakova O; Karelkina E; Lebedeva V; Lubimtseva T; Semenov A; Nikitin A; Speshilov G; Kozyreva A; Sokolnikova P; Zhuk S; Fomicheva Y; Moiseeva O; Kostareva A
Front Genet; 2022; 13():743472. PubMed ID: 35273634
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]