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The Journal of Pediatrics|December 1, 1994
Adult and infantile Gaucher disease in one family: mutational studies and clinical updateM Shahinfar, D A WengerClinica Chimica Acta; International Journal of Clinical Chemistry|March 15, 1985
Studies on a sphingolipid activator protein (SAP-2) in fibroblasts from patients with lysosomal storage diseases, including Niemann-Pick disease Type CS Fujibayashi, D A WengerDevelopmental Neuroscience|January 1, 1991
Pseudodeficiencies of arylsulfatase A and galactocerebrosidase activitiesD A Wenger, E LouieVeterinary Pathology|April 22, 2008
Sphingomyelinase deficiency (Niemann-Pick disease) in a Hereford calfG K Saunders, D A WengerPrenatal Diagnosis|July 1, 1987
Use of 4-methylumbelliferyl-6-sulpho-2-acetamido-2-deoxy-beta- D-glucopyranoside for prenatal diagnosis of Tay-Sachs disease using chorionic villiE E Grebner, D A WengerBiochimica Et Biophysica Acta|September 29, 1993
Galactocerebrosidase from human urine: purification and partial characterizationY Q Chen, D A WengerClinica Chimica Acta; International Journal of Clinical Chemistry|February 5, 1981
Mucolipidosis I: studies of sialidase activity and a prenatal diagnosisO T Mueller, D A WengerClinical Genetics|January 1, 1985
Late onset GM2 gangliosidosis: an alpha-locus genetic compound with near normal hexosaminidase activityJ Charrow, K Inui, D A WengerProceedings of the National Academy of Sciences of the United States of America|May 1, 1983
Immunological evidence for deficiency in an activator protein for sulfatide sulfatase in a variant form of metachromatic leukodystrophyK Inui, M Emmett, D A WengerProceedings of the National Academy of Sciences of the United States of America|March 1, 1974
Globoid cell leukodystrophy: deficiency of lactosyl ceramide beta-galactosidaseD A Wenger, M Sattler, W HiattPageof 116