Results 61 to 70 of about 47,935 (263)

Transient elevation of serum ferritin in a Sri Lankan with homozygosity for H63D mutation in the HFE gene: a case report

open access: yesJournal of Medical Case Reports, 2020
Introduction Hereditary hemochromatosis is an inherited disorder of iron metabolism, characterized by excessive iron deposition in major organs of the body, leading to multi-organ dysfunction. It is a genetically heterogeneous disease caused by mutations
Wasanthi Wickramasinghe   +3 more
doaj   +1 more source

Hepatocarcinoma with tumor thrombus occupying the right atrium and portal vein in a patient with hereditary hemochromatosis and liver cirrhosis [PDF]

open access: yes, 2018
We present the case of a 46-year old patient with Child-Pugh class C cirrhosis with MEDL-Score 16, and hepatocellular carcinoma invading the inferior vena cava and the right atrium.
Breaban, Iulia   +11 more
core   +1 more source

The effect of amino acid deprivation on the transfer of iron through Caco-2 cell monolayers [PDF]

open access: yes, 2017
Funding Source Rural and Environmental Scientific and Analytical Services, the Scottish Government Acknowledgments We thank Dr Helen Hayes for her technical support during this project.
Cottin, Sarah   +3 more
core   +3 more sources

Type 4B hereditary hemochromatosis associated with a novel mutation in the SLC40A1 gene

open access: yesMedicine, 2017
Rationale: Hereditary hemochromatosis can be divided into HFE- and non-HFE-related based on genetic mutations in different genes. HFE-related hemochromatosis is the most common inherited genetic disease in European populations but rare in Asia-pacific ...
Wei Zhang, Tingxia Lv, Jian Huang, X. Ou
semanticscholar   +1 more source

Association between high serum ferritin and periodontitis: A population‐based cross‐sectional preliminary study

open access: yesJournal of Periodontology, EarlyView.
Abstract Background The aim of this study was to investigate the association between high serum ferritin levels and periodontitis considering pathways induced by sociodemographic and behavioral factors, serum inflammation, and metabolic risk. Methods Data from 7283 individuals who participated in the Third National Health and Nutrition Examination ...
Susilena Arouche Costa   +4 more
wiley   +1 more source

Hemochromatosis Patients as Voluntary Blood Donors

open access: yesCanadian Journal of Gastroenterology, 2004
The present study was designed to investigate hemochromatosis patients' suitability as blood donors as well as their perceptions and experience with the current public donation system.
Tara E Power, Paul C Adams
doaj   +1 more source

Neogenin-mediated hemojuvelin shedding occurs after hemojuvelin traffics to the plamsa membrane [PDF]

open access: yes, 2008
Hemochromatosis type 2 gene (HFE2) is highly expressed in skeletal muscle and liver hepatocytes. Its encoded protein, hemojuvelin (HJV), is a co-receptor for the bone morphogenetic proteins 2 and 4 (BMP2 and BMP4) and enhances the BMP-induced hepcidin ...
Altschuler   +51 more
core   +3 more sources

Clinical Features and Dental Pathologies in Maxillary Sinus Fungal Balls and Odontogenic Sinusitis

open access: yesThe Laryngoscope, EarlyView.
This international, multicenter study compared clinical and dental characteristics of maxillary sinus fungal balls (MSFB), odontogenic MSFB (MSFBO), and odontogenic sinusitis (ODS). When MSFB and MSFBO were compared, MSFBO was associated with extruded root canal material and dental implant protrusion; when MSFBOs and ODS were compared, ODS was ...
Eunice Im   +32 more
wiley   +1 more source

Idiopathic brain calcification in a patient with hereditary hemochromatosis

open access: yesBMC Neurology, 2020
Background Detection of brain-MRI T2/T2* gradient echo images (T2*GRE)-hypointensity can be compatible with iron accumulation and leads to a differential diagnosis work-up including neurodegeneration with brain iron accumulation (NBIA) and Wilson Disease.
Stefania Scarlini   +10 more
doaj   +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

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