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November 1, 1991Annals of Neurology

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

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Authors

CSCharles A. StanleySDSusan DeleeuwPCPaul M. Coates

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Cite This Study

Stanley et al. (1991) studied this question.

synapsesocial.com/papers/6a962bcd924fb82095bad1dehttps://doi.org/10.1002/ana.410300512
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Medium‐chain acyl‐CoA dehydrogenase deficiency: Metabolic effects and therapeutic efficacy of long‐term l ‐carnitine supplementation1988 · 32 citations
  2. 2Carnitine--metabolism and functions1983 · 1,690 citations
  3. 3Observations on the affinity for carnitine, and malonyl-CoA sensitivity, of carnitine palmitoyltransferase I in animal and human tissues. Demonstration of the presence of malonyl-CoA in non-hepatic tissues of the rat1983 · 558 citations