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	381.	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)
	382.	Brain magnetic resonance imaging in suspected extrapyramidal cerebral palsy: observations in distinguishing genetic-metabolic from acquired causes. [electronic resource] by Hoon, A H Reinhardt, E M Kelley, R I Breiter, S N Morton, D H Naidu, S B Johnston, M V Producer: 19971002 In: The Journal of pediatrics vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	383.	A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I. [electronic resource] by Scharfe, C Hauschild, M Klopstock, T Janssen, A J Heidemann, P H Meitinger, T Jaksch, M Producer: 20001116 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	384.	[Metabolic diseases--a new challenge for pediatric intensive care]. [electronic resource] by Reichel, Annette George, Mathias Producer: 20051110 In: Kinderkrankenschwester : Organ der Sektion Kinderkrankenpflege vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	385.	[Enzymopathic congenital hyperlactacidemia]. [electronic resource] by Leroux, J P Marsac, C Saudubray, J M Producer: 19761201 In: Annales de biologie clinique vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	386.	Deficiency of pyruvate dehydrogenase activity in pancreatic islets of diabetic GK rats. [electronic resource] by Zhou, Y P Ostenson, C G Ling, Z C Grill, V Producer: 19950901 In: Endocrinology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	387.	Acetyl-CoA production from pyruvate is not necessary for preservation of myelin. [electronic resource] by Della-Flora Nunes, Gustavo Mueller, Lauren Silvestri, Nicholas Patel, Mulchand S Wrabetz, Lawrence Feltri, M Laura Poitelon, Yannick Producer: 20180502 In: Glia vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	388.	An overview of a cohort of South African patients with mitochondrial disorders. [electronic resource] by Smuts, Izelle Louw, Roan du Toit, Hanli Klopper, Brenda Mienie, Lodewyk J van der Westhuizen, Francois H Producer: 20140408 In: Journal of inherited metabolic disease vol. 33 Suppl 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	389.	[Congenital enzyme deficiency in carbohydrate metabolism. Its significance for clinical pediatrics and human biochemical genetics (author's transl)]. [electronic resource] by Schaub, J Osang, M Producer: 19760823 In: MMW, Munchener medizinische Wochenschrift vol. 118 Availability: No items available. Save to lists Add to cart (remove)
	390.	Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency. [electronic resource] by Shevell, M I Matthews, P M Scriver, C R Brown, R M Otero, L J Legris, M Brown, G K Arnold, D L Producer: 19950412 In: Pediatric neurology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	391.	Lacticacidemia. [electronic resource] by Robinson, B H Producer: 19931122 In: Biochimica et biophysica acta vol. 1182 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	392.	Evoked potentials in children with oxidative metabolic defects leading to Leigh syndrome. [electronic resource] by Taylor, M J Robinson, B H Producer: 19920511 In: Pediatric neurology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	393.	Disorders of the pyruvate dehydrogenase complex. [electronic resource] by Stansbie, D Wallace, S J Marsac, C Producer: 19861010 In: Journal of inherited metabolic disease vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	394.	Nuclear complementation restores mtDNA levels in cultured cells from a patient with mtDNA depletion. [electronic resource] by Bodnar, A G Cooper, J M Holt, I J Leonard, J V Schapira, A H Producer: 19930916 In: American journal of human genetics vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	395.	Recombinant adeno-associated virus vector-based gene transfer for defects in oxidative metabolism. [electronic resource] by Owen R, I V Lewin, A P Peel, A Wang, J Guy, J Hauswirth, W W Stacpoole, P W Flotte, T R Producer: 20001109 In: Human gene therapy vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	396.	Dihydrolipoamide dehydrogenase (DLD) deficiency in a Spanish patient with myopathic presentation due to a new mutation in the interface domain. [electronic resource] by Quintana, Ester Pineda, Mercé Font, Aida Vilaseca, Maria Antonia Tort, Frederic Ribes, Antonia Briones, Paz Producer: 20140408 In: Journal of inherited metabolic disease vol. 33 Suppl 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	397.	A novel mutation in the dihydrolipoamide dehydrogenase E3 subunit gene (DLD) resulting in an atypical form of alpha-ketoglutarate dehydrogenase deficiency. [electronic resource] by Odièvre, Marie-Hélène Chretien, Dominique Munnich, Arnold Robinson, Brian H Dumoulin, Renée Masmoudi, Sahben Kadhom, Noman Rötig, Agnès Rustin, Pierre Bonnefont, Jean-Paul Producer: 20060516 In: Human mutation vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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