出版事項（掲載誌）The Japanese Society of Internal Medicine
DOI10.2169/internalmedicine.55.6565
参照The mechanisms of systemic iron homeostasis and etiology, diagnosis, and treatment of hereditary hemochromatosis
Long-term phlebotomy successfully alleviated hepatic iron accumulation in a ferroportin disease patient with a mutation in SLC40A1: a case report
参照Non-<i>HFE</i>Hepatic Iron Overload
Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload
A Mutation, in the Iron-Responsive Element of H Ferritin mRNA, Causing Autosomal Dominant Iron Overload
Hereditary hemochromatosis is characterized by a clinically definable arthropathy that correlates with iron load
Lens Opacities in Thalassemia
Ferroportin-mediated mobilization of ferritin iron precedes ferritin degradation by the proteasome
Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders
Hepcidin Regulates Cellular Iron Efflux by Binding to Ferroportin and Inducing Its Internalization
Global Sequencing Approach for Characterizing the Molecular Background of Hereditary Iron Disorders
The ferritins: molecular properties, iron storage function and cellular regulation
Comprehensive Mutational Screening in a Cohort of Danish Families with Hereditary Congenital Cataract
Identification of Mutations in SLC40A1 That Affect Ferroportin Function and Phenotype of Human Ferroportin Iron Overload
Sex and Acquired Cofactors Determine Phenotypes of Ferroportin Disease
Ferritin functions as a proinflammatory cytokine via iron‐independent protein kinase C zeta/nuclear factor kappaB–regulated signaling in rat hepatic stellate cells†
Hereditary hyperferritinaemia cataract syndrome
Development of lens opacities with peculiar characteristics in patients affected by thalassemia major on chelating treatment with deferasirox (ICL670) at the Pediatric Clinic in Monza, Italy
Hemochromatosis with Mutation of the Ferroportin 1 (IREG1) Gene
A Japanese Family with Ferroportin Disease Caused by a Novel Mutation of SLC40A1 Gene: Hyperferritinemia Associated with a Relatively Low Transferrin Saturation of Iron
連携機関・データベース国立情報学研究所 : CiNii Research