256 related articles for article (PubMed ID: 18651846)
1. Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology.
Menon SC; Michels VV; Pellikka PA; Ballew JD; Karst ML; Herron KJ; Nelson SM; Rodeheffer RJ; Olson TM
Clin Genet; 2008 Nov; 74(5):445-54. PubMed ID: 18651846
[TBL] [Abstract][Full Text] [Related]
2. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes.
Kaski JP; Syrris P; Burch M; Tomé-Esteban MT; Fenton M; Christiansen M; Andersen PS; Sebire N; Ashworth M; Deanfield JE; McKenna WJ; Elliott PM
Heart; 2008 Nov; 94(11):1478-84. PubMed ID: 18467357
[TBL] [Abstract][Full Text] [Related]
3. Inherited cardiomyopathies as a troponin disease.
Harada K; Morimoto S
Jpn J Physiol; 2004 Aug; 54(4):307-18. PubMed ID: 15631686
[TBL] [Abstract][Full Text] [Related]
4. Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy.
Mouton JM; Pellizzon AS; Goosen A; Kinnear CJ; Herbst PG; Brink PA; Moolman-Smook JC
Cardiovasc J Afr; 2015; 26(2):63-9. PubMed ID: 25940119
[TBL] [Abstract][Full Text] [Related]
5. A novel nonsense mutation in TNNT2 in a Chinese pedigree with hypertrophic cardiomyopathy: A case report.
Gao G; Liu G; Chen W; Tong Y; Mao C; Liu J; Zhang X; He MM; Yang P
Medicine (Baltimore); 2020 Aug; 99(34):e21843. PubMed ID: 32846832
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects.
Monserrat L; Hermida-Prieto M; Fernandez X; Rodríguez I; Dumont C; Cazón L; Cuesta MG; Gonzalez-Juanatey C; Peteiro J; Alvarez N; Penas-Lado M; Castro-Beiras A
Eur Heart J; 2007 Aug; 28(16):1953-61. PubMed ID: 17611253
[TBL] [Abstract][Full Text] [Related]
8. Cardiac troponin T Arg92Trp mutation and progression from hypertrophic to dilated cardiomyopathy.
Fujino N; Shimizu M; Ino H; Okeie K; Yamaguchi M; Yasuda T; Kokado H; Mabuchi H
Clin Cardiol; 2001 May; 24(5):397-402. PubMed ID: 11346248
[TBL] [Abstract][Full Text] [Related]
9. [Mutations in genes for sarcomeric proteins].
Kimura A
Nihon Rinsho; 2000 Jan; 58(1):117-22. PubMed ID: 10885298
[TBL] [Abstract][Full Text] [Related]
10. Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.
Zhao Y; Cao H; Song Y; Feng Y; Ding X; Pang M; Zhang Y; Zhang H; Ding J; Xia X
Int J Mol Med; 2016 Jun; 37(6):1511-20. PubMed ID: 27082122
[TBL] [Abstract][Full Text] [Related]
11. Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy.
Hanson EL; Jakobs PM; Keegan H; Coates K; Bousman S; Dienel NH; Litt M; Hershberger RE
J Card Fail; 2002 Feb; 8(1):28-32. PubMed ID: 11862580
[TBL] [Abstract][Full Text] [Related]
12. Hypertrophic cardiomyopathy: two homozygous cases with "typical" hypertrophic cardiomyopathy and three new mutations in cases with progression to dilated cardiomyopathy.
Nanni L; Pieroni M; Chimenti C; Simionati B; Zimbello R; Maseri A; Frustaci A; Lanfranchi G
Biochem Biophys Res Commun; 2003 Sep; 309(2):391-8. PubMed ID: 12951062
[TBL] [Abstract][Full Text] [Related]
13. Mutations in the cardiac troponin T gene show various prognoses in Japanese patients with hypertrophic cardiomyopathy.
Fujita E; Nakanishi T; Nishizawa T; Hagiwara N; Matsuoka R
Heart Vessels; 2013 Nov; 28(6):785-94. PubMed ID: 23494605
[TBL] [Abstract][Full Text] [Related]
14. Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.
Fernlund E; Österberg AW; Kuchinskaya E; Gustafsson M; Jansson K; Gunnarsson C
Pediatr Cardiol; 2017 Aug; 38(6):1262-1268. PubMed ID: 28669108
[TBL] [Abstract][Full Text] [Related]
15. Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
Purevjav E; Arimura T; Augustin S; Huby AC; Takagi K; Nunoda S; Kearney DL; Taylor MD; Terasaki F; Bos JM; Ommen SR; Shibata H; Takahashi M; Itoh-Satoh M; McKenna WJ; Murphy RT; Labeit S; Yamanaka Y; Machida N; Park JE; Alexander PM; Weintraub RG; Kitaura Y; Ackerman MJ; Kimura A; Towbin JA
Hum Mol Genet; 2012 May; 21(9):2039-53. PubMed ID: 22286171
[TBL] [Abstract][Full Text] [Related]
16. Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy.
Petropoulou E; Soltani M; Firoozabadi AD; Namayandeh SM; Crockford J; Maroofian R; Jamshidi Y
Eur J Med Genet; 2017 Sep; 60(9):485-488. PubMed ID: 28642161
[TBL] [Abstract][Full Text] [Related]
17. Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.
Selvi Rani D; Nallari P; Dhandapany PS; Rani J; Meraj K; Ganesan M; Narasimhan C; Thangaraj K
DNA Cell Biol; 2015 May; 34(5):350-9. PubMed ID: 25607779
[TBL] [Abstract][Full Text] [Related]
18. Autopsy findings in siblings with hypertrophic cardiomyopathy caused by Arg92Trp mutation in the cardiac troponin T gene showing dilated cardiomyopathy-like features.
Shimizu M; Ino H; Yamaguchi M; Terai H; Uchiyama K; Inoue M; Ikeda M; Kawashima A; Mabuchi H
Clin Cardiol; 2003 Nov; 26(11):536-9. PubMed ID: 14640471
[TBL] [Abstract][Full Text] [Related]
19. Familial dilated cardiomyopathy with troponin T K210del mutation.
Martins E; Silva-Cardoso J; Alves C; Pereira H; Soares B; Damasceno A; Abreu-Lima C; Amorim A; Rocha-Gonçalves F
Rev Port Cardiol; 2006 Mar; 25(3):295-300. PubMed ID: 16789403
[TBL] [Abstract][Full Text] [Related]
20. A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy.
Fujino N; Shimizu M; Ino H; Yamaguchi M; Yasuda T; Nagata M; Konno T; Mabuchi H
Am J Cardiol; 2002 Jan; 89(1):29-33. PubMed ID: 11779518
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
