{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,31]],"date-time":"2026-03-31T16:46:08Z","timestamp":1774975568566,"version":"3.50.1"},"reference-count":13,"publisher":"Elsevier BV","issue":"6","license":[{"start":{"date-parts":[[2020,12,1]],"date-time":"2020-12-01T00:00:00Z","timestamp":1606780800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,12,1]],"date-time":"2020-12-01T00:00:00Z","timestamp":1606780800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2021,12,8]],"date-time":"2021-12-08T00:00:00Z","timestamp":1638921600000},"content-version":"am","delay-in-days":372,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Seminars in Arthritis and Rheumatism"],"published-print":{"date-parts":[[2020,12]]},"DOI":"10.1016\/j.semarthrit.2020.03.005","type":"journal-article","created":{"date-parts":[[2020,3,19]],"date-time":"2020-03-19T03:11:34Z","timestamp":1584587494000},"page":"1370-1373","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":23,"title":["AA amyloidosis revealing mevalonate kinase deficiency: A report of 20 cases including two new French cases and a comprehensive review of literature"],"prefix":"10.1016","volume":"50","author":[{"given":"Fran\u00e7ois","family":"Rodrigues","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jean-Baptiste","family":"Philit","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Irina","family":"Giurgea","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dany","family":"Anglicheau","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jean-Jacques","family":"Roux","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nadia","family":"Hoyeau","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gilles","family":"Grateau","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Laurence","family":"Cuisset","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sophie","family":"Georgin-Lavialle","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.semarthrit.2020.03.005_bib0001","doi-asserted-by":"crossref","first-page":"101","DOI":"10.2147\/TACG.S93933","article-title":"Mevalonate kinase deficiency: current perspectives","volume":"9","author":"Schulert","year":"2016","journal-title":"Appl Clin Genet"},{"issue":"9","key":"10.1016\/j.semarthrit.2020.03.005_bib0002","doi-asserted-by":"crossref","first-page":"2966","DOI":"10.1002\/art.20490","article-title":"First report of systemic reactive (AA) amyloidosis in a patient with the hyperimmunoglobulinemia D with periodic fever syndrome","volume":"50","author":"Obici","year":"2004","journal-title":"Arthritis Rheum"},{"issue":"6","key":"10.1016\/j.semarthrit.2020.03.005_bib0003","first-page":"865","article-title":"Renal amyloidosis due to hyper-IgD syndrome","volume":"32","author":"Li Cavoli","year":"2012","journal-title":"Nefrologia"},{"issue":"4","key":"10.1016\/j.semarthrit.2020.03.005_bib0004","doi-asserted-by":"crossref","first-page":"1116","DOI":"10.1002\/art.37827","article-title":"AA amyloidosis complicating the hereditary periodic fever syndromes","volume":"65","author":"Lane","year":"2013","journal-title":"Arthritis Rheum"},{"issue":"Suppl 1","key":"10.1016\/j.semarthrit.2020.03.005_bib0005","doi-asserted-by":"crossref","first-page":"A122","DOI":"10.1186\/1546-0096-11-S1-A122","article-title":"P02-015 - A novel MVK mutation in a child with AA amyloid","volume":"11","author":"Kolsky","year":"2013","journal-title":"Pediatr Rheumatol"},{"issue":"1","key":"10.1016\/j.semarthrit.2020.03.005_bib0006","first-page":"43","article-title":"Amyloid a amyloidosis secondary to hyper IGD syndrome and response to IL-1 blockage therapy","volume":"74","author":"Kallianidis","year":"2016","journal-title":"Neth J Med"},{"issue":"6","key":"10.1016\/j.semarthrit.2020.03.005_bib0007","doi-asserted-by":"crossref","first-page":"2010","DOI":"10.1002\/art.21901","article-title":"AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: a report of two cases","volume":"54","author":"Lachmann","year":"2006","journal-title":"Arthritis Rheum"},{"key":"10.1016\/j.semarthrit.2020.03.005_bib0008","series-title":"Poster session presented at: 9th International Congress of Familial and Mediterranean Fever and Systemic Auto-Inflammatory Diseases (ISSAID 2017)","article-title":"Two cases of AA amyloidosis complication hyper-IGD and periodic fever syndrome (HIDS) diagnosed at the UK national amyloidosis centre","author":"Rowczenio","year":"2017"},{"issue":"6","key":"10.1016\/j.semarthrit.2020.03.005_bib0009","doi-asserted-by":"crossref","first-page":"610","DOI":"10.1007\/BF02238553","article-title":"Atypical hypergammaglobulinaemia D syndrome with amyloidosis: an overlap with familial Mediterranean fever?","volume":"15","author":"Ostuni","year":"1996","journal-title":"Clin Rheumatol"},{"issue":"3","key":"10.1016\/j.semarthrit.2020.03.005_bib0010","doi-asserted-by":"crossref","first-page":"e41","DOI":"10.1053\/j.ajkd.2006.05.027","article-title":"Hereditary periodic fever with systemic amyloidosis: is hyper-IGD syndrome really a benign disease?","volume":"48","author":"Siewert","year":"2006","journal-title":"Am J Kidney Dis"},{"issue":"Suppl 1","key":"10.1016\/j.semarthrit.2020.03.005_bib0011","doi-asserted-by":"crossref","first-page":"P2","DOI":"10.1186\/1546-0096-9-S1-P2","article-title":"Amyloidosis in a child with hyperimmunoglobulin D syndrome","volume":"9","author":"Dusunsel","year":"2011","journal-title":"Pediatr Rheumatol Online J"},{"issue":"11","key":"10.1016\/j.semarthrit.2020.03.005_bib0012","doi-asserted-by":"crossref","first-page":"2795","DOI":"10.1002\/art.39763","article-title":"The phenotype and genotype of mevalonate kinase deficiency: a series of 114 cases from the eurofever registry: phenotype and genotype of MKD","volume":"68","author":"ter Haar","year":"2016","journal-title":"Arthritis Rheumatol"},{"issue":"9","key":"10.1016\/j.semarthrit.2020.03.005_bib0013","doi-asserted-by":"crossref","first-page":"1636","DOI":"10.1136\/annrheumdis-2015-207546","article-title":"Recommendations for the management of autoinflammatory diseases","volume":"74","author":"ter Haar","year":"2015","journal-title":"Ann Rheum Dis"}],"container-title":["Seminars in Arthritis and Rheumatism"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0049017220300780?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0049017220300780?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,24]],"date-time":"2025-09-24T17:05:49Z","timestamp":1758733549000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0049017220300780"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,12]]},"references-count":13,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2020,12]]}},"alternative-id":["S0049017220300780"],"URL":"https:\/\/doi.org\/10.1016\/j.semarthrit.2020.03.005","relation":{},"ISSN":["0049-0172"],"issn-type":[{"value":"0049-0172","type":"print"}],"subject":[],"published":{"date-parts":[[2020,12]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"AA amyloidosis revealing mevalonate kinase deficiency: A report of 20 cases including two new French cases and a comprehensive review of literature","name":"articletitle","label":"Article Title"},{"value":"Seminars in Arthritis and Rheumatism","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.semarthrit.2020.03.005","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 Published by Elsevier Inc.","name":"copyright","label":"Copyright"}]}}