These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
173 related articles for article (PubMed ID: 24880466)
1. Novel and highly lethal NKX2.5 missense mutation in a family with sudden death and ventricular arrhythmia. Perera JL; Johnson NM; Judge DP; Crosson JE Pediatr Cardiol; 2014 Oct; 35(7):1206-12. PubMed ID: 24880466 [TBL] [Abstract][Full Text] [Related]
2. Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature. Ellesøe SG; Johansen MM; Bjerre JV; Hjortdal VE; Brunak S; Larsen LA Congenit Heart Dis; 2016 May; 11(3):283-90. PubMed ID: 26679770 [TBL] [Abstract][Full Text] [Related]
3. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome. Elliott DA; Kirk EP; Yeoh T; Chandar S; McKenzie F; Taylor P; Grossfeld P; Fatkin D; Jones O; Hayes P; Feneley M; Harvey RP J Am Coll Cardiol; 2003 Jun; 41(11):2072-6. PubMed ID: 12798584 [TBL] [Abstract][Full Text] [Related]
4. R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease. Beffagna G; Cecchetto A; Dal Bianco L; Lorenzon A; Angelini A; Padalino M; Vida V; Bhattacharya S; Stellin G; Rampazzo A; Daliento L J Cardiovasc Med (Hagerstown); 2013 Aug; 14(8):582-6. PubMed ID: 22964646 [TBL] [Abstract][Full Text] [Related]
5. NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity. Abou Hassan OK; Fahed AC; Batrawi M; Arabi M; Refaat MM; DePalma SR; Seidman JG; Seidman CE; Bitar FF; Nemer GM Sci Rep; 2015 Mar; 5():8848. PubMed ID: 25742962 [TBL] [Abstract][Full Text] [Related]
6. Importance of ventricular tachycardia storms not terminated by implantable cardioverter defibrillators shocks in patients with CASQ2 associated catecholaminergic polymorphic ventricular tachycardia. Marai I; Khoury A; Suleiman M; Gepstein L; Blich M; Lorber A; Boulos M Am J Cardiol; 2012 Jul; 110(1):72-6. PubMed ID: 22481011 [TBL] [Abstract][Full Text] [Related]
7. Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease. Stallmeyer B; Fenge H; Nowak-Göttl U; Schulze-Bahr E Clin Genet; 2010 Dec; 78(6):533-40. PubMed ID: 20456451 [TBL] [Abstract][Full Text] [Related]
8. Novel NKX2-5 mutations responsible for congenital heart disease. Wang J; Liu XY; Yang YQ Genet Mol Res; 2011 Nov; 10(4):2905-15. PubMed ID: 22179962 [TBL] [Abstract][Full Text] [Related]
9. NKX2-5 genetic mutation in a young woman with an atrial septal defect presenting with complete heart block: ICD or bradycardia pacemaker? El-Medany A; Aziz S; Duncan E BMJ Case Rep; 2023 Jan; 16(1):. PubMed ID: 36609421 [TBL] [Abstract][Full Text] [Related]
10. Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardia. Sy RW; Gollob MH; Klein GJ; Yee R; Skanes AC; Gula LJ; Leong-Sit P; Gow RM; Green MS; Birnie DH; Krahn AD Heart Rhythm; 2011 Jun; 8(6):864-71. PubMed ID: 21315846 [TBL] [Abstract][Full Text] [Related]
11. A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death. Ouyang P; Saarel E; Bai Y; Luo C; Lv Q; Xu Y; Wang F; Fan C; Younoszai A; Chen Q; Tu X; Wang QK Clin Chim Acta; 2011 Jan; 412(1-2):170-5. PubMed ID: 20932824 [TBL] [Abstract][Full Text] [Related]
12. NKX2.5 mutations in patients with congenital heart disease. McElhinney DB; Geiger E; Blinder J; Benson DW; Goldmuntz E J Am Coll Cardiol; 2003 Nov; 42(9):1650-5. PubMed ID: 14607454 [TBL] [Abstract][Full Text] [Related]
14. Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect. Hirayama-Yamada K; Kamisago M; Akimoto K; Aotsuka H; Nakamura Y; Tomita H; Furutani M; Imamura S; Takao A; Nakazawa M; Matsuoka R Am J Med Genet A; 2005 May; 135(1):47-52. PubMed ID: 15810002 [TBL] [Abstract][Full Text] [Related]
15. Wenckebach periodicity at rest that normalizes with tachycardia in a family with a NKX2.5 mutation. Guntheroth W; Chun L; Patton KK; Matsushita MM; Page RL; Raskind WH Am J Cardiol; 2012 Dec; 110(11):1646-50. PubMed ID: 22920929 [TBL] [Abstract][Full Text] [Related]
17. Familial atrial septal defect and atrioventricular conduction disturbance associated with a point mutation in the cardiac homeobox gene CSX/NKX2-5 in a Japanese patient. Hosoda T; Komuro I; Shiojima I; Hiroi Y; Harada M; Murakawa Y; Hirata Y; Yazaki Y Jpn Circ J; 1999 May; 63(5):425-6. PubMed ID: 10943630 [TBL] [Abstract][Full Text] [Related]
18. Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in the CSX/NKX2-5 gene. Gutierrez-Roelens I; Sluysmans T; Gewillig M; Devriendt K; Vikkula M Hum Mutat; 2002 Jul; 20(1):75-6. PubMed ID: 12112663 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects. Salazar M; Consoli F; Villegas V; Caicedo V; Maddaloni V; Daniele P; Caianiello G; Pachón S; Nuñez F; Limongelli G; Pacileo G; Marino B; Bernal JE; De Luca A; Dallapiccola B Eur J Med Genet; 2011; 54(3):306-9. PubMed ID: 21276881 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]