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American Journal of Medical Genetics|January 1, 1977
Mucolipidosis I--a sialidosisJ Sphranger, J Gehler, M CantzHuman Genetics|June 29, 1976
The mucopolysaccharidoses: inborn errors of glycosaminoglycan catabolismM Cantz, J GehlerEuropean Journal of Pediatrics|June 8, 1976
Prenatal diagnosis of mucolipidosis II (I-cell disease)J Gehler, M Cantz, M Stoeckenius, et al.Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|June 1, 1978
Increased urinary excretion of keratan sulfate in fucosidosisH Greiling, H W Stuhlsatz, M Cantz, et al.European Journal of Pediatrics|August 17, 1978
Mucopolysaccharidosis II (Hunter disease) with corneal opacities. Report on two patients at the extremes of a wide clinical spectrumJ Spranger, M Cantz, J Gehler, et al.Human Genetics|January 1, 1985
N-Acetylneuraminic acid storage diseaseJ Baumkötter, M Cantz, K Mendla, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|November 1, 1981
[Phenotypes in heteroglycanoses and sphingolipidoses (author's transl)]J GehlerBiochimica Et Biophysica Acta|December 13, 1983
Decreased ganglioside neuraminidase activity in fibroblasts from mucopolysaccharidosis patients. Inhibition of the activity in vitro by sulfated glycosaminoglycans and other compoundsJ Baumkötter, M CantzThe Biochemical Journal|March 1, 1984
Specificity studies on the oligosaccharide neuraminidase of human fibroblastsK Mendla, M CantzPageof 7