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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2006 | 3 |
2007 | 1 |
2011 | 1 |
2018 | 1 |
2019 | 1 |
2024 | 0 |
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Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy.
Circulation. 2006 Mar 7;113(9):1171-9. doi: 10.1161/CIRCULATIONAHA.105.583674. Epub 2006 Feb 27.
Circulation. 2006.
PMID: 16505173
DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Awad MM, Dalal D, Cho E, Amat-Alarcon N, James C, Tichnell C, Tucker A, Russell SD, Bluemke DA, Dietz HC, Calkins H, Judge DP.
Awad MM, et al.
Am J Hum Genet. 2006 Jul;79(1):136-42. doi: 10.1086/504393. Epub 2006 Apr 28.
Am J Hum Genet. 2006.
PMID: 16773573
Free PMC article.
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Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease.
Syrris P, Ward D, Asimaki A, Evans A, Sen-Chowdhry S, Hughes SE, McKenna WJ.
Syrris P, et al.
Eur Heart J. 2007 Mar;28(5):581-8. doi: 10.1093/eurheartj/ehl380. Epub 2006 Nov 14.
Eur Heart J. 2007.
PMID: 17105751
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Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy.
Lahtinen AM, Lehtonen E, Marjamaa A, Kaartinen M, Heliö T, Porthan K, Oikarinen L, Toivonen L, Swan H, Jula A, Peltonen L, Palotie A, Salomaa V, Kontula K.
Lahtinen AM, et al.
Heart Rhythm. 2011 Aug;8(8):1214-21. doi: 10.1016/j.hrthm.2011.03.015. Epub 2011 Mar 10.
Heart Rhythm. 2011.
PMID: 21397041
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Usefulness of Genetic Study by Next-generation Sequencing in High-risk Arrhythmogenic Cardiomyopathy.
Ruiz Salas A, Peña Hernández J, Medina Palomo C, Barrera Cordero A, Cabrera Bueno F, García Pinilla JM, Guijarro A, Morcillo-Hidalgo L, Jiménez Navarro M, Gómez Doblas JJ, de Teresa E, Alzueta J.
Ruiz Salas A, et al.
Rev Esp Cardiol (Engl Ed). 2018 Dec;71(12):1018-1026. doi: 10.1016/j.rec.2018.03.001. Epub 2018 Mar 30.
Rev Esp Cardiol (Engl Ed). 2018.
PMID: 29606362
English, Spanish.
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Prevalence and Electronic Health Record-Based Phenotype of Loss-of-Function Genetic Variants in Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Genes.
Carruth ED, Young W, Beer D, James CA, Calkins H, Jing L, Raghunath S, Hartzel DN, Leader JB, Kirchner HL, Smelser DT, Carey DJ, Kelly MA, Sturm AC, Alsaid A, Fornwalt BK, Haggerty CM.
Carruth ED, et al.
Circ Genom Precis Med. 2019 Nov;12(11):e002579. doi: 10.1161/CIRCGEN.119.002579. Epub 2019 Oct 22.
Circ Genom Precis Med. 2019.
PMID: 31638835
Free PMC article.
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