MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F

Known as: LGMD1F 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2004-2015
01220042015

Papers overview

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2015
2015
Limb-girdle muscular dystrophy (LGMD) type 1F (MIM # 608423) is a rare autosomal dominant disorder whose locus was mapped and… (More)
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2014
2014
Limb-girdle muscular dystrophies (LGMD) are a heterogeneous group of genetically determined muscle disorders with a primary or… (More)
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Review
2014
Review
2014
Limb-girdle muscular dystrophies (LGMD) are a highly heterogeneous group of muscle disorders, which first affect the voluntary… (More)
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2014
2014
  • Josep Gamez
  • Neuropathology : official journal of the Japanese…
  • 2014
I read with interest the article by Cenacchi et al., reporting the ultrastructural findings in two patients (mother and daughter… (More)
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2013
2013
Of the seven autosomal dominant genetically distinct forms of LGMD so far described, in only four the causative gene has been… (More)
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2013
2013
A large Italo-Spanish kindred with autosomal-dominant inheritance has been reported with proximal limb and axial muscle weakness… (More)
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2004
2004
Gliedergürteldystrophien (limb girdle muscular dystrophies, LGMD) sind genetisch heterogene, primäre Myopathien mit progredienten… (More)
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Review
2004
Review
2004
Limb girdle muscular dystrophies (LGMDs) are a genetically heterogeneous group of primary myopathies involving progressive… (More)
Is this relevant?