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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

190 related articles for article (PubMed ID: 27085656)

  • 1. Brugada Syndrome and PKP2: Evidences and uncertainties.
    Campuzano O; Fernández-Falgueras A; Iglesias A; Brugada R
    Int J Cardiol; 2016 Jul; 214():403-5. PubMed ID: 27085656
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype.
    Cerrone M; Lin X; Zhang M; Agullo-Pascual E; Pfenniger A; Chkourko Gusky H; Novelli V; Kim C; Tirasawadichai T; Judge DP; Rothenberg E; Chen HS; Napolitano C; Priori SG; Delmar M
    Circulation; 2014 Mar; 129(10):1092-103. PubMed ID: 24352520
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Desmosomes and the sodium channel complex: implications for arrhythmogenic cardiomyopathy and Brugada syndrome.
    Cerrone M; Delmar M
    Trends Cardiovasc Med; 2014 Jul; 24(5):184-90. PubMed ID: 24656989
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and Molecular Data Define a Diagnosis of Arrhythmogenic Cardiomyopathy in a Carrier of a Brugada-Syndrome-Associated
    Persampieri S; Pilato CA; Sommariva E; Maione AS; Stadiotti I; Ranalletta A; Torchio M; Dello Russo A; Basso C; Pompilio G; Tondo C; Casella M
    Genes (Basel); 2020 May; 11(5):. PubMed ID: 32443836
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular Autopsy of Desmosomal Protein Plakophilin-2 in Sudden Unexplained Nocturnal Death Syndrome.
    Huang L; Tang S; Peng L; Chen Y; Cheng J
    J Forensic Sci; 2016 May; 61(3):687-91. PubMed ID: 27122407
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Is Brugada syndrome a variant of arrhythmogenic cardiomyopathy?
    Peters S
    Int J Cardiol; 2015; 189():88-90. PubMed ID: 25889434
    [No Abstract]   [Full Text] [Related]  

  • 7. Epicardial Ventricular Tachycardia Ablation in a Patient With Brugada ECG Pattern and Mutation of PKP2 and DSP Genes.
    Forkmann M; Tomala J; Huo Y; Mayer J; Christoph M; Wunderlich C; Salmas J; Gaspar T; Piorkowski C
    Circ Arrhythm Electrophysiol; 2015 Apr; 8(2):505-7. PubMed ID: 25900994
    [No Abstract]   [Full Text] [Related]  

  • 8. Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.
    Allegue C; Coll M; Mates J; Campuzano O; Iglesias A; Sobrino B; Brion M; Amigo J; Carracedo A; Brugada P; Brugada J; Brugada R
    PLoS One; 2015; 10(7):e0133037. PubMed ID: 26230511
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Arrhythmogenic cardiomyopathy and provocable Brugada ECG in a patient caused by missense mutation in plakophilin-2.
    Peters S
    Int J Cardiol; 2014 May; 173(2):317-8. PubMed ID: 24681023
    [No Abstract]   [Full Text] [Related]  

  • 10. Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?
    Campuzano O; Sarquella-Brugada G; Cesar S; Arbelo E; Brugada J; Brugada R
    Int J Mol Sci; 2020 Sep; 21(19):. PubMed ID: 32998306
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pleiotropic Phenotypes Associated With PKP2 Variants.
    Novelli V; Malkani K; Cerrone M
    Front Cardiovasc Med; 2018; 5():184. PubMed ID: 30619891
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Arrhythmogenic cardiomyopathy and Brugada syndrome: diseases of the connexome.
    Agullo-Pascual E; Cerrone M; Delmar M
    FEBS Lett; 2014 Apr; 588(8):1322-30. PubMed ID: 24548564
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Left-dominant arrhythmogenic cardiomyopathy in a large family: associated desmosomal or nondesmosomal genotype?
    Groeneweg JA; van der Zwaag PA; Jongbloed JD; Cox MG; Vreeker A; de Boer RA; van der Heijden JF; van Veen TA; McKenna WJ; van Tintelen JP; Dooijes D; Hauer RN
    Heart Rhythm; 2013 Apr; 10(4):548-59. PubMed ID: 23270881
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathies.
    Bissay V; Van Malderen SC; Keymolen K; Lissens W; Peeters U; Daneels D; Jansen AC; Pappaert G; Brugada P; De Keyser J; Van Dooren S
    Eur J Hum Genet; 2016 Mar; 24(3):400-7. PubMed ID: 26036855
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic interpretation and clinical translation of minor genes related to Brugada syndrome.
    Campuzano O; Sarquella-Brugada G; Fernandez-Falgueras A; Cesar S; Coll M; Mates J; Arbelo E; Perez-Serra A; Del Olmo B; Jordá P; Fiol V; Iglesias A; Puigmulé M; Lopez L; Pico F; Brugada J; Brugada R
    Hum Mutat; 2019 Jun; 40(6):749-764. PubMed ID: 30821013
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Genetic modulation of brugada syndrome by a common polymorphism.
    Lizotte E; Junttila MJ; Dube MP; Hong K; Benito B; DE Zutter M; Henkens S; Sarkozy A; Huikuri HV; Towbin J; Vatta M; Brugada P; Brugada J; Brugada R
    J Cardiovasc Electrophysiol; 2009 Oct; 20(10):1137-41. PubMed ID: 19549036
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family.
    Kannankeril PJ; Bhuiyan ZA; Darbar D; Mannens MM; Wilde AA; Roden DM
    Heart Rhythm; 2006 Aug; 3(8):939-44. PubMed ID: 16876743
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.