ERNEST BEUTLER

SELECTED BIBLIOGRAPHY
1996
The cost of treating Gaucher disease. Nat. Med. 2:523-524.
With J. Sipe, J. Romine, R. McMillan, J. Zyroff, and J. Koziol. Treatment of
multiple sclerosis and other autoimmune diseases with cladribine. Semin.
Hematol. 33(suppl. 1):45-52.
2003
The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical
hereditary hemochromatosis. Blood 101:3347-3350.
2006
Disorders of red cells resulting from enzyme abnormalities. In Williams Hematology,
eds. M. A. Lichtman, E. Beutler, T. J. Kipps, U. Seligsohn, K.
Kaushansky, and J. T. Prchal, pp.603-632. New York: McGraw-Hill.
Hemochromatosis: Genetics and pathophysiology. Annu. Rev. Med. 57:331-347.
Lysosomal storage diseases: Natural history and ethical and economic aspects.
Mol. Genet. Metab. 88:208-215.
2007
Iron storage disease: Facts, fiction and progress. Blood Cells Mol. Dis. 39:140-147.
2008
With X. Du, E. She, T. Gelbart, J. Truksa, P. Lee, Y. Xia, K. Khovananth, S.
Mudd, N. Mann, E. M. Moresco, and B. Beutler. 2008. The serine protease
TMPRSS6 is required to sense iron deficiency. Science 320:1088-1092.
2010
Disorders of iron metabolism. In Williams Hematology, eds. K. Kaushansky,
M. A. Lichtman, E. Beutler, T. J. Kipps, U. Seligsohn, and J. T. Prchal, pp.
565-606. New York: McGraw-Hill.