{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,4]],"date-time":"2022-04-04T13:45:15Z","timestamp":1649079915137},"reference-count":13,"publisher":"Elsevier BV","issue":"7","license":[{"start":{"date-parts":[[2014,7,1]],"date-time":"2014-07-01T00:00:00Z","timestamp":1404172800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.fr","em-consulte.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Archives de P\u00e9diatrie"],"published-print":{"date-parts":[[2014,7]]},"DOI":"10.1016\/j.arcped.2014.04.024","type":"journal-article","created":{"date-parts":[[2014,6,13]],"date-time":"2014-06-13T18:15:27Z","timestamp":1402683327000},"page":"765-767","update-policy":"http:\/\/dx.doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"title":["Le syndrome d\u2019hyper-immunoglobulines D (HIGDS) avec fi\u00e8vre p\u00e9riodique. \u00c0 propos de deux observations"],"prefix":"10.1016","volume":"21","author":[{"given":"K.-P.","family":"Agbo-kpati","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Condor","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Hollenberg","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Chalvon Demersay","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Cuisset","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.","family":"Quartier","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.arcped.2014.04.024_bib0005","doi-asserted-by":"crossref","first-page":"178","DOI":"10.1038\/9696","article-title":"Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group","volume":"22","author":"Drenth","year":"1999","journal-title":"Nat Genet"},{"key":"10.1016\/j.arcped.2014.04.024_bib0010","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1038\/9691","article-title":"Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome","volume":"22","author":"Houten","year":"1999","journal-title":"Nat Genet"},{"key":"10.1016\/j.arcped.2014.04.024_bib0015","first-page":"163","article-title":"Aspect nosologique des formes syst\u00e9mique d\u2019arthrite juv\u00e9nile \u00e0 d\u00e9but tr\u00e8s pr\u00e9coce. \u00c0 propos de dix-sept observations","volume":"60","author":"Prieur","year":"1984","journal-title":"Sem Hop"},{"key":"10.1016\/j.arcped.2014.04.024_bib0020","doi-asserted-by":"crossref","first-page":"1087","DOI":"10.1016\/S0140-6736(84)92505-4","article-title":"Hyperimmunoglobulinaemia D and periodic fever: a new syndrome","volume":"1","author":"van der Meer","year":"1984","journal-title":"Lancet"},{"key":"10.1016\/j.arcped.2014.04.024_bib0025","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1097\/MD.0b013e318190cfb7","article-title":"Long-term follow-up, clinical features and quality of life in a series of 103\u00a0patients with hyperimmunoglobulinemia D syndrome","volume":"87","author":"van der Hilst","year":"2008","journal-title":"Medicine (Baltimore)"},{"key":"10.1016\/j.arcped.2014.04.024_bib0030","doi-asserted-by":"crossref","first-page":"e152","DOI":"10.1542\/peds.2010-3639","article-title":"Mevalonate kinase deficiency: a survey of 50\u00a0patients","volume":"128","author":"Bader-Meunier","year":"2011","journal-title":"Pediatrics"},{"key":"10.1016\/j.arcped.2014.04.024_bib0035","doi-asserted-by":"crossref","first-page":"260","DOI":"10.1038\/sj.ejhg.5200614","article-title":"Molecular analysis of MVK mutations and enzymatic activity in hyper-IgD and periodic fever syndrome","volume":"9","author":"Cuisset","year":"2001","journal-title":"Eur J Hum Genet"},{"key":"10.1016\/j.arcped.2014.04.024_bib0040","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1186\/1750-1172-1-13","article-title":"Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndrome","volume":"1","author":"Haas","year":"2006","journal-title":"Orphanet J Rare Dis"},{"key":"10.1016\/j.arcped.2014.04.024_bib0045","doi-asserted-by":"crossref","first-page":"411","DOI":"10.1023\/A:1010525206818","article-title":"Mevalonate kinase deficiency in a child with periodic fever and without hyperimmunoglobulinaemia D","volume":"24","author":"Di Rocco","year":"2001","journal-title":"J Inherit Metab Dis"},{"key":"10.1016\/j.arcped.2014.04.024_bib0050","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1016\/S0022-3476(03)00212-9","article-title":"Hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) in a child with normal serum IgD, but increased serum IgA concentration","volume":"143","author":"Saulsbury","year":"2003","journal-title":"J Pediatr"},{"key":"10.1016\/j.arcped.2014.04.024_bib0055","doi-asserted-by":"crossref","first-page":"1597","DOI":"10.1093\/rheumatology\/kem200","article-title":"Diagnostic value of serum immunoglobulinaemia D level in patients with a clinical suspicion of hyper-IgD syndrome","volume":"46","author":"Ammouri","year":"2007","journal-title":"Rheumatology (Oxford)"},{"key":"10.1016\/j.arcped.2014.04.024_bib0060","doi-asserted-by":"crossref","first-page":"1855","DOI":"10.1093\/rheumatology\/kes097","article-title":"Efficacy of interleukin-1-targeting drugs in mevalonate kinase deficiency","volume":"51","author":"Galeotti","year":"2012","journal-title":"Rheumatology (Oxford)"},{"key":"10.1016\/j.arcped.2014.04.024_bib0065","doi-asserted-by":"crossref","first-page":"2700","DOI":"10.1056\/NEJMoa070715","article-title":"Allogeneic bone marrow transplantation in mevalonic aciduria","volume":"356","author":"Neven","year":"2007","journal-title":"N Engl J Med"}],"container-title":["Archives de P\u00e9diatrie"],"original-title":[],"language":"fr","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0929693X14001791?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0929693X14001791?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,10,3]],"date-time":"2018-10-03T11:52:31Z","timestamp":1538567551000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0929693X14001791"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,7]]},"references-count":13,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2014,7]]}},"alternative-id":["S0929693X14001791"],"URL":"https:\/\/doi.org\/10.1016\/j.arcped.2014.04.024","relation":{},"ISSN":["0929-693X"],"issn-type":[{"value":"0929-693X","type":"print"}],"subject":[],"published":{"date-parts":[[2014,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Le syndrome d\u2019hyper-immunoglobulines D (HIGDS) avec fi\u00e8vre p\u00e9riodique. \u00c0 propos de deux observations","name":"articletitle","label":"Article Title"},{"value":"Archives de P\u00e9diatrie","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.arcped.2014.04.024","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2014 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}