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Results: 1 to 20 of 170

Similar articles for PubMed (Select 20206892)

1.

Familial dilated cardiomyopathy secondary to dystrophin splice site mutation.

Obler D, Wu BL, Lip V, Estrella E, Keck S, Haggan C, Semigran M, Smoot LB.

J Card Fail. 2010 Mar;16(3):194-9. doi: 10.1016/j.cardfail.2009.11.009.

PMID:
20206892
2.

[Genetics of dilated cardiomyopathy].

Osterziel KJ, Scheffold T, Perrot A, Dietz R; Netzwerk Myokardiale Erkrankungen.

Z Kardiol. 2001 Jul;90(7):461-9. Review. German.

PMID:
11515275
3.

A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy.

Milasin J, Muntoni F, Severini GM, Bartoloni L, Vatta M, Krajinovic M, Mateddu A, Angelini C, Camerini F, Falaschi A, Mestroni L, Giacca M.

Hum Mol Genet. 1996 Jan;5(1):73-9.

4.

Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy.

Feng J, Yan J, Buzin CH, Towbin JA, Sommer SS.

Mol Genet Metab. 2002 Sep-Oct;77(1-2):119-26.

PMID:
12359139
5.

Genetics of idiopathic dilated cardiomyopathy.

Arbustini E, Morbini P, Pilotto A, Gavazzi A, Tavazzi L.

Herz. 2000 May;25(3):156-60. Review.

PMID:
10904833
6.

X-linked dilated cardiomyopathy. Novel mutation of the dystrophin gene.

Franz WM, Cremer M, Herrmann R, Grünig E, Fogel W, Scheffold T, Goebel HH, Kircheisen R, Kübler W, Voit T, et al.

Ann N Y Acad Sci. 1995 Mar 27;752:470-91.

PMID:
7755293
7.

[Familial dilated cardiomyopathy].

Osterziel KJ, Hassfeld S, Geier C, Perrot A.

Herz. 2005 Sep;30(6):529-34. Review. German.

PMID:
16170685
8.

A missense mutation in the CHRM2 gene is associated with familial dilated cardiomyopathy.

Zhang L, Hu A, Yuan H, Cui L, Miao G, Yang X, Wang L, Liu J, Liu X, Wang S, Zhang Z, Liu L, Zhao R, Shen Y.

Circ Res. 2008 Jun 6;102(11):1426-32. doi: 10.1161/CIRCRESAHA.107.167783. Epub 2008 May 1.

9.

Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group.

Mestroni L, Rocco C, Gregori D, Sinagra G, Di Lenarda A, Miocic S, Vatta M, Pinamonti B, Muntoni F, Caforio AL, McKenna WJ, Falaschi A, Giacca M, Camerini.

J Am Coll Cardiol. 1999 Jul;34(1):181-90.

10.

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations.

Taylor MR, Fain PR, Sinagra G, Robinson ML, Robertson AD, Carniel E, Di Lenarda A, Bohlmeyer TJ, Ferguson DA, Brodsky GL, Boucek MM, Lascor J, Moss AC, Li WL, Stetler GL, Muntoni F, Bristow MR, Mestroni L; Familial Dilated Cardiomyopathy Registry Research Group.

J Am Coll Cardiol. 2003 Mar 5;41(5):771-80. Erratum in: J Am Coll Cardiol. 2003 Aug 6;42(3):590.

11.

Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy.

Feng J, Yan JY, Buzin CH, Sommer SS, Towbin JA.

J Am Coll Cardiol. 2002 Sep 18;40(6):1120-4.

12.

A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy.

Bies RD, Maeda M, Roberds SL, Holder E, Bohlmeyer T, Young JB, Campbell KP.

J Mol Cell Cardiol. 1997 Dec;29(12):3175-88.

PMID:
9441825
13.

Molecular basis of hypertrophic and dilated cardiomyopathy.

Marian AJ, Roberts R.

Tex Heart Inst J. 1994;21(1):6-15. Review.

14.

Novel mutation in splicing donor of dystrophin gene first exon in a patient with dilated cardiomyopathy but no clinical signs of skeletal myopathy.

Kimura S, Ikezawa M, Ozasa S, Ito K, Ueno H, Yoshioka K, Ijiri S, Nomura K, Nakamura K, Matuskura M, Miike T.

J Child Neurol. 2007 Jul;22(7):901-6.

PMID:
17715288
15.

A novel missense mutation in the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and dilation in elderly patients.

Konno T, Shimizu M, Ino H, Matsuyama T, Yamaguchi M, Terai H, Hayashi K, Mabuchi T, Kiyama M, Sakata K, Hayashi T, Inoue M, Kaneda T, Mabuchi H.

J Am Coll Cardiol. 2003 Mar 5;41(5):781-6.

16.

[Familial predisposition and microbial etiology in dilated cardiomyopathy].

Pankuweit S, Richter A, Ruppert V, Maisch B.

Herz. 2009 Mar;34(2):110-6. doi: 10.1007/s00059-009-3200-2. German.

PMID:
19370326
17.

Gene mutations in adult Japanese patients with dilated cardiomyopathy.

Shimizu M, Ino H, Yasuda T, Fujino N, Uchiyama K, Mabuchi T, Konno T, Kaneda T, Fujita T, Masuta E, Katoh M, Funada A, Mabuchi H.

Circ J. 2005 Feb;69(2):150-3.

18.

Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy.

Muntoni F, Di Lenarda A, Porcu M, Sinagra G, Mateddu A, Marrosu G, Ferlini A, Cau M, Milasin J, Melis MA, Marrosu MG, Cianchetti C, Sanna A, Falaschi A, Camerini F, Giacca M, Mestroni L.

Heart. 1997 Dec;78(6):608-12.

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.

PMID:
16789403
20.

Prevalence and characteristics of dystrophin defects in adult male patients with dilated cardiomyopathy.

Arbustini E, Diegoli M, Morbini P, Dal Bello B, Banchieri N, Pilotto A, Magani F, Grasso M, Narula J, Gavazzi A, Viganò M, Tavazzi L.

J Am Coll Cardiol. 2000 Jun;35(7):1760-8. Review.

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