Your search returned 23 results.

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	1.	Towards the professional status of dental hygiene in Alberta. [electronic resource] by Lautar, C Kirby, D M Producer: 19980616 In: Probe (Ottawa, Ont.) vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	2.	Urinary-free amino acids in osteogenesis imperfecta. [electronic resource] by Cole, W G Kirby, D M Producer: 19860613 In: Bone vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Respiratory chain enzyme analysis in muscle and liver. [electronic resource] by Thorburn, D R Chow, C W Kirby, D M Producer: 20051013 In: Mitochondrion vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Maternal tyrosinaemia II: management and successful outcome. [electronic resource] by Francis, D E Kirby, D M Thompson, G N Producer: 19920710 In: European journal of pediatrics vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Pregnancy in phenylketonuria: dietary treatment aimed at normalising maternal plasma phenylalanine concentration. [electronic resource] by Thompson, G N Francis, D E Kirby, D M Compton, R Producer: 19920130 In: Archives of disease in childhood vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A Family of Single-Isomer Chiral Resolving Agents for Capillary Electrophoresis. 2. Hepta-6-sulfato-β-cyclodextrin. [electronic resource] by Vincent, J B Kirby, D M Nguyen, T V Vigh, G Producer: 20121002 In: Analytical chemistry vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	The importance of liver biopsy in the investigation of possible mitochondrial respiratory chain disease. [electronic resource] by Panetta, J Gibson, K Kirby, D M Thorburn, D R Boneh, A Producer: 20051202 In: Neuropediatrics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Characterization of the mutations in three patients with pyruvate dehydrogenase E1 alpha deficiency. [electronic resource] by Hansen, L L Brown, G K Kirby, D M Dahl, H H Producer: 19911004 In: Journal of inherited metabolic disease vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Difficulties in assessing the effect of strychnine on the outcome of non-ketotic hyperglycinaemia. Observations on sisters with a mild T-protein defect. [electronic resource] by Haan, E A Kirby, D M Tada, K Hayasaka, K Danks, D M Producer: 19861211 In: European journal of pediatrics vol. 145 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families. [electronic resource] by Kirby, D M Kahler, S G Freckmann, M L Reddihough, D Thorburn, D R Producer: 20000731 In: Annals of neurology vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	11.	The clinical and biochemical spectrum of human pyruvate dehydrogenase complex deficiency. [electronic resource] by Brown, G K Brown, R M Scholem, R D Kirby, D M Dahl, H H Producer: 19900531 In: Annals of the New York Academy of Sciences vol. 573 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Respiratory chain complex III [correction of complex] in deficiency with pruritus: a novel vitamin responsive clinical feature. [electronic resource] by Mowat, D Kirby, D M Kamath, K R Kan, A Thorburn, D R Christodoulou, J Producer: 19990325 In: The Journal of pediatrics vol. 134 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder. [electronic resource] by Kirby, D M Crawford, M Cleary, M A Dahl, H H Dennett, X Thorburn, D R Producer: 19990512 In: Neurology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Mitochondrial electron transport chain defect presenting as hypoglycemia. [electronic resource] by Freckmann, M L Thorburn, D R Kirby, D M Kamath, K R Hammond, J Dennett, X Christodoulou, J Producer: 19970408 In: The Journal of pediatrics vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	HIV-1 protein Vpr causes gross mitochondrial dysfunction in the yeast Saccharomyces cerevisiae. [electronic resource] by Macreadie, I G Thorburn, D R Kirby, D M Castelli, L A de Rozario, N L Azad, A A Producer: 19970903 In: FEBS letters vol. 410 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Continuous venovenous hemofiltration in the management of acute decompensation in inborn errors of metabolism. [electronic resource] by Thompson, G N Butt, W W Shann, F A Kirby, D M Henning, R D Howells, D W Osborne, A Producer: 19910710 In: The Journal of pediatrics vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis. [electronic resource] by Brown, G K Haan, E A Kirby, D M Scholem, R D Wraith, J E Rogers, J G Danks, D M Producer: 19880302 In: European journal of pediatrics vol. 147 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Leigh syndrome: clinical features and biochemical and DNA abnormalities. [electronic resource] by Rahman, S Blok, R B Dahl, H H Danks, D M Kirby, D M Chow, C W Christodoulou, J Thorburn, D R Producer: 19960509 In: Annals of neurology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Mitochondrial myopathy with tRNA(Leu(UUR)) mutation and complex I deficiency responsive to riboflavin. [electronic resource] by Ogle, R F Christodoulou, J Fagan, E Blok, R B Kirby, D M Seller, K L Dahl, H H Thorburn, D R Producer: 19970214 In: The Journal of pediatrics vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Mutations of the mitochondrial ND1 gene as a cause of MELAS. [electronic resource] by Kirby, D M McFarland, R Ohtake, A Dunning, C Ryan, M T Wilson, C Ketteridge, D Turnbull, D M Thorburn, D R Taylor, R W Producer: 20050804 In: Journal of medical genetics vol. 41 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.