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Genomics|March 20, 1995
Structure and organization of the human galactocerebrosidase (GALC) geneP Luzi, M A Rafi, D A WengerAmerican Journal of Diseases of Children (1960)|September 1, 1977
Nine cases of sphingomyelin lipidosis, a new variant in Spanish-American Children. Juvenile variant of Niemann-Pick Disease with foamy and sea-blue histiocytesD A Wenger, G Barth, J H GithensAnnals of Neurology|July 1, 1996
Multiple mutations in the GALC gene in a patient with adult-onset Krabbe diseaseP Luzi, M A Rafi, D A WengerEuropean Journal of Pharmacology|March 12, 1982
Ketamine inhibition of ligand binding to cholinergic receptors and ion channelsR S Aronstam, L Narayanan, D A WengerAmerican Journal of Human Genetics|June 1, 1994
Mutations in the lysosomal beta-galactosidase gene that cause the adult form of GM1 gangliosidosisS Chakraborty, M A Rafi, D A WengerClinical Genetics|February 1, 1987
Pseudodeficiency of arylsulfatase A: a counseling dilemmaS Baldinger, M E Pierpont, D A WengerHuman Mutation|January 1, 1997
Molecular genetics of Krabbe disease (globoid cell leukodystrophy): diagnostic and clinical implicationsD A Wenger, M A Rafi, P LuziJournal of Inherited Metabolic Disease|January 1, 1990
Quantitative analysis of disaccharides in the urine of beta-mannosidosis patientsS Tjoa, D A Wenger, P V FennesseyGenomics|May 1, 1996
Cloning of the canine GALC cDNA and identification of the mutation causing globoid cell leukodystrophy in West Highland White and Cairn terriersT Victoria, M A Rafi, D A WengerMovement Disorders : Official Journal of the Movement Disorder Society|December 5, 2000
Niemann-Pick disease type C: two cases and an updateE Y Uc, D A Wenger, J JankovicPageof 116