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Items: 17

1.

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.

Helbling-Leclerc A, Zhang X, Topaloglu H, Cruaud C, Tesson F, Weissenbach J, Tomé FM, Schwartz K, Fardeau M, Tryggvason K, et al.

Nat Genet. 1995 Oct;11(2):216-8.

PMID:
7550355
2.
3.

Congenital muscular dystrophies: 1997 update.

Voit T.

Brain Dev. 1998 Mar;20(2):65-74. Review.

PMID:
9545174
4.

The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review.

Jones KJ, Morgan G, Johnston H, Tobias V, Ouvrier RA, Wilkinson I, North KN.

J Med Genet. 2001 Oct;38(10):649-57. Review.

5.

[Non-Fukuyama type congenital muscular dystrophy--merosin deficient and positive forms].

Nonaka I.

Nihon Rinsho. 1997 Dec;55(12):3176-80. Review. Japanese.

PMID:
9436431
6.

Merosin and congenital muscular dystrophy.

Miyagoe-Suzuki Y, Nakagawa M, Takeda S.

Microsc Res Tech. 2000 Feb 1-15;48(3-4):181-91. Review.

PMID:
10679965
7.

[Molecular genetics and merosin abnormality in Fukuyama-type congenital muscular dystrophy (FCMD)].

Toda T, Kobayashi K.

Nihon Rinsho. 1997 Dec;55(12):3169-75. Review. Japanese.

PMID:
9436430
8.

Beyond dystrophin: current progress in the muscular dystrophies.

Bönnemann CG, McNally EM, Kunkel LM.

Curr Opin Pediatr. 1996 Dec;8(6):569-82. Review. Erratum in: Curr Opin Pediatr 1997 Apr;9(2):196.

PMID:
9018440
9.
10.

Merosin/laminin-2 and muscular dystrophy.

Wewer UM, Engvall E.

Neuromuscul Disord. 1996 Dec;6(6):409-18. Review.

PMID:
9027848
11.

Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse.

Matsumura K, Yamada H, Saito F, Sunada Y, Shimizu T.

Neuromuscul Disord. 1997 Jan;7(1):7-12. Review.

PMID:
9132144
12.

Congenital myopathies and congenital muscular dystrophies.

Tubridy N, Fontaine B, Eymard B.

Curr Opin Neurol. 2001 Oct;14(5):575-82. Review.

PMID:
11562568
13.
14.

[Congenital muscular dystrophies in children].

Scavone-Mauro C, Barros G.

Rev Neurol. 2013 Sep 6;57 Suppl 1:S47-52. Review. Spanish.

15.

Laminin-α2 Chain-Deficient Congenital Muscular Dystrophy: Pathophysiology and Development of Treatment.

Durbeej M.

Curr Top Membr. 2015;76:31-60. doi: 10.1016/bs.ctm.2015.05.002. Review.

PMID:
26610911
16.

Congenital muscular dystrophies: toward molecular therapeutic interventions.

Collins J, Bönnemann CG.

Curr Neurol Neurosci Rep. 2010 Mar;10(2):83-91. doi: 10.1007/s11910-010-0092-8. Review.

PMID:
20425232
17.

Congenital muscular dystrophies.

Sparks SE, Escolar DM.

Handb Clin Neurol. 2011;101:47-79. doi: 10.1016/B978-0-08-045031-5.00004-9. Review.

PMID:
21496624

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