Results 61 to 70 of about 25,688 (240)
Genetic disorders in gastroenterology and hepatology - HFE gene and hemochromatosis
, 2004 Hereditary hemochromatosis (HH) is the most common inherited disorder of iron metabolism. It is characterized by elevated intestinal iron absorption and the progressive deposition of iron in tissues throughout the body, notably in the parenchymal cells ...
Ramm, G. A. +6 more
core +1 more source
, 2009 Review on HFE (hemochromatosis), with data on DNA, on the protein encoded, and where the gene is ...
Dorak, MT, MT Dorak
core +1 more source
The Development of Hemochromatosis after Treatment for Celiac Sprue
Canadian Journal of Gastroenterology, 1994 Celiac sprue is a chronic disease characterized by maldigestion and malabsorption. Whereas many diseases have been reported in association with celiac sprue, hemochromatosis has not.
Mang Ma, Edmond A Ryan, Vincent G Bain
doaj +1 more source
Developmental Trends in Serum Iron, Transferrin, and Transferrin Saturation From Birth to 12 Months
Acta Paediatrica, EarlyView.ABSTRACT Aim There is a need for updated reference intervals for iron status biomarkers during infancy. This study aimed to investigate reference interval trends and diurnal variation of iron, transferrin, and transferrin saturation in infants subjected to delayed cord clamping at birth (DCC). Methods Data analysis from population‐based Swedish studies,
Sara Marie Larsson +5 more
wiley +1 more source
Journal of Education, Health and SportIntroduction: Hereditary hemochromatosis is the most common genetic disorder in Northern Europe. It involves an overload of iron in the tissues due to a deficiency of the protein hepcidin.
Dominika Prystacka-Szar +9 more
doaj +1 more source
A Rare Presentation of Transfusional Hemochromatosis: Hypogonadotropic Hypogonadism
Case Reports in Endocrinology, 2015 Hemochromatosis is a disease caused by extraordinary iron deposition in parenchymal cells leading to cellular damage and organ dysfunction. β-thalassemia major is one of the causes of secondary hemochromatosis due to regular transfusional treatment for ...
Rifki Ucler +6 more
doaj +1 more source
Patients and blood donors with hemochromatosis: A survey conducted in Førde Health Trust
Bioingeniøren, 2021 Introduction: To allow eligible persons with hemochromatosis to become blood donors will be advantageous for these individuals and for the blood supply.
Turid Aarhus Braseth +2 more
doaj
Mechanisms of Thrombocytosis in Iron‐Deficiency Anemia
European Journal of Haematology, EarlyView.ABSTRACT Iron‐deficiency anemia is frequently accompanied by reactive thrombocytosis, yet the mechanisms underlying this association remain incompletely understood. Beyond impaired erythropoiesis, iron availability has emerged as an active regulator of hematopoietic lineage decisions.
João Vitor Facco +2 more
wiley +1 more source
Should the Children of Patients with Hemochromatosis be Screened for the Disease?
Canadian Journal of Gastroenterology, 1988 Idiopathic hemochromatosis is an underdiagnosed treatable condition inherited in an autosomal recessive pattern. Since early treatment is of demonstrated value, screening of high risk groups of individuals in a valuable exercise in preventive medicine ...
Donald G. MacIntosh +5 more
doaj +1 more source
Hepatology Research, EarlyView.ABSTRACT Aim Steatotic liver disease (SLD), including metabolic dysfunction–associated SLD (MASLD) and metabolic dysfunction–associated alcohol‐related liver disease (MetALD), is a growing global health burden. Although impaired mastication is linked to metabolic disorders, its role in SLD remains unclear.
Takashi Miyano +4 more
wiley +1 more source