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2. [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]
3. 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]
4. A novel mutation in LAMIN A/C is associated with isolated early-onset atrial fibrillation and progressive atrioventricular block followed by cardiomyopathy and sudden cardiac death. Pan H; Richards AA; Zhu X; Joglar JA; Yin HL; Garg V Heart Rhythm; 2009 May; 6(5):707-10. PubMed ID: 19328042 [No Abstract] [Full Text] [Related]
5. 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]
6. A novel LMNA nonsense mutation causes two distinct phenotypes of cardiomyopathy with high risk of sudden cardiac death in a large five-generation family. Glöcklhofer CR; Steinfurt J; Franke G; Hoppmann A; Glantschnig T; Perez-Feliz S; Alter S; Fischer J; Brunner M; Rainer PP; Köttgen A; Bode C; Odening KE Europace; 2018 Dec; 20(12):2003-2013. PubMed ID: 29947763 [TBL] [Abstract][Full Text] [Related]
9. Risk prediction of ventricular arrhythmias and myocardial function in Lamin A/C mutation positive subjects. Hasselberg NE; Edvardsen T; Petri H; Berge KE; Leren TP; Bundgaard H; Haugaa KH Europace; 2014 Apr; 16(4):563-71. PubMed ID: 24058181 [TBL] [Abstract][Full Text] [Related]
10. A cardio-neurological form of laminopathy: dilated cardiomyopathy with permanent partial atrial standstill and axonal neuropathy. Duparc A; Cintas P; Somody E; Bieth E; Richard P; Maury P; Delay M Pacing Clin Electrophysiol; 2009 Mar; 32(3):410-5. PubMed ID: 19272076 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. A novel c.563 T>G, p.L189R lamin A/C mutation in identical twins with dilated cardiomyopathy. Lee E; Park KT; Kang J; Park H; Park JJ; Oh IY; Yoon YE Korean J Intern Med; 2017 Jan; 32(1):178-181. PubMed ID: 26951916 [No Abstract] [Full Text] [Related]
13. Primary prevention of sudden death in patients with lamin A/C gene mutations. Meune C; Van Berlo JH; Anselme F; Bonne G; Pinto YM; Duboc D N Engl J Med; 2006 Jan; 354(2):209-10. PubMed ID: 16407522 [No Abstract] [Full Text] [Related]
14. Malignant mutation in the lamin A/C gene causing progressive conduction system disease and early sudden death in a family with mild form of limb-girdle muscular dystrophy. Antoniades L; Eftychiou C; Kyriakides T; Christodoulou K; Katritsis DG J Interv Card Electrophysiol; 2007 Jun; 19(1):1-7. PubMed ID: 17605093 [TBL] [Abstract][Full Text] [Related]
15. Novel human pathological mutations. Gene symbol: LMNA. Disease: cardiomyopathy, dilated with conduction defects. Arbustini E; Pilotto A; Grasso M; Marziliano N; Serio A; Gambarin F; Pasotti M; Serafini E; Cassini P; Digiorgio B Hum Genet; 2009 Apr; 125(3):350. PubMed ID: 19320036 [No Abstract] [Full Text] [Related]
17. A novel overlapping phenotype characterized by lipodystrophy, mandibular dysplasia, and dilated cardiomyopathy associated with a new mutation in the LMNA gene. Ambrosi P; Kreitmann B; Lepidi H; Habib G; Levy N; Philip N; De Sandre-Giovannoli A Int J Cardiol; 2016 Apr; 209():317-8. PubMed ID: 26922292 [No Abstract] [Full Text] [Related]
18. Sudden cardiac death in a patient with lamin A/C mutation in the absence of dilated cardiomyopathy or conduction disease. Ehlermann P; Lehrke S; Papavassiliu T; Meder B; Borggrefe M; Katus HA; Schimpf R Clin Res Cardiol; 2011 Jun; 100(6):547-51. PubMed ID: 21327842 [No Abstract] [Full Text] [Related]
19. Dilated cardiomyopathy with profound segmental wall motion abnormalities and ventricular arrhythmia caused by the R541C mutation in the LMNA gene. Saj M; Jankowska A; Lewandowski M; Szwed H; Szperl M; Płoski R; Bilińska ZT Int J Cardiol; 2010 Oct; 144(3):e51-3. PubMed ID: 19167105 [TBL] [Abstract][Full Text] [Related]
20. Laminopathies: a Pandora's box of heart failure, bradyarrhythmias and sudden death. Cabanelas N; Martins VP Rev Port Cardiol; 2015 Feb; 34(2):139.e1-5. PubMed ID: 25656816 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]