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Expert Commentary & Five-year View Many significant advances have been made in our understanding of HH in recent years. It has become clear that the primary physiologic defect in this disorder is ...
Wang, J. (2016) Nursing of a Patient with Primary Hemochromatosis Treated with Erythrocyte Apheresis. Nursing Practice and Research, 13, 156-157. has been cited by the following article: TITLE: ...
Article citations More>> Xu, P., Zhou, Y.D. and Li, Y. (2008) Efficacy of Phlebotomy in Patients with Primary Hemochromatosis. Journal of Clinical Hematology (Transfusion and Laboratory Edition), 21, ...
People with hemochromatosis currently make up 2.5% of the Australian donor panel, with 15,000 donors already making 37,000 donations every year at Australian Red Cross Lifeblood donor centers.
Hemochromatosis is anticipated to witness a CAGR of 6% during the forecast period 2024-2031, owing to growing diagnosis and treatment rates. On the basis of type, primary hemochromatosis segment is ...
The third possibility is that this subject has classic primary hemochromatosis and that this disease is due to the failure of xanthine oxidase to reduce ferric-ferritin to ferrous-ferritin.
This was a homozygous HAMP c.166C > G (p.Arg56Gly) mutation. This patient was considered to have primary hemochromatosis due to a mutation in the HAMP gene. To further confirm that the gene mutation ...
Representative Andy Kim is the frontrunner in a three-way Democratic race for the seat held by Robert Menendez, who is on trial on federal bribery charges. Mr. Menendez is not on the primary ...
TOPLINE: Many patients with hereditary hemochromatosis (HH) present with diverse skin manifestations, including hyperpigmentation, hypertrichosis of the face, and pruritus, according to a ...
Primary Hemochromatosis: A Genetic Mutation Primary hemochromatosis occurs due to an alteration of normal iron absorption, usually caused by an inherited genetic mutation. With primary hemochromatosis ...
There are two types of hemochromatosis: primary and secondary. Primary hemochromatosis is genetic, while secondary hemochromatosis can result from health conditions, such as liver disease and anemia.
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