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Items: 1 to 20 of 85

1.

Dystrophinopathy, the expanding phenotype. Dystrophin abnormalities in X-linked dilated cardiomyopathy.

Beggs AH.

Circulation. 1997 May 20;95(10):2344-7. Review. No abstract available.

2.

[X-linked dilated cardiomyopathy: a cardiospecific phenotype of dystrophinopathy].

Yoshida K, Takeda S.

Ryoikibetsu Shokogun Shirizu. 2001;(35):23-7. Review. Japanese. No abstract available.

PMID:
11555918
3.

[The heartache of muscular dystrophy].

Hoogerwaard EM, Ginjaar HB, Wilde AA, Leschot NJ, de Voogt WG, de Visser M.

Ned Tijdschr Geneeskd. 2000 Nov 11;144(46):2181-4. Review. Dutch.

PMID:
11103252
4.

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.

5.

Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.

Ortiz-Lopez R, Li H, Su J, Goytia V, Towbin JA.

Circulation. 1997 May 20;95(10):2434-40.

6.

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.

7.

X-linked dilated cardiomyopathy and the dystrophin gene.

Ferlini A, Sewry C, Melis MA, Mateddu A, Muntoni F.

Neuromuscul Disord. 1999 Jul;9(5):339-46. Review.

PMID:
10407857
8.

X-linked dilated cardiomyopathy with a large hot-spot deletion in the dystrophin gene.

Tasaki N, Yoshida K, Haruta SI, Kouno H, Ichinose H, Fujimoto Y, Urasawa N, Kawakami T, Taniguchi M, Kurushima S, Shimakura T.

Intern Med. 2001 Dec;40(12):1215-21.

9.

X-linked dilated cardiomyopathy.

Towbin JA, Ortiz-Lopez R.

N Engl J Med. 1994 Feb 3;330(5):369-70. No abstract available.

PMID:
8123157
10.

X-linked dilated cardiomyopathy.

Bies RD.

N Engl J Med. 1994 Feb 3;330(5):368-9; author reply 370. No abstract available.

11.

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
12.

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.

13.

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
14.

Progress in defining the causes of idiopathic dilated cardiomyopathy.

Michels VV.

N Engl J Med. 1993 Sep 23;329(13):960-1. No abstract available.

PMID:
8361512
15.

Insertional mutation by transposable element, L1, in the DMD gene results in X-linked dilated cardiomyopathy.

Yoshida K, Nakamura A, Yazaki M, Ikeda S, Takeda S.

Hum Mol Genet. 1998 Jul;7(7):1129-32.

PMID:
9618170
16.

[Mutations of the dystrophin gene in dilated cardiomyopathy].

Shiga N, Akita H, Yokoyama M.

Nihon Rinsho. 2000 Jan;58(1):123-7. Review. Japanese.

PMID:
10885299
17.

A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy.

Ferlini A, GaliƩ N, Merlini L, Sewry C, Branzi A, Muntoni F.

Am J Hum Genet. 1998 Aug;63(2):436-46.

18.

A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotype.

Goldberg LR, Hausmanowa-Petrusewicz I, Fidzianska A, Duggan DJ, Steinberg LS, Hoffman EP.

Ann Neurol. 1998 Dec;44(6):971-6.

PMID:
9851445
19.

[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
20.

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

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