Iron can accumulate in the liver in a variety of conditions, including congenital, systemic iron- loading conditions (hereditary hemochromatosis), conditions associated with systemic …
V Niederkofler, R Salie, S Arber - The Journal of clinical …, 2005 - Am Soc Clin Investig
Iron homeostasis plays a critical role in many physiological processes, notably synthesis of heme proteins. Dietary iron sensing and inflammation converge in the control of iron …
P Guggenbuhl, Y Deugnier, JF Boisdet… - Osteoporosis …, 2005 - Springer
Genetic hemochromatosis (GH) is an iron overload disorder mainly due to the C282Y mutation of the HFE gene. The possibility of bone involvement was only recently recognized …
Iron overload diseases of genetic origin are an ever changing world, due to major advances in genetics and molecular biology. Five major categories are now established: HFE-related …
PCJL Santos, JE Krieger, AC Pereira - International journal of molecular …, 2012 - mdpi.com
Hereditary hemochromatosis (HH) is an autosomal recessive disorder characterized by enhanced intestinal absorption of dietary iron. Without therapeutic intervention, iron …
S Taketani - The Tohoku journal of experimental medicine, 2005 - jstage.jst.go.jp
205 (4), 297-318── Iron is fastidiously utilized by living cells, since it is an essential element, but is toxic in excess. Cells take up iron via a transferrin-transferrin receptor …
P Brissot, F de Bels - ASH Education Program Book, 2006 - ashpublications.org
The term hemochromatosis encompasses at least four types of genetic iron overload conditions, most of them recently distinguished from one another as a result of the …
P Aguilar-Martinez, JF Schved… - Official journal of the …, 2005 - journals.lww.com
The number of new genes implicated in iron metabolism has dramatically increased during the last few years. Alterations of these genes may cause hyperferritinemia associated or not …
C Koyama, H Hayashi, S Wakusawa, T Ueno… - Journal of …, 2005 - Elsevier
Hemochromatosis is a genetically heterogeneous condition. Mutations in the recently described hemojuvelin gene were found in patients with juvenile hemochromatosis, who …