Bone mineral density in men with genetic hemochromatosis and HFE gene mutation

The diagnosis of osteoporosis

John A. Professor Kanis, L. Joseph Melton, Claus Christiansen et al. · Journal of Bone and Mineral Research · 1994 · 3.8K citations

Bone Disease, Bone Health, Diagnosis +4

A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

John N. Feder, Andreas Gnirke, Zenta Tsuchihashi et al. · Nature Genetics · 1996 · 3.7K citations

Histocompatibility, Immunogenetics, Autoimmune Disease +11

Non-invasive assessment of hepatic iron stores by MRI

Y. Gandon, Damien Olivié, Dominique Guyader et al. · The Lancet · 2004 · 665 citations

Hepatic Iron Stores, Engineering, Hepatology +10

Disrupted hepcidin regulation in HFE -associated haemochromatosis and the liver as a regulator of body iron homoeostasis

Kim R. Bridle, David M. Frazer, Sarah J. Wilkins et al. · The Lancet · 2003 · 615 citations

Body Iron Homoeostasis, Pathology, Iron Deficiency +16

Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosis

Dominique Guyader, Christian Jacquelinet, Romain Moirand et al. · Gastroenterology · 1998 · 342 citations · Full text

Fibrosis, Medicine, Histopathology +5