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A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiency

Authors

  • E H Touma aLaboratory of Professor Loiselet, Faculty of Medicine, University St Joseph, Damascus Street, PO Box 11-5076, Beirut, Lebanon, bMetabolic Screening Laboratory, King Faisal Specialist Hospital, Riyadh, Saudi Arabia, cLaboratory of Pediatric Biochemistry, Hôpital Debrousse, Lyon, France, dAnalytical Testing Laboratory, Beirut, Lebanon, eResearch Unit for Molecular Medicine and Aarhus University Hospital, Aarhus, Denmark PubMed articlesGoogle scholar articles
  • M S Rashed aLaboratory of Professor Loiselet, Faculty of Medicine, University St Joseph, Damascus Street, PO Box 11-5076, Beirut, Lebanon, bMetabolic Screening Laboratory, King Faisal Specialist Hospital, Riyadh, Saudi Arabia, cLaboratory of Pediatric Biochemistry, Hôpital Debrousse, Lyon, France, dAnalytical Testing Laboratory, Beirut, Lebanon, eResearch Unit for Molecular Medicine and Aarhus University Hospital, Aarhus, Denmark PubMed articlesGoogle scholar articles
  • C Vianey-Saban aLaboratory of Professor Loiselet, Faculty of Medicine, University St Joseph, Damascus Street, PO Box 11-5076, Beirut, Lebanon, bMetabolic Screening Laboratory, King Faisal Specialist Hospital, Riyadh, Saudi Arabia, cLaboratory of Pediatric Biochemistry, Hôpital Debrousse, Lyon, France, dAnalytical Testing Laboratory, Beirut, Lebanon, eResearch Unit for Molecular Medicine and Aarhus University Hospital, Aarhus, Denmark PubMed articlesGoogle scholar articles
  • A Sakr aLaboratory of Professor Loiselet, Faculty of Medicine, University St Joseph, Damascus Street, PO Box 11-5076, Beirut, Lebanon, bMetabolic Screening Laboratory, King Faisal Specialist Hospital, Riyadh, Saudi Arabia, cLaboratory of Pediatric Biochemistry, Hôpital Debrousse, Lyon, France, dAnalytical Testing Laboratory, Beirut, Lebanon, eResearch Unit for Molecular Medicine and Aarhus University Hospital, Aarhus, Denmark PubMed articlesGoogle scholar articles
  • P Divry aLaboratory of Professor Loiselet, Faculty of Medicine, University St Joseph, Damascus Street, PO Box 11-5076, Beirut, Lebanon, bMetabolic Screening Laboratory, King Faisal Specialist Hospital, Riyadh, Saudi Arabia, cLaboratory of Pediatric Biochemistry, Hôpital Debrousse, Lyon, France, dAnalytical Testing Laboratory, Beirut, Lebanon, eResearch Unit for Molecular Medicine and Aarhus University Hospital, Aarhus, Denmark PubMed articlesGoogle scholar articles
  • N Gregersen aLaboratory of Professor Loiselet, Faculty of Medicine, University St Joseph, Damascus Street, PO Box 11-5076, Beirut, Lebanon, bMetabolic Screening Laboratory, King Faisal Specialist Hospital, Riyadh, Saudi Arabia, cLaboratory of Pediatric Biochemistry, Hôpital Debrousse, Lyon, France, dAnalytical Testing Laboratory, Beirut, Lebanon, eResearch Unit for Molecular Medicine and Aarhus University Hospital, Aarhus, Denmark PubMed articlesGoogle scholar articles
  • B S Andresen aLaboratory of Professor Loiselet, Faculty of Medicine, University St Joseph, Damascus Street, PO Box 11-5076, Beirut, Lebanon, bMetabolic Screening Laboratory, King Faisal Specialist Hospital, Riyadh, Saudi Arabia, cLaboratory of Pediatric Biochemistry, Hôpital Debrousse, Lyon, France, dAnalytical Testing Laboratory, Beirut, Lebanon, eResearch Unit for Molecular Medicine and Aarhus University Hospital, Aarhus, Denmark PubMed articlesGoogle scholar articles
  1. Dr Touma email:loiselet{at}dm.net.lb
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Citation

Touma EH, Rashed MS, Vianey-Saban C, et al
A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiency

Publication history

  • Accepted June 1, 2000
  • First published January 1, 2001.
Online issue publication 
January 10, 2022

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