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	1.	Cerebral ketone body metabolism. [electronic resource] by Morris, A A M Producer: 20050804 In: Journal of inherited metabolic disease vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Urea cycle disorders. [electronic resource] by Leonard, J V Morris, A A M Producer: 20021002 In: Seminars in neonatology : SN vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Rhabdomyolysis in glutaric aciduria type I. [electronic resource] by Chow, S L Rohan, C Morris, A A M Producer: 20040728 In: Journal of inherited metabolic disease vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	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. [electronic resource] by Knowles, L Morris, A A M Walter, J H Publication details: JIMD reports 2016 In: JIMD reports vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Treatment with Mefolinate (5-Methyltetrahydrofolate), but Not Folic Acid or Folinic Acid, Leads to Measurable 5-Methyltetrahydrofolate in Cerebrospinal Fluid in Methylenetetrahydrofolate Reductase Deficiency. [electronic resource] by Knowles, L Morris, A A M Walter, J H Publication details: JIMD reports 2016 In: JIMD reports vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Hyperlipidaemia due to carnitine palmitoyltransferase I deficiency. [electronic resource] by Worthington, H Olpin, S E Blumenthal, I Morris, A A M Producer: 20070313 In: Journal of inherited metabolic disease vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Recurrent Ventricular Tachycardia in Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency. [electronic resource] by Bala, P Ferdinandusse, S Olpin, S E Chetcuti, P Morris, A A M Producer: 20160512 In: JIMD reports vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Biotinidase deficiency: a treatable leukoencephalopathy. [electronic resource] by Grünewald, S Champion, M P Leonard, J V Schaper, J Morris, A A M Producer: 20041130 In: Neuropediatrics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Plasma and erythrocyte fatty acid concentrations in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. [electronic resource] by Lund, A M Dixon, M A Vreken, P Leonard, J V Morris, A A M Producer: 20040401 In: Journal of inherited metabolic disease vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	What is the role of medium-chain triglycerides in the management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency? [electronic resource] by Lund, A M Dixon, M A Vreken, P Leonard, J V Morris, A A M Producer: 20040401 In: Journal of inherited metabolic disease vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	N-carbamylglutamate for neonatal hyperammonaemia in propionic acidaemia. [electronic resource] by Jones, S Reed, C A B Vijay, S Walter, J H Morris, A A M Producer: 20120111 In: Journal of inherited metabolic disease vol. 31 Suppl 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Cerebral edema associated with betaine treatment in classical homocystinuria. [electronic resource] by Devlin, A M Hajipour, L Gholkar, A Fernandes, H Ramesh, V Morris, A A M Producer: 20040601 In: The Journal of pediatrics vol. 144 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Cholestatic Jaundice Associated with Carnitine Palmitoyltransferase IA Deficiency. [electronic resource] by Morris, A A M Olpin, S E Bennett, M J Santani, A Stahlschmidt, J McClean, P Producer: 20130225 In: JIMD reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	The significance of a high plasma ammonia value. [electronic resource] by Chow, S L Gandhi, V Krywawych, S Clayton, P T Leonard, J V Morris, A A M Producer: 20040615 In: Archives of disease in childhood vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Are tablets a practical source of protein substitute in phenylketonuria? [electronic resource] by MacDonald, A Ferguson, C Rylance, G Morris, A A M Asplin, D Hall, S K Booth, I W Producer: 20030416 In: Archives of disease in childhood vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Cataract in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). [electronic resource] by Russell-Eggitt, I M Leonard, J V Lund, A M Manoj, B Thompson, D A Morris, A A M Producer: 20030418 In: Ophthalmic genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Lathosterolosis: A Relatively Mild Case with Cataracts and Learning Difficulties. [electronic resource] by Anderson, R Rust, S Ashworth, J Clayton-Smith, J Taylor, R L Clayton, P T Morris, A A M Publication details: JIMD reports 2019 In: JIMD reports vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Acute respiratory distress syndrome in long-chain 3-hydroxyacyl-CoA dehydrogenase and mitochondrial trifunctional protein deficiencies. [electronic resource] by Lundy, C T Shield, J P H Kvittingen, E A Vinorum, O J Trimble, E R Morris, A A M Producer: 20040617 In: Journal of inherited metabolic disease vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Unsuccessful treatment of severe pyruvate carboxylase deficiency with triheptanoin. [electronic resource] by Breen, C White, F J Scott, C A B Heptinstall, L Walter, J H Jones, S A Morris, A A M Producer: 20150102 In: European journal of pediatrics vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiency. [electronic resource] by Olsen, R K J Pourfarzam, M Morris, A A M Dias, R C Knudsen, I Andresen, B S Gregersen, N Olpin, S E Producer: 20050324 In: Journal of inherited metabolic disease vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 23 results.