Your search returned 1243 results.

Results
	961.	[Lipid and lectin histochemical studies of neurolipidosis]. [electronic resource] by Dietzmann, K Producer: 19891208 In: Zentralblatt fur allgemeine Pathologie u. pathologische Anatomie vol. 135 Availability: No items available. Save to lists Add to cart (remove)
	962.	Comparison of enzymatic activity with evidence of engraftment in patients with inborn errors of metabolism receiving allogeneic marrow transplantation. [electronic resource] by Blazar, B R Whitley, C B Desnick, R J Pierpont, M E Filipovich, A H Ramsay, N K Kersey, J H Orr, H T Yasmineh, W G Tsai, M Y Producer: 19860530 In: Birth defects original article series vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	963.	Lipid storage disease: Part II. Ultrastructural pathology of lipid storage cells in sphingolipidoses. [electronic resource] by Takahashi, K Naito, M Producer: 19850904 In: Acta pathologica japonica vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	964.	Electron microscopic investigation of inclusion material in a case of adult metachromatic leukodystrophy; observations on kidney biopsy, peripheral nerve and cerebral white matter. [electronic resource] by Joosten, E Hoes, M Gabreëls-Festen, A Hommes, O Schuurmans Stekhoven, H Slooff, J L Producer: 19760301 In: Acta neuropathologica vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	965.	[Pathogenesis and pathomorphology of human leukodystrophies]. [electronic resource] by Zhabotinskiĭ, Iu M Shefer, V F Producer: 19820222 In: Arkhiv patologii vol. 43 Availability: No items available. Save to lists Add to cart (remove)
	966.	Population carrier rates of pathogenic ARSA gene mutations: is metachromatic leukodystrophy underdiagnosed? [electronic resource] by Ługowska, Agnieszka Ponińska, Joanna Krajewski, Paweł Broda, Grażyna Płoski, Rafał Producer: 20111102 In: PloS one vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	967.	Single exon mutation in arylsulfatase A gene has two effects: loss of enzyme activity and aberrant splicing. [electronic resource] by Hasegawa, Y Kawame, H Ida, H Ohashi, T Eto, Y Producer: 19940601 In: Human genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	968.	Metachromatic leukodystrophy: a scoring system for brain MR imaging observations. [electronic resource] by Eichler, F Grodd, W Grant, E Sessa, M Biffi, A Bley, A Kohlschuetter, A Loes, D J Kraegeloh-Mann, I Producer: 20100205 In: AJNR. American journal of neuroradiology vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	969.	SPECULATIONS ON THE NATURE OF THE METABOLIC DEFECTS IN TAY-SACHS, NIEMANN-PICK, GAUCHER'S AND ALZHEIMER'S DISEASES, AND METACHROMATIC LEUCODYSTROPHY. [electronic resource] by ROUSER, G KRITCHEVSKY, G GALLI, C Producer: 19961201 In: Journal of the American Oil Chemists' Society vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	970.	Novel mutations in arylsulfatase A gene in three Ukrainian families with metachromatic leukodystrophy. [electronic resource] by Olkhovich, Natalia V Takamura, Noboru Pichkur, Natalia A Gorovenko, Natalia G Aoyagi, Kiyoshi Yamashita, Shunichi Producer: 20040802 In: Molecular genetics and metabolism vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	971.	Long-term outcomes after allogeneic hematopoietic stem cell transplantation for metachromatic leukodystrophy: the largest single-institution cohort report. [electronic resource] by Boucher, Alexander A Miller, Weston Shanley, Ryan Ziegler, Richard Lund, Troy Raymond, Gerald Orchard, Paul J Producer: 20160425 In: Orphanet journal of rare diseases vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	972.	Brain galactolipid content in a patient with pseudoarylsulfatase A deficiency and coincidental diffuse disseminated sclerosis, and in patients with metachromatic, adreno-, and other leukodystrophies. [electronic resource] by Harzer, K Kustermann-Kuhn, B Producer: 19870129 In: Journal of neurochemistry vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	973.	[Enzyme deficiencies detected on cultured fibroblasts and amniotic cells. Application to prenatal diagnosis]. [electronic resource] by Dreyfus, J C Poenaru, L Producer: 19760802 In: Annales de biologie clinique vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	974.	A therapeutic trial of amniotic epithelial cell implantation in patients with lysosomal storage diseases. [electronic resource] by Yeager, A M Singer, H S Buck, J R Matalon, R Brennan, S O'Toole, S O Moser, H W Producer: 19851118 In: American journal of medical genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	975.	[Function and relevance of activator proteins for glycolipid degradation]. [electronic resource] by Sandhoff, K Producer: 19850819 In: Seikagaku. The Journal of Japanese Biochemical Society vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	976.	Spectrum of mutations in the arylsulfatase A gene in a Canadian DNA collection including two novel frameshift mutations, a new missense mutation (C488R) and an MLD mutation (R84Q) in cis with a pseudodeficiency allele. [electronic resource] by Coulter-Mackie, Marion B Gagnier, Liane Producer: 20040204 In: Molecular genetics and metabolism vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	977.	An Asn > Lys substitution in saposin B involving a conserved amino acidic residue and leading to the loss of the single N-glycosylation site in a patient with metachromatic leukodystrophy and normal arylsulphatase A activity. [electronic resource] by Regis, S Filocamo, M Corsolini, F Caroli, F Keulemans, J L van Diggelen, O P Gatti, R Producer: 19990615 In: European journal of human genetics : EJHG vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	978.	Imaging of complex sulfatides SM3 and SB1a in mouse kidney using MALDI-TOF/TOF mass spectrometry. [electronic resource] by Marsching, Christian Eckhardt, Matthias Gröne, Hermann-Josef Sandhoff, Roger Hopf, Carsten Producer: 20111025 In: Analytical and bioanalytical chemistry vol. 401 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	979.	Challenging symptom profiles of life-limiting conditions in children: a survey of care professionals and families. [electronic resource] by Malcolm, Cari Forbat, Liz Anderson, Gillian Gibson, Faith Hain, Richard Producer: 20110830 In: Palliative medicine vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	980.	Computerized cranial tomography in cerebral diseases of white matter. [electronic resource] by Lane, B Carroll, B A Pedley, T A Producer: 19780724 In: Neurology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 1243 results.