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American Journal of Hematology|September 2, 1998
Coincidence of Gaucher's disease due to a private mutation and Ph' positive chronic myeloid leukemiaP E Petrides, P leCoutre, J Müller-Höcker, et al.Blood Cells, Molecules & Diseases|October 13, 2009
Polymorphisms and mutations of human TMPRSS6 in iron deficiency anemiaE Beutler, C Van Geet, D M W M te Loo, et al.The New England Journal of Medicine|December 3, 1992
A less costly regimen of alglucerase to treat Gaucher's diseaseM L Figueroa, B E Rosenbloom, A C Kay, et al.British Journal of Haematology|February 13, 2001
Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studiesJ L Corrons, R Alvarez, A Pujades, et al.Proceedings of the National Academy of Sciences of the United States of America|June 15, 1993
Gaucher disease as a paradigm of current issues regarding single gene mutations of humansE BeutlerAmerican Journal of Hematology|January 1, 1993
Study of glucose-6-phosphate dehydrogenase: history and molecular biologyE BeutlerProceedings of the National Academy of Sciences of the United States of America|June 1, 1983
Selectivity of proteases as a basis for tissue distribution of enzymes in hereditary deficienciesE BeutlerAnnual Review of Medicine|January 1, 1992
The molecular biology of G6PD variants and other red cell enzyme defectsE BeutlerPageof 58