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Clinica Chimica Acta; International Journal of Clinical Chemistry|July 5, 2005
Beware of multiple comparisons: a study of symptoms associated with mutations of the HFE hemochromatosis geneJill Waalen, Ernest Beutler
Annual Review of Genomics and Human Genetics|September 1, 2009
Genetic screening for low-penetrance variants in protein-coding genesJill Waalen, Ernest Beutler
Current Hematology Reports|March 16, 2006
Hereditary hemochromatosis: screening and managementJill Waalen, Ernest Beutler
Blood Cells, Molecules & Diseases|September 13, 2005
Chronic inflammation does not appear to modify the homozygous hereditary hemochromatosis phenotypeErnest Beutler, Jill Waalen, Terri Gelbart
Best Practice & Research. Clinical Haematology|March 2, 2005
The penetrance of hereditary hemochromatosisJill Waalen, Børge G Nordestgaard, Ernest Beutler
British Journal of Haematology|March 5, 2003
Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestryErnest Beutler, Vincent Felitti, Terri Gelbart, et al.
Blood Cells, Molecules & Diseases|August 5, 2008
The anemia of ageing is not associated with increased plasma hepcidin levelsPauline Lee, Terri Gelbart, Jill Waalen, et al.
Blood|November 21, 2007
Screening for hemochromatosis by measuring ferritin levels: a more effective approachJill Waalen, Vincent J Felitti, Terri Gelbart, et al.
Blood Cells, Molecules & Diseases|August 19, 2007
Human chitotriosidase polymorphisms G354R and A442V associated with reduced enzyme activityPauline Lee, Jill Waalen, Karen Crain, et al.
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