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Items: 1 to 20 of 25

1.

Re-examination of the electrocardiogram in boys with Duchenne muscular dystrophy and correlation with its dilated cardiomyopathy.

Thrush PT, Allen HD, Viollet L, Mendell JR.

Am J Cardiol. 2009 Jan 15;103(2):262-5. doi: 10.1016/j.amjcard.2008.08.064. Epub 2008 Oct 30.

PMID:
19121448
2.

Cardiac expression of a mini-dystrophin that normalizes skeletal muscle force only partially restores heart function in aged Mdx mice.

Bostick B, Yue Y, Long C, Marschalk N, Fine DM, Chen J, Duan D.

Mol Ther. 2009 Feb;17(2):253-61. doi: 10.1038/mt.2008.264. Epub 2008 Dec 9.

3.

Follow-up of three patients with a large in-frame deletion of exons 45-55 in the Duchenne muscular dystrophy (DMD) gene.

Nakamura A, Yoshida K, Fukushima K, Ueda H, Urasawa N, Koyama J, Yazaki Y, Yazaki M, Sakai T, Haruta S, Takeda S, Ikeda S.

J Clin Neurosci. 2008 Jul;15(7):757-63. doi: 10.1016/j.jocn.2006.12.012. Epub 2008 Feb 7.

PMID:
18261911
4.

Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy.

Jefferies JL, Eidem BW, Belmont JW, Craigen WJ, Ware SM, Fernbach SD, Neish SR, Smith EO, Towbin JA.

Circulation. 2005 Nov 1;112(18):2799-804. Epub 2005 Oct 24.

5.

Analysis of dystrophin gene deletions indicates that the hinge III region of the protein correlates with disease severity.

Carsana A, Frisso G, Tremolaterra MR, Lanzillo R, Vitale DF, Santoro L, Salvatore F.

Ann Hum Genet. 2005 May;69(Pt 3):253-9.

6.

Effect of perindopril on the onset and progression of left ventricular dysfunction in Duchenne muscular dystrophy.

Duboc D, Meune C, Lerebours G, Devaux JY, Vaksmann G, Bécane HM.

J Am Coll Cardiol. 2005 Mar 15;45(6):855-7.

7.

Independent movement, dimerization and stability of tandem repeats of chicken brain alpha-spectrin.

Kusunoki H, Minasov G, Macdonald RI, Mondragón A.

J Mol Biol. 2004 Nov 19;344(2):495-511.

PMID:
15522301
8.
9.

Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy.

Harper SQ, Hauser MA, DelloRusso C, Duan D, Crawford RW, Phelps SF, Harper HA, Robinson AS, Engelhardt JF, Brooks SV, Chamberlain JS.

Nat Med. 2002 Mar;8(3):253-61.

PMID:
11875496
10.

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.

11.

Clinical characteristics of aged Becker muscular dystrophy patients with onset after 30 years.

Yazaki M, Yoshida K, Nakamura A, Koyama J, Nanba T, Ohori N, Ikeda S.

Eur Neurol. 1999;42(3):145-9.

PMID:
10529540
12.

Could utrophin rescue the myocardium of patients with dystrophin gene mutations?

Fanin M, Melacini P, Angelini C, Danieli GA.

J Mol Cell Cardiol. 1999 Aug;31(8):1501-8.

PMID:
10423348
13.

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.

14.

Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy.

Melacini P, Fanin M, Danieli GA, Villanova C, Martinello F, Miorin M, Freda MP, Miorelli M, Mostacciuolo ML, Fasoli G, Angelini C, Dalla Volta S.

Circulation. 1996 Dec 15;94(12):3168-75.

15.

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.

16.

Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

Muntoni F, Cau M, Ganau A, Congiu R, Arvedi G, Mateddu A, Marrosu MG, Cianchetti C, Realdi G, Cao A, et al.

N Engl J Med. 1993 Sep 23;329(13):921-5. No abstract available.

17.

Cardiac involvement in Becker muscular dystrophy.

Melacini P, Fanin M, Danieli GA, Fasoli G, Villanova C, Angelini C, Vitiello L, Miorelli M, Buja GF, Mostacciuolo ML, et al.

J Am Coll Cardiol. 1993 Dec;22(7):1927-34.

PMID:
8245351
18.

Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates.

Comi GP, Prelle A, Bresolin N, Moggio M, Bardoni A, Gallanti A, Vita G, Toscano A, Ferro MT, Bordoni A, et al.

Brain. 1994 Feb;117 ( Pt 1):1-14.

PMID:
8149204
19.

Mutation of dystrophin gene and cardiomyopathy.

Nigro G, Politano L, Nigro V, Petretta VR, Comi LI.

Neuromuscul Disord. 1994 Jul;4(4):371-9.

PMID:
7981594
20.

Cardiac dystrophin abnormalities in Becker muscular dystrophy assessed by endomyocardial biopsy.

Maeda M, Nakao S, Miyazato H, Setoguchi M, Arima S, Higuchi I, Osame M, Taira A, Nomoto K, Toda H, et al.

Am Heart J. 1995 Apr;129(4):702-7.

PMID:
7900621
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