138 related articles for article (PubMed ID: 15689433)
1. The importance of seeking ALMS1 mutations in infants with dilated cardiomyopathy.
Bond J; Flintoff K; Higgins J; Scott S; Bennet C; Parsons J; Mannon J; Jafri H; Rashid Y; Barrow M; Trembath R; Woodruff G; Rossa E; Lynch S; Sheilds J; Newbury-Ecob R; Falconer A; Holland P; Cockburn D; Karbani G; Malik S; Ahmed M; Roberts E; Taylor G; Woods CG
J Med Genet; 2005 Feb; 42(2):e10. PubMed ID: 15689433
[No Abstract] [Full Text] [Related]
2. Mutations in the cardiac Troponin C gene are a cause of idiopathic dilated cardiomyopathy in childhood.
Kaski JP; Burch M; Elliott PM
Cardiol Young; 2007 Dec; 17(6):675-7. PubMed ID: 17977476
[TBL] [Abstract][Full Text] [Related]
3. Atypical Alstrom syndrome with novel ALMS1 mutations precluded by current diagnostic criteria.
Casey J; McGettigan P; Brosnahan D; Curtis E; Treacy E; Ennis S; Lynch SA
Eur J Med Genet; 2014 Feb; 57(2-3):55-9. PubMed ID: 24503146
[TBL] [Abstract][Full Text] [Related]
4. Expanded spectrum of gene causing both hypertrophic cardiomyopathy and dilated cardiomyopathy.
Morimoto S
Circ Res; 2009 Aug; 105(4):313-5. PubMed ID: 19679850
[No Abstract] [Full Text] [Related]
5. [Familial dilated cardiomyopathy with autosomal mode of inheritance. Case report].
Dzielińska Z; Michalak E; Bilińska ZT; Walczak E; Demkow M; Chojnowska L; Ruzyłło W; Rydlewska-Sadowska W; Popławska W; Lewicki Z
Kardiol Pol; 1993 Dec; 39(12):473-7. PubMed ID: 8289434
[TBL] [Abstract][Full Text] [Related]
6. Molecular analysis and long-term clinical evaluation of three siblings with Alström syndrome.
Ozgül RK; Satman I; Collin GB; Hinman EG; Marshall JD; Kocaman O; Tütüncü Y; Yilmaz T; Naggert JK
Clin Genet; 2007 Oct; 72(4):351-6. PubMed ID: 17850632
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Dilated cardiomyopathy caused by LMNA mutations. Clinical and morphological studies.
Bilińska ZT; Sylvius N; Grzybowski J; Fidziańska A; Michalak E; Walczak E; Walski M; Bieganowska K; Szymaniak E; Kuśmierczyk-Droszcz B; Lubiszewska B; Wagner T; Tesson F; Ruzyłło W
Kardiol Pol; 2006 Aug; 64(8):812-9; discussion 820-1. PubMed ID: 16981056
[TBL] [Abstract][Full Text] [Related]
9. Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutation.
Müller T; Krasnianski M; Witthaut R; Deschauer M; Zierz S
Neuromuscul Disord; 2005 May; 15(5):372-6. PubMed ID: 15833432
[TBL] [Abstract][Full Text] [Related]
10. Phospholamban R14 deletion results in late-onset, mild, hereditary dilated cardiomyopathy.
DeWitt MM; MacLeod HM; Soliven B; McNally EM
J Am Coll Cardiol; 2006 Oct; 48(7):1396-8. PubMed ID: 17010801
[TBL] [Abstract][Full Text] [Related]
11. [Correlation between desmin gene, platelet-activating factor acetylhydrolase gene and dilated cardiomyopathy].
Wang B; Rao L; Zhang L; Zhou B; Wang YP; Chen XY
Sichuan Da Xue Xue Bao Yi Xue Ban; 2006 May; 37(3):391-4. PubMed ID: 16761416
[TBL] [Abstract][Full Text] [Related]
12. Familial dilated cardiomyopathy--study in two families.
Bansal RK; Bhardwaj RP; Thaper RK; Ahmad M; Varma CM; Singhal SS; Jain PC
Indian Heart J; 1988; 40(2):99-102. PubMed ID: 3192264
[No Abstract] [Full Text] [Related]
13. Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition.
Davey KM; Parboosingh JS; McLeod DR; Chan A; Casey R; Ferreira P; Snyder FF; Bridge PJ; Bernier FP
J Med Genet; 2006 May; 43(5):385-93. PubMed ID: 16055927
[TBL] [Abstract][Full Text] [Related]
14. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics.
van Tintelen JP; Hofstra RM; Katerberg H; Rossenbacker T; Wiesfeld AC; du Marchie Sarvaas GJ; Wilde AA; van Langen IM; Nannenberg EA; van der Kooi AJ; Kraak M; van Gelder IC; van Veldhuisen DJ; Vos Y; van den Berg MP;
Am Heart J; 2007 Dec; 154(6):1130-9. PubMed ID: 18035086
[TBL] [Abstract][Full Text] [Related]
15. Novel mutations in the lamin A/C gene in heart transplant recipients with end stage dilated cardiomyopathy.
Kärkkäinen S; Reissell E; Heliö T; Kaartinen M; Tuomainen P; Toivonen L; Kuusisto J; Kupari M; Nieminen MS; Laakso M; Peuhkurinen K
Heart; 2006 Apr; 92(4):524-6. PubMed ID: 16537768
[No Abstract] [Full Text] [Related]
16. Homozygous loss-of-function mutation in ALMS1 causes the lethal disorder mitogenic cardiomyopathy in two siblings.
Louw JJ; Corveleyn A; Jia Y; Iqbal S; Boshoff D; Gewillig M; Peeters H; Moerman P; Devriendt K
Eur J Med Genet; 2014 Sep; 57(9):532-5. PubMed ID: 24972238
[TBL] [Abstract][Full Text] [Related]
17. Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.
Kushner JD; Nauman D; Burgess D; Ludwigsen S; Parks SB; Pantely G; Burkett E; Hershberger RE
J Card Fail; 2006 Aug; 12(6):422-9. PubMed ID: 16911908
[TBL] [Abstract][Full Text] [Related]
18. A W148R mutation in the human FOXD4 gene segregating with dilated cardiomyopathy, obsessive-compulsive disorder, and suicidality.
Minoretti P; Arra M; Emanuele E; Olivieri V; Aldeghi A; Politi P; Martinelli V; Pesenti S; Falcone C
Int J Mol Med; 2007 Mar; 19(3):369-72. PubMed ID: 17273782
[TBL] [Abstract][Full Text] [Related]
19. Cardiology patient page. Familial dilated cardiomyopathy.
Ku L; Feiger J; Taylor M; Mestroni L;
Circulation; 2003 Oct; 108(17):e118-21. PubMed ID: 14581388
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]