Search research articles
Contact Us
Filters
Showing results (1-10 of 24) with videos related to
Page
of 3
Sort By:
Journal of Inherited Metabolic Disease
|
May 7, 2005
Cerebral ketone body metabolism
A A M Morris
Seminars in Neonatology : SN
|
June 19, 2002
Urea cycle disorders
J 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 Deficiency
L 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 Deficiency
L Knowles, A A M Morris, J H Walter
Journal of Inherited Metabolic Disease
|
January 7, 2004
Rhabdomyolysis in glutaric aciduria type I
S L Chow, C Rohan, A A M Morris
Journal of Inherited Metabolic Disease
|
December 13, 2006
Hyperlipidaemia due to carnitine palmitoyltransferase I deficiency
H Worthington, S E Olpin, I Blumenthal, et al.
JIMD Reports
|
September 26, 2015
Recurrent Ventricular Tachycardia in Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
P Bala, S Ferdinandusse, S E Olpin, et al.
Neuropediatrics
|
August 26, 2004
Biotinidase deficiency: a treatable leukoencephalopathy
S 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 deficiency
A M Lund, M A Dixon, P Vreken, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Journal of Inherited Metabolic Disease
|
May 7, 2005
Cerebral ketone body metabolism
A A M Morris
Seminars in Neonatology : SN
|
June 19, 2002
Urea cycle disorders
J 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 Deficiency
L 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 Deficiency
L Knowles, A A M Morris, J H Walter
Journal of Inherited Metabolic Disease
|
January 7, 2004
Rhabdomyolysis in glutaric aciduria type I
S L Chow, C Rohan, A A M Morris
Journal of Inherited Metabolic Disease
|
December 13, 2006
Hyperlipidaemia due to carnitine palmitoyltransferase I deficiency
H Worthington, S E Olpin, I Blumenthal, et al.
JIMD Reports
|
September 26, 2015
Recurrent Ventricular Tachycardia in Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
P Bala, S Ferdinandusse, S E Olpin, et al.
Neuropediatrics
|
August 26, 2004
Biotinidase deficiency: a treatable leukoencephalopathy
S 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 deficiency
A M Lund, M A Dixon, P Vreken, et al.
Page
of 3