351 related articles for article (PubMed ID: 27504452)
21. Cardiomyopathies and their role in sudden death.
Brandenburg RO
J Am Coll Cardiol; 1985 Jun; 5(6 Suppl):185B-189B. PubMed ID: 3158692
[TBL] [Abstract][Full Text] [Related]
22. A case of sporadic infantile histiocytoid cardiomyopathy caused by the A8344G (MERRF) mitochondrial DNA mutation.
Vallance HD; Jeven G; Wallace DC; Brown MD
Pediatr Cardiol; 2004; 25(5):538-40. PubMed ID: 15164143
[TBL] [Abstract][Full Text] [Related]
23. Mitochondrial defects in cardiomyopathy and neuromuscular disease.
Wallace DC
Am Heart J; 2000 Feb; 139(2 Pt 3):S70-85. PubMed ID: 10650320
[TBL] [Abstract][Full Text] [Related]
24. Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies.
Ortiz-Genga MF; Cuenca S; Dal Ferro M; Zorio E; Salgado-Aranda R; Climent V; Padrón-Barthe L; Duro-Aguado I; Jiménez-Jáimez J; Hidalgo-Olivares VM; García-Campo E; Lanzillo C; Suárez-Mier MP; Yonath H; Marcos-Alonso S; Ochoa JP; Santomé JL; García-Giustiniani D; Rodríguez-Garrido JL; Domínguez F; Merlo M; Palomino J; Peña ML; Trujillo JP; Martín-Vila A; Stolfo D; Molina P; Lara-Pezzi E; Calvo-Iglesias FE; Nof E; Calò L; Barriales-Villa R; Gimeno-Blanes JR; Arad M; García-Pavía P; Monserrat L
J Am Coll Cardiol; 2016 Dec; 68(22):2440-2451. PubMed ID: 27908349
[TBL] [Abstract][Full Text] [Related]
25. Mitochondrial dysfunction in cardiovascular disease: Current status of translational research/clinical and therapeutic implications.
Manolis AS; Manolis AA; Manolis TA; Apostolaki NE; Apostolopoulos EJ; Melita H; Katsiki N
Med Res Rev; 2021 Jan; 41(1):275-313. PubMed ID: 32959403
[TBL] [Abstract][Full Text] [Related]
26. Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.
Marín-García J; Goldenthal MJ; Filiano JJ
J Child Neurol; 2002 Oct; 17(10):759-65. PubMed ID: 12546431
[TBL] [Abstract][Full Text] [Related]
27. Mitochondrial medicine--molecular pathology of defective oxidative phosphorylation.
Fosslien E
Ann Clin Lab Sci; 2001 Jan; 31(1):25-67. PubMed ID: 11314862
[TBL] [Abstract][Full Text] [Related]
28. Milder clinical course of Type IV 3-methylglutaconic aciduria due to a novel mutation in TMEM70.
Shchelochkov OA; Li FY; Wang J; Zhan H; Towbin JA; Jefferies JL; Wong LJ; Scaglia F
Mol Genet Metab; 2010; 101(2-3):282-5. PubMed ID: 20728387
[TBL] [Abstract][Full Text] [Related]
29. Overview of Cardiomyopathies in Childhood.
Rath A; Weintraub R
Front Pediatr; 2021; 9():708732. PubMed ID: 34368032
[TBL] [Abstract][Full Text] [Related]
30. Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options.
Lioncino M; Monda E; Caiazza M; Fusco A; Cirillo A; Dongiglio F; Simonelli V; Sampaolo S; Ruggiero L; Scarano G; Pota V; Frisso G; Mazzaccara C; D'Amati G; Nigro G; Russo MG; Wahbi K; Limongelli G
Heart Fail Clin; 2022 Jan; 18(1):51-60. PubMed ID: 34776083
[TBL] [Abstract][Full Text] [Related]
31. A mitochondrial paradigm for degenerative diseases and ageing.
Wallace DC
Novartis Found Symp; 2001; 235():247-63; discussion 263-6. PubMed ID: 11280029
[TBL] [Abstract][Full Text] [Related]
32. Systematic review of pregnancy in women with inherited cardiomyopathies.
Krul SP; van der Smagt JJ; van den Berg MP; Sollie KM; Pieper PG; van Spaendonck-Zwarts KY
Eur J Heart Fail; 2011 Jun; 13(6):584-94. PubMed ID: 21482599
[TBL] [Abstract][Full Text] [Related]
33. Mitochondrial DNA Variation Dictates Expressivity and Progression of Nuclear DNA Mutations Causing Cardiomyopathy.
McManus MJ; Picard M; Chen HW; De Haas HJ; Potluri P; Leipzig J; Towheed A; Angelin A; Sengupta P; Morrow RM; Kauffman BA; Vermulst M; Narula J; Wallace DC
Cell Metab; 2019 Jan; 29(1):78-90.e5. PubMed ID: 30174309
[TBL] [Abstract][Full Text] [Related]
34. [Ambulatory ECG in cardiomyopathies].
Mestroni L; Miani D; Neri R; Di Lenarda A; Camerini F
G Ital Cardiol; 1987 Dec; 17(12):1139-44. PubMed ID: 3503812
[TBL] [Abstract][Full Text] [Related]
35. [Cardiomyopathy associated with mitochondrial disorders].
Matsushita T; Okada S
Nihon Rinsho; 2000 Jan; 58(1):196-9. PubMed ID: 10885313
[TBL] [Abstract][Full Text] [Related]
36. Animal models for mitochondrial disease.
Wallace DC
Methods Mol Biol; 2002; 197():3-54. PubMed ID: 12013805
[TBL] [Abstract][Full Text] [Related]
37. Cardiomyopathy and pregnancy.
Schaufelberger M
Heart; 2019 Oct; 105(20):1543-1551. PubMed ID: 31308064
[TBL] [Abstract][Full Text] [Related]
38. [Clinical practice guidelines for hereditary cardiomyopathy].
Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association ; Sun J; Han S; Hu J; Jiang C; Wang Q; Zheng L; Zhou Z; Qi M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Mar; 37(3):300-307. PubMed ID: 32128748
[TBL] [Abstract][Full Text] [Related]
39. Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.
Arbustini E; Diegoli M; Fasani R; Grasso M; Morbini P; Banchieri N; Bellini O; Dal Bello B; Pilotto A; Magrini G; Campana C; Fortina P; Gavazzi A; Narula J; Viganò M
Am J Pathol; 1998 Nov; 153(5):1501-10. PubMed ID: 9811342
[TBL] [Abstract][Full Text] [Related]
40. Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies.
Hoedemaekers YM; Caliskan K; Majoor-Krakauer D; van de Laar I; Michels M; Witsenburg M; ten Cate FJ; Simoons ML; Dooijes D
Eur Heart J; 2007 Nov; 28(22):2732-7. PubMed ID: 17947214
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]