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Unsolved problems in hemochromatosisCROSBY, W. H.Annals of the New York Academy of Sciences. 1988, Vol 526, pp 323-327, issn 0077-8923Conference Paper

Manifestations articulaires de l'hémocromatose. Revue de la littérature à propos de deux cas avec manifestations articulaires révélatrices = Arthropathies of hemochromatosis. Review of literature about two cases with revealing arthropathiesCLERC, D; SALLIERE, D; MEDICIS, P et al.Rhumatologie (Aix-les-Bains). 1984, Vol 36, Num 4, pp 95-102, issn 0249-7581Article

Arthropathie bei idiopathischer Hämochromatose = Arthropathie dans l'hémochromatose idiopathique = Arthropathy in idiopathic hemochromatosisZOGG, T; FUCHS, W; KISSLING, R et al.Zeitschrift für Orthopädie und ihre Grenzgebiete. 1987, Vol 125, Num 2, pp 206-208, issn 0044-3220Article

L'arthropathie dans l'hémochromatose idiopathique = Joint disease in idiopathic hemochromatosisURBINA, B; DE MIGUEL MENDIETA, E; GIJON BANOS, J et al.Revue du rhumatisme et des maladies ostéo-articulaires. 1983, Vol 50, Num 8-9, pp 585-587, issn 0035-2659Article

Juvenile idiopathic haemochromatosis: a life-threatening disorder presenting as hypogonadotropic hypogonadismCAZZOLA, M; ASCARI, E; BAROSI, G et al.Human genetics. 1983, Vol 65, Num 2, pp 149-154, issn 0340-6717Article

Arthritis in hereditary hemochromatosisMATHEWS, J. L; WILLIAMS, H. J.Arthritis and rheumatism. 1987, Vol 30, Num 10, pp 1137-1141, issn 0004-3591Article

Expression of the hemochromatosis (HFE) gene modulates the cellular uptake of ⁶⁷GaCHITAMBAR, Christopher R; WERELEY, Janine P.The Journal of nuclear medicine (1978). 2003, Vol 44, Num 6, pp 943-946, issn 0161-5505, 4 p.Article

Comment interprétez-vous ce cas anatamo-clinique? = Anatomo-clinical interpretation of a histologic sectionBROUSSE, N; HENIN, D.Concours médical (Paris). 1984, Vol 106, Num 14, pp 1233-1234, issn 0010-5309Article

An HLA-all association with the hemochromatosis allele?LE MIGNON, L; SIMON, M; FAUCHET, R et al.Clinical genetics. 1983, Vol 24, Num 3, pp 171-176, issn 0009-9163Article

The Southern French registry of genetic hemochromatosis: a tool for determining clinical prevalence of the disorder and genotype penetranceAGUILAR-MARTINEZ, Patricia; BISMUTH, Michael; LARREY, Dominique et al.Haematologica (Roma). 2010, Vol 95, Num 4, pp 551-556, issn 0390-6078, 6 p.Article

Association of hemochromatosis with infectious diseases : expanding spectrumKHAN, Fida A; FISHER, Melanie A; KHAKOO, Rashida A et al.International journal of infectious diseases. 2007, Vol 11, Num 6, pp 482-487, issn 1201-9712, 6 p.Article

Les hémochromatoses héréditaires : partie II. L'hémochromatose héréditaire liée au HFE (HFE1) = Hereditary hemochromatosis: part II - HFE hemochromatosisBOUIZEGARENE, P; COULHON, M.-P; DEYBACH, J.-C et al.Immuno analyse & biologie spécialisée. 2006, Vol 21, Num 3, pp 128-137, issn 0923-2532, 10 p.Article

Iron overload in HFE C282Y heterozygotes at first genetic testing: a strategy for identifying rare HFE variantsAGUILAR-MARTINEZ, Patricia; GRANDCHAMP, Bernard; CUNAT, Séverine et al.Haematologica (Roma). 2011, Vol 96, Num 4, pp 507-514, issn 0390-6078, 8 p.Article

Iron-Overload-Related Disease in HFE Hereditary HemochromatosisALIEN, Katrina J; GURRIN, Lyle C; ANDERSON, Gregory J et al.The New England journal of medicine. 2008, Vol 358, Num 3, pp 221-230, issn 0028-4793, 10 p.Article

Physiopathologie et génétique de l'hémochromatose HFE de type 1 = Pathophysiology and genetics of classic HFE (type 1) hemochromatosisLOREAL, Olivier; ROPERT, Martine; MOSSER, Annick et al.La Presse médicale (1983). 2007, Vol 36, Num 9, pp 1271-1277, issn 0755-4982, 7 p., CAH2Article

Pathways for the regulation of body iron homeostasis in response to experimental iron overloadTHEURL, Igor; LUDWICZEK, Susanne; ELLER, Philipp et al.Journal of hepatology. 2005, Vol 43, Num 4, pp 711-719, issn 0168-8278, 9 p.Article

Hepcidin assay in serum by SELDI-TOF-MS and other approachesCASTAGNA, Annalisa; CAMPOSTRINI, Natascia; ZANINOTTO, Federica et al.Journal of proteomics (Print). 2010, Vol 73, Num 3, pp 527-536, issn 1874-3919, 10 p.Article

Blunted hepcidin response to oral iron challenge in HFE-related hemochromatosisPIPERNO, Alberto; GIRELLI, Domenico; NEMETH, Elizabeta et al.Blood. 2007, Vol 110, Num 12, pp 4096-4100, issn 0006-4971, 5 p.Article

Hemojuvelin N-terminal mutants reach the plasma membrane but do not activate the hepcidin responsePAGANI, Alessia; SILVESTRI, Laura; NAI, Antonella et al.Haematologica (Roma). 2008, Vol 93, Num 10, pp 1466-1472, issn 0390-6078, 7 p.Article

Hemojuvelin (HJV)-associated hemochromatosis: analysis of HJV and HFE mutations and iron overload in three familiesWALLACE, Daniel F; DIXON, Jeannette L; RAMM, Grant A et al.Haematologica (Roma). 2005, Vol 90, Num 2, pp 254-255, issn 0390-6078, 2 p.Article

Significance of H63D homozygosity in a Basque population with hemochroniatosisCASTIELLA, Agustin; ZAPTA, Eva; DE JUAN, Maria Dolores et al.Journal of gastroenterology and hepatology. 2010, Vol 25, Num 7, pp 1295-1298, issn 0815-9319, 4 p.Article

Anemia of inflammation: the hepcidin link : Erythroid system and its diseasesROY, Cindy N; ANDREWS, Nancy C.Current opinion in hematology. 2005, Vol 12, Num 2, pp 107-111, issn 1065-6251, 5 p.Article

A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosisDELATYCKI, M. B; ALLEN, K. J; GOW, P et al.Clinical genetics. 2004, Vol 65, Num 5, pp 378-383, issn 0009-9163, 6 p.Article

The hemochromatosis proteins HFE, TfR2, and HJV form a membrane-associated protein complex for hepcidin regulationD'ALESSIO, Flavia; HENTZE, Matthias W; MUCKENTHALER, Martina U et al.Journal of hepatology. 2012, Vol 57, Num 5, pp 1052-1060, issn 0168-8278, 9 p.Article