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	61.	Acylcarnitine analysis in the investigation of myopathy. [electronic resource] by Moore, S J Haites, N E Broom, I White, I Coleman, R J Pourfarzam, M Morris, A A Producer: 19981130 In: Journal of inherited metabolic disease vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	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)
	63.	Glucose and leucine kinetics in idiopathic ketotic hypoglycaemia. [electronic resource] by Bodamer, O A Hussein, K Morris, A A Langhans, C-D Rating, D Mayatepek, E Leonard, J V Producer: 20060609 In: Archives of disease in childhood vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Expanding the forensic German mitochondrial DNA control region database: genetic diversity as a function of sample size and microgeography. [electronic resource] by Pfeiffer, H Brinkmann, B Hühne, J Rolf, B Morris, A A Steighner, R Holland, M M Forster, P Producer: 19991029 In: International journal of legal medicine vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	Glutaric aciduria and suspected child abuse. [electronic resource] by Morris, A A Hoffmann, G F Naughten, E R Monavari, A A Collins, J E Leonard, J V Producer: 19991013 In: Archives of disease in childhood vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	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)
	67.	MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA. [electronic resource] by Taylor, R W Chinnery, P F Haldane, F Morris, A A Bindoff, L A Wilson, J Turnbull, D M Producer: 19961112 In: Annals of neurology vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	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)
	69.	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)
	70.	Molecular mechanisms in mitochondrial DNA depletion syndrome. [electronic resource] by Taanman, J W Bodnar, A G Cooper, J M Morris, A A Clayton, P T Leonard, J V Schapira, A H Producer: 19970729 In: Human molecular genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	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)
	72.	ARC syndrome: an expanding range of phenotypes. [electronic resource] by Eastham, K M McKiernan, P J Milford, D V Ramani, P Wyllie, J van't Hoff, W Lynch, S A Morris, A A Producer: 20011204 In: Archives of disease in childhood vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Impaired ketogenesis in fructose-1,6-bisphosphatase deficiency: a pitfall in the investigation of hypoglycaemia. [electronic resource] by Morris, A A Deshphande, S Ward-Platt, M P Whitfield, A E Aynsley-Green, A Leonard, J V Pourfarzam, M Bartlett, K Producer: 19950828 In: Journal of inherited metabolic disease vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	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)
	75.	Pyruvate dehydrogenase E3 binding protein (protein X) deficiency. [electronic resource] by Brown, R M Head, R A Morris, A A M Raiman, J A J Walter, J H Whitehouse, W P Brown, G K Producer: 20060928 In: Developmental medicine and child neurology vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	76.	Respiratory chain dysfunction in progressive neuronal degeneration of childhood with liver disease. [electronic resource] by Morris, A A Singh-Kler, R Perry, R H Griffiths, P D Burt, A D Wong, C P Gardner-Medwin, D Turnbull, D M Producer: 19970116 In: Journal of child neurology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	77.	Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain. [electronic resource] by Morris, A A Taylor, R W Birch-Machin, M A Jackson, M J Coulthard, M G Bindoff, L A Welch, R J Howell, N Turnbull, D M Producer: 19951219 In: Pediatric nephrology (Berlin, Germany) vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	78.	Liver failure associated with mitochondrial DNA depletion. [electronic resource] by Morris, A A Taanman, J W Blake, J Cooper, J M Lake, B D Malone, M Love, S Clayton, P T Leonard, J V Schapira, A H Producer: 19980618 In: Journal of hepatology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	79.	Effect of N-[(S)-1-carboxy-3-phenylpropyl]-L-Ala-L-Pro and its ethyl ester (MK-421) on angiotensin converting enzyme in vitro and angiotensin I pressor responses in vivo. [electronic resource] by Gross, D M Sweet, C S Ulm, E H Backlund, E P Morris, A A Weitz, D Bohn, D L Wenger, H C Vassil, T C Stone, C A Producer: 19810513 In: The Journal of pharmacology and experimental therapeutics vol. 216 Availability: No items available. Save to lists Add to cart (remove)
	80.	Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathy. [electronic resource] by Morris, A A M Appleton, R E Power, B Isherwood, D M Abernethy, L J Taylor, R W Turnbull, D M Verhoeven, N M Salomons, G S Jakobs, C 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)

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Your search returned 84 results.