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	21.	Medium-chain acyl-CoA dehydrogenase deficiency is not a cause of previously diagnosed Reye syndrome. [electronic resource] by Rupar, C A Frewen, T W Gordon, B A Producer: 19951213 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)
	22.	Ultrastructure and peroxidase of leucocytes in five patients with juvenile form of ceroid lipofuscinoses. [electronic resource] by Haust, M D Gordon, B A Hinton, G G Producer: 19760823 In: Advances in experimental medicine and biology vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Defective heparan sulfate metabolism in the Sanfilippo syndrome and assay of this defect in the assessment of the mucopolysaccharidoses patient. [electronic resource] by Gordon, B A Feleki, V Budreau, C H Tyler, L Producer: 19751021 In: Clinical biochemistry vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Defective heparan sulfate metabolism in the Sanfilippo syndrome and assay of this defect in the assessment of the mucopolysaccharidoses patient. [electronic resource] by Gordon, B A Feleki, V Budreau, C H Tyler, L Producer: 19751021 In: Clinical biochemistry vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Deficiency of the hexosaminidase A activator protein in a case of GM2 gangliosidosis; variant AB. [electronic resource] by Hechtman, P Gordon, B A Ng Ying Kin, N M Producer: 19820512 In: Pediatric research vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Use of a genetic variant to study the hexose transport properties of human skin fibroblasts. [electronic resource] by Mesmer, O T Gordon, B A Rupar, C A Lo, T C Producer: 19900327 In: The Biochemical journal vol. 265 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH)-syndrome. Ultrastructural changes of mitochondria in cultured dermal fibroblasts of three patients. [electronic resource] by Haust, M D Dewar, R A Gatfield, D P Gordon, B A Producer: 19970114 In: Pathology, research and practice vol. 192 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Insulin sensitivity in response to a single resistance exercise session in apparently healthy individuals. [electronic resource] by Gordon, B A Fraser, S F Bird, S R Benson, A C Producer: 20130118 In: Journal of endocrinological investigation vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Resistance training improves metabolic health in type 2 diabetes: a systematic review. [electronic resource] by Gordon, B A Benson, A C Bird, S R Fraser, S F Producer: 20090402 In: Diabetes research and clinical practice vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Reproducibility of multiple repeated oral glucose tolerance tests. [electronic resource] by Gordon, B A Fraser, S F Bird, S R Benson, A C Producer: 20120508 In: Diabetes research and clinical practice vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	A variant form of metachromatic leukodystrophy without arylsulfatase deficiency. [electronic resource] by Hahn, A F Gordon, B A Hinton, G G Gilbert, J J Producer: 19821029 In: Annals of neurology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	The AB-variant of metachromatic leukodystrophy (postulated activator protein deficiency). Light and electron microscopic findings in a sural nerve biopsy. [electronic resource] by Hahn, A F Gordon, B A Gilbert, J J Hinton, G G Producer: 19820422 In: Acta neuropathologica vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Insulin sensitivity not modulated 24 to 78 h after acute resistance exercise in type 2 diabetes patients. [electronic resource] by Gordon, B A Fraser, S F Bird, S R Benson, A C Producer: 20131105 In: Diabetes, obesity & metabolism vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Purification and structure of human liver aspartylglucosaminidase. [electronic resource] by Rip, J W Coulter-Mackie, M B Rupar, C A Gordon, B A Producer: 19930128 In: The Biochemical journal vol. 288 ( Pt 3) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Metachromatic leukodystrophy (MLD) in hospitalized adult schizophrenic patients resistant to drug treatment. [electronic resource] by Galbraith, D A Gordon, B A Feleki, V Gordon, N Cooper, A J Producer: 19890731 In: Canadian journal of psychiatry. Revue canadienne de psychiatrie vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Pharmacy medication refill clinics. [electronic resource] by Rodriquez, L R Weber, C E Halperin, A K Gordon, B A Montano, A Producer: 19870724 In: American journal of hospital pharmacy vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	37.	Retrospective diagnosis of medium chain acyl-CoA dehydrogenase deficiency. [electronic resource] by Christodoulou, J Clarke, J T Rupar, C A Gordon, B A Kelly, D P Producer: 19930727 In: Journal of paediatrics and child health vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemia. [electronic resource] by Hommes, F A Ho, C K Roesel, R A Coryell, M E Gordon, B A Producer: 19830610 In: Journal of inherited metabolic disease vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Tay-Sachs disease: B1 variant. [electronic resource] by Gordon, B A Gordon, K E Hinton, G G Cadera, W Feleki, V Bayleran, J Hechtman, P Producer: 19890510 In: Pediatric neurology vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Fucosidosis with dystonia. [electronic resource] by Gordon, B A Gordon, K E Seo, H C Yang, M DiCioccio, R A O'Brien, J S Producer: 19961028 In: Neuropediatrics vol. 26 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 48 results.