451 related articles for article (PubMed ID: 21214875)
1. Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy.
Christensen AH; Andersen CB; Tybjaerg-Hansen A; Haunso S; Svendsen JH
Clin Genet; 2011 Sep; 80(3):256-64. PubMed ID: 21214875
[TBL] [Abstract][Full Text] [Related]
2. Wide spectrum of desmosomal mutations in Danish patients with arrhythmogenic right ventricular cardiomyopathy.
Christensen AH; Benn M; Bundgaard H; Tybjaerg-Hansen A; Haunso S; Svendsen JH
J Med Genet; 2010 Nov; 47(11):736-44. PubMed ID: 20864495
[TBL] [Abstract][Full Text] [Related]
3. Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy.
Quarta G; Syrris P; Ashworth M; Jenkins S; Zuborne Alapi K; Morgan J; Muir A; Pantazis A; McKenna WJ; Elliott PM
Eur Heart J; 2012 May; 33(9):1128-36. PubMed ID: 22199124
[TBL] [Abstract][Full Text] [Related]
4. Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy.
van Tintelen JP; Entius MM; Bhuiyan ZA; Jongbloed R; Wiesfeld AC; Wilde AA; van der Smagt J; Boven LG; Mannens MM; van Langen IM; Hofstra RM; Otterspoor LC; Doevendans PA; Rodriguez LM; van Gelder IC; Hauer RN
Circulation; 2006 Apr; 113(13):1650-8. PubMed ID: 16567567
[TBL] [Abstract][Full Text] [Related]
5. Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.
Fressart V; Duthoit G; Donal E; Probst V; Deharo JC; Chevalier P; Klug D; Dubourg O; Delacretaz E; Cosnay P; Scanu P; Extramiana F; Keller D; Hidden-Lucet F; Simon F; Bessirard V; Roux-Buisson N; Hebert JL; Azarine A; Casset-Senon D; Rouzet F; Lecarpentier Y; Fontaine G; Coirault C; Frank R; Hainque B; Charron P
Europace; 2010 Jun; 12(6):861-8. PubMed ID: 20400443
[TBL] [Abstract][Full Text] [Related]
6. Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis.
Antoniades L; Tsatsopoulou A; Anastasakis A; Syrris P; Asimaki A; Panagiotakos D; Zambartas C; Stefanadis C; McKenna WJ; Protonotarios N
Eur Heart J; 2006 Sep; 27(18):2208-16. PubMed ID: 16893920
[TBL] [Abstract][Full Text] [Related]
7. The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus.
Milting H; Klauke B; Christensen AH; Müsebeck J; Walhorn V; Grannemann S; Münnich T; Šarić T; Rasmussen TB; Jensen HK; Mogensen J; Baecker C; Romaker E; Laser KT; zu Knyphausen E; Kassner A; Gummert J; Judge DP; Connors S; Hodgkinson K; Young TL; van der Zwaag PA; van Tintelen JP; Anselmetti D
Eur Heart J; 2015 Apr; 36(14):872-81. PubMed ID: 24598986
[TBL] [Abstract][Full Text] [Related]
8. Molecular insights into arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 missense mutations.
Kirchner F; Schuetz A; Boldt LH; Martens K; Dittmar G; Haverkamp W; Thierfelder L; Heinemann U; Gerull B
Circ Cardiovasc Genet; 2012 Aug; 5(4):400-11. PubMed ID: 22781308
[TBL] [Abstract][Full Text] [Related]
9. Desmosomal gene evaluation in Boxers with arrhythmogenic right ventricular cardiomyopathy.
Meurs KM; Ederer MM; Stern JA
Am J Vet Res; 2007 Dec; 68(12):1338-41. PubMed ID: 18052738
[TBL] [Abstract][Full Text] [Related]
10. Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications.
Alcalde M; Campuzano O; Allegue C; Torres M; Arbelo E; Partemi S; Iglesias A; Brugada J; Oliva A; Carracedo A; Brugada R
Int J Legal Med; 2015 Jan; 129(1):1-10. PubMed ID: 24832006
[TBL] [Abstract][Full Text] [Related]
11. Role of genetic testing in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Barahona-Dussault C; Benito B; Campuzano O; Iglesias A; Leung TL; Robb L; Talajic M; Brugada R
Clin Genet; 2010 Jan; 77(1):37-48. PubMed ID: 19863551
[TBL] [Abstract][Full Text] [Related]
12. Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy.
Syrris P; Ward D; Asimaki A; Sen-Chowdhry S; Ebrahim HY; Evans A; Hitomi N; Norman M; Pantazis A; Shaw AL; Elliott PM; McKenna WJ
Circulation; 2006 Jan; 113(3):356-64. PubMed ID: 16415378
[TBL] [Abstract][Full Text] [Related]
13. Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter study.
Bhuiyan ZA; Jongbloed JD; van der Smagt J; Lombardi PM; Wiesfeld AC; Nelen M; Schouten M; Jongbloed R; Cox MG; van Wolferen M; Rodriguez LM; van Gelder IC; Bikker H; Suurmeijer AJ; van den Berg MP; Mannens MM; Hauer RN; Wilde AA; van Tintelen JP
Circ Cardiovasc Genet; 2009 Oct; 2(5):418-27. PubMed ID: 20031616
[TBL] [Abstract][Full Text] [Related]
14. TMEM43 mutations associated with arrhythmogenic right ventricular cardiomyopathy in non-Newfoundland populations.
Baskin B; Skinner JR; Sanatani S; Terespolsky D; Krahn AD; Ray PN; Scherer SW; Hamilton RM
Hum Genet; 2013 Nov; 132(11):1245-52. PubMed ID: 23812740
[TBL] [Abstract][Full Text] [Related]
15. Lower than expected desmosomal gene mutation prevalence in endurance athletes with complex ventricular arrhythmias of right ventricular origin.
La Gerche A; Robberecht C; Kuiperi C; Nuyens D; Willems R; de Ravel T; Matthijs G; Heidbüchel H
Heart; 2010 Aug; 96(16):1268-74. PubMed ID: 20525856
[TBL] [Abstract][Full Text] [Related]
16. Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells.
Asimaki A; Protonotarios A; James CA; Chelko SP; Tichnell C; Murray B; Tsatsopoulou A; Anastasakis A; te Riele A; Kléber AG; Judge DP; Calkins H; Saffitz JE
Circ Arrhythm Electrophysiol; 2016 Feb; 9(2):e003688. PubMed ID: 26850880
[TBL] [Abstract][Full Text] [Related]
17. Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations.
Bauce B; Basso C; Rampazzo A; Beffagna G; Daliento L; Frigo G; Malacrida S; Settimo L; Danieli G; Thiene G; Nava A
Eur Heart J; 2005 Aug; 26(16):1666-75. PubMed ID: 15941723
[TBL] [Abstract][Full Text] [Related]
18. De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy.
Klauke B; Kossmann S; Gaertner A; Brand K; Stork I; Brodehl A; Dieding M; Walhorn V; Anselmetti D; Gerdes D; Bohms B; Schulz U; Zu Knyphausen E; Vorgerd M; Gummert J; Milting H
Hum Mol Genet; 2010 Dec; 19(23):4595-607. PubMed ID: 20829228
[TBL] [Abstract][Full Text] [Related]
19. Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression.
Sen-Chowdhry S; Syrris P; Ward D; Asimaki A; Sevdalis E; McKenna WJ
Circulation; 2007 Apr; 115(13):1710-20. PubMed ID: 17372169
[TBL] [Abstract][Full Text] [Related]
20. Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Dalal D; James C; Devanagondi R; Tichnell C; Tucker A; Prakasa K; Spevak PJ; Bluemke DA; Abraham T; Russell SD; Calkins H; Judge DP
J Am Coll Cardiol; 2006 Oct; 48(7):1416-24. PubMed ID: 17010805
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
