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	61.	Enzyme replacement therapy in mucopolysaccharidosis type I. [electronic resource] by Miebach, E Producer: 20050825 In: Acta paediatrica (Oslo, Norway : 1992). Supplement vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Impact of 144 weeks of laronidase therapy on body functions, endurance and general well-being in a Hurler-Scheie patient. [electronic resource] by Soutar, R L Mercer, J Wraith, J E Producer: 20070108 In: Journal of inherited metabolic disease vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	Capturing phenotypic heterogeneity in MPS I: results of an international consensus procedure. [electronic resource] by de Ru, Minke H Teunissen, Quirine Ga van der Lee, Johanna H Beck, Michael Bodamer, Olaf A Clarke, Lorne A Hollak, Carla E Lin, Shuan-Pei Rojas, Maria-Verónica Muñoz Pastores, Gregory M Raiman, Julian A Scarpa, Maurizio Treacy, Eileen P Tylki-Szymanska, Anna Wraith, J Edmond Zeman, Jiri Wijburg, Frits A Producer: 20121026 In: Orphanet journal of rare diseases vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Role of rehabilitation in Hurler's syndrome. [electronic resource] by Mishra, Sudhir Ramkishore Shastri, Mona Ramesh, Jaishree Producer: 20171218 In: Journal of back and musculoskeletal rehabilitation vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	Phenotype prediction for mucopolysaccharidosis type I by in silico analysis. [electronic resource] by Ou, Li Przybilla, Michael J Whitley, Chester B Producer: 20180430 In: Orphanet journal of rare diseases vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	Characteristics of leukocyte and plasma methylumbelliferyl-alpha-L-iduronide iduronidase. [electronic resource] by Den Tandt, W R Scharpe, S Producer: 19890622 In: Biochemical medicine and metabolic biology vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Post- and pre-natal assessment of alpha-L-iduronidase deficiency with a radiolabelled natural substrate. [electronic resource] by Hopwood, J J Muller, V Pollard, A C Producer: 19791129 In: Clinical science (London, England : 1979) vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	alpha-L-iduronidase activity in leukocytes: diagnosis of homozygotes and heterozygotes of the Hurler syndrome. [electronic resource] by Omura, K Higami, S Tada, K Producer: 19760802 In: European journal of pediatrics vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	Maturation of alpha-L-iduronidase in cultured human fibroblasts. [electronic resource] by Myerowitz, R Neufeld, E F Producer: 19810526 In: The Journal of biological chemistry vol. 256 Availability: No items available. Save to lists Add to cart (remove)
	70.	[Overview of enzyme replacement therapy in mucopolysaccharidosis]. [electronic resource] by Fouilhoux, Alain Guffon, Nathalie Producer: 20070628 In: Presse medicale (Paris, France : 1983) vol. 36 Spec No 1 Availability: No items available. Save to lists Add to cart (remove)
	71.	Enzyme measurements of hair follicles in the study of some inborn erros of metabolism, with particular reference to Hurler's disease. [electronic resource] by Gibbs, D A Producer: 19770729 In: Annals of clinical biochemistry vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	A new phenotypic variant of alpha-L-iduronidase deficiency. [electronic resource] by Kohn, G Bach, G Lasch, E Massri, M E Legum, C Cohen, M M Producer: 19790223 In: Monographs in human genetics vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	73.	Hurler-Scheie phenotype with parental consanguinity. Report of an additional case supporting the concept of genetic heterogeneity. [electronic resource] by Kaibara, N Katsuki, I Hotokebuchi, T Takagishi, K Kure, T Producer: 19830617 In: Clinical orthopaedics and related research no. 175 Availability: No items available. Save to lists Add to cart (remove)
	74.	USAN Council. List No. 439. New names. Laronidase. [electronic resource] Producer: 20010809 In: Clinical pharmacology and therapeutics vol. 70 Availability: No items available. Save to lists Add to cart (remove)
	75.	Bone marrow transplantation for feline mucopolysaccharidosis I. [electronic resource] by Ellinwood, N Matthew Colle, Marie-Anne Weil, Margaret A Casal, Margret L Vite, Charles H Wiemelt, Staci Hasson, Christopher W O'Malley, Thomas M He, Xingxuan Prociuk, Ulana Verot, Lucie Melniczek, John R Lannon, Anne Aguirre, Gustavo D Knox, Van W Evans, Sydney M Vanier, Marie T Schuchman, Edward H Walkley, Steven U Haskins, Mark E Producer: 20070926 In: Molecular genetics and metabolism vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	76.	[Hurler syndrome. Early diagnosis and successful enzyme replacement therapy: a new therapeutic approach. Case report]. [electronic resource] by Dupont, C El Hachem, C Harchaoui, S Ribault, V Amiour, M Guillot, M Maire, I Froissart, R Guffon-Fouilhoux, N Producer: 20080521 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	77.	Mucopolysaccharidosis type I (Hurler syndrome): linkage disequilibrium indicates the presence of a major allele. [electronic resource] by Scott, H S Nelson, P V Cooper, A Wraith, J E Hopwood, J J Morris, C P Producer: 19920427 In: Human genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	78.	The application of the Milner-Avigad method for the quantitative determination of endouronidase activities. [electronic resource] by Majima, M Takagaki, K Igarashi, S Nakamura, T Endo, M Producer: 19850520 In: Journal of biochemical and biophysical methods vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	79.	Mucopolysaccharidosis type I: identification of 13 novel mutations of the alpha-L-iduronidase gene. [electronic resource] by Bunge, S Kleijer, W J Steglich, C Beck, M Schwinger, E Gal, A Producer: 19951121 In: Human mutation vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	80.	Standardization of α-L-iduronidase enzyme assay with Michaelis-Menten kinetics. [electronic resource] by Ou, Li Herzog, Tyler L Wilmot, Carrie M Whitley, Chester B Producer: 20140923 In: Molecular genetics and metabolism vol. 111 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 640 results.