[Hereditary hemochromatosis: physiopathological, clinical and therapeutical considerations]

scientific article published on 01 February 2002

[Hereditary hemochromatosis: physiopathological, clinical and therapeutical considerations] is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.1016/S0025-7753(02)72299-9
P698PubMed publication ID11825553

P2093author name stringFernando Pérez-Aguilar
P2860cites workPrevalence of Hemochromatosis among 11,065 Presumably Healthy Blood DonorsQ68352478
Prevalence of genetic haemochromatosis among diabetic patientsQ69372230
Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosisQ69995807
Hepatic iron overload: paramagnetic pathologyQ70137185
Long-term survival in patients with hereditary hemochromatosisQ71035591
HEMOCHROMATOSIS AND ARTHRITISQ76716647
Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosisQ77350070
Molecular medicine and hemochromatosis: at the crossroadsQ77738423
Waiting for frataxinQ93899465
A novel mammalian iron-regulated protein involved in intracellular iron metabolismQ22253435
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosisQ24310146
The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expressionQ24323216
A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulationQ28140006
Disorders of iron metabolismQ28141020
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporterQ28145559
Cloning and characterization of a mammalian proton-coupled metal-ion transporterQ28245045
Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouseQ28297185
Haemochromatosis in the new millennium.Q33870226
A population-based study of the clinical expression of the hemochromatosis geneQ33872904
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.Q33901224
Coordinate post-transcriptional regulation of ferritin and transferrin receptor expression: the role of regulated RNA-protein interactionQ37845182
Characterization and partial purification of a ferrireductase from human duodenal microvillus membranesQ41772474
Estimation of available dietary ironQ41981809
Expression of the duodenal iron transporters divalent-metal transporter 1 and ferroportin 1 in iron deficiency and iron overloadQ43582807
Primary liver cancer in genetic hemochromatosis: a clinical, pathological, and pathogenetic study of 54 casesQ50128215
Distribution of transferrin saturation in an Australian population: relevance to the early diagnosis of hemochromatosis.Q51571372
Intestinal iron uptake determined by divalent metal transporter is enhanced in HFE-deficient mice with hemochromatosis.Q52542851
P433issue3
P304page(s)103-110
P577publication date2002-02-01
P1433published inMedicina clínicaQ26854009
P1476title[Hereditary hemochromatosis: physiopathological, clinical and therapeutical considerations]
P478volume118

Reverse relations

cites work (P2860)
Q45151263Study of patients referred for elevated ferritin levels and/or transferrin saturation: significance of non-alcoholic fatty liver disease
Q78593736[Ceruloplasmine and iron metabolism: their implications in hemochromatosis, Wilson's disease and aceruloplasminemia]
Q73466414[Iron overload. More than hereditary hemochromatosis]

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