{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,26]],"date-time":"2026-03-26T16:27:56Z","timestamp":1774542476610,"version":"3.50.1"},"reference-count":10,"publisher":"Codon Publications","issue":"3","license":[{"start":{"date-parts":[[2016,5,1]],"date-time":"2016-05-01T00:00:00Z","timestamp":1462060800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","elsevier.es","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Allergologia et Immunopathologia"],"published-print":{"date-parts":[[2016,5]]},"DOI":"10.1016\/j.aller.2015.07.007","type":"journal-article","created":{"date-parts":[[2016,3,3]],"date-time":"2016-03-03T06:51:40Z","timestamp":1456987900000},"page":"257-262","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":7,"title":["Humoral deficiency in three paediatric patients with genetic diseases"],"prefix":"10.15586","volume":"44","author":[{"given":"K.","family":"Calvo Campoverde","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Gean","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Piquer Gibert","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Martinez Valdez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Dey\u00e0-Mart\u00ednez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Rojas Volquez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Esteve-Sole","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Juan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.M.","family":"Plaza","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Alsina","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"6228","reference":[{"key":"10.1016\/j.aller.2015.07.007_bib0055","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1182\/blood-2007-06-091744","article-title":"The EUROclass trial: defining subgroups in common variable immunodeficiency","volume":"111","author":"Wher","year":"2008","journal-title":"Blood"},{"key":"10.1016\/j.aller.2015.07.007_bib0060","doi-asserted-by":"crossref","first-page":"190","DOI":"10.1006\/clim.1999.4799","article-title":"Diagnostic criteria for primary immunodeficiencies","volume":"93","author":"Conley","year":"1999","journal-title":"Clin Immunol"},{"key":"10.1016\/j.aller.2015.07.007_bib0065","series-title":"ESID Registry \u2013 Working definitions for clinical diagnosis of PID","author":"European Society for Immunodeficiencies","year":"2014"},{"key":"10.1016\/j.aller.2015.07.007_bib0070","doi-asserted-by":"crossref","first-page":"1651","DOI":"10.1016\/j.jaci.2014.02.034","article-title":"Early-onset inflammatory bowel disease and common variable immunodeficiency-like disease caused by IL-21 deficiency","volume":"133","author":"Salzer","year":"2014","journal-title":"J Allergy Clin Immun"},{"key":"10.1016\/j.aller.2015.07.007_bib0075","doi-asserted-by":"crossref","first-page":"452","DOI":"10.1016\/j.anai.2014.04.024","article-title":"Pulmonary radiologic findings in common variable immunodeficiency: clinical and immunological correlations","volume":"113","author":"Maglione","year":"2014","journal-title":"Ann Allergy Asthma Immunol"},{"key":"10.1016\/j.aller.2015.07.007_bib0080","doi-asserted-by":"crossref","first-page":"587","DOI":"10.1080\/714037692","article-title":"Syndromic Immunodeficiencies: genetic syndromes associated with immune abnormalities","volume":"40","author":"Ming","year":"2003","journal-title":"Crit Rev Clin Lab Sci"},{"key":"10.1016\/j.aller.2015.07.007_bib0085","doi-asserted-by":"crossref","first-page":"278","DOI":"10.1002\/ajmg.a.30722","article-title":"Immune abnormalities are a frequent manifestation of Kabuki syndrome","volume":"135A","author":"Hoffman","year":"2005","journal-title":"Am J Med Genet"},{"issue":"Suppl. 1","key":"10.1016\/j.aller.2015.07.007_bib0090","first-page":"S329","article-title":"Lymphoid interstitial pneumonia and Kabuki-syndrome in a young man","volume":"7","author":"Zimmermann","year":"2006","journal-title":"Paediatr Respir Rev"},{"key":"10.1016\/j.aller.2015.07.007_bib0095","doi-asserted-by":"crossref","first-page":"38","DOI":"10.1002\/ajmg.a.30774","article-title":"Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter","volume":"136A","author":"Archer","year":"2005","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.aller.2015.07.007_bib0100","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1016\/S1059-1311(03)00086-4","article-title":"Carbamazepine-induced IgG1 and IgG2 deficiency associated with B cell maturation defect","volume":"13","author":"Go","year":"2004","journal-title":"Seizure"}],"container-title":["Allergologia et Immunopathologia"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0301054616000021?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0301054616000021?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2020,12,31]],"date-time":"2020-12-31T22:50:30Z","timestamp":1609455030000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0301054616000021"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,5]]},"references-count":10,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2016,5]]}},"alternative-id":["S0301054616000021"],"URL":"https:\/\/doi.org\/10.1016\/j.aller.2015.07.007","relation":{},"ISSN":["0301-0546"],"issn-type":[{"value":"0301-0546","type":"print"}],"subject":[],"published":{"date-parts":[[2016,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Humoral deficiency in three paediatric patients with genetic diseases","name":"articletitle","label":"Article Title"},{"value":"Allergologia et Immunopathologia","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.aller.2015.07.007","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2016 SEICAP. Published by Elsevier Espa\u00f1a, S.L.U. All rights reserved.","name":"copyright","label":"Copyright"}]}}