Results 211 to 220 of about 33,546 (266)
The Iron Enigma: Expounding Iron Deficiency in a Pregnant Woman With Hemochromatosis and Celiac Disease. [PDF]
CureusIdrees Z, Khan H, Akhtar MZ, Khan U.
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Hemochromatosis: Hereditary hemochromatosis and HFE gene
Vitamins and hormones, 2019Hereditary Hemochromatosis (HH) is an autosomal recessive genetic disease, characterized by an excessively increased absorption of dietary iron. Excess iron can be accumulated because of the lack of an effective excretory mechanism leading to toxic effects. HH is one of the most common genetic disorders in individuals of European descent.
Nikolaos Drakoulis +3 more
openaire +3 more sources
Clinics in Liver Disease, 2000
The recent cloning of the hemochromatosis gene (HFE) and the demonstration that a single missense mutation is responsible for 90% or more of patients with the disease, have stimulated renewed interest in all aspects of this common disease. The molecular tests for identifying mutations in HFE provide improved means for diagnosis, family screening, and ...
Powell, Lawrie W., Yapp, Thomas R.
+17 more sources
The recent cloning of the hemochromatosis gene (HFE) and the demonstration that a single missense mutation is responsible for 90% or more of patients with the disease, have stimulated renewed interest in all aspects of this common disease. The molecular tests for identifying mutations in HFE provide improved means for diagnosis, family screening, and ...
Powell, Lawrie W., Yapp, Thomas R.
+17 more sources
Expert Review of Gastroenterology & Hepatology, 2018
Introduction: Hereditary hemochromatosis (HH) is an autosomal recessive disorder that occurs in approximately 1 in 200–250 individuals. Mutations in the HFE gene lead to excess iron absorption. Excess iron in the form of non-transferrin-bound iron (NTBI)
Shmuel Golfeyz, S. Lewis, I. Weisberg
semanticscholar +1 more source
Introduction: Hereditary hemochromatosis (HH) is an autosomal recessive disorder that occurs in approximately 1 in 200–250 individuals. Mutations in the HFE gene lead to excess iron absorption. Excess iron in the form of non-transferrin-bound iron (NTBI)
Shmuel Golfeyz, S. Lewis, I. Weisberg
semanticscholar +1 more source