2009
DOI: 10.1016/j.ando.2008.05.001
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Rhabdomyolyse sévère révélant une myopathie hypothyroïdienne d’origine auto-immune

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Cited by 6 publications
(1 citation statement)
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“…Various hypotheses have been postulated, such as mitochondrial oxidative metabolism, induction of insulin-resistant state, and decreased muscle carnitine levels, including autoimmune mechanism. 11,13 Also, deficiency in thyroxine leads to abnormal glycogenolysis and increased triglyceride turnover, thus leading to the impairment of muscle function by causing a transition from fast-twitching type 2 muscle fibers to slow-twitching type 1 fibers, low myosin ATPase activity, and low ATP turnover in the skeletal muscles. 14…”
Section: Discussionmentioning
confidence: 99%
“…Various hypotheses have been postulated, such as mitochondrial oxidative metabolism, induction of insulin-resistant state, and decreased muscle carnitine levels, including autoimmune mechanism. 11,13 Also, deficiency in thyroxine leads to abnormal glycogenolysis and increased triglyceride turnover, thus leading to the impairment of muscle function by causing a transition from fast-twitching type 2 muscle fibers to slow-twitching type 1 fibers, low myosin ATPase activity, and low ATP turnover in the skeletal muscles. 14…”
Section: Discussionmentioning
confidence: 99%