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Article

[Sarcoglycanopathies].

Revista de neurologia - 1 Jan 2000

Colomer J

Abstract excerpt

INTRODUCTION: Identification of several clinical pictures in relation to a deficit of various protein components of the sarcoglycan complex, has allowed a new classification to be established for muscular dystrophies, correlating the protein alpha, beta, gamma, sigma deficit with a type of girdle dystrophy ('Limb-Girdle Muscular Dystrophy', LGMD) and the genomic identification respectively: 2D/17, 2E/4q12,...

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PMID: 10101783

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[Sarcoglycanopathies].PMID 10101783Read ↗

[Sarcoglycanopathies: state of the art and therapeutic perspectives].Semantic proximity Read ↗

[Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation].Semantic proximity Read ↗

[Sarcoglycanopathies, a particular limb-girdle muscular dystrophy type (phenotype in three Polish families): initial report].Semantic proximity Read ↗

Sarcoglycanopathies: molecular pathogenesis and therapeutic prospectsSemantic proximity Read ↗

From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.Semantic proximity Read ↗

Invited commentary. Sarcoglycanopathies: a clinico-pathological study.Semantic proximity Read ↗

Phenotypic and immunohistochemical characterization of sarcoglycanopathies.Semantic proximity Read ↗

[Muscular dystrophies].Semantic proximity Read ↗

Sarcoglycanopathies: an update.Semantic proximity Read ↗

[Gamma-sarcoglycanopathy: clinico-pathological and genetic study of 11 cases].Semantic proximity Read ↗

Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian populationSemantic proximity Read ↗

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