194 related articles for article (PubMed ID: 22413764)
1. Variants of the lamin A/C (LMNA) gene in non-valvular atrial fibrillation patients: a possible pathogenic role of the Thr528Met mutation.
Saj M; Dabrowski R; Labib S; Jankowska A; Szperl M; Broda G; Szwed H; Tesson F; Bilinska ZT; Ploski R
Mol Diagn Ther; 2012 Apr; 16(2):99-107. PubMed ID: 22413764
[TBL] [Abstract][Full Text] [Related]
2.
Hoorntje ET; Bollen IA; Barge-Schaapveld DQ; van Tienen FH; Te Meerman GJ; Jansweijer JA; van Essen AJ; Volders PG; Constantinescu AA; van den Akker PC; van Spaendonck-Zwarts KY; Oldenburg RA; Marcelis CL; van der Smagt JJ; Hennekam EA; Vink A; Bootsma M; Aten E; Wilde AA; van den Wijngaard A; Broers JL; Jongbloed JD; van der Velden J; van den Berg MP; van Tintelen JP
Circ Cardiovasc Genet; 2017 Aug; 10(4):. PubMed ID: 28790152
[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. LMNA mutations in Polish patients with dilated cardiomyopathy: prevalence, clinical characteristics, and in vitro studies.
Saj M; Bilinska ZT; Tarnowska A; Sioma A; Bolongo P; Sobieszczanska-Malek M; Michalak E; Golen D; Mazurkiewicz L; Malek L; Walczak E; Fidzianska A; Grzybowski J; Przybylski A; Zielinski T; Korewicki J; Tesson F; Ploski R
BMC Med Genet; 2013 May; 14():55. PubMed ID: 23702046
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A novel nonsense mutation in LMNA gene identified by Exome Sequencing in an atrial fibrillation family.
Zhao J; Yao H; Li Z; Wang L; Liu G; Wang DW; Wang DW; Liang Z
Eur J Med Genet; 2016 Aug; 59(8):396-400. PubMed ID: 27373676
[TBL] [Abstract][Full Text] [Related]
7. Implantable cardioverter-defibrillators in lamin A/C mutation carriers with cardiac conduction disorders.
Anselme F; Moubarak G; Savouré A; Godin B; Borz B; Drouin-Garraud V; Gay A
Heart Rhythm; 2013 Oct; 10(10):1492-8. PubMed ID: 23811080
[TBL] [Abstract][Full Text] [Related]
8. Gene-Based Risk Stratification for Cardiac Disorders in
Nishiuchi S; Makiyama T; Aiba T; Nakajima K; Hirose S; Kohjitani H; Yamamoto Y; Harita T; Hayano M; Wuriyanghai Y; Chen J; Sasaki K; Yagihara N; Ishikawa T; Onoue K; Murakoshi N; Watanabe I; Ohkubo K; Watanabe H; Ohno S; Doi T; Shizuta S; Minamino T; Saito Y; Oginosawa Y; Nogami A; Aonuma K; Kusano K; Makita N; Shimizu W; Horie M; Kimura T
Circ Cardiovasc Genet; 2017 Dec; 10(6):. PubMed ID: 29237675
[TBL] [Abstract][Full Text] [Related]
9. Non-syndromic cardiac progeria in a patient with the rare pathogenic p.Asp300Asn variant in the LMNA gene.
Marian AJ
BMC Med Genet; 2017 Oct; 18(1):116. PubMed ID: 29047356
[TBL] [Abstract][Full Text] [Related]
10. Intrinsic Atrial Myopathy Precedes Left Ventricular Dysfunction and Predicts Atrial Fibrillation in
Tremblay-Gravel M; Ichimura K; Picard K; Kawano Y; Dries AM; Haddad F; Lakdawala NK; Wheeler MT; Parikh VN
Circ Genom Precis Med; 2023 Feb; 16(1):e003480. PubMed ID: 36548481
[TBL] [Abstract][Full Text] [Related]
11. Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation.
Hasselberg NE; Haland TF; Saberniak J; Brekke PH; Berge KE; Leren TP; Edvardsen T; Haugaa KH
Eur Heart J; 2018 Mar; 39(10):853-860. PubMed ID: 29095976
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.
Sébillon P; Bouchier C; Bidot LD; Bonne G; Ahamed K; Charron P; Drouin-Garraud V; Millaire A; Desrumeaux G; Benaïche A; Charniot JC; Schwartz K; Villard E; Komajda M
J Med Genet; 2003 Aug; 40(8):560-7. PubMed ID: 12920062
[TBL] [Abstract][Full Text] [Related]
14. Comprehensive mutation scanning of LMNA in 268 patients with lone atrial fibrillation.
Brauch KM; Chen LY; Olson TM
Am J Cardiol; 2009 May; 103(10):1426-8. PubMed ID: 19427440
[TBL] [Abstract][Full Text] [Related]
15. Complex phenotype linked to a mutation in exon 11 of the lamin A/C gene: Hypertrophic cardiomyopathy, atrioventricular block, severe dyslipidemia and diabetes.
Francisco ARG; Santos Gonçalves I; Veiga F; Mendes Pedro M; Pinto FJ; Brito D
Rev Port Cardiol; 2017 Sep; 36(9):669.e1-669.e4. PubMed ID: 28874324
[TBL] [Abstract][Full Text] [Related]
16. Lamin A/C cardiomyopathy presenting as high-grade atrioventricular (AV) block, atrial fibrillation, heart failure and ventricular tachycardia in a single-family cluster.
Lubin SR; Paulraj S; Ahmed J
BMJ Case Rep; 2023 Jun; 16(6):. PubMed ID: 37348923
[TBL] [Abstract][Full Text] [Related]
17. Cardiac effects of the c.1583 C→G LMNA mutation in two families with Emery-Dreifuss muscular dystrophy.
Zhang L; Shen H; Zhao Z; Bing Q; Hu J
Mol Med Rep; 2015 Oct; 12(4):5065-71. PubMed ID: 26165385
[TBL] [Abstract][Full Text] [Related]
18. Lamin A/C gene mutations in familial cardiomyopathy with advanced atrioventricular block and arrhythmia.
Saga A; Karibe A; Otomo J; Iwabuchi K; Takahashi T; Kanno H; Kikuchi J; Keitoku M; Shinozaki T; Shimokawa H
Tohoku J Exp Med; 2009 Aug; 218(4):309-16. PubMed ID: 19638735
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Use of machine learning to classify high-risk variants of uncertain significance in lamin A/C cardiac disease.
Bennett JS; Gordon DM; Majumdar U; Lawrence PJ; Matos-Nieves A; Myers K; Kamp AN; Leonard JC; McBride KL; White P; Garg V
Heart Rhythm; 2022 Apr; 19(4):676-685. PubMed ID: 34958940
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
