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	101.	Cardiovascular risk factors in multi-ethnic middle school students: the HEALTHY primary prevention trial. [electronic resource] by Willi, S M Hirst, K Jago, R Buse, J Kaufman, F El Ghormli, L Bassin, S Elliot, D Hale, D E Producer: 20120904 In: Pediatric obesity vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	102.	Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant death. [electronic resource] by Bennett, M J Allison, F Pollitt, R J Manning, N J Gray, R G Green, A Hale, D E Coates, P M Producer: 19870324 In: Lancet (London, England) vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	103.	Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. [electronic resource] by Treem, W R Rinaldo, P Hale, D E Stanley, C A Millington, D S Hyams, J S Jackson, S Turnbull, D M Producer: 19940302 In: Hepatology (Baltimore, Md.) vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	104.	New clinical phenotype of branched-chain acyl-CoA oxidation defect. [electronic resource] by Burlina, A Zacchello, F Dionisi-Vici, C Bertini, E Sabetta, G Bennet, M J Hale, D E Schmidt-Sommerfeld, E Rinaldo, P Producer: 19920115 In: Lancet (London, England) vol. 338 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	105.	Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency. [electronic resource] by Bennett, M J Coates, P M Hale, D E Millington, D S Pollitt, R J Rinaldo, P Roe, C R Tanaka, K Producer: 19910110 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)
	106.	The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy. [electronic resource] by Sims, H F Brackett, J C Powell, C K Treem, W R Hale, D E Bennett, M J Gibson, B Shapiro, S Strauss, A W Producer: 19950303 In: Proceedings of the National Academy of Sciences of the United States of America vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	107.	Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. [electronic resource] by Treem, W R Shoup, M E Hale, D E Bennett, M J Rinaldo, P Millington, D S Stanley, C A Riely, C A Hyams, J S Producer: 19961224 In: The American journal of gastroenterology vol. 91 Availability: No items available. Save to lists Add to cart (remove)
	108.	A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts. [electronic resource] by Burlina, A B Dionisi-Vici, C Bennett, M J Gibson, K M Servidei, S Bertini, E Hale, D E Schmidt-Sommerfeld, E Sabetta, G Zacchello, F Producer: 19940214 In: The Journal of pediatrics vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	Growth hormone deficiency associated in the 18q deletion syndrome. [electronic resource] by Ghidoni, P D Hale, D E Cody, J D Gay, C T Thompson, N M McClure, E B Danney, M M Leach, R J Kaye, C I Producer: 19970624 In: American journal of medical genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	110.	Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels. [electronic resource] by Stanley, C A Hale, D E Coates, P M Hall, C L Corkey, B E Yang, W Kelley, R I Gonzales, E L Williamson, J R Baker, L Producer: 19840107 In: Pediatric research vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	111.	Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q. [electronic resource] by Cody, J D Ghidoni, P D DuPont, B R Hale, D E Hilsenbeck, S G Stratton, R F Hoffman, D S Muller, S Schaub, R L Leach, R J Kaye, C I Producer: 19990830 In: American journal of medical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	112.	The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype? [electronic resource] by Andresen, B S Bross, P Udvari, S Kirk, J Gray, G Kmoch, S Chamoles, N Knudsen, I Winter, V Wilcken, B Yokota, I Hart, K Packman, S Harpey, J P Saudubray, J M Hale, D E Bolund, L Kølvraa, S Gregersen, N Producer: 19970721 In: Human molecular genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	Metabolites as novel biomarkers for childhood obesity-related traits in Mexican-American children. [electronic resource] by Farook, V S Reddivari, L Chittoor, G Puppala, S Arya, R Fowler, S P Hunt, K J Curran, J E Comuzzie, A G Lehman, D M Jenkinson, C P Lynch, J L DeFronzo, R A Blangero, J Hale, D E Duggirala, R Vanamala, J Producer: 20160518 In: Pediatric obesity vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	114.	Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduria. [electronic resource] by Gregersen, N Winter, V S Corydon, M J Corydon, T J Rinaldo, P Ribes, A Martinez, G Bennett, M J Vianey-Saban, C Bhala, A Hale, D E Lehnert, W Kmoch, S Roig, M Riudor, E Eiberg, H Andresen, B S Bross, P Bolund, L A Kølvraa, S Producer: 19980512 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	115.	Localization of a major susceptibility locus influencing preterm birth. [electronic resource] by Chittoor, G Farook, V S Puppala, S Fowler, S P Schneider, J Dyer, T D Cole, S A Lynch, J L Curran, J E Almasy, L Maccluer, J W Comuzzie, A G Hale, D E Ramamurthy, R S Dudley, D J Moses, E K Arya, R Lehman, D M Jenkinson, C P Bradshaw, B S Defronzo, R A Blangero, J Duggirala, R Producer: 20140418 In: Molecular human reproduction vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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