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Items: 1 to 20 of 28

1.

Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E).

Bönnemann CG, Passos-Bueno MR, McNally EM, Vainzof M, de Sá Moreira E, Marie SK, Pavanello RC, Noguchi S, Ozawa E, Zatz M, Kunkel LM.

Hum Mol Genet. 1996 Dec;5(12):1953-61.

3.
4.

Sarcoglycans in muscular dystrophy.

Hack AA, Groh ME, McNally EM.

Microsc Res Tech. 2000 Feb 1-15;48(3-4):167-80. Review.

PMID:
10679964
5.

[The frequency of patients with adhalin deficiency in a muscular dystrophy patient population].

Hayashi YK, Arahata K.

Nihon Rinsho. 1997 Dec;55(12):3165-8. Review. Japanese.

PMID:
9436429
6.

[Significance of merosin and sarcoglycan in manifestations of certain forms of muscular dystrophy].

Medić S, Rakocević-Stojanović V.

Srp Arh Celok Lek. 1998 Jan-Feb;126(1-2):34-9. Review. Serbian.

PMID:
9525081
7.

Sarcoglycan complex: a muscular supporter of dystroglycan-dystrophin interplay?

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

Cell Mol Biol (Noisy-le-grand). 1999 Sep;45(6):751-62. Review.

PMID:
10541473
8.
9.

[Sarcoglycanopathies].

Colomer J.

Rev Neurol. 1999 Jan 16-31;28(2):150-3. Review. Spanish.

PMID:
10101783
10.

[Severe childhood autosomal recessive muscular dystrophy].

Matsumura K, Shimizu T.

Rinsho Shinkeigaku. 1995 Dec;35(12):1422-4. Review. Japanese.

PMID:
8752417
11.

The sarcoglycan complex in limb-girdle muscular dystrophy.

Lim LE, Campbell KP.

Curr Opin Neurol. 1998 Oct;11(5):443-52. Review.

PMID:
9847993
13.

[Muscular dystrophy and dystrophin and its associated proteins].

Ozawa E.

No To Hattatsu. 1996 Mar;28(2):102-8. Review. Japanese.

PMID:
8851278
14.
15.

The differential diagnosis of the human dystrophinopathies and related disorders.

Kakulas BA.

Curr Opin Neurol. 1996 Oct;9(5):380-8. Review.

PMID:
8894415
17.

Molecular bases of autosomal recessive limb-girdle muscular dystrophies.

Nigro V.

Acta Myol. 2003 Sep;22(2):35-42. Review.

PMID:
14959561
18.

Understanding the heterogeneity of the limb-girdle muscular dystrophies.

Bushby K.

Biochem Soc Trans. 1996 May;24(2):489-96. Review. No abstract available.

PMID:
8736790
19.

The ABC's of limb-girdle muscular dystrophy: alpha-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more.

Gordon ES, Hoffman EP.

Curr Opin Neurol. 2001 Oct;14(5):567-73. Review.

PMID:
11562567
20.

Functional roles of dystrophin and of associated proteins. New insights for the sarcoglycans.

Betto R, Biral D, Sandonà D.

Ital J Neurol Sci. 1999 Dec;20(6):371-9. Review.

PMID:
10937856
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