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Journal of Inherited Metabolic Disease|January 1, 1990
Disorders of glycoprotein degradationM Cantz, B Ulrich-BottAmerican Journal of Medical Genetics|March 1, 1985
The clinical spectrum of alpha-L-iduronidase deficiencyM Roubicek, J Gehler, J SprangerBiological Chemistry Hoppe-Seyler|June 1, 1991
Lysosomal and plasma membrane ganglioside GM3 sialidases of cultured human fibroblasts. Differentiation by detergents and inhibitorsH R Schneider-Jakob, M CantzFEBS Letters|March 10, 2001
Desialylation of extracellular GD1a-neoganglioprotein suggests cell surface orientation of the plasma membrane-bound ganglioside sialidase activity in human neuroblastoma cellsJ Kopitz, C Oehler, M CantzKlinische Wochenschrift|June 1, 1979
Comprehensive urinary screening for inborn errors of complex carbohydrate metabolismA C Sewell, J Gehler, J SprangerEuropean Journal of Pediatrics|May 1, 1980
Urinary oligosaccharide screening in patients with beta-galactosidase deficiencyA C Sewell, J Gehler, J SprangerJournal of Medical Genetics|April 1, 1978
Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromesB Zabel, W Baumann, J Gehler, et al.Birth Defects Original Article Series|January 1, 1975
Sandhoff disease: impaired catabolism of sulfated glycosaminoglycans in cultured fibroblastsM Cantz, J F O'Brien, H KresseGeburtshilfe Und Frauenheilkunde|November 1, 1988
[Prenatal diagnosis of sialidosis, a defect of the lysosomal enzyme neuraminidase]H Heyes, J Gehler, U Töllner, et al.European Journal of Pediatrics|April 1, 1986
Childhood neuromuscular disease with rimmed vacuolesH H Goebel, S von Loh, J GehlerPageof 7