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	101.	Prenatal diagnosis of Hurler's syndrome--biochemical studies on the affected fetus. [electronic resource] by Ikeno, T Minami, R Wagatsuma, K Fujibayashi, S Nakao, T Abo, K Tsugawa, S Taniguchi, S Takasago, Y Producer: 19820527 In: Human genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	102.	Effect of discontinuing of laronidase in a patient with mucopolysaccharidosis type I. [electronic resource] by Anbu, A T Mercer, J Wraith, J E Producer: 20061016 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)
	103.	A general model for genetic regulation of turnover of glycosaminoglycans suggests a possible procedure for prediction of severity and clinical progress of mucopolysaccharidoses. [electronic resource] by Wegrzyn, G Wegrzyn, A Tylki-Szymańska, A Producer: 20041221 In: Medical hypotheses vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	104.	Mucopolysaccharidosis type I and craniosynostosis. [electronic resource] by Ziyadeh, Jawad Le Merrer, Martine Robert, Matthieu Arnaud, Eric Valayannopoulos, Vassili Di Rocco, Federico Producer: 20140422 In: Acta neurochirurgica vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	105.	Bone marrow transplantation in canine mucopolysaccharidosis I. Effects within the central nervous system. [electronic resource] by Shull, R M Hastings, N E Selcer, R R Jones, J B Smith, J R Cullen, W C Constantopoulos, G Producer: 19870312 In: The Journal of clinical investigation vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	106.	A nonpathologic allele (IW) for low alpha-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome. [electronic resource] by Whitley, C B Gorlin, R J Krivit, W Producer: 19871203 In: American journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	107.	The clinical spectrum of alpha-L-iduronidase deficiency. [electronic resource] by Roubicek, M Gehler, J Spranger, J Producer: 19850528 In: American journal of medical genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	108.	Hybridization studies of fibroblasts from Hurler, Scheie, and Hurler/Scheie compound patients: support for the hypothesis of allelic mutants. [electronic resource] by Fortuin, J J Kleijer, W J Producer: 19800514 In: Human genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	Diagnosis of alpha-L-iduronidase deficiency in dried blood spots on filter paper: the possibility of newborn diagnosis. [electronic resource] by Chamoles, N A Blanco, M Gaggioli, D Producer: 20010419 In: Clinical chemistry vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	110.	Towards gene therapy of Hurler syndrome. [electronic resource] by Fairbairn, L J Lashford, L S Spooncer, E McDermott, R H Lebens, G Arrand, J E Arrand, J R Bellantuono, I Holt, R Hatton, C E Cooper, A Besley, G T Wraith, J E Anson, D S Hopwood, J J Dexter, T M Producer: 19970514 In: Casopis lekaru ceskych vol. 136 Availability: No items available. Save to lists Add to cart (remove)
	111.	[Use of 4-methylumbelliferryl-alpha-L-iduronide and 4-trifluoromethylumbelliferryl-alpha-L-iduronide for detecting alpha-L-iduronidase deficiencies in human tissue and for rapid prenatal diagnosis of Hurler disease]. [electronic resource] by Tsvetkova, I V Karpova, E A Voznyĭ, Ia V Zolotukhina, T V Biriukov, V B Semiachkina, A N Producer: 19910829 In: Voprosy meditsinskoi khimii vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	112.	An 86-bp VNTR within IDUA is the basis of the D4S111 polymorphic locus. [electronic resource] by Scott, H S Nelson, P V MacDonald, M E Gusella, J F Hopwood, J J Morris, C P Producer: 19930210 In: Genomics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	A fluorometric assay using 4-methylumbelliferyl alpha-L-iduronide for the estimation of alpha-L-iduronidase activity and the detection of Hurler and Scheie syndromes. [electronic resource] by Hopwood, J J Muller, V Smithson, A Baggett, N Producer: 19791229 In: Clinica chimica acta; international journal of clinical chemistry vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	114.	[Metabolism of the basic component of connective tissue at various stages of developing experimental liver cirrhosis]. [electronic resource] by Skobeleva, T V Producer: 19950301 In: Voprosy meditsinskoi khimii vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	115.	[Ocular Manifestation of Mucopolysaccharidosis I-S (Scheie's Syndrome)]. [electronic resource] by Viestenz, Arne Shin, Yoon S Viestenz, Anja Naumann, Gottfried O H Producer: 20030424 In: Klinische Monatsblatter fur Augenheilkunde vol. 219 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	116.	alpha-L-iduronidase forms semi-crystalline spherulites with amyloid-like properties. [electronic resource] by Ruth, L Eisenberg, D Neufeld, E F Producer: 20000605 In: Acta crystallographica. Section D, Biological crystallography vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	117.	Mutational analysis of the alpha-L-iduronidase gene in 10 unrelated Korean type I mucopolysaccharidosis patients: Identification of four novel mutations. [electronic resource] by Lee, I J Hwang, S H Jeon, B H Song, S M Kim, J S Paik, K H Kwon, E K Jin, D-K Producer: 20051114 In: Clinical genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	118.	Uptake of a recombinant human alpha-L-iduronidase (laronidase) by cultured fibroblasts and osteoblasts. [electronic resource] by Tsukimura, Takahiro Tajima, Youichi Kawashima, Ikuo Fukushige, Tomoko Kanzaki, Tamotsu Kanekura, Takuro Ikekita, Masahiko Sugawara, Kanako Suzuki, Toshihiro Togawa, Tadayasu Sakuraba, Hitoshi Producer: 20081020 In: Biological & pharmaceutical bulletin vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	119.	Developmental outcomes in children with Hurler syndrome after stem cell transplantation. [electronic resource] by Dusing, Stacey C Producer: 20071002 In: Developmental medicine and child neurology vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	120.	Enzyme replacement therapy with laronidase (Aldurazyme) for treating mucopolysaccharidosis type I. [electronic resource] by Jameson, Elisabeth Jones, Simon Wraith, James E Producer: 20140423 In: The Cochrane database of systematic reviews no. 9 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.