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	661.	A sensitive fluorescence assay for the simultaneous and separate determination of arylsulphatases A and B. [electronic resource] by Christomanou, H Sandhoff, K Producer: 19771031 In: Clinica chimica acta; international journal of clinical chemistry vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	662.	Myelination of mouse axons by Schwann cells transplanted from normal and abnormal human nerves. [electronic resource] by Aguayo, A J Kasarjian, J Skamene, E Kongshavn, P Bray, G M Producer: 19771031 In: Nature vol. 268 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	663.	Sequence of morphological alterations in the nervous system of metachromatic leucodystrophy. Light- and electronmicroscopic observations in the central and peripheral nervous system in a prenatally diagnosed foetus of 22 weeks. [electronic resource] by Meier, C Bischoff, A Producer: 19770321 In: Acta neuropathologica vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	664.	[Metachromatic leukodystrophy (MLD) and Multiple sulphatase deficiency (MSD)]. [electronic resource] by Eto, Y Hasegawa, Y Tsuda, T Producer: 19960312 In: Nihon rinsho. Japanese journal of clinical medicine vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	665.	Overexpression of arylsulfatase A gene in fibroblasts from metachromatic leukodystrophy patients does not induce a new phenotype. [electronic resource] by Ohashi, T Matalon, R Barranger, J A Eto, Y Producer: 19951204 In: Gene therapy vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	666.	[Allogeneic bone marrow transplantation in the treatment of (lysosomal) storage diseases]. [electronic resource] by Maaswinkel-Mooij, P D Poorthuis, B J Hoogerbrugge, P M Brouwer, O F Vossen, J M Producer: 19980717 In: Nederlands tijdschrift voor geneeskunde vol. 142 Availability: No items available. Save to lists Add to cart (remove)
	667.	Complex arylsulfatase A alleles causing metachromatic leukodystrophy. [electronic resource] by Kappler, J Sommerlade, H J von Figura, K Gieselmann, V Producer: 19941230 In: Human mutation vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	668.	Metachromatic leukodystrophy: clinical, histochemical, and cerebrospinal fluid abnormalities. [electronic resource] by ALLEN, R J McCUSKER, J J TOURTELLOTTE, W W Producer: 19981101 In: Pediatrics vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	669.	Multifocal slowing of nerve conduction in metachromatic leukodystrophy. [electronic resource] by Cameron, Carol L Kang, Peter B Burns, Ted M Darras, Basil T Jones, H Royden Producer: 20040429 In: Muscle & nerve vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	670.	Developing treatment options for metachromatic leukodystrophy. [electronic resource] by Batzios, Spyros P Zafeiriou, Dimitrios I Producer: 20120531 In: Molecular genetics and metabolism vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	671.	Whole-exome sequencing identifies compound heterozygous mutations in ARSA of two siblings presented with atypical onset of metachromatic leukodystrophy from a Chinese pedigree. [electronic resource] by Wang, Zhihong Lin, Yanhong Zheng, Dezhu Yan, Aizhen Tu, Xiangdong Lin, Juan Lan, Fenghua Producer: 20170202 In: Clinica chimica acta; international journal of clinical chemistry vol. 460 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	672.	Metabolism of cerebroside sulfate and subcellular distribution of its metabolites in cultured skin fibroblasts from controls, metachromatic leukodystrophy, and globoid cell leukodystrophy. [electronic resource] by Inui, K Furukawa, M Okada, S Yabuuchi, H Producer: 19880318 In: The Journal of clinical investigation vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	673.	Four cases of late onset metachromatic leucodystrophy in a family: clinical, biochemical and neuropathological studies. [electronic resource] by Alves, D Pires, M M Guimarães, A Miranda, M C Producer: 19870320 In: Journal of neurology, neurosurgery, and psychiatry vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	674.	Metachromatic leucodystrophy: review of 38 cases. [electronic resource] by MacFaul, R Cavanagh, N Lake, B D Stephens, R Whitfield, A E Producer: 19820621 In: Archives of disease in childhood vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	675.	Association of alcoholism with the N-glycosylation polymorphism of pseudodeficient human arylsulfatase A. [electronic resource] by Park, D S Poretz, R D Stein, S Nora, R Manowitz, P Producer: 19961002 In: Alcoholism, clinical and experimental research vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	676.	Different molecular mechanisms leading to white matter hypomyelination in infantile onset lysosomal disorders. [electronic resource] by Di Rocco, M Rossi, A Parenti, G Allegri, A E M Filocamo, M Pessagno, A Tortori-Donati, P Minetti, C Biancheri, R Producer: 20051202 In: Neuropediatrics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	677.	Metachromatic leukodystrophy: consequences of sulphatide accumulation. [electronic resource] by Gieselmann, V Franken, S Klein, D Mansson, J E Sandhoff, R Lüllmann Rauch, R Hartmann, D Saravanan, V P M De Deyn, P P D'Hooge, R Van Der Linden, A M Schaeren-Wiemers, N Producer: 20040602 In: Acta paediatrica (Oslo, Norway : 1992). Supplement vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	678.	4H syndrome: a rare cause of leukodystrophy. [electronic resource] by Outteryck, Olivier Devos, David Jissendi, Patrice Boespflug-Tanguy, Odile Hopes, Lucie Renard, Dimitri Ferri, Joël Vermersch, Patrick Labauge, Pierre Producer: 20110126 In: Journal of neurology vol. 257 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	679.	An Italian cohort study identifies four new pathologic mutations in the ARSA gene. [electronic resource] by Galla, Daniela de Gemmis, Paola Anesi, Laura Berto, Silvia Dolcetta, Diego Hladnik, Uroš Producer: 20131205 In: Journal of molecular neuroscience : MN vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	680.	Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation. [electronic resource] by Di Bella, Daniela Pareyson, Davide Savoiardo, Mario Farina, Laura Ciano, Claudia Caldarazzo, Serena Sagnelli, Anna Bonato, Sara Nava, Simone Bresolin, Nereo Tedeschi, Gioacchino Taroni, Franco Salsano, Ettore Producer: 20141125 In: Neurology vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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