Hemochromatosis

Hemochromatosis is a genetic disorder characterized by excessive intestinal absorption of dietary iron, resulting in a pathological increase in total body iron stores. It leads to massive iron deposits in parenchymal cells of liver, adrenal glands, heart, skin, gonads, joints and pancreas, which disrupts the normal function of these organs. Discover the latest research on hemochromatosis here

January 14, 2022
Review

Neuropathological Mechanisms of β-N-Methylamino-L-Alanine (BMAA) with a Focus on Iron Overload and Ferroptosis.

Neurotoxicity Research
Hamed Kazemi Shariat PanahiVanessa X Tan
January 12, 2022

Association of Habitual Dietary Intake with Liver Iron-A Population-Based Imaging Study.

Nutrients
Jule FillerSusanne Rospleszcz
January 12, 2022
Review
Open Access

Hearing Loss in Beta-Thalassemia: Systematic Review.

Journal of Clinical Medicine
Immacolata TartaglioneRenzo Manara
January 10, 2022

Iron supplementation ameliorates aloin-induced iron deficiency anemia in rats.

Experimental and Molecular Pathology
Mostafa M Abdel-MoniemAmr Y Esmat
January 10, 2022

Busulfan-fludarabine- or treosulfan-fludarabine-based myeloablative conditioning for children with thalassemia major.

Annals of Hematology
Roswitha LüftingerEBMT Pediatric Diseases, Inborn Errors Working Parties
January 11, 2022
Case Report

Hereditary Hemochromatosis Associated With Idiopathic Refractory Aplastic Anemia in a Five-Year-Old Boy: A Case Report.

Curēus
Ibrahim AlharbiAbdulrahman A Baabdullah
January 9, 2022

Iron dysregulation in COVID-19 and reciprocal evolution of SARS-CoV-2: Natura nihil frustra facit.

Journal of Cellular Biochemistry
Yash GuptaPrakasha Kempaiah
January 8, 2022

Disruption of Hfe leads to skeletal muscle iron loading and reduction of hemoproteins involved in oxidative metabolism in a mouse model of hereditary hemochromatosis.

Biochimica Et Biophysica Acta. General Subjects
Francesca M AlvesRené Koopman
January 7, 2022
Case Report
Open Access

Hepatitis B-Associated Symptomatic Iron Overload, with Complete Resolution after Nucleoside Analogue Treatment.

Case Reports in Gastrointestinal Medicine
Tze Tong TeyWei Qiang Leow
January 7, 2022
Review

Hereditary Hemochromatosis: A Cardiac Perspective.

Curēus
Pranay K JoshiIbrahim Sange
January 7, 2022
Open Access

Health Status of Patients With β-Thalassemia in the West Bank: A Retrospective-Cohort Study.

Frontiers in Medicine
Reem AldwaikRania Abu Seir
January 7, 2022

Effect of iron overload on endothelial cell calcification and its mechanism.

Annals of Translational Medicine
Lili ZhaoZhigang Guo
January 7, 2022

Brain iron deposition and movement disorders in hereditary haemochromatosis without liver failure: A cross-sectional study.

European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies
Soumya SharmaMandar S Jog

Sign up to follow this feed and discover related papers.

Related Feeds

AAV-based Gene Therapy

Adeno-associated virus (AAV)-based gene therapy is a biological vector that is being researched to be used as a potential therapeutic option. This gene therapy is designed to insert fragments of DNA into targeted cells to help treat diseases, such as hemophilia a. Discover the latest research on AAV-based gene therapy here.

ALS: Genetics

Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. ALS is a genetically heterogeneous disorder with several causative genes. Here are the latest discoveries pertaining to the genetics of this disease.

Acute Myeloid Leukaemia & RNA

Acute myeloid leukaemia (AML) is a common hematological type of cancer. As the population ages, there has been a rise in the frequency of AML. RNA expression has been used to see if there are different genetic profiles that exist within AML and whether these may underpin the variations in survival rates. Here is the latest research on AML and RNA.

Alzheimer's Disease: Genetics

Alzheimer's disease is a neurodegenerative disease. Discover genetic and epigenetic aspects of Alzheimer’s disease, including genetic markers and genomic structural variations with this feed.

Antisense Oligonucleotide Therapies: ND

Antisense oligonucleotides are synthetic DNA oligomers that hybridize to a target RNA. This feed focuses on antisense oligonucleotide therapies such as Inotersen, Nusinursen, and Patisiran, in neurodegenerative diseases.

Antisense Oligonucleotides: ND

This feed focuses on antisense oligonucleotide therapies such as Inotersen, Nusinursen, and Patisiran, in neurodegenerative diseases including amyotrophic lateral sclerosis.

Birth Defects

Birth defects encompass structural and functional alterations that occur during embryonic or fetal development and are present since birth. The cause may be genetic, environmental or unknown and can result in physical and/or mental impairment. Here is the latest research on birth defects.

Breast Cancer: Risk Factors

Breast cancer is a multifactorial disease that is influenced by both environmental and genetic factors. Discover the latest research on the environmental and genetic risk factors for breast cancer here.

CREs: Gene & Cell Therapy

Gene and cell therapy advances have shown promising outcomes for several diseases. The role of cis-regulatory elements (CREs) is crucial in the design of gene therapy vectors. Here is the latest research on CREs in gene and cell therapy.

Cell-Type-Specific Viral Vectors

Viral vectors are used in biological research and therapy to deliver genetic material into cells. However, the efficiency of viral vectors varies depending on the cell type. Here is the latest research on cell-type-specific viral vectors.

© 2022 Meta ULC. All rights reserved
/feed-previews/hemochromatosis/686ee11d-9259-421a-8fe8-735b618e1f7e