{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T01:06:46Z","timestamp":1790384806519,"version":"4.1.0"},"reference-count":56,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2021,3,1]],"date-time":"2021-03-01T00:00:00Z","timestamp":1614556800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2021,3,1]],"date-time":"2021-03-01T00:00:00Z","timestamp":1614556800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2021,3,1]],"date-time":"2021-03-01T00:00:00Z","timestamp":1614556800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2021,3,1]],"date-time":"2021-03-01T00:00:00Z","timestamp":1614556800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2021,3,1]],"date-time":"2021-03-01T00:00:00Z","timestamp":1614556800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2021,3,1]],"date-time":"2021-03-01T00:00:00Z","timestamp":1614556800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2021,3,1]],"date-time":"2021-03-01T00:00:00Z","timestamp":1614556800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"funder":[{"DOI":"10.13039\/100006108","name":"National Center for Advancing Translational Sciences","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100006108","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100007172","name":"Cincinnati Children's Hospital Medical Center","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100007172","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000050","name":"National Heart, Lung, and Blood Institute","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000050","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Blood Cells, Molecules, and Diseases"],"published-print":{"date-parts":[[2021,3]]},"DOI":"10.1016\/j.bcmd.2020.102534","type":"journal-article","created":{"date-parts":[[2020,12,25]],"date-time":"2020-12-25T04:19:53Z","timestamp":1608869993000},"page":"102534","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":13,"special_numbering":"C","title":["Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR)"],"prefix":"10.1016","volume":"87","author":[{"given":"Omar","family":"Niss","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert B.","family":"Lorsbach","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mikaela","family":"Berger","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Satheesh","family":"Chonat","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Morgan","family":"McLemore","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Buchbinder","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Timothy","family":"McCavit","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Linda G.","family":"Shaffer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jessica","family":"Simpson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jeffrey H.","family":"Schwartz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jessica","family":"Meznarich","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Myesa","family":"Emberesh","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katie G.","family":"Seu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wenying","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Theodosia A.","family":"Kalfa","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ammar","family":"Husami","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Theodosia","family":"Kalfa","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert","family":"Lorsbach","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carolyn","family":"Lutzko","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Adam","family":"Nelson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Omar","family":"Niss","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Charles","family":"Quinn","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katie G.","family":"Seu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wenying","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Satheesh","family":"Chonat","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Buchbinder","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Clarissa","family":"Johnson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Timothy","family":"McCavit","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Linda G.","family":"Shaffer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jennifer A.","family":"Rothman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sweta","family":"Gupta","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mara Nu\u00f1ez","family":"Toscano","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Melissa","family":"Forouhar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vinod K.","family":"Gidvani-Diaz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"James B.","family":"Ball","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gavin D.","family":"Roach","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"KayeLyn","family":"Wagner","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sam","family":"Milanovich","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"James","family":"Boyer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jane","family":"Chawla","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christine Moore","family":"Smith","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Adrienne","family":"Lee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jessica","family":"Simpson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jeffrey H.","family":"Schwartz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vlad C.","family":"Radulescu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yasmina L.","family":"Abajas","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A. Kim","family":"Ritchey","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jessica","family":"Meznarich","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hunter R.","family":"Underhill","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yaddanapudi","family":"Ravindranath","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Morgan","family":"McLemore","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Niketa C.","family":"Shah","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"issue":"10","key":"10.1016\/j.bcmd.2020.102534_bb0005","doi-asserted-by":"crossref","first-page":"613","DOI":"10.1007\/s00277-004-0892-5","article-title":"Congenital dyserythropoietic anemias: epidemiology, clinical significance, and progress in understanding their pathogenesis","volume":"83","author":"Heimpel","year":"2004","journal-title":"Ann. Hematol."},{"issue":"2","key":"10.1016\/j.bcmd.2020.102534_bb0010","first-page":"103","article-title":"Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts","volume":"34","author":"Heimpel","year":"1968","journal-title":"Helv Med Acta."},{"issue":"12","key":"10.1016\/j.bcmd.2020.102534_bb0015","doi-asserted-by":"crossref","first-page":"1786","DOI":"10.3324\/haematol.2012.072207","article-title":"Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach","volume":"97","author":"Iolascon","year":"2012","journal-title":"Haematologica."},{"issue":"4","key":"10.1016\/j.bcmd.2020.102534_bb0020","doi-asserted-by":"crossref","first-page":"431","DOI":"10.1111\/j.1365-2141.2005.05757.x","article-title":"Advances in the understanding of the congenital dyserythropoietic anaemias","volume":"131","author":"Wickramasinghe","year":"2005","journal-title":"Br. J. Haematol."},{"issue":"11","key":"10.1016\/j.bcmd.2020.102534_bb0025","doi-asserted-by":"crossref","first-page":"1274","DOI":"10.1182\/blood.2019000948","article-title":"Congenital dyserythropoietic anemias","volume":"136","author":"Iolascon","year":"2020","journal-title":"Blood."},{"issue":"13","key":"10.1016\/j.bcmd.2020.102534_bb0030","doi-asserted-by":"crossref","first-page":"2162","DOI":"10.1182\/blood-2013-05-468223","article-title":"Congenital dyserythropoietic anemias: molecular insights and diagnostic approach","volume":"122","author":"Iolascon","year":"2013","journal-title":"Blood."},{"issue":"1","key":"10.1016\/j.bcmd.2020.102534_bb0035","doi-asserted-by":"crossref","first-page":"334","DOI":"10.1182\/blood-2005-01-0421","article-title":"Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation","volume":"107","author":"Heimpel","year":"2006","journal-title":"Blood."},{"issue":"1","key":"10.1016\/j.bcmd.2020.102534_bb0040","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1111\/ejh.12778","article-title":"Morbidity and mortality of adult patients with congenital dyserythropoietic anemia type I","volume":"98","author":"Shalev","year":"2017","journal-title":"Eur. J. Haematol."},{"issue":"6","key":"10.1016\/j.bcmd.2020.102534_bb0045","doi-asserted-by":"crossref","first-page":"1467","DOI":"10.1086\/344781","article-title":"Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1","volume":"71","author":"Dgany","year":"2002","journal-title":"Am. J. Hum. Genet."},{"issue":"9","key":"10.1016\/j.bcmd.2020.102534_bb0050","doi-asserted-by":"crossref","first-page":"1383","DOI":"10.3324\/haematol.2013.089490","article-title":"Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I","volume":"98","author":"Babbs","year":"2013","journal-title":"Haematologica."},{"issue":"23","key":"10.1016\/j.bcmd.2020.102534_bb0055","doi-asserted-by":"crossref","first-page":"4791","DOI":"10.1182\/blood-2012-10-461392","article-title":"Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23","volume":"121","author":"Liljeholm","year":"2013","journal-title":"Blood."},{"issue":"3","key":"10.1016\/j.bcmd.2020.102534_bb0060","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1016\/j.hoc.2019.01.002","article-title":"Rare hereditary hemolytic anemias: diagnostic approach and considerations in management","volume":"33","author":"Risinger","year":"2019","journal-title":"Hematol. Oncol. Clin. North Am."},{"issue":"16","key":"10.1016\/j.bcmd.2020.102534_bb0065","doi-asserted-by":"crossref","first-page":"4434","DOI":"10.1073\/pnas.1521754113","article-title":"Insight into GATA1 transcriptional activity through interrogation of cis elements disrupted in human erythroid disorders","volume":"113","author":"Wakabayashi","year":"2016","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"issue":"5","key":"10.1016\/j.bcmd.2020.102534_bb0070","doi-asserted-by":"crossref","first-page":"599","DOI":"10.3324\/haematol.2009.005785","article-title":"Close to unraveling the secrets of congenital dyserythropoietic anemia types I and II","volume":"94","author":"Iolascon","year":"2009","journal-title":"Haematologica."},{"issue":"4","key":"10.1016\/j.bcmd.2020.102534_bb0075","doi-asserted-by":"crossref","first-page":"785","DOI":"10.1046\/j.1365-2141.1997.2513065.x","article-title":"Dyserythropoiesis and congenital dyserythropoietic anaemias","volume":"98","author":"Wickramasinghe","year":"1997","journal-title":"Br. J. Haematol."},{"issue":"11","key":"10.1016\/j.bcmd.2020.102534_bb0080","doi-asserted-by":"crossref","first-page":"746","DOI":"10.1097\/00043426-200411000-00011","article-title":"A comprehensive study of the neonatal manifestations of congenital dyserythropoietic anemia type I","volume":"26","author":"Shalev","year":"2004","journal-title":"J. Pediatr. Hematol. Oncol."},{"issue":"13","key":"10.1016\/j.bcmd.2020.102534_bb0085","doi-asserted-by":"crossref","first-page":"4576","DOI":"10.1182\/blood-2003-02-0613","article-title":"Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation","volume":"102","author":"Heimpel","year":"2003","journal-title":"Blood."},{"issue":"4","key":"10.1016\/j.bcmd.2020.102534_bb0090","doi-asserted-by":"crossref","first-page":"1258","DOI":"10.1182\/blood.V98.4.1258","article-title":"Natural history of congenital dyserythropoietic anemia type II","volume":"98","author":"Iolascon","year":"2001","journal-title":"Blood."},{"key":"10.1016\/j.bcmd.2020.102534_bb0095","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1016\/j.bcmd.2018.03.002","article-title":"Fetal presentation of congenital dyserythropoietic anemia type 1 with novel compound heterozygous CDAN1 mutations","volume":"71","author":"Meznarich","year":"2018","journal-title":"Blood Cells Mol. Dis."},{"issue":"1","key":"10.1016\/j.bcmd.2020.102534_bb0100","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1111\/bjh.15217","article-title":"Congenital dyserythropoietic anaemia type I diagnosed in a young adult with a history of splenectomy in childhood for presumed haemolytic anaemia","volume":"182","author":"Chonat","year":"2018","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2020.102534_bb0105","doi-asserted-by":"crossref","unstructured":"Seu KG, Trump LR, Emberesh S, et al. VPS4A mutations in humans cause syndromic congenital dyserythropoietic anemia due to cytokinesis and trafficking defects. Am J Hum Genet. 2020;in press.","DOI":"10.1016\/j.ajhg.2020.10.013"},{"key":"10.1016\/j.bcmd.2020.102534_bb0110","doi-asserted-by":"crossref","unstructured":"Emberesh M, Giger Seu K, Emberesh S, et al. Peroxiredoxin II (PRDX2) is a novel candidate gene for congenital dyserythropoietic anemia. Blood. 2018;132(Supplement 1):3605\u20133605.","DOI":"10.1182\/blood-2018-99-120056"},{"issue":"1","key":"10.1016\/j.bcmd.2020.102534_bb0115","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1097\/MOH.0000000000000558","article-title":"Severe chronic neutropenia international R. registries for study of nonmalignant hematological diseases: the example of the severe chronic neutropenia international registry","volume":"27","author":"Dale","year":"2020","journal-title":"Curr. Opin. Hematol."},{"issue":"8","key":"10.1016\/j.bcmd.2020.102534_bb0120","doi-asserted-by":"crossref","first-page":"936","DOI":"10.1038\/ng.405","article-title":"Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II","volume":"41","author":"Schwarz","year":"2009","journal-title":"Nat. Genet."},{"issue":"4","key":"10.1016\/j.bcmd.2020.102534_bb0125","doi-asserted-by":"crossref","first-page":"628","DOI":"10.1111\/j.1365-2141.2005.05642.x","article-title":"Clinical and molecular variability in congenital dyserythropoietic anaemia type I","volume":"130","author":"Tamary","year":"2005","journal-title":"Br. J. Haematol."},{"issue":"5","key":"10.1016\/j.bcmd.2020.102534_bb0130","doi-asserted-by":"crossref","first-page":"708","DOI":"10.3324\/haematol.2009.014985","article-title":"Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship","volume":"95","author":"Iolascon","year":"2010","journal-title":"Haematologica."},{"issue":"4","key":"10.1016\/j.bcmd.2020.102534_bb0135","doi-asserted-by":"crossref","first-page":"220","DOI":"10.3816\/SCT.2006.n.020","article-title":"The severe chronic neutropenia international registry: 10-year follow-up report","volume":"3","author":"Dale","year":"2006","journal-title":"Supportive cancer therapy."},{"issue":"6","key":"10.1016\/j.bcmd.2020.102534_bb0140","doi-asserted-by":"crossref","first-page":"377","DOI":"10.1097\/00043426-200108000-00015","article-title":"The Diamond Blackfan Anemia Registry: tool for investigating the epidemiology and biology of Diamond-Blackfan anemia","volume":"23","author":"Vlachos","year":"2001","journal-title":"J. Pediatr. Hematol. Oncol."},{"issue":"3","key":"10.1016\/j.bcmd.2020.102534_bb0145","doi-asserted-by":"crossref","first-page":"368","DOI":"10.1111\/ejh.13112","article-title":"Clinical and genetic features of congenital dyserythropoietic anemia (CDA)","volume":"101","author":"Moreno-Carralero","year":"2018","journal-title":"Eur. J. Haematol."},{"issue":"5","key":"10.1016\/j.bcmd.2020.102534_bb0150","doi-asserted-by":"crossref","first-page":"672","DOI":"10.1002\/ajh.25058","article-title":"Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias","volume":"93","author":"Russo","year":"2018","journal-title":"Am. J. Hematol."},{"issue":"3","key":"10.1016\/j.bcmd.2020.102534_bb0155","doi-asserted-by":"crossref","first-page":"436","DOI":"10.1111\/bjh.15817","article-title":"The pathogenesis, diagnosis and management of congenital dyserythropoietic anaemia type I","volume":"185","author":"Roy","year":"2019","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2020.102534_bb0160","doi-asserted-by":"crossref","unstructured":"Rothman JA, Stevens JL, Gray FL, Kalfa TA. How I approach hereditary hemolytic anemia and splenectomy. Pediatr Blood Cancer. 2020:e28337.","DOI":"10.1002\/pbc.28337"},{"issue":"11","key":"10.1016\/j.bcmd.2020.102534_bb0165","doi-asserted-by":"crossref","first-page":"1250","DOI":"10.1182\/blood.2019000946","article-title":"Red cell membrane disorders: structure meets function","volume":"136","author":"Risinger","year":"2020","journal-title":"Blood."},{"issue":"4","key":"10.1016\/j.bcmd.2020.102534_bb0170","doi-asserted-by":"crossref","first-page":"352","DOI":"10.3109\/01443615.2013.859238","article-title":"Intrauterine therapy in a fetus with congenital dyserythropoietic anaemia type I","volume":"34","author":"Lin","year":"2014","journal-title":"Journal of Obstetrics and Gynaecology"},{"key":"10.1016\/j.bcmd.2020.102534_bb0175","doi-asserted-by":"crossref","unstructured":"al-Fawaz IM, al-Mashhadani SA. Congenital dyserythropoietic anaemia type I. Report of two siblings from Saudi Arabia. Acta Haematol. 1995;93(1):50\u201353.","DOI":"10.1159\/000204092"},{"issue":"4","key":"10.1016\/j.bcmd.2020.102534_bb0180","doi-asserted-by":"crossref","first-page":"929","DOI":"10.1111\/j.1365-2141.1995.tb08442.x","article-title":"Alpha-interferon therapy for congenital dyserythropoiesis type I","volume":"89","author":"Lavabre-Bertrand","year":"1995","journal-title":"Br. J. Haematol."},{"issue":"5","key":"10.1016\/j.bcmd.2020.102534_bb0185","doi-asserted-by":"crossref","first-page":"380","DOI":"10.1111\/j.1600-0609.2004.00310.x","article-title":"Long-term alpha interferon treatment is effective on anaemia and significantly reduces iron overload in congenital dyserythropoiesis type I","volume":"73","author":"Lavabre-Bertrand","year":"2004","journal-title":"Eur. J. Haematol."},{"issue":"8","key":"10.1016\/j.bcmd.2020.102534_bb0190","doi-asserted-by":"crossref","first-page":"416","DOI":"10.1097\/01.mph.0000175406.42427.c9","article-title":"Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in a cohort of French children","volume":"27","author":"Bader-Meunier","year":"2005","journal-title":"J. Pediatr. Hematol. Oncol."},{"key":"10.1016\/j.bcmd.2020.102534_bb0195","doi-asserted-by":"crossref","unstructured":"Rathe M, M\u00f8ller MB, Greisen PW, Fisker N. Successful management of transfusion-dependent congenital dyserythropoietic anemia type 1b with interferon alfa-2a. Pediatric Blood & Cancer. 2018;65(3):https:\/\/doi.org\/10.1002\/pbc.26866.","DOI":"10.1002\/pbc.26866"},{"key":"10.1016\/j.bcmd.2020.102534_bb0200","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1111\/j.1600-0609.1997.tb00935.x","article-title":"Response of CDA type I to alpha-interferon","volume":"58","author":"Wickramasinghe","year":"1997","journal-title":"Eur J Haematol"},{"issue":"2","key":"10.1016\/j.bcmd.2020.102534_bb0205","doi-asserted-by":"crossref","first-page":"295","DOI":"10.1046\/j.1365-2141.1997.1993016.x","article-title":"Reduced interferon-alpha production by Epstein-Barr virus transformed B-lymphoblastoid cell lines and lectin-stimulated lymphocytes in congenital dyserythropoietic anaemia type I","volume":"98","author":"Wickramasinghe","year":"1997","journal-title":"Br. J. Haematol."},{"issue":"3","key":"10.1016\/j.bcmd.2020.102534_bb0210","doi-asserted-by":"crossref","first-page":"825","DOI":"10.1046\/j.1365-2141.1998.01071.x","article-title":"Effects of four species of interferon-alpha on cultured erythroid progenitors from congenital dyserythropoietic anaemia type I","volume":"103","author":"Menike","year":"1998","journal-title":"Br. J. Haematol."},{"issue":"3 Pt 1","key":"10.1016\/j.bcmd.2020.102534_bb0215","doi-asserted-by":"crossref","first-page":"527","DOI":"10.1016\/S0022-3476(98)70034-4","article-title":"Spastic diplegia as a complication of interferon Alfa-2a treatment of hemangiomas of infancy","volume":"132","author":"Barlow","year":"1998","journal-title":"J. Pediatr."},{"issue":"22","key":"10.1016\/j.bcmd.2020.102534_bb0220","doi-asserted-by":"crossref","first-page":"1456","DOI":"10.1056\/NEJM199205283262203","article-title":"Interferon alfa-2a therapy for life-threatening hemangiomas of infancy","volume":"326","author":"Ezekowitz","year":"1992","journal-title":"N. Engl. J. Med."},{"issue":"3","key":"10.1016\/j.bcmd.2020.102534_bb0225","doi-asserted-by":"crossref","first-page":"382","DOI":"10.1016\/S0022-3476(99)70474-9","article-title":"Spastic diplegia and interferon","volume":"134","author":"Deb","year":"1999","journal-title":"J. Pediatr."},{"issue":"2","key":"10.1016\/j.bcmd.2020.102534_bb0230","doi-asserted-by":"crossref","first-page":"216","DOI":"10.1111\/ejh.13428","article-title":"Treatment of transfusion-dependent congenital dyserythropoietic anemia type I patients with pegylated interferon alpha-2a","volume":"105","author":"Abu-Quider","year":"2020","journal-title":"Eur. J. Haematol."},{"issue":"3","key":"10.1016\/j.bcmd.2020.102534_bb0235","doi-asserted-by":"crossref","first-page":"170","DOI":"10.1034\/j.1600-0609.2002.01663.x","article-title":"Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in young adults","volume":"68","author":"Shalev","year":"2002","journal-title":"Eur. J. Haematol."},{"issue":"11","key":"10.1016\/j.bcmd.2020.102534_bb0240","doi-asserted-by":"crossref","first-page":"E283","DOI":"10.1002\/ajh.23543","article-title":"Tissue iron evaluation in chronically transfused children shows significant levels of iron loading at a very young age","volume":"88","author":"Berdoukas","year":"2013","journal-title":"Am. J. Hematol."},{"issue":"13","key":"10.1016\/j.bcmd.2020.102534_bb0245","doi-asserted-by":"crossref","first-page":"5241","DOI":"10.1182\/blood-2008-06-165738","article-title":"Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I","volume":"112","author":"Tamary","year":"2008","journal-title":"Blood."},{"issue":"6","key":"10.1016\/j.bcmd.2020.102534_bb0250","doi-asserted-by":"crossref","first-page":"506","DOI":"10.7326\/0003-4819-130-6-199903160-00014","article-title":"Pulmonary hypertension after splenectomy?","volume":"130","author":"Hoeper","year":"1999","journal-title":"Ann. Intern. Med."},{"issue":"8","key":"10.1016\/j.bcmd.2020.102534_bb0255","doi-asserted-by":"crossref","first-page":"e335","DOI":"10.3324\/haematol.2018.206623","article-title":"Stem cell transplantation for congenital dyserythropoietic anemia: an analysis from the European Society for Blood and Marrow Transplantation","volume":"104","author":"Miano","year":"2019","journal-title":"Haematologica."},{"issue":"8","key":"10.1016\/j.bcmd.2020.102534_bb0260","doi-asserted-by":"crossref","first-page":"1460","DOI":"10.1002\/pbc.24945","article-title":"Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension with pigeon chest deformity","volume":"61","author":"El-Sheikh","year":"2014","journal-title":"Pediatr. Blood Cancer"},{"issue":"4","key":"10.1016\/j.bcmd.2020.102534_bb0265","doi-asserted-by":"crossref","first-page":"553","DOI":"10.1016\/S0022-3476(00)90025-8","article-title":"Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newborn","volume":"136","author":"Shalev","year":"2000","journal-title":"J. Pediatr."},{"issue":"1","key":"10.1016\/j.bcmd.2020.102534_bb0270","doi-asserted-by":"crossref","first-page":"60","DOI":"10.1097\/MPH.0000000000000064","article-title":"Persistent pulmonary hypertension of the newborn associated with severe congenital anemia of various etiologies","volume":"37","author":"Landau","year":"2015","journal-title":"J. Pediatr. Hematol. Oncol."},{"issue":"8","key":"10.1016\/j.bcmd.2020.102534_bb0275","doi-asserted-by":"crossref","first-page":"2013","DOI":"10.1038\/emboj.2012.55","article-title":"Codanin-1, mutated in the anaemic disease CDAI, regulates Asf1 function in S-phase histone supply","volume":"31","author":"Ask","year":"2012","journal-title":"EMBO J."},{"issue":"4","key":"10.1016\/j.bcmd.2020.102534_bb0280","doi-asserted-by":"crossref","first-page":"418","DOI":"10.1111\/joa.12361","article-title":"How the embryo makes a limb: determination, polarity and identity","volume":"227","author":"Tickle","year":"2015","journal-title":"J. Anat."}],"container-title":["Blood Cells, Molecules, and Diseases"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1079979620305714?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1079979620305714?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,21]],"date-time":"2025-10-21T12:36:44Z","timestamp":1761050204000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1079979620305714"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,3]]},"references-count":56,"alternative-id":["S1079979620305714"],"URL":"https:\/\/doi.org\/10.1016\/j.bcmd.2020.102534","relation":{},"ISSN":["1079-9796"],"issn-type":[{"value":"1079-9796","type":"print"}],"subject":[],"published":{"date-parts":[[2021,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR)","name":"articletitle","label":"Article Title"},{"value":"Blood Cells, Molecules, and Diseases","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.bcmd.2020.102534","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}],"article-number":"102534"}}