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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: May 31, 2023. (Total: 217454Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Iron Overload and HFE2[original query]
HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.
Genetic testing 2007 11 (3): 269-75.
Barton James C, Acton Ronald T, Leiendecker-Foster Catherine, Lovato Laura, Adams Paul C, McLaren Gordon D, Eckfeldt John H, McLaren Christine E, Reboussin David M, Gordeuk Victor R, Speechley Mark R, Reiss Jacob A, Press Richard D, Dawkins Fitzroy W,
Cardiac iron overload in transfusion-dependent patients with myelodysplastic syndromes.
British journal of haematology 2011 Jun .
Roy NB, Myerson S, Schuh AH, Bignell P, Patel R, Wainscoat JS, McGowan S, Marchi E, Atoyebi W, Littlewood T, Chacko J, Vyas P, Killick SB
The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data.
Genetics in medicine : official journal of the American College of Medical Genetics 2015 Dec .
Wallace Daniel F, Subramaniam V Nath
The role of genetic factors in patients with hepatocellular carcinoma and iron overload - a prospective series of 234 patients.
Liver international : official journal of the International Association for the Study of the Liver 2015 Oct .
Funakoshi Natalie, Chaze Iphigénie, Alary Anne-Sophie, Tachon Gaëlle, Cunat Séverine, Giansily-Blaizot Muriel, Bismuth Michael, Larrey Dominique, Pageaux Georges-Philippe, Schved Jean-François, Donnadieu-Rigole Hélène, Blanc Pierre, Aguilar-Martinez Patric
Rare HFE variants are the most frequent cause of hemochromatosis in non-c282y homozygous patients with hemochromatosis.
American journal of hematology 2016 Aug .
Hamdi-Rozé Houda, Beaumont-Epinette Marie-Pascale, Ben Ali Zeineb, Le Lan Caroline, Loustaud Ratti Véronique, Causse Xavier, Loreal Olivier, Deugnier Yves, Brissot Pierre, Jouanolle Anne-Marie, Bardou-Jacquet Edoua
Causes of iron overload in blood donors - a clinical study.
Vox sanguinis 2017 12 113 (2): 110-119.
Laursen A H, Bjerrum O W, Friis-Hansen L, Hansen T O, Marott J L, Magnussen
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