{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,17]],"date-time":"2026-07-17T16:45:16Z","timestamp":1784306716392,"version":"3.55.0"},"reference-count":23,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2013,5]]},"DOI":"10.1097\/mph.0b013e31828be602","type":"journal-article","created":{"date-parts":[[2013,4,23]],"date-time":"2013-04-23T13:24:02Z","timestamp":1366723442000},"page":"311-314","source":"Crossref","is-referenced-by-count":7,"title":["Transient Effect of Anti-CD20 Therapy in a Child With 22q11.2 Deletion Syndrome and Severe Steroid Refractory Cytopenias"],"prefix":"10.1097","volume":"35","author":[{"given":"Alexandra","family":"Soldatou","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Theodora","family":"Anastassiou","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Olga","family":"Vougiouka","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Evgenios","family":"Goussetis","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lydia","family":"Kossiva","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-14-20210227","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1016\/j.spen.2007.07.005","article-title":"Deletion 22q11: spectrum of associated disorders.","volume":"14","author":"Hay","year":"2007","journal-title":"Semin Pediatr Neurol"},{"key":"R2-14-20210227","doi-asserted-by":"crossref","first-page":"1443","DOI":"10.1016\/S0140-6736(07)61601-8","article-title":"Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes.","volume":"370","author":"Kobrynski","year":"2007","journal-title":"Lancet"},{"key":"R3-14-20210227","doi-asserted-by":"crossref","first-page":"353","DOI":"10.1016\/j.iac.2008.01.003","article-title":"Chromosome 22q11.2 deletion syndrome: DiGeorge syndromevelocardiofacial syndrome.","volume":"28","author":"Sullivan","year":"2008","journal-title":"Immunol Allergy Clin North Am"},{"key":"R4-14-20210227","doi-asserted-by":"crossref","first-page":"505","DOI":"10.1097\/00130832-200412000-00006","article-title":"The clinical, immunological, and molecular spectrum of chromosome 22q11.2 deletion syndrome and DiGeorge syndrome.","volume":"4","author":"Sullivan","year":"2004","journal-title":"Curr Opin Allergy Clin Immunol"},{"key":"R5-14-20210227","doi-asserted-by":"crossref","first-page":"734","DOI":"10.1016\/j.jaci.2004.01.766","article-title":"Complete DiGeorge syndrome: development of rash, lymphadenopathy, and oligoclonal T cells in 5 cases.","volume":"113","author":"Markert","year":"2004","journal-title":"J Allergy Clin Immunol"},{"key":"R6-14-20210227","doi-asserted-by":"crossref","first-page":"422","DOI":"10.1136\/adc.86.6.422","article-title":"Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.","volume":"86","author":"Gennery","year":"2002","journal-title":"Arch Dis Child"},{"key":"R7-14-20210227","doi-asserted-by":"crossref","first-page":"362","DOI":"10.1016\/j.jaci.2008.03.033","article-title":"Immunologic defects in 22q11.2 deletion syndrome.","volume":"122","author":"McLean-Tooke","year":"2008","journal-title":"J Allergy Clin Immunol"},{"key":"R8-14-20210227","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1111\/j.1365-3083.2007.01949.x","article-title":"Immunodeficiency and autoimmunity in 22q11.2 deletion syndrome.","volume":"66","author":"McLean-Tooke","year":"2007","journal-title":"Scand J Immunol"},{"key":"R9-14-20210227","doi-asserted-by":"crossref","first-page":"409","DOI":"10.1016\/j.clim.2010.04.011","article-title":"Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndromevelocardiofacial syndrome).","volume":"136","author":"Zemble","year":"2010","journal-title":"Clin Immunol"},{"key":"R10-14-20210227","doi-asserted-by":"crossref","first-page":"1115","DOI":"10.1016\/j.jaci.2011.06.043","article-title":"Autoimmunity in a cohort of 130 pediatric patients with partial DiGeorge syndrome.","volume":"128","author":"Tison","year":"2011","journal-title":"J Allergy Clin Immunol"},{"key":"R11-14-20210227","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1111\/j.1365-2141.2008.07054.x","article-title":"Rituximab in the treatment of autoimmune haematological disorders.","volume":"141","author":"Garvey","year":"2008","journal-title":"Br J Haematol"},{"key":"R12-14-20210227","doi-asserted-by":"crossref","first-page":"318","DOI":"10.1159\/000102157","article-title":"Chromosome 22q11.2 deletion presenting with immune-mediated cytopenias, macrothrombocytopenia and platelet dysfunction.","volume":"16","author":"Akar","year":"2007","journal-title":"Med Princ Pract"},{"key":"R13-14-20210227","doi-asserted-by":"crossref","first-page":"390","DOI":"10.1007\/s00431-002-0976-y","article-title":"Autoimmune pancytopenia in a child with DiGeorge syndrome.","volume":"161","author":"Bruno","year":"2002","journal-title":"Eur J Pediatr"},{"key":"R14-14-20210227","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1046\/j.1365-2257.2003.00508.x","article-title":"Autoimmune cytopenias in the 22q11.2 deletion syndrome.","volume":"25","author":"Davies","year":"2003","journal-title":"Clin Lab Haem"},{"key":"R15-14-20210227","doi-asserted-by":"crossref","first-page":"484","DOI":"10.1016\/S0022-3476(97)80085-6","article-title":"Recurrent immune cytopenias in two patients with DiGeorgevelocadiofacial syndrome.","volume":"131","author":"De Piero","year":"1997","journal-title":"J Pediatr"},{"key":"R16-14-20210227","doi-asserted-by":"crossref","first-page":"167","DOI":"10.1080\/0880010390158685","article-title":"Evans syndrome in a patient with chromosome 22q11.2 deletion syndrome: a case report.","volume":"20","author":"Kratz","year":"2003","journal-title":"Pediatr Hematol Oncol"},{"key":"R17-14-20210227","doi-asserted-by":"crossref","first-page":"1692","DOI":"10.3324\/haematol.11540","article-title":"Rituximab therapy for childhood Evans syndrome.","volume":"92","author":"Bader-Meunier","year":"2007","journal-title":"Haematologica"},{"key":"R18-14-20210227","doi-asserted-by":"crossref","first-page":"1589","DOI":"10.3324\/haematol.11312","article-title":"Rituximab for the treatment of autoimmune cytopenias.","volume":"92","author":"Berentsen","year":"2007","journal-title":"Haematologica"},{"key":"R19-14-20210227","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1111\/j.1365-2141.2007.06616.x","article-title":"Rituximab for the treatment of autoimmune cytopenias in children with immune deficiency.","volume":"138","author":"Kim","year":"2007","journal-title":"Br J Haematol"},{"key":"R20-14-20210227","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1002\/ajh.20180","article-title":"Rituximab for refractory Evans syndrome and other immune-mediated hematologic diseases.","volume":"77","author":"Mantadakis","year":"2004","journal-title":"American Journal of Hematology"},{"key":"R21-14-20210227","doi-asserted-by":"crossref","first-page":"822","DOI":"10.1002\/pbc.21264","article-title":"Safety, efficacy, and immune reconstitution after rituximab therapy in pediatric patients with chronic or refractory hematologic autoimmune cytopenias.","volume":"50","author":"Rao","year":"2008","journal-title":"Pediatr Blood Cancer"},{"key":"R22-14-20210227","doi-asserted-by":"crossref","first-page":"164","DOI":"10.1016\/j.clim.2008.03.524","article-title":"Immune constitution monitoring after PBMC transplantation in complete DiGeorge syndrome: an eight-year follow-up.","volume":"128","author":"Daguindau","year":"2008","journal-title":"Clin Immunol"},{"key":"R23-14-20210227","doi-asserted-by":"crossref","first-page":"2229","DOI":"10.1182\/blood-2010-03-275966","article-title":"Multicenter survey on the outcome of transplantation of hematopoietic cells in patients with the complete form of DiGeorge anomaly.","volume":"116","author":"Janda","year":"2010","journal-title":"Blood"}],"container-title":["Journal of Pediatric Hematology\/Oncology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.lww.com\/10.1097\/MPH.0b013e31828be602","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,5,14]],"date-time":"2021-05-14T04:15:04Z","timestamp":1620965704000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/00043426-201305000-00014"}},"subtitle":["A Case Report"],"short-title":[],"issued":{"date-parts":[[2013,5]]},"references-count":23,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2013]]}},"URL":"https:\/\/doi.org\/10.1097\/mph.0b013e31828be602","relation":{},"ISSN":["1077-4114"],"issn-type":[{"value":"1077-4114","type":"print"}],"subject":[],"published":{"date-parts":[[2013,5]]}}}