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	401.	Computed tomography in late-onset metachromatic leucodystrophy. [electronic resource] by Schipper, H I Seidel, D Producer: 19840813 In: Neuroradiology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	402.	Morquio's syndrome: deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase. [electronic resource] by Matalon, R Arbogast, B Justice, P Brandt, I K Dorfman, A Producer: 19750604 In: Biochemical and biophysical research communications vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	403.	A single origin for the most frequent mutation causing late infantile metachromatic leucodystrophy. [electronic resource] by Zlotogora, J Furman-Shaharabani, Y Harris, A Barth, M L von Figura, K Gieselmann, V Producer: 19950209 In: Journal of medical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	404.	Ichthyosis: the skin manifestation of multiple sulfatase deficiency. [electronic resource] by Castaño Suárez, E Segurado Rodríguez, A Guerra Tapia, A Simón de las Heras, R López-Ríos, F Coll Rosell, M J Producer: 19980112 In: Pediatric dermatology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	405.	Two new polymorphisms in the arylsulfatase A gene and their haplotype associations with normal, metachromatic leukodystrophy and pseudodeficiency alleles. [electronic resource] by Coulter-Mackie, M Gagnier, L Producer: 19980123 In: American journal of medical genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	406.	Metachromatic leukodystrophy: a novel mutation (c237delC) and extension of the haplotype associated with the P426L mutation. [electronic resource] by Gort, L Coll, M J Chabás, A Producer: 20001027 In: Human mutation vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	407.	Adult metachromatic leukodystrophy: disorganized schizophrenia-like symptoms and postpartum depression in 2 sisters. [electronic resource] by Kumperscak, Hojka Gregoric Paschke, Eduard Gradisnik, Peter Vidmar, Jernej Bradac, Stanislava Umek Producer: 20050303 In: Journal of psychiatry & neuroscience : JPN vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	408.	[LESIONS OF THE PREGENICULATE OPTIC SYSTEM IN ORTHOCHROMATIC AND METACHROMATIC LEUKODYSTROPHIES]. [electronic resource] by VANBOGAERT, L Producer: 19961201 In: Archiv fur Psychiatrie und Nervenkrankheiten vol. 206 Availability: No items available. Save to lists Add to cart (remove)
	409.	INTRANEURONAL LIPID DEPOSITS IN METACHROMATIC LEUKODYSTROPHY. HISTOCHEMICAL AND TOPOGRAPHIC OBSERVATIONS. [electronic resource] by ABRAHAM, K LAMPERT, P Producer: 19961201 In: Neurology vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	410.	Sublingual atropine drops for the treatment of pediatric sialorrhea. [electronic resource] by Rapoport, Adam Producer: 20110225 In: Journal of pain and symptom management vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	411.	Gallbladder abnormalities in children with metachromatic leukodystrophy. [electronic resource] by Kim, Jina Sun, Zhifei Ezekian, Brian Schooler, Gary R Prasad, Vinod K Kurtzberg, Joanne Rice, Henry E Tracy, Elisabeth T Producer: 20170718 In: The Journal of surgical research vol. 208 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	412.	Hematopoietic Stem Cell Transplantation to Treat Leukodystrophies: Clinical Practice Guidelines from the Hunter's Hope Leukodystrophy Care Network. [electronic resource] by Page, Kristin M Stenger, Elizabeth O Connelly, James A Shyr, David West, Tara Wood, Susan Case, Laura Kester, Maureen Shim, Soo Hammond, Lauren Hammond, Matthew Webb, Christin Biffi, Alessandra Bambach, Barbara Fatemi, Ali Kurtzberg, Joanne Producer: 20200908 In: Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	413.	Detection of homozygotes and heterozygotes for metachromatic leukodystrophy in lymphoid cell lines and peripheral leukocytes. [electronic resource] by Beratis, N G Danesino, C Hirschhorn, K Producer: 19760117 In: Annals of human genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	414.	Genetic complementation studies of multiple sulfatase deficiency. [electronic resource] by Horwitz, A L Producer: 19800327 In: Proceedings of the National Academy of Sciences of the United States of America vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	415.	HPLC analysis of urinary sulfatide: an aid in the diagnosis of metachromatic leukodystrophy. [electronic resource] by Strasberg, P M Warren, I Skomorowski, M A Lowden, J A Producer: 19850923 In: Clinical biochemistry vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	416.	Magnetic resonance imaging in leukodystrophies of childhood. [electronic resource] by Young, R S Osbakken, M D Alger, P M Ramer, J C Weidner, W A Daigh, J D Producer: 19890623 In: Pediatric neurology vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	417.	Metachromatic leukodystrophy. II. Direct determination of arylsulphatase A activity in amniotic fluid. [electronic resource] by Borresen, A L van der Hagen, C B Producer: 19740114 In: Clinical genetics vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	418.	The molecular detection of the pseudodeficiency allele for arylsulphatase A in patients with neurological symptoms and low arylsulphatase A activity. [electronic resource] by Goldenfum, S Malcolm, S Young, E Winchester, B Producer: 19940411 In: Journal of inherited metabolic disease vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	419.	Arylsulfatase A pseudodeficiency incidence in Turkey. [electronic resource] by Emre, S Topçu, M Terzioğlu, M Renda, Y Producer: 20000915 In: The Turkish journal of pediatrics vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	420.	Mutations in the arylsulfatase A gene of Japanese patients with metachromatic leukodystrophy. [electronic resource] by Hasegawa, Y Kawame, H Eto, Y Producer: 19930817 In: DNA and cell biology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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