Literature DB >> 7623461

Ketonuria and medium-chain acyl-CoA dehydrogenase deficiency.

J S Patel1, J V Leonard.   

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Year:  1995        PMID： 7623461     DOI： 10.1007/bf00711392

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  1 in total

1.  Production and disposal of medium-chain fatty acids in children with medium-chain acyl-CoA dehydrogenase deficiency.

Authors:  S J Heales; G N Thompson; A F Massoud; S Rahman; D Halliday; J V Leonard
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982
  1 in total
  2 in total

Review 1.  Laboratory diagnostic approaches in metabolic disorders.

Authors:  Ruben Bonilla Guerrero; Denise Salazar; Pranoot Tanpaiboon
Journal:  Ann Transl Med       Date:  2018-12

Review 2.  Disorders of mitochondrial fatty acyl-CoA beta-oxidation.

Authors:  R J Wanders; P Vreken; M E den Boer; F A Wijburg; A H van Gennip; L IJlst
Journal:  J Inherit Metab Dis       Date:  1999-06       Impact factor: 4.982
  2 in total

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