Results of search for 'au:"ROE, C"' › مکتبة رقمیه للعلوم الطبيه catalog

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- Carson, K D
- Carson, P P
- Chen, Y T
- Ding, J H
- Maltby, D A
- Millington, D S
- Nada, M A
- ROE, C F
- Roe, C
- Roe, C A
- Roe, C F
- Roe, C J
- Roe, C K
- Roe, C M
- Roe, C R
- Roe, C W
- Roe, D S
- Røe, C
- Vianey-Saban, C
- Yang, B Z
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- Carnitine
- Creatine Kinase
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- Humans
- Infant
- Infant, Newborn
- Isoenzymes
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- analogs & derivatives
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	221.	Creatine kinase brain isoenzyme: relationship of cerebrospinal fluid concentration to the neurologic condition of newborns and cellular localization in the human brain. [electronic resource] by Worley, G Lipman, B Gewolb, I H Green, J A Schmechel, D E Roe, C R Gross, S J Producer: 19850812 In: Pediatrics vol. 76 Availability: No items available. Save to lists Add to cart (remove)
	222.	Computer-aided diagnosis of pulmonary nodules: results of a large-scale observer test. [electronic resource] by MacMahon, H Engelmann, R Behlen, F M Hoffmann, K R Ishida, T Roe, C Metz, C E Doi, K Producer: 19991217 In: Radiology vol. 213 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	223.	Cytomegalovirus infection in dialysis patients. [electronic resource] by Hardiman, A E Butter, K C Roe, C J Cunningham, J Baker, L R Kangro, H O Heath, R B Producer: 19850426 In: Clinical nephrology vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	224.	The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiency. [electronic resource] by Andresen, B S Vianey-Saban, C Bross, P Divry, P Roe, C R Nada, M A Knudsen, I Gregersen, N Producer: 19961004 In: Journal of inherited metabolic disease vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	225.	Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria. [electronic resource] by Bartholomew, D W Batshaw, M L Allen, R H Roe, C R Rosenblatt, D Valle, D L Francomano, C A Producer: 19880223 In: The Journal of pediatrics vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	226.	Macrophage and myofibroblast proliferation in remnant kidney: role of angiotensin II. [electronic resource] by Wu, L L Yang, N Roe, C J Cooper, M E Gilbert, R E Atkins, R C Lan, H Y Producer: 19980205 In: Kidney international. Supplement vol. 63 Availability: No items available. Save to lists Add to cart (remove)
	227.	Very long chain acyl-CoA dehydrogenase deficiency: successful treatment of acute cardiomyopathy. [electronic resource] by Brown-Harrison, M C Nada, M A Sprecher, H Vianey-Saban, C Farquhar, J Gilladoga, A C Roe, C R Producer: 19970303 In: Biochemical and molecular medicine vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	228.	Alzheimer disease identification using amyloid imaging and reserve variables: proof of concept. [electronic resource] by Roe, C M Mintun, M A Ghoshal, N Williams, M M Grant, E A Marcus, D S Morris, J C Producer: 20100720 In: Neurology vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	229.	The L-3-hydroxyacyl-CoA dehydrogenase deficiency. [electronic resource] by Hale, D E Thorpe, C Braat, K Wright, J H Roe, C R Coates, P M Hashimoto, T Glasgow, A M Producer: 19900517 In: Progress in clinical and biological research vol. 321 Availability: No items available. Save to lists Add to cart (remove)
	230.	L-Carnitine insufficiency in disorders of organic acid metabolism: response to L-carnitine by patients with methylmalonic aciduria and 3-hydroxy-3-methylglutaric aciduria. [electronic resource] by Chalmers, R A Stacey, T E Tracey, B M de Sousa, C Roe, C R Millington, D S Hoppel, C L Producer: 19841119 In: Journal of inherited metabolic disease vol. 7 Suppl 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	231.	Retrospective diagnosis of carnitine-acylcarnitine translocase deficiency by acylcarnitine analysis in the proband Guthrie card and enzymatic studies in the parents. [electronic resource] by Brivet, M Slama, A Millington, D S Roe, C R Demaugre, F Legrand, A Boutron, A Poggi, F Saudubray, J M Producer: 19961004 In: Journal of inherited metabolic disease vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	232.	Effects of direct periaqueductal grey administration of a cannabinoid receptor agonist on nociceptive and aversive responses in rats. [electronic resource] by Finn, D P Jhaveri, M D Beckett, S R G Roe, C H Kendall, D A Marsden, C A Chapman, V Producer: 20031219 In: Neuropharmacology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	233.	Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency. [electronic resource] by Yang, B Z Ding, J H Zhou, C Dimachkie, M M Sweetman, L Dasouki, M J Wilkinson, J Roe, C R Producer: 20000531 In: Molecular genetics and metabolism vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	234.	Identification of two novel mutations in the hypoglycemic phenotype of very long chain acyl-CoA dehydrogenase deficiency. [electronic resource] by He, G Yang, B Z Roe, D S Teramoto, R Aleck, K Grebe, T A Roe, C R Ding, J H Producer: 19991207 In: Biochemical and biophysical research communications vol. 264 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	235.	Pedigree testing in Duchenne muscular dystrophy. [electronic resource] by Roses, A D Roses, M J Metcalf, B S Hull, K L Nicholson, G A Hartwig, G B Roe, C R Producer: 19790126 In: Annals of neurology vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	236.	Genetic heterogeneity in MCAD deficiency: frequency of K329E allele and identification of three additional mutant alleles. [electronic resource] by Ding, J H Bross, P Yang, B Z Iafolla, A K Millington, D S Roe, C R Gregersen, N Chen, Y T Producer: 19921218 In: Progress in clinical and biological research vol. 375 Availability: No items available. Save to lists Add to cart (remove)
	237.	Acute profound dystonia in infants with glutaric acidemia. [electronic resource] by Bergman, I Finegold, D Gartner, J C Zitelli, B J Claassen, D Scarano, J Roe, C R Stanley, C Goodman, S I Producer: 19890301 In: Pediatrics vol. 83 Availability: No items available. Save to lists Add to cart (remove)
	238.	Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated alpha-fetoprotein and cystic renal changes. [electronic resource] by Chisholm, C A Vavelidis, F Lovell, M A Sweetman, L Roe, C R Roe, D S Frerman, F E Wilson, W G Producer: 20020131 In: Prenatal diagnosis vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	239.	2,4-Dienoyl-coenzyme A reductase deficiency: a possible new disorder of fatty acid oxidation. [electronic resource] by Roe, C R Millington, D S Norwood, D L Kodo, N Sprecher, H Mohammed, B S Nada, M Schulz, H McVie, R Producer: 19900606 In: The Journal of clinical investigation vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	240.	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)

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