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Human Genetics|April 1, 1989
Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implicationsC Hohenschutz, P Eich, W Friedl, et al.Journal of Lipid Research|September 19, 1998
Degradation of blood group A glycolipid A-6-2 by normal and mutant human skin fibroblastsB Asfaw, D Schindler, J Ledvinová, et al.American Journal of Human Genetics|January 1, 1985
Hereditary heat-labile hexosaminidase B: a variant whose homozygotes synthesize a functional HEX AR Navon, R Kopel, J Nutman, et al.Prenatal Diagnosis|May 18, 1999
Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical, immunocytochemical and DNA analysesE M Maier, A A Roscher, S Kammerer, et al.European Journal of Pediatrics|February 1, 1991
Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophyJ Kappler, R W Watts, E Conzelmann, et al.Archives of Biochemistry and Biophysics|December 1, 1987
Identity of the activator proteins for the enzymatic hydrolysis of sulfatide, ganglioside GM1, and globotriaosylceramideA Vogel, W Fürst, M A Abo-Hashish, et al.American Journal of Medical Genetics|September 1, 1988
Probable metachromatic leukodystrophy/pseudodeficiency compound heterozygote at the arylsulfatase A locus with neurological and psychiatric symptomatologyC Hohenschutz, W Friedl, K H Schlör, et al.Kidney International|April 14, 1999
Lp(a) and LDL induce apoptosis in human endothelial cells and in rabbit aorta: role of oxidative stressJ Galle, R Schneider, A Heinloth, et al.Atherosclerosis|July 25, 1998
Glyc-oxidized LDL impair endothelial function more potently than oxidized LDL: role of enhanced oxidative stressJ Galle, R Schneider, B Winner, et al.Human Genetics|November 1, 1986
The influence of low arylsulfatase A activity on neuropsychiatric morbidity: a large-scale screening in patientsP Propping, W Friedl, M Huschka, et al.Pageof 5