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International Journal of Clinical Pharmacology and Therapeutics|December 31, 2009
Krabbe disease: an overviewG M PastoresDrugs of Today (Barcelona, Spain : 1998)|May 28, 2003
Gaucher disease: Genetics, diagnosis and managementM. Levin, I. Pleskova, G. M. PastoresGenetics and Molecular Research : GMR|December 1, 2007
Laronidase for treating mucopolysaccharidosis type IR P El Dib, G M PastoresJournal of Inherited Metabolic Disease|May 22, 2007
Very long chain acyl-CoA dehydrogenase deficiency in a pair of mildly affected monozygotic twin sister in their late fiftiesA Zia, E H Kolodny, G M PastoresCurrent Rheumatology Reports|December 21, 2000
Bone and joint complications related to Gaucher diseaseG M Pastores, M J Patel, H FiroozniaBlood|July 15, 1993
Enzyme therapy in Gaucher disease type 1: dosage efficacy and adverse effects in 33 patients treated for 6 to 24 monthsG M Pastores, A R Sibille, G A GrabowskiThe Journal of Clinical Investigation|May 15, 1997
Identification and expression of acid beta-glucosidase mutations causing severe type 1 and neurologic type 2 Gaucher disease in non-Jewish patientsM E Grace, R J Desnick, G M PastoresBiochemistry. Biokhimiia|September 10, 2013
Animal models for lysosomal storage disordersG M Pastores, P A Torres, B-J ZengQuality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|August 6, 1998
The health-related quality of life of adults with Gaucher's disease receiving enzyme replacement therapy: results from a retrospective studyA M Damiano, G M Pastores, J E WarePageof 7