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2. Proteomic identification of putative biomarkers for early detection of sudden cardiac death in a family with a LMNA gene mutation causing dilated cardiomyopathy. Izquierdo I; Rosa I; Bravo SB; Guitián E; Pérez-Serra A; Campuzano O; Brugada R; Mangas A; García Á; Toro R J Proteomics; 2016 Oct; 148():75-84. PubMed ID: 27457270 [TBL] [Abstract][Full Text] [Related]
3. A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy. Kärkkäinen S; Heliö T; Miettinen R; Tuomainen P; Peltola P; Rummukainen J; Ylitalo K; Kaartinen M; Kuusisto J; Toivonen L; Nieminen MS; Laakso M; Peuhkurinen K Eur Heart J; 2004 May; 25(10):885-93. PubMed ID: 15140538 [TBL] [Abstract][Full Text] [Related]
4. Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death. Yokokawa T; Ichimura S; Hijioka N; Kaneshiro T; Yoshihisa A; Kunii H; Nakazato K; Ishida T; Suzuki O; Ohno S; Aiba T; Ohtani H; Takeishi Y BMC Cardiovasc Disord; 2019 Dec; 19(1):298. PubMed ID: 31847799 [TBL] [Abstract][Full Text] [Related]
5. [A novel lamin A/C mutation in a family with dilated cardiomyopathy and a strong history of sudden cardiac death]. Andreassi MG; Botto N; Vittorini S; Pulignani S; Aquaro G; Sicari R Recenti Prog Med; 2010 Mar; 101(3):127-30. PubMed ID: 20461955 [TBL] [Abstract][Full Text] [Related]
6. Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy. Forleo C; Carmosino M; Resta N; Rampazzo A; Valecce R; Sorrentino S; Iacoviello M; Pisani F; Procino G; Gerbino A; Scardapane A; Simone C; Calore M; Torretta S; Svelto M; Favale S PLoS One; 2015; 10(4):e0121723. PubMed ID: 25837155 [TBL] [Abstract][Full Text] [Related]
7. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics. van Tintelen JP; Hofstra RM; Katerberg H; Rossenbacker T; Wiesfeld AC; du Marchie Sarvaas GJ; Wilde AA; van Langen IM; Nannenberg EA; van der Kooi AJ; Kraak M; van Gelder IC; van Veldhuisen DJ; Vos Y; van den Berg MP; Am Heart J; 2007 Dec; 154(6):1130-9. PubMed ID: 18035086 [TBL] [Abstract][Full Text] [Related]
8. Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications. van Rijsingen IA; Bakker A; Azim D; Hermans-van Ast JF; van der Kooi AJ; van Tintelen JP; van den Berg MP; Christiaans I; Lekanne Dit Deprez RH; Wilde AA; Zwinderman AH; Meijers JC; Grootemaat AE; Nieuwland R; Pinto YM; Pinto-Sietsma SJ Int J Cardiol; 2013 Sep; 168(1):472-7. PubMed ID: 23073275 [TBL] [Abstract][Full Text] [Related]
9. Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience. van Spaendonck-Zwarts KY; van Rijsingen IA; van den Berg MP; Lekanne Deprez RH; Post JG; van Mil AM; Asselbergs FW; Christiaans I; van Langen IM; Wilde AA; de Boer RA; Jongbloed JD; Pinto YM; van Tintelen JP Eur J Heart Fail; 2013 Jun; 15(6):628-36. PubMed ID: 23349452 [TBL] [Abstract][Full Text] [Related]
10. Identification of novel mutations in LMNA associated with familial forms of dilated cardiomyopathy. Stallmeyer B; Koopmann M; Schulze-Bahr E Genet Test Mol Biomarkers; 2012 Jun; 16(6):543-9. PubMed ID: 22224630 [TBL] [Abstract][Full Text] [Related]
11. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. Fatkin D; MacRae C; Sasaki T; Wolff MR; Porcu M; Frenneaux M; Atherton J; Vidaillet HJ; Spudich S; De Girolami U; Seidman JG; Seidman C; Muntoni F; Müehle G; Johnson W; McDonough B N Engl J Med; 1999 Dec; 341(23):1715-24. PubMed ID: 10580070 [TBL] [Abstract][Full Text] [Related]
12. Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy. Millat G; Bouvagnet P; Chevalier P; Sebbag L; Dulac A; Dauphin C; Jouk PS; Delrue MA; Thambo JB; Le Metayer P; Seronde MF; Faivre L; Eicher JC; Rousson R Eur J Med Genet; 2011; 54(6):e570-5. PubMed ID: 21846512 [TBL] [Abstract][Full Text] [Related]
13. Clinical and Genetic Investigations of 109 Index Patients With Dilated Cardiomyopathy and 445 of Their Relatives. Hey TM; Rasmussen TB; Madsen T; Aagaard MM; Harbo M; Mølgaard H; Nielsen SK; Haas J; Meder B; Møller JE; Eiskjær H; Mogensen J Circ Heart Fail; 2020 Oct; 13(10):e006701. PubMed ID: 33019804 [TBL] [Abstract][Full Text] [Related]
15. A novel mutation of the LMNA gene in a family with dilated cardiomyopathy, conduction system disease, and sudden cardiac death of young females. Chen W; Huo J; Ma A; Bai L; Liu P Mol Cell Biochem; 2013 Oct; 382(1-2):307-11. PubMed ID: 23793583 [TBL] [Abstract][Full Text] [Related]
16. Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy. Perrot A; Hussein S; Ruppert V; Schmidt HH; Wehnert MS; Duong NT; Posch MG; Panek A; Dietz R; Kindermann I; Böhm M; Michalewska-Wludarczyk A; Richter A; Maisch B; Pankuweit S; Ozcelik C Basic Res Cardiol; 2009 Jan; 104(1):90-9. PubMed ID: 18795223 [TBL] [Abstract][Full Text] [Related]
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18. Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death. Fernlund E; Österberg AW; Kuchinskaya E; Gustafsson M; Jansson K; Gunnarsson C Pediatr Cardiol; 2017 Aug; 38(6):1262-1268. PubMed ID: 28669108 [TBL] [Abstract][Full Text] [Related]
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