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Items: 1 to 20 of 186

1.

Cardiomyopathy of limb-girdle muscular dystrophy.

Mascarenhas DA, Spodick DH, Chad DA, Gilchrist J, Townes PL, DeGirolami U, Mudge GH, Maki DW, Bishop RL.

J Am Coll Cardiol. 1994 Nov 1;24(5):1328-33.

2.

The heart in limb girdle muscular dystrophy.

van der Kooi AJ, de Voogt WG, Barth PG, Busch HF, Jennekens FG, Jongen PJ, de Visser M.

Heart. 1998 Jan;79(1):73-7.

3.

Malignant mutation in the lamin A/C gene causing progressive conduction system disease and early sudden death in a family with mild form of limb-girdle muscular dystrophy.

Antoniades L, Eftychiou C, Kyriakides T, Christodoulou K, Katritsis DG.

J Interv Card Electrophysiol. 2007 Jun;19(1):1-7.

PMID:
17605093
4.

A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3.

Driss A, Amouri R, Ben Hamida C, Souilem S, Gouider-Khouja N, Ben Hamida M, Hentati F.

Neuromuscul Disord. 2000 Jun;10(4-5):240-6.

PMID:
10838249
5.

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.

Weiler T, Greenberg CR, Zelinski T, Nylen E, Coghlan G, Crumley MJ, Fujiwara TM, Morgan K, Wrogemann K.

Am J Hum Genet. 1998 Jul;63(1):140-7.

6.

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.

Circulation. 1993 Jun;87(6):1854-65.

PMID:
8504498
7.

Dilated cardiomyopathy and the dystrophin gene: an illustrated review.

Oldfors A, Eriksson BO, Kyllerman M, Martinsson T, Wahlström J.

Br Heart J. 1994 Oct;72(4):344-8. Review.

8.

[Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family].

Horváth R, Walter MC, Lochmüller H, Hübner A, Karcagi V, Pikó H, Timár L, Komoly S.

Ideggyogy Sz. 2005 Jan 20;58(1-2):52-8. Hungarian.

PMID:
15884399
9.

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.

PMID:
18261911
10.

A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy.

Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SK, Pereira L, Akiyama J, Roberds SL, Campbell KP, Zatz M.

Hum Mol Genet. 1995 Jul;4(7):1163-7.

PMID:
8528203
11.

Hereditary muscular dystrophies and the heart.

Hermans MC, Pinto YM, Merkies IS, de Die-Smulders CE, Crijns HJ, Faber CG.

Neuromuscul Disord. 2010 Aug;20(8):479-92. doi: 10.1016/j.nmd.2010.04.008. Review.

PMID:
20627570
12.

Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathy.

Mehta SG, Watts GD, McGillivray B, Mumm S, Hamilton SJ, Ramdeen S, Novack D, Briggs C, Whyte MP, Kimonis VE.

Am J Med Genet A. 2006 Feb 15;140(4):322-30.

PMID:
16419137
13.

A scapular onset muscular dystrophy without facial involvement: possible allelism with facioscapulohumeral muscular dystrophy.

Jardine PE, Upadhyaya M, Maynard J, Harper P, Lunt PW.

Neuromuscul Disord. 1994 Sep-Nov;4(5-6):477-82.

PMID:
7881292
14.

A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement.

van der Kooi AJ, Ledderhof TM, de Voogt WG, Res CJ, Bouwsma G, Troost D, Busch HF, Becker AE, de Visser M.

Ann Neurol. 1996 May;39(5):636-42.

PMID:
8619549
15.

Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy.

Illarioshkin SN, Ivanova-Smolenskaya IA, Tanaka H, Vereshchagin NV, Markova ED, Poleshchuk VV, Lozhnikova SM, Sukhorukov VS, Limborska SA, Slominsky PA, Bulayeva KB, Tsuji S.

Brain. 1996 Dec;119 ( Pt 6):1895-909.

PMID:
9009996
16.

R25G mutation in exon 1 of LMNA gene is associated with dilated cardiomyopathy and limb-girdle muscular dystrophy 1B.

Yuan WL, Huang CY, Wang JF, Xie SL, Nie RQ, Liu YM, Liu PM, Zhou SX, Chen SQ, Huang WJ.

Chin Med J (Engl). 2009 Dec 5;122(23):2840-5.

PMID:
20092787
17.

Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.

van der Kooi AJ, van Meegen M, Ledderhof TM, McNally EM, de Visser M, Bolhuis PA.

Am J Hum Genet. 1997 Apr;60(4):891-5.

18.

Electron microscopic findings of cardiomyopathy with limb girdle muscular dystrophy.

Funabiki K, Onishi K, Tanabe M, Kuru S, Konagaya M, Sato F, Ito M, Nakano T.

Int J Cardiol. 2005 Jan;98(1):161-2.

PMID:
15676184
19.

Limb girdle muscular dystrophy: reappraisal of a rejected entity.

van der Kooi AJ, de Visser M, Barth PG.

Clin Neurol Neurosurg. 1994 Aug;96(3):209-18. Review.

PMID:
7988088
20.

The 10 autosomal recessive limb-girdle muscular dystrophies.

Zatz M, de Paula F, Starling A, Vainzof M.

Neuromuscul Disord. 2003 Sep;13(7-8):532-44. Review.

PMID:
12921790
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