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Journal of Inherited Metabolic Disease|January 5, 2002
Gaucher disease: understanding the molecular pathogenesis of sphingolipidosesT M CoxFASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 1, 1994
Aldolase B and fructose intoleranceT M CoxActa Paediatrica (Oslo, Norway : 1992). Supplement|May 18, 2005
Substrate reduction therapy for lysosomal storage diseasesT M CoxJournal of the Royal College of Physicians of London|April 1, 1993
The MB PhD programme. Training to be a clinician-scientist in the UKT M Cox, R WakefordThe Journal of Biological Chemistry|January 14, 1994
Purple acid phosphatase of the human macrophage and osteoclast. Characterization, molecular properties, and crystallization of the recombinant di-iron-oxo protein secreted by baculovirus-infected insect cellsA R Hayman, T M CoxAmerican Journal of Human Genetics|July 1, 1990
Partial aldolase B gene deletions in hereditary fructose intoleranceN C Cross, T M CoxBailliere'S Clinical Haematology|March 14, 1998
Gaucher's disease: clinical features and natural historyT M Cox, J P SchofieldBritish Journal of Haematology|January 1, 1980
Cellular mechanisms in the regulation of iron absorption by the human intestine: studies in patients with iron deficiency before and after treatmentT M Cox, T J PetersThe Journal of Biological Chemistry|May 15, 1988
Biosynthesis of heme in immature erythroid cells. The regulatory step for heme formation in the human erythronL C Gardner, T M CoxPageof 12