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Outward- and inward-facing structures of a putative bacterial transition-metal transporter with homology to ferroportin.Distribution of manganese and other biometals in flatiron miceIron-regulatory gene expression during liver regenerationHuman macrophage ferroportin biology and the basis for the ferroportin disease.Deletion of hemojuvelin, an iron-regulatory protein, in mice results in abnormal angiogenesis and vasculogenesis in retina along with reactive gliosis.Novel bioimaging techniques of metals by laser ablation inductively coupled plasma mass spectrometry for diagnosis of fibrotic and cirrhotic liver disorders.Molecular diagnosis of hemochromatosis.Regulation of the cholesterol efflux transporters ABCA1 and ABCG1 in retina in hemochromatosis and by the endogenous siderophore 2,5-dihydroxybenzoic acid.Examining the clinical use of hemochromatosis genetic testing.Naotaifang extract treatment results in increased ferroportin expression in the hippocampus of rats subjected to cerebral ischemia.Ferroportin deficiency impairs manganese metabolism in flatiron mice.Oral iron prophylaxis in pregnancy: not too little and not too much!CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients.Disrupted iron homeostasis causes dopaminergic neurodegeneration in mice.A late presentation of a fatal disease: juvenile hemochromatosis.Telomere length and elevated iron: the influence of phenotype and HFE genotypeIron metabolism: interactions with normal and disordered erythropoiesisNeuroimaging, nutrition, and iron-related genes.Diagnosis and treatment of hereditary hemochromatosis: an update.Application of Modified Spin-Echo-based Sequences for Hepatic MR Elastography: Evaluation, Comparison with the Conventional Gradient-Echo Sequence, and Preliminary Clinical Experience.Clinical evaluation of a hemochromatosis next-generation sequencing gene panel.Bone morphogenetic protein-binding endothelial regulator of liver sinusoidal endothelial cells induces iron overload in a fatty liver mouse model.Ferroportin-related haemochromatosis associated with novel Y64H mutation of the SCL40A1 gene.A novel mutation in the SLC40A1 gene associated with reduced iron export in vitro.Ferroportin disease: pathogenesis, diagnosis and treatment.Iron status in pregnant women and women of reproductive age in Europe.Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.Iron refractory iron deficiency anemia: a heterogeneous disease that is not always iron refractory.Causes of iron overload in blood donors - a clinical study.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Non-HFE hepatic iron overload.
@en
Non-HFE hepatic iron overload.
@nl
type
label
Non-HFE hepatic iron overload.
@en
Non-HFE hepatic iron overload.
@nl
prefLabel
Non-HFE hepatic iron overload.
@en
Non-HFE hepatic iron overload.
@nl
P2093
P356
P1476
Non-HFE hepatic iron overload.
@en
P2093
Angela Caleffi
Antonello Pietrangelo
Elena Corradini
P304
P356
10.1055/S-0031-1286061
P577
2011-08-01T00:00:00Z