Your search returned 28 results.

Results
	1.	Inhibition of human alkaline phosphatases by vanadate. [electronic resource] by Seargeant, L E Stinson, R A Producer: 19791121 In: The Biochemical journal vol. 181 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Evidence that three structural genes code for human alkaline phosphatases. [electronic resource] by Seargeant, L E Stinson, R A Producer: 19791026 In: Nature vol. 281 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Affinity elution from a phosphonic acid-Sepharose derivative in the purification of human liver alkaline phosphatase. [electronic resource] by Seargeant, L E Stinson, R A Producer: 19800825 In: Journal of chromatography vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Phosphoester specificity of purified human liver alkaline phosphatase. [electronic resource] by Seargeant, L E Stinson, R A Producer: 19791220 In: Canadian journal of biochemistry vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	5.	Comparative studies of pure alkaline phosphatases from five human tissues. [electronic resource] by Stinson, R A Seargeant, L E Producer: 19810720 In: Clinica chimica acta; international journal of clinical chemistry vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Aspartylglycosaminuria presenting with hepatosplenomegaly in early infancy. [electronic resource] by Haworth, J C Seargeant, L E Dilling, L A Producer: 19930408 In: Journal of inherited metabolic disease vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Increased prevalence of hereditary metabolic diseases among native Indians in Manitoba and northwestern Ontario. [electronic resource] by Haworth, J C Dilling, L A Seargeant, L E Producer: 19910905 In: CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne vol. 145 Availability: No items available. Save to lists Add to cart (remove)
	8.	Affinity purification and some molecular properties of human liver alkaline phosphatase. [electronic resource] by Trépanier, J M Seargeant, L E Stinson, R A Producer: 19761001 In: The Biochemical journal vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A rare case of Niemann-Pick disease type C without neurological involvement in a 66-year-old patient. [electronic resource] by Greenberg, C R Barnes, J G Kogan, S Seargeant, L E Producer: 20160303 In: Molecular genetics and metabolism reports vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	In vitro stability and compatibility of daunorubicin, cytarabine, and etoposide. [electronic resource] by Seargeant, L E Kobrinsky, N L Sus, C J Nazeravich, D R Producer: 19880203 In: Cancer treatment reports vol. 71 Availability: No items available. Save to lists Add to cart (remove)
	11.	A simple screening test for fatty acid oxidation defects using whole-blood palmitate oxidation. [electronic resource] by Seargeant, L E Balachandra, K Mallory, C Dilling, L A Greenberg, C R Producer: 19991004 In: Journal of inherited metabolic disease vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Primary oxaluria type 2 (L-glyceric aciduria): a rare cause of nephrolithiasis in children. [electronic resource] by Seargeant, L E deGroot, G W Dilling, L A Mallory, C J Haworth, J C 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)
	13.	Carrier detection in glutaric aciduria type I using interleukin-2-dependent cultured lymphocytes. [electronic resource] by Seargeant, L E Chudley, A E Dilling, L A Mallory, C J Haworth, J C Producer: 19921223 In: Journal of inherited metabolic disease vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Increased plasma pyridoxal-5'-phosphate levels before and after pyridoxine loading in carriers of perinatal/infantile hypophosphatasia. [electronic resource] by Chodirker, B N Coburn, S P Seargeant, L E Whyte, M P Greenberg, C R Producer: 19910502 In: Journal of inherited metabolic disease vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Hyperphosphatemia in infantile hypophosphatasia: implications for carrier diagnosis and screening. [electronic resource] by Chodirker, B N Evans, J A Seargeant, L E Cheang, M S Greenberg, C R Producer: 19900312 In: American journal of human genetics vol. 46 Availability: No items available. Save to lists Add to cart (remove)
	16.	Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, Pennsylvania. [electronic resource] by Morton, D H Bennett, M J Seargeant, L E Nichter, C A Kelley, R I Producer: 19911223 In: American journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Newborn screening for galactosemia: a new method used in Manitoba. [electronic resource] by Greenberg, C R Dilling, L A Thompson, R Ford, J D Seargeant, L E Haworth, J C Producer: 19890825 In: Pediatrics vol. 84 Availability: No items available. Save to lists Add to cart (remove)
	18.	Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantation. [electronic resource] by Laitinen, A Hietala, M Haworth, J C Schroeder, M L Seargeant, L E Greenberg, C R Aula, P Producer: 19970612 In: Clinical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	A homoallelic Gly317-->Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian mennonites. [electronic resource] by Greenberg, C R Taylor, C L Haworth, J C Seargeant, L E Philipps, S Triggs-Raine, B Chodirker, B N Producer: 19931022 In: Genomics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism. [electronic resource] by Schuh, S Rosenblatt, D S Cooper, B A Schroeder, M L Bishop, A J Seargeant, L E Haworth, J C Producer: 19840327 In: The New England journal of medicine vol. 310 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search

Availability

Authors

Topics

Languages

Your search returned 28 results.