{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,25]],"date-time":"2026-03-25T14:10:09Z","timestamp":1774447809280,"version":"3.50.1"},"reference-count":19,"publisher":"Elsevier BV","issue":"8","license":[{"start":{"date-parts":[[2002,8,1]],"date-time":"2002-08-01T00:00:00Z","timestamp":1028160000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2002,8,1]],"date-time":"2002-08-01T00:00:00Z","timestamp":1028160000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["ard.eular.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Annals of the Rheumatic Diseases"],"published-print":{"date-parts":[[2002,8]]},"DOI":"10.1136\/ard.61.8.745","type":"journal-article","created":{"date-parts":[[2002,7,28]],"date-time":"2002-07-28T23:08:40Z","timestamp":1027897720000},"page":"745-747","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":31,"title":["Genetic testing for haemochromatosis in patients with chondrocalcinosis"],"prefix":"10.1016","volume":"61","author":[{"given":"A E","family":"Timms","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R","family":"Sathananthan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L","family":"Bradbury","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N A","family":"Athanasou","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M A","family":"Brown","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1136\/ard.61.8.745_bib1","doi-asserted-by":"crossref","first-page":"1355","DOI":"10.1056\/NEJM198805263182103","article-title":"Prevalence of hemochromatosis among 11 065 presumably healthy blood donors","volume":"318","author":"Edwards","year":"1988","journal-title":"N Engl J Med"},{"key":"10.1136\/ard.61.8.745_bib2","doi-asserted-by":"crossref","first-page":"1388","DOI":"10.1086\/302379","article-title":"Juvenile hemochromatosis locus maps to chromosome 1q","volume":"64","author":"Roetto","year":"1999","journal-title":"Am J Hum Genet"},{"key":"10.1136\/ard.61.8.745_bib3","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1038\/75534","article-title":"The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22","volume":"25","author":"Camaschella","year":"2000","journal-title":"Nat Genet"},{"key":"10.1136\/ard.61.8.745_bib4","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1038\/90038","article-title":"A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis","volume":"28","author":"Njajou","year":"2001","journal-title":"Nat Genet"},{"key":"10.1136\/ard.61.8.745_bib5","doi-asserted-by":"crossref","first-page":"191","DOI":"10.1086\/321261","article-title":"A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload","volume":"69","author":"Kato","year":"2001","journal-title":"Am J Hum Genet"},{"key":"10.1136\/ard.61.8.745_bib6","doi-asserted-by":"crossref","first-page":"399","DOI":"10.1038\/ng0896-399","article-title":"A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis","volume":"13","author":"Feder","year":"1996","journal-title":"Nat Genet"},{"key":"10.1136\/ard.61.8.745_bib7","doi-asserted-by":"crossref","first-page":"14025","DOI":"10.1074\/jbc.272.22.14025","article-title":"The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression","volume":"272","author":"Feder","year":"1997","journal-title":"J Biol Chem"},{"key":"10.1136\/ard.61.8.745_bib8","doi-asserted-by":"crossref","first-page":"375","DOI":"10.1038\/ng1297-375","article-title":"Haemochromatosis, HFE and genetic complexity","volume":"17","author":"Risch","year":"1997","journal-title":"Nat Genet"},{"key":"10.1136\/ard.61.8.745_bib9","doi-asserted-by":"crossref","first-page":"1327","DOI":"10.1056\/NEJM199705013361817","article-title":"Mutations of the hereditary hemochromatosis candidate gene HLA-H in porphyria cutanea tarda","volume":"336","author":"Santos","year":"1997","journal-title":"N Engl J Med"},{"key":"10.1136\/ard.61.8.745_bib10","doi-asserted-by":"crossref","first-page":"739","DOI":"10.1016\/S0021-9150(00)00623-7","article-title":"A prospective study of coronary heart disease and the hemochromatosis gene (HFE) C282Y mutation: the atherosclerosis risk in communities (ARIC) study","volume":"154","author":"Rasmussen","year":"2001","journal-title":"Atherosclerosis"},{"key":"10.1136\/ard.61.8.745_bib11","doi-asserted-by":"crossref","first-page":"170","DOI":"10.1067\/mlc.2000.104464","article-title":"Prevalence of HFE (hemochromatosis gene) mutations in unselected male patients with type 2 diabetes","volume":"135","author":"Sampson","year":"2000","journal-title":"J Lab Clin Med"},{"key":"10.1136\/ard.61.8.745_bib12","doi-asserted-by":"crossref","first-page":"188","DOI":"10.1016\/0049-0172(92)90019-A","article-title":"Diseases associated with calcium pyrophosphate deposition disease","volume":"22","author":"Jones","year":"1992","journal-title":"Semin Arthritis Rheum"},{"key":"10.1136\/ard.61.8.745_bib13","doi-asserted-by":"crossref","first-page":"566","DOI":"10.1136\/gut.42.4.566","article-title":"A rapid method of haplotyping HFE mutations and linkage disequilibrium in a Caucasoid population","volume":"42","author":"Mullighan","year":"1998","journal-title":"Gut"},{"key":"10.1136\/ard.61.8.745_bib14","doi-asserted-by":"crossref","first-page":"325","DOI":"10.1038\/11892","article-title":"Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis","volume":"22","author":"Jeffrey","year":"1999","journal-title":"Nat Genet"},{"key":"10.1136\/ard.61.8.745_bib15","doi-asserted-by":"crossref","first-page":"718","DOI":"10.1056\/NEJM199909023411002","article-title":"A population-based study of the clinical expression of the hemochromatosis gene","volume":"341","author":"Olynyk","year":"1999","journal-title":"N Engl J Med"},{"key":"10.1136\/ard.61.8.745_bib16","doi-asserted-by":"crossref","first-page":"160","DOI":"10.1111\/j.1399-0039.1983.tb01183.x","article-title":"Estimating genotype relative risks","volume":"22","author":"Lathrop","year":"1983","journal-title":"Tissue Antigens"},{"key":"10.1136\/ard.61.8.745_bib17","first-page":"71","article-title":"Chondrocalcinosis and arthropathy: studies in haemochromatosis and in idiopathic chondrocalcinosis","volume":"39","author":"Atkins","year":"1970","journal-title":"Q J Med"},{"key":"10.1136\/ard.61.8.745_bib18","doi-asserted-by":"crossref","first-page":"317","DOI":"10.1007\/BF02054248","article-title":"The arthritis of hemochromatosis. A review of 25 cases with special reference to chondrocalcinosis, and a comparison with patients with primary hyperparathyroidism and controls","volume":"5","author":"Huaux","year":"1986","journal-title":"Clin Rheumatol"},{"key":"10.1136\/ard.61.8.745_bib19","doi-asserted-by":"crossref","first-page":"769","DOI":"10.1001\/archinte.1994.00420070087010","article-title":"Cost-effectiveness of screening for hereditary hemochromatosis","volume":"154","author":"Phatak","year":"1994","journal-title":"Arch Intern Med"}],"container-title":["Annals of the Rheumatic Diseases"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S000349672409280X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S000349672409280X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/ard.61.8.745","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,1,21]],"date-time":"2025-01-21T07:49:16Z","timestamp":1737445756000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S000349672409280X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2002,8]]},"references-count":19,"journal-issue":{"issue":"8","published-print":{"date-parts":[[2002,8]]}},"alternative-id":["S000349672409280X"],"URL":"https:\/\/doi.org\/10.1136\/ard.61.8.745","relation":{},"ISSN":["0003-4967"],"issn-type":[{"value":"0003-4967","type":"print"}],"subject":[],"published":{"date-parts":[[2002,8]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Genetic testing for haemochromatosis in patients with chondrocalcinosis","name":"articletitle","label":"Article Title"},{"value":"Annals of the Rheumatic Diseases","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1136\/ard.61.8.745","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2002 Copyright 2002 by Annals of the Rheumatic Diseases, Published by Elsevier Inc. Published by Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.","name":"copyright","label":"Copyright"}]}}