{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T16:09:18Z","timestamp":1786118958890,"version":"build-2736575974"},"reference-count":24,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2008,5]]},"DOI":"10.1097\/mph.0b013e318168e7a0","type":"journal-article","created":{"date-parts":[[2008,5,5]],"date-time":"2008-05-05T03:21:27Z","timestamp":1209957687000},"page":"396-400","source":"Crossref","is-referenced-by-count":30,"title":["Maternal T-cell Engraftment Associated With Severe Hemophagocytosis of the Bone Marrow in Untreated X-linked Severe Combined Immunodeficiency"],"prefix":"10.1097","volume":"30","author":[{"given":"Christopher C.","family":"Dvorak","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amanda","family":"Sandford","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Abraham","family":"Fong","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Morton J.","family":"Cowan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tracy I.","family":"George","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David B.","family":"Lewis","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-14-20210227","doi-asserted-by":"crossref","first-page":"378","DOI":"10.1016\/S0022-3476(97)70199-9","article-title":"Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants","volume":"130","author":"Buckley","year":"1997","journal-title":"J Pediatr"},{"key":"R2-14-20210227","doi-asserted-by":"crossref","first-page":"564","DOI":"10.1016\/S0022-3476(05)80951-5","article-title":"Severe combined immunodeficiency: a retrospective single-center study of clinical presentation and outcome in 117 patients","volume":"123","author":"Stephan","year":"1993","journal-title":"J Pediatr"},{"key":"R3-14-20210227","doi-asserted-by":"crossref","first-page":"1847","DOI":"10.1182\/blood.V98.6.1847","article-title":"Transplacentally acquired maternal T lymphocytes in severe combined immunodeficiency: a study of 121 patients","volume":"98","author":"Muller","year":"2001","journal-title":"Blood"},{"key":"R4-14-20210227","doi-asserted-by":"crossref","first-page":"227","DOI":"10.1038\/sj.bmt.1703128","article-title":"Cutaneous manifestations of maternal engraftment in patients with severe combined immunodeficiency: a clinicopathologic study","volume":"28","author":"Denianke","year":"2001","journal-title":"Bone Marrow Transplant"},{"key":"R5-14-20210227","doi-asserted-by":"crossref","first-page":"834","DOI":"10.1046\/j.1365-2141.2000.01923.x","article-title":"Haemophagocytic lymphohistiocytosis in X-linked severe combined immunodeficiency","volume":"108","author":"Grunebaum","year":"2000","journal-title":"Br J Haematol"},{"key":"R6-14-20210227","first-page":"366","article-title":"Gene abnormalities in patients with hemophagocytic lymphohistiocytosis","volume":"4","author":"Grunebaum","year":"2002","journal-title":"Isr Med Assoc J"},{"key":"R7-14-20210227","first-page":"1968","article-title":"Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency","volume":"89","author":"Puck","year":"1997","journal-title":"Blood"},{"key":"R8-14-20210227","doi-asserted-by":"crossref","first-page":"124","DOI":"10.1002\/pbc.21039","article-title":"HLH-2004: diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis","volume":"48","author":"Henter","year":"2007","journal-title":"Pediatr Blood Cancer"},{"key":"R9-14-20210227","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1002\/(SICI)1098-1004(200001)15:1<7::AID-HUMU4>3.0.CO;2-N","article-title":"Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion","volume":"15","author":"Den Dunnen","year":"2000","journal-title":"Hum Mutat"},{"key":"R10-14-20210227","doi-asserted-by":"crossref","first-page":"340","DOI":"10.1097\/00043426-199611000-00002","article-title":"Characteristic immune abnormalities in hemophagocytic lymphohistiocytosis","volume":"18","author":"Egeler","year":"1996","journal-title":"J Pediatr Hematol Oncol"},{"key":"R11-14-20210227","doi-asserted-by":"crossref","first-page":"586","DOI":"10.1046\/j.1365-2141.1998.00721.x","article-title":"Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1)","volume":"101","author":"Wengler","year":"1998","journal-title":"Br J Haematol"},{"key":"R12-14-20210227","doi-asserted-by":"crossref","first-page":"737","DOI":"10.1136\/jmg.2004.029538","article-title":"Splicing in action: assessing disease causing sequence changes","volume":"42","author":"Baralle","year":"2005","journal-title":"J Med Genet"},{"key":"R13-14-20210227","doi-asserted-by":"crossref","first-page":"4157","DOI":"10.4049\/jimmunol.146.12.4157","article-title":"Limited T cell receptor diversity of transplacentally acquired maternal T cells in severe combined immunodeficiency","volume":"146","author":"Knobloch","year":"1991","journal-title":"J Immunol"},{"key":"R14-14-20210227","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1016\/j.jpeds.2004.09.010","article-title":"Long-term survival in severe combined immune deficiency: the role of persistent maternal engraftment","volume":"146","author":"Tezcan","year":"2005","journal-title":"J Pediatr"},{"key":"R15-14-20210227","doi-asserted-by":"crossref","first-page":"20","DOI":"10.1080\/07853890500465189","article-title":"Hemophagocytic lymphohistiocytosis: diagnosis, pathophysiology, treatment, and future perspectives","volume":"38","author":"Verbsky","year":"2006","journal-title":"Ann Med"},{"key":"R16-14-20210227","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1097\/00043426-200206000-00017","article-title":"Hemophagocytic lymphohistiocytosis presenting with thrombocytopenia in the newborn","volume":"24","author":"Levendoglu-Tugal","year":"2002","journal-title":"J Pediatr Hematol Oncol"},{"key":"R17-14-20210227","doi-asserted-by":"crossref","first-page":"1435","DOI":"10.1016\/S0140-6736(84)91932-9","article-title":"Maternal isoimmunisation resulting in combined immunodeficiency and fatal graft-versus-host disease in an infant","volume":"1","author":"Bastian","year":"1984","journal-title":"Lancet"},{"key":"R18-14-20210227","doi-asserted-by":"crossref","first-page":"423","DOI":"10.1016\/j.jaci.2007.02.047","article-title":"Unusual clinical and immunologic manifestations of transplacentally acquired maternal T cells in severe combined immunodeficiency","volume":"120","author":"Palmer","year":"2007","journal-title":"J Allergy Clin Immunol"},{"key":"R19-14-20210227","doi-asserted-by":"crossref","first-page":"340","DOI":"10.1136\/adc.74.4.340","article-title":"Severe combined immunodeficiency (SCID) associated neutropenia: a lesson from monozygotic twins","volume":"74","author":"Niehues","year":"1996","journal-title":"Arch Dis Child"},{"key":"R20-14-20210227","doi-asserted-by":"crossref","first-page":"519","DOI":"10.1038\/sj.bmt.1703396","article-title":"Allogeneic bone marrow transplantation for active Epstein-Barr virus-related lymphoproliferative disease and hemophagocytic lymphohistiocytosis in an infant with severe combined immunodeficiency syndrome","volume":"29","author":"Schmid","year":"2002","journal-title":"Bone Marrow Transplant"},{"key":"R21-14-20210227","doi-asserted-by":"crossref","first-page":"703","DOI":"10.1038\/sj.bmt.1702831","article-title":"Bone marrow transplantation for T\u2212B\u2212 severe combined immunodeficiency disease in Athabascan-speaking native Americans","volume":"27","author":"O'Marcaigh","year":"2001","journal-title":"Bone Marrow Transplant"},{"key":"R22-14-20210227","doi-asserted-by":"crossref","first-page":"2021","DOI":"10.1182\/blood.V81.8.2021.2021","article-title":"Immune reconstitution in severe combined immunodeficiency disease after lectin-treated, T-cell-depleted haplocompatible bone marrow transplantation","volume":"81","author":"Dror","year":"1993","journal-title":"Blood"},{"key":"R23-14-20210227","doi-asserted-by":"crossref","first-page":"2825","DOI":"10.1002\/eji.1830221111","article-title":"Classical transplantation tolerance in the adult: the interaction between myeloablation and immunosuppression","volume":"22","author":"Leong","year":"1992","journal-title":"Eur J Immunol"},{"key":"R24-14-20210227","doi-asserted-by":"crossref","first-page":"6133","DOI":"10.4049\/jimmunol.169.11.6133","article-title":"Multilineage engraftment with minimal graft-versus-host disease following in utero transplantation of S-59 psoralen\/ultraviolet a light-treated, sensitized T cells and adult T cell-depleted bone marrow in fetal mice","volume":"169","author":"Bhattacharyya","year":"2002","journal-title":"J Immunol"}],"container-title":["Journal of Pediatric Hematology\/Oncology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.1097\/MPH.0b013e318168e7a0","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,6]],"date-time":"2026-08-06T17:02:37Z","timestamp":1786035757000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/00043426-200805000-00014"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,5]]},"references-count":24,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2008]]}},"URL":"https:\/\/doi.org\/10.1097\/mph.0b013e318168e7a0","relation":{},"ISSN":["1077-4114"],"issn-type":[{"value":"1077-4114","type":"print"}],"subject":[],"published":{"date-parts":[[2008,5]]}}}