Similar articles for PMID: 10841222

Year	Number of Results
1984	1
1985	1
1993	4
1994	2
1995	1
1997	4
1998	2
1999	3
2000	5
2001	2
2002	4
2003	4
2004	2
2005	2
2006	4
2007	3
2008	1
2009	1
2010	2
2011	3
2012	3
2013	2
2014	2
2015	3
2016	4
2017	5
2018	3
2021	1
2024	0

1

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. Arbustini E, et al. J Am Coll Cardiol. 2000 Jun;35(7):1760-8. doi: 10.1016/s0735-1097(00)00650-1. J Am Coll Cardiol. 2000. PMID: 10841222 Free article. Review.

2

Diagnostic work-up and risk stratification in X-linked dilated cardiomyopathies caused by dystrophin defects.

Diegoli M, Grasso M, Favalli V, Serio A, Gambarin FI, Klersy C, Pasotti M, Agozzino E, Scelsi L, Ferlini A, Febo O, Piccolo G, Tavazzi L, Narula J, Arbustini E. Diegoli M, et al. J Am Coll Cardiol. 2011 Aug 23;58(9):925-34. doi: 10.1016/j.jacc.2011.01.072. J Am Coll Cardiol. 2011. PMID: 21851881 Free article.

3

Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease.

Arbustini E, Pilotto A, Repetto A, Grasso M, Negri A, Diegoli M, Campana C, Scelsi L, Baldini E, Gavazzi A, Tavazzi L. Arbustini E, et al. J Am Coll Cardiol. 2002 Mar 20;39(6):981-90. doi: 10.1016/s0735-1097(02)01724-2. J Am Coll Cardiol. 2002. PMID: 11897440 Free article.

4

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. Franz WM, et al. Ann N Y Acad Sci. 1995 Mar 27;752:470-91. doi: 10.1111/j.1749-6632.1995.tb17457.x. Ann N Y Acad Sci. 1995. PMID: 7755293

5

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. Mestroni L, et al. J Am Coll Cardiol. 1999 Jul;34(1):181-90. doi: 10.1016/s0735-1097(99)00172-2. J Am Coll Cardiol. 1999. PMID: 10400009 Free article.

6

Dystrophin analysis in idiopathic dilated cardiomyopathy.

Michels VV, Pastores GM, Moll PP, Driscoll DJ, Miller FA, Burnett JC, Rodeheffer RJ, Tajik JA, Beggs AH, Kunkel LM, et al. Michels VV, et al. J Med Genet. 1993 Nov;30(11):955-7. doi: 10.1136/jmg.30.11.955. J Med Genet. 1993. PMID: 8301653 Free PMC article.

7

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. Obler D, et al. J Card Fail. 2010 Mar;16(3):194-9. doi: 10.1016/j.cardfail.2009.11.009. J Card Fail. 2010. PMID: 20206892

8

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. Muntoni F, et al. Heart. 1997 Dec;78(6):608-12. doi: 10.1136/hrt.78.6.608. Heart. 1997. PMID: 9470882 Free PMC article.

9

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. Bies RD, et al. J Mol Cell Cardiol. 1997 Dec;29(12):3175-88. doi: 10.1006/jmcc.1997.0568. J Mol Cell Cardiol. 1997. PMID: 9441825

10

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.

Towbin JA, Hejtmancik JF, Brink P, Gelb B, Zhu XM, Chamberlain JS, McCabe ER, Swift M. Towbin JA, et al. Circulation. 1993 Jun;87(6):1854-65. doi: 10.1161/01.cir.87.6.1854. Circulation. 1993. PMID: 8504498

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