Showing results (31-40 of 327) with videos related to

Sort By:
Pageof 33
Annual Review of Pathology|April 30, 2009
Regulation of hepcidin and iron-overload diseasePauline L Lee, Ernest Beutler
Haematologica|May 18, 2006
The genetic basis of human erythrocyte pyridoxal kinase activity variationJonathan M Flanagan, Ernest Beutler
Science (New York, N.Y.)|May 3, 2008
The serine protease TMPRSS6 is required to sense iron deficiencyXin Du, Ellen She, Terri Gelbart, et al.
Acta Haematologica|December 22, 2007
A new case of human atransferrinemia with a previously undescribed mutation in the transferrin geneDeniz Aslan, Karen Crain, Ernest Beutler
Clinical Chemistry|November 26, 2002
Haptoglobin polymorphism and iron homeostasisErnest Beutler, Terri Gelbart, Pauline Lee
The Journal of Laboratory and Clinical Medicine|August 24, 2004
Mutations in the gene encoding cytosolic beta-glucosidase in Gaucher diseaseErnest Beutler, Lisa Beutler, Carol West
Blood Cells, Molecules & Diseases|June 18, 2002
Severe jaundice in a patient with a previously undescribed glucose-6-phosphate dehydrogenase (G6PD) mutation and Gilbert syndromeErnest Beutler, Terri Gelbart, William Miller
Blood Cells, Molecules & Diseases|September 13, 2005
Chronic inflammation does not appear to modify the homozygous hereditary hemochromatosis phenotypeErnest Beutler, Jill Waalen, Terri Gelbart
Pageof 33