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Blood|April 1, 1992
Mutations in Jewish patients with Gaucher diseaseE Beutler, T Gelbart, W Kuhl, et al.Clinical Genetics|August 25, 2004
A previously undescribed frameshift deletion mutation of HFE (c.del277; G93fs) associated with hemochromatosis and iron overload in a C282Y heterozygoteJ C Barton, C West, P L Lee, et al.Acta Haematologica|January 1, 1978
Acid hydrolases in normal B and T blood lymphocytesG A Pangalis, W Kuhl, S R Waldman, et al.Blood|April 1, 1980
Plasma blood group glycosyltransferase activities after bone marrow transplantationA Yoshida, G M Schmidt, K G Blume, et al.The Journal of Laboratory and Clinical Medicine|August 1, 1975
Nonenzymatic conversion of human hexosaminidase AE Beutler, D Villacorte, W Kuhl, et al.Proceedings of the National Academy of Sciences of the United States of America|October 1, 1977
Enzyme replacement therapy in Gaucher's disease: preliminary clinical trial of a new enzyme preparationE Beutler, G L Dale, D E Guinto, et al.Journal of Pain and Symptom Management|August 1, 1990
Behavior, affect, and cognition among psychogenic pain patients in group expressive psychotherapyM A Corbishley, R Hendrickson, L E Beutler, et al.Blood|January 1, 1990
Gamma-glutamylcysteine synthetase deficiency and hemolytic anemiaE Beutler, R Moroose, L Kramer, et al.Biochemical and Biophysical Research Communications|May 18, 2000
NADH-ferric reductase activity associated with dihydropteridine reductaseP L Lee, C Halloran, A R Cross, et al.Blood Cells, Molecules & Diseases|February 8, 2000
The effect of transferrin polymorphisms on iron metabolismP L Lee, N J Ho, R Olson, et al.Pageof 668