Results 141 to 150 of about 198,942 (291)
Molecular Genetics & Genomic Medicine, 2015 Hereditary hemochromatosis (HH) type 3 is an autosomal recessive disorder of iron metabolism characterized by excessive iron deposition in the liver and caused by mutations in the transferrin receptor 2 (TFR2) gene.
Ricky S. Joshi +11 more
semanticscholar +1 more source
PLoS ONE, 2019 Hepatic iron overload, a hallmark of hereditary hemochromatosis, triggers progressive liver disease. There is also increasing evidence for a pathogenic role of iron in non-alcoholic fatty liver disease (NAFLD), which may progress to non-alcoholic ...
John Wagner +7 more
doaj +1 more source
Erythrocytapheresis, a treatment modality in hereditary hemochromatosis [PDF]
, 2016 Eva Rombout‐Sestrienkova
openalex +1 more source
Update on Hereditary Hemochromatosis and the HFE Gene [PDF]
, 1999 David J. Brandhagen +3 more
openalex +1 more source
A 1.1-Mb Transcript Map of the Hereditary Hemochromatosis Locus [PDF]
, 1997 David A. Ruddy +18 more
openalex +1 more source
Hereditary Hemochromatosis Type 3, Analysis of M172k Mutational Sequence in A Single Male Patient [PDF]
, 2020 Consuelo Fabi
openalex +1 more source
Tumor Necrosis Factor-α −308G>A Allelic Variant Modulates Iron Accumulation in Patients with Hereditary Hemochromatosis [PDF]
, 2006 Pierre‐Alexandre Krayenbuehl +8 more
openalex +1 more source
The HFE 5569A allele defines a low-risk haplotype for hereditary hemochromatosis [PDF]
, 2000 Martin J. Somerville +4 more
openalex +1 more source
Cognitive event-related potentials in patient with hereditary hemochromatosis: A case report
, 2020 openalex +1 more source
Expression of hepcidin is down-regulated in TfR2 mutant mice manifesting a phenotype of hereditary hemochromatosis [PDF]
, 2004 Hiroshi Kawabata +9 more
openalex +1 more source