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A A M Morris

Showing results (1-10 of 24) with videos related to

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Journal of Inherited Metabolic Disease|May 7, 2005
Cerebral ketone body metabolismA A M Morris
Seminars in Neonatology : SN|June 19, 2002
Urea cycle disordersJ V Leonard, A A M Morris
JIMD Reports|June 22, 2016
Erratum to: Treatment with Mefolinate (5-Methyltetrahydrofolate), but Not Folic Acid or Folinic Acid, Leads to Measurable 5-Methyltetrahydrofolate in Cerebrospinal Fluid in Methylenetetrahydrofolate Reductase DeficiencyL Knowles, A A M Morris, J H Walter
JIMD Reports|February 23, 2016
Treatment with Mefolinate (5-Methyltetrahydrofolate), but Not Folic Acid or Folinic Acid, Leads to Measurable 5-Methyltetrahydrofolate in Cerebrospinal Fluid in Methylenetetrahydrofolate Reductase DeficiencyL Knowles, A A M Morris, J H Walter
Journal of Inherited Metabolic Disease|January 7, 2004
Rhabdomyolysis in glutaric aciduria type IS L Chow, C Rohan, A A M Morris
Journal of Inherited Metabolic Disease|December 13, 2006
Hyperlipidaemia due to carnitine palmitoyltransferase I deficiencyH Worthington, S E Olpin, I Blumenthal, et al.
JIMD Reports|September 26, 2015
Recurrent Ventricular Tachycardia in Medium-Chain Acyl-Coenzyme A Dehydrogenase DeficiencyP Bala, S Ferdinandusse, S E Olpin, et al.
Neuropediatrics|August 26, 2004
Biotinidase deficiency: a treatable leukoencephalopathyS Grünewald, M P Champion, J V Leonard, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
What is the role of medium-chain triglycerides in the management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency?A M Lund, M A Dixon, P Vreken, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
Plasma and erythrocyte fatty acid concentrations in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyA M Lund, M A Dixon, P Vreken, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Journal of Inherited Metabolic Disease|May 7, 2005
Cerebral ketone body metabolismA A M Morris
Seminars in Neonatology : SN|June 19, 2002
Urea cycle disordersJ V Leonard, A A M Morris
JIMD Reports|June 22, 2016
Erratum to: Treatment with Mefolinate (5-Methyltetrahydrofolate), but Not Folic Acid or Folinic Acid, Leads to Measurable 5-Methyltetrahydrofolate in Cerebrospinal Fluid in Methylenetetrahydrofolate Reductase DeficiencyL Knowles, A A M Morris, J H Walter
JIMD Reports|February 23, 2016
Treatment with Mefolinate (5-Methyltetrahydrofolate), but Not Folic Acid or Folinic Acid, Leads to Measurable 5-Methyltetrahydrofolate in Cerebrospinal Fluid in Methylenetetrahydrofolate Reductase DeficiencyL Knowles, A A M Morris, J H Walter
Journal of Inherited Metabolic Disease|January 7, 2004
Rhabdomyolysis in glutaric aciduria type IS L Chow, C Rohan, A A M Morris
Journal of Inherited Metabolic Disease|December 13, 2006
Hyperlipidaemia due to carnitine palmitoyltransferase I deficiencyH Worthington, S E Olpin, I Blumenthal, et al.
JIMD Reports|September 26, 2015
Recurrent Ventricular Tachycardia in Medium-Chain Acyl-Coenzyme A Dehydrogenase DeficiencyP Bala, S Ferdinandusse, S E Olpin, et al.
Neuropediatrics|August 26, 2004
Biotinidase deficiency: a treatable leukoencephalopathyS Grünewald, M P Champion, J V Leonard, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
What is the role of medium-chain triglycerides in the management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency?A M Lund, M A Dixon, P Vreken, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
Plasma and erythrocyte fatty acid concentrations in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyA M Lund, M A Dixon, P Vreken, et al.
Pageof 3