Učitavanje...
McArdle disease: a case report and review
McArdle disease (glycogen storage disease type V) is a pure myopathy caused by an inherited deficit of myophosphorylase. The disease exhibits clinical heterogeneity, but patients typically experience exercise intolerance, acute crises of early fatigue, and contractures, sometimes with rhabdomyolysis...
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| Glavni autori: | , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Dove Medical Press
2012
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3658246/ https://ncbi.nlm.nih.gov/pubmed/23754915 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/IMCRJ.S28664 |
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