Results 141 to 150 of about 192,458 (292)

Liver Involvement in Celiac Disease and Immune‐Mediated Diseases of the Small Bowel

open access: yesLiver International, Volume 45, Issue 8, August 2025.
ABSTRACT Disorders of the hepatobiliary system are commonly associated with gastrointestinal (GI) diseases. The GI and hepatobiliary systems interact through the portal vein system and enterohepatic circulation, creating a gut–liver axis that allows for a complex multidirectional interplay between immune, hormonal, dietary and environmental luminal ...
Nicoletta Nandi   +8 more
wiley   +1 more source

A rare cause of osteonecrosis

open access: yesItalian Journal of Medicine, 2012
IntroductionHereditary hemochromatosis (HH) is an autosomal recessive disorder caused by mutations in the HFE gene, which increase intestinal iron absorption.
Paolo Agostinis   +8 more
doaj   +1 more source

THE PATHOGENESIS OF HEREDITARY HEMOCHROMATOSIS

open access: yesThe FASEB Journal, 2009
Hereditary hemochromatosis (HH) is an iron overload disease which can result from mutations in HFE, transferrin receptor 2 (TfR2), hemojuvelin (HJV) or hepcidin, all of which lead to inadequate synthesis of the iron‐regulatory hormone hepcidin. Hepcidin deficiency in HH results in excessive iron absorption. In normal homeostasis, hepcidin production is
Emilio Ramos   +2 more
openaire   +2 more sources

Identification of New Key Players for Ferrous Iron Export in the Asymmetric Inner Gate of Human Ferroportin 1

open access: yesThe FASEB Journal, Volume 39, Issue 14, 31 July 2025.
Ferroportin 1 is an iron exporter belonging to the Major Facilitator Superfamily. Its unusual intracellular gate is formed by asymmetric networks of non‐covalent bonds. We analyzed these networks using Molecular Dynamics simulations and experimental tests and identified novel amino acids as key players in inter‐lobe connections.
Marlène Le Tertre   +8 more
wiley   +1 more source

Hemochromatosis and Heart Involvement

open access: yesАрхивъ внутренней медицины
Hemochromatosis is a life-threatening condition if left untreated, that is caused by excess iron in the body. It can be primary (hereditary) hemochromatosis, resulting from genes mutations, and secondary (acquired) as a result of excessive intake of iron
E. V. Reznik   +3 more
doaj   +1 more source

Therapeutic Depletion of Iron Stores Is Not Associated with a Reduced Hemoglobin Mass in a Hemochromatosis Patient

open access: yesCase Reports in Gastroenterology, 2016
Introduction: Hereditary hemochromatosis features a dysregulated iron absorption leading to iron overload and organ damage. The regulation of total hemoglobin mass during depletion of iron deposits by therapeutic phlebotomy has not been studied.
Nina Wrobel   +4 more
doaj   +1 more source

Evaluation of a Nucleic Acid-based Cross-Linking Assay to Screen for Hereditary Hemochromatosis in Healthy Blood Donors [PDF]

open access: bronze, 2000
Christiane Wylenzek   +5 more
openalex   +1 more source

Genetic Information and the Workplace - Full Report [PDF]

open access: yes, 1998
Joint Agency ReportGeneticInfoWorkplace1998.pdf: 800 downloads, before Oct.
Department of Health and Human Services, U.S.   +2 more
core   +1 more source

HFE Gene Mutations as Predisposing Factors for Childhood Acute Lymphoblastic Leukaemia in Iraqi Patients

open access: yesمجلة علوم ذي قار
Hemochromatosis is a prevalent hereditary disorder that causes excess iron to build up in the body to dangerous levels. Hereditary hemochromatosis, also known as HFE-related hemochromatosis is carried on by changes in the HFE gene.
Thanaa Kalil Ibrahim   +3 more
doaj   +1 more source

Improved Molecular Diagnosis of Hereditary Hemochromatosis Using a DNA Enzyme Immunoassay [PDF]

open access: bronze, 2000
Mara Biasin   +5 more
openalex   +1 more source

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