203 related articles for article (PubMed ID: 33290826)
21. Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity.
Sen-Chowdhry S; Syrris P; Prasad SK; Hughes SE; Merrifield R; Ward D; Pennell DJ; McKenna WJ
J Am Coll Cardiol; 2008 Dec; 52(25):2175-87. PubMed ID: 19095136
[TBL] [Abstract][Full Text] [Related]
22. Prevalence of desmin mutations in dilated cardiomyopathy.
Taylor MR; Slavov D; Ku L; Di Lenarda A; Sinagra G; Carniel E; Haubold K; Boucek MM; Ferguson D; Graw SL; Zhu X; Cavanaugh J; Sucharov CC; Long CS; Bristow MR; Lavori P; Mestroni L; ;
Circulation; 2007 Mar; 115(10):1244-51. PubMed ID: 17325244
[TBL] [Abstract][Full Text] [Related]
23. Familial screening in case of acute myocarditis reveals inherited arrhythmogenic left ventricular cardiomyopathies.
Piriou N; Marteau L; Kyndt F; Serfaty JM; Toquet C; Le Gloan L; Warin-Fresse K; Guijarro D; Le Tourneau T; Conan E; Thollet A; Probst V; Trochu JN
ESC Heart Fail; 2020 Aug; 7(4):1520-1533. PubMed ID: 32356610
[TBL] [Abstract][Full Text] [Related]
24. Dual color photoactivation localization microscopy of cardiomyopathy-associated desmin mutants.
Brodehl A; Hedde PN; Dieding M; Fatima A; Walhorn V; Gayda S; Šarić T; Klauke B; Gummert J; Anselmetti D; Heilemann M; Nienhaus GU; Milting H
J Biol Chem; 2012 May; 287(19):16047-57. PubMed ID: 22403400
[TBL] [Abstract][Full Text] [Related]
25. Distinct fibrosis pattern in desmosomal and phospholamban mutation carriers in hereditary cardiomyopathies.
Sepehrkhouy S; Gho JMIH; van Es R; Harakalova M; de Jonge N; Dooijes D; van der Smagt JJ; Buijsrogge MP; Hauer RNW; Goldschmeding R; de Weger RA; Asselbergs FW; Vink A
Heart Rhythm; 2017 Jul; 14(7):1024-1032. PubMed ID: 28365402
[TBL] [Abstract][Full Text] [Related]
26. Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.
Lin X; Ma Y; Cai Z; Wang Q; Wang L; Huo Z; Hu D; Wang J; Xiang M
BMC Cardiovasc Disord; 2020 Feb; 20(1):74. PubMed ID: 32046637
[TBL] [Abstract][Full Text] [Related]
27. [Arrhythmogenic cardiomyopathy. Patterns of ventricular involvement using cardiac magnetic resonance].
Igual B; Zorio E; Maceira A; Estornell J; Lopez-Lereu MP; Monmeneu JV; Quesada A; Navarro J; Mas F; Salvador A
Rev Esp Cardiol; 2011 Dec; 64(12):1114-22. PubMed ID: 22030343
[TBL] [Abstract][Full Text] [Related]
28. Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (
Brodehl A; Pour Hakimi SA; Stanasiuk C; Ratnavadivel S; Hendig D; Gaertner A; Gerull B; Gummert J; Paluszkiewicz L; Milting H
Genes (Basel); 2019 Nov; 10(11):. PubMed ID: 31718026
[TBL] [Abstract][Full Text] [Related]
29. Autophagic vacuolar pathology in desminopathies.
Weihl CC; Iyadurai S; Baloh RH; Pittman SK; Schmidt RE; Lopate G; Pestronk A; Harms MB
Neuromuscul Disord; 2015 Mar; 25(3):199-206. PubMed ID: 25557463
[TBL] [Abstract][Full Text] [Related]
30. A series of Chinese patients with desminopathy associated with six novel and one reported mutations in the desmin gene.
Hong D; Wang Z; Zhang W; Xi J; Lu J; Luan X; Yuan Y
Neuropathol Appl Neurobiol; 2011 Apr; 37(3):257-70. PubMed ID: 20696008
[TBL] [Abstract][Full Text] [Related]
31. AAV9-mediated gene transfer of desmin ameliorates cardiomyopathy in desmin-deficient mice.
Heckmann MB; Bauer R; Jungmann A; Winter L; Rapti K; Strucksberg KH; Clemen CS; Li Z; Schröder R; Katus HA; Müller OJ
Gene Ther; 2016 Aug; 23(8-9):673-9. PubMed ID: 27101257
[TBL] [Abstract][Full Text] [Related]
32. Characteristics of Patients With Arrhythmogenic Left Ventricular Cardiomyopathy: Combining Genetic and Histopathologic Findings.
Casella M; Gasperetti A; Sicuso R; Conte E; Catto V; Sommariva E; Bergonti M; Vettor G; Rizzo S; Pompilio G; Andreini D; Saguner AM; Duru F; Natale A; Thiene G; Basso C; Dello Russo A; Tondo C
Circ Arrhythm Electrophysiol; 2020 Dec; 13(12):e009005. PubMed ID: 33197325
[TBL] [Abstract][Full Text] [Related]
33. Structural and functional analysis of a new desmin variant causing desmin-related myopathy.
Goudeau B; Dagvadorj A; Rodrigues-Lima F; Nédellec P; Casteras-Simon M; Perret E; Langlois S; Goldfarb L; Vicart P
Hum Mutat; 2001 Nov; 18(5):388-96. PubMed ID: 11668632
[TBL] [Abstract][Full Text] [Related]
34. Desminopathy: Novel Desmin Variants, a New Cardiac Phenotype, and Further Evidence for Secondary Mitochondrial Dysfunction.
Kubánek M; Schimerová T; Piherová L; Brodehl A; Krebsová A; Ratnavadivel S; Stanasiuk C; Hansíková H; Zeman J; Paleček T; Houštěk J; Drahota Z; Nůsková H; Mikešová J; Zámečník J; Macek M; Ridzoň P; Malusková J; Stránecký V; Melenovský V; Milting H; Kmoch S
J Clin Med; 2020 Mar; 9(4):. PubMed ID: 32235386
[No Abstract] [Full Text] [Related]
35. Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Yang Z; Bowles NE; Scherer SE; Taylor MD; Kearney DL; Ge S; Nadvoretskiy VV; DeFreitas G; Carabello B; Brandon LI; Godsel LM; Green KJ; Saffitz JE; Li H; Danieli GA; Calkins H; Marcus F; Towbin JA
Circ Res; 2006 Sep; 99(6):646-55. PubMed ID: 16917092
[TBL] [Abstract][Full Text] [Related]
36. Mouse model of desmin-related cardiomyopathy.
Wang X; Osinska H; Dorn GW; Nieman M; Lorenz JN; Gerdes AM; Witt S; Kimball T; Gulick J; Robbins J
Circulation; 2001 May; 103(19):2402-7. PubMed ID: 11352891
[TBL] [Abstract][Full Text] [Related]
37. Discovery of a new mutation in the desmin gene in a young patient with cardiomyopathy and muscular weakness.
JurcuŢ RO; Bastian AE; Militaru S; Popa A; Manole E; Popescu BA; Tallila J; Popescu BO; Ginghină CD
Rom J Morphol Embryol; 2017; 58(1):225-230. PubMed ID: 28523323
[TBL] [Abstract][Full Text] [Related]
38. Patient-specific induced-pluripotent stem cells-derived cardiomyocytes recapitulate the pathogenic phenotypes of dilated cardiomyopathy due to a novel DES mutation identified by whole exome sequencing.
Tse HF; Ho JC; Choi SW; Lee YK; Butler AW; Ng KM; Siu CW; Simpson MA; Lai WH; Chan YC; Au KW; Zhang J; Lay KW; Esteban MA; Nicholls JM; Colman A; Sham PC
Hum Mol Genet; 2013 Apr; 22(7):1395-403. PubMed ID: 23300193
[TBL] [Abstract][Full Text] [Related]
39. Phenotypic Patterns of Cardiomyopathy Caused by Mutations in the Desmin Gene. A Clinical and Genetic Study in Two Inherited Heart Disease Units.
Ripoll-Vera T; Zorio E; Gámez JM; Molina P; Govea N; Crémer D
Rev Esp Cardiol (Engl Ed); 2015 Nov; 68(11):1027-9. PubMed ID: 26431784
[No Abstract] [Full Text] [Related]
40. Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy.
Norman M; Simpson M; Mogensen J; Shaw A; Hughes S; Syrris P; Sen-Chowdhry S; Rowland E; Crosby A; McKenna WJ
Circulation; 2005 Aug; 112(5):636-42. PubMed ID: 16061754
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
