Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
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Hemojuvelin and bone morphogenetic protein (BMP) signaling in iron homeostasisExtracellular matrix and liver diseaseNon-HFE hemochromatosisTaurine supplementation reduces oxidative stress and protects the liver in an iron-overload murine model.HFE gene mutation and oxidative damage biomarkers in patients with myelodysplastic syndromes and its relation to transfusional iron overload: an observational cross-sectional studyEvaluation of a high throughput method for the detection of mutations associated with thrombosis and hereditary hemochromatosis in Brazilian blood donors.Exome sequencing for molecular characterization of non-HFE hereditary hemochromatosis.Increased Retinal Expression of the Pro-Angiogenic Receptor GPR91 via BMP6 in a Mouse Model of Juvenile HemochromatosisPersonalized medicine for osteoarthritis: where are we now?Variation in an Iron Metabolism Gene Moderates the Association Between Blood Lead Levels and Attention-Deficit/Hyperactivity Disorder in Children.Out of balance--systemic iron homeostasis in iron-related disordersA late presentation of a fatal disease: juvenile hemochromatosis.Profound morphological changes in the erythrocytes and fibrin networks of patients with hemochromatosis or with hyperferritinemia, and their normalization by iron chelators and other agents.De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis.Iron homeostasis in the liver.Mutations in the HFE gene and sporadic amyotrophic lateral sclerosis risk: a meta-analysis of observational studies.An update on laboratory diagnosis of liver inherited diseases.Genetic diseases that predispose to early liver cirrhosis.Invariant Natural Killer T Cells are Reduced in Hereditary Hemochromatosis Patients.Proteomic analysis and molecular modelling characterize the iron-regulatory protein haemojuvelin/repulsive guidance molecule cFerroportin-related haemochromatosis associated with novel Y64H mutation of the SCL40A1 gene.Design and validation of a colorimetric test for the genetic diagnosis of hemochromatosis using α-phosphorothioate nucleotides.Variables Related to Iron Status and Genetic Background Among Korean Populations: Ironing Out the Differences.Juvenile hemochromatosis: HAMP mutation and severe iron overload treated with phlebotomies and deferasirox.Autopsy relevance determining hemochromatosis: Case report.Quality of life scores differs between genotypic groups of patients with suspected hereditary hemochromatosis.A novel germline PIGA mutation in Ferro-Cerebro-Cutaneous syndrome: a neurodegenerative X-linked epileptic encephalopathy with systemic iron-overload.Personalized lifestyle medicine: relevance for nutrition and lifestyle recommendations
P2860
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P2860
Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
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
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name
Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
@en
Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
@nl
type
label
Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
@en
Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
@nl
prefLabel
Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
@en
Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
@nl
P2860
P921
P356
P1476
Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
@en
P2093
Alexandre C Pereira
Paulo C J L Santos
P2860
P304
P356
10.3390/IJMS13021497
P407
P5008
P577
2012-02-01T00:00:00Z