{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,11]],"date-time":"2026-07-11T10:18:41Z","timestamp":1783765121987,"version":"3.55.0"},"reference-count":22,"publisher":"Springer Science and Business Media LLC","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["International Journal of Hematology"],"published-print":{"date-parts":[[2005,10,1]]},"DOI":"10.1532\/ijh97.a20505","type":"journal-article","created":{"date-parts":[[2005,10,4]],"date-time":"2005-10-04T21:02:44Z","timestamp":1128459764000},"page":"201-205","source":"Crossref","is-referenced-by-count":19,"title":["Neonatal Anemia Associated with Southeast Asian Ovalocytosis"],"prefix":"10.1007","volume":"82","author":[{"given":"Vichai","family":"Laosombat","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Supaporn","family":"Dissaneevate","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Malai","family":"Wongchanchailert","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Benjamas","family":"Satayasevanaa","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","reference":[{"key":"E00001","doi-asserted-by":"crossref","first-page":"489","DOI":"10.1016\/S0095-5108(18)30930-8","volume":"11","author":"Blanchette, VS","year":"1984","unstructured":"Blanchette VS, Zipursky A. Assessment of anemia in newborn infants. Clin Perinatol. 1984;11:489-510.","journal-title":"Clin Perinatol."},{"key":"E00002","doi-asserted-by":"crossref","first-page":"841","DOI":"10.1016\/S0031-3955(16)32769-9","volume":"19","author":"Gill, FM","year":"1972","unstructured":"Gill FM, Schwartz E. Anemia in early infancy. Pediatr Clin North Am. 1972;19:841-853.","journal-title":"Pediatr Clin North Am."},{"key":"E00003","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1002\/(SICI)1096-8652(199902)60:2<136::AID-AJH9>3.0.CO;2-E","volume":"60","author":"Laosombat, V","year":"1999","unstructured":"Laosombat V, Dissaneevate S, Peerapittayamongkol C, Matsuo M. Neonatal hyperbilirubinemia associated with Southeast Asian ovalocytosis. Am J Hematol. 1999;60:136-139.","journal-title":"Am J Hematol."},{"key":"E00004","doi-asserted-by":"crossref","first-page":"196","DOI":"10.1542\/peds.44.2.196","volume":"44","author":"Austin, RF","year":"1969","unstructured":"Austin RF, Desforges JF. Hereditary elliptocytosis: an unusual presentation of hemolysis in the newborn associated with transient morphologic abnormalities. Pediatrics. 1969;44:196-200.","journal-title":"Pediatrics."},{"key":"E00005","doi-asserted-by":"crossref","first-page":"307","DOI":"10.3109\/00313027609101493","volume":"8","author":"Harrison, KL","year":"1976","unstructured":"Harrison KL, Collins KA, McKenna HW. Hereditary elliptical stomatocytosis: a case report. Pathology. 1976;8:307-311.","journal-title":"Pathology."},{"key":"E00006","doi-asserted-by":"crossref","first-page":"159","DOI":"10.1203\/00006450-197104000-00003","volume":"5","author":"Honig, GR","year":"1971","unstructured":"Honig GR, Lacson PS, Maurer HS. A new familial disorder with abnormal erythrocyte morphology and increased permeability of the erythrocytes to sodium and potassium. Pediatric Res. 1971;5: 159-166.","journal-title":"Pediatric Res."},{"key":"E00007","first-page":"1","volume":"30","author":"Palek, J","year":"1993","unstructured":"Palek J. Introduction: red blood cell membrane proteins, their genes and mutations. Semin Hematol. 1993;30:1-3.","journal-title":"Semin Hematol."},{"key":"E00008","doi-asserted-by":"crossref","first-page":"228","DOI":"10.1016\/S0035-9203(96)90223-0","volume":"90","author":"Mgone, CS","year":"1996","unstructured":"Mgone CS, Koki G, Paniu MM, et al. Occurrence of the erythrocyte band 3 (AE1) gene deletion in relation to malaria endemicity in Papua New Guinea. Trans R Soc Trop Med Hyg. 1996;90:228-231.","journal-title":"Trans R Soc Trop Med Hyg."},{"key":"E00009","doi-asserted-by":"crossref","first-page":"11022","DOI":"10.1073\/pnas.88.24.11022","volume":"88","author":"Jarolim, P","year":"1991","unstructured":"Jarolim P, Palek J, Amato D, et al. Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis. Proc Natl Acad Sci U S A. 1991;88:11022-11026.","journal-title":"Proc Natl Acad Sci U S A."},{"key":"E00010","doi-asserted-by":"crossref","first-page":"853","DOI":"10.1016\/S0092-8674(00)80160-9","volume":"86","author":"Jay, DG","year":"1996","unstructured":"Jay DG. Role of band 3 in homeostasis and cell shape. Cell. 1996; 86:853-854.","journal-title":"Cell."},{"key":"E00011","first-page":"26","volume":"20","author":"Amato, D","year":"1977","unstructured":"Amato D, Booth PB. Hereditary ovalocytosis in Melanesians. P N G Med J. 1977;20:26-32.","journal-title":"P N G Med J."},{"key":"E00012","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1111\/j.1365-2141.1993.tb08670.x","volume":"85","author":"Reardon, DM","year":"1993","unstructured":"Reardon DM, Seymour CA, Cox TM, Pinder JC, Schofield AE, Tanner MJ. Hereditary ovalocytosis with compensated haemolysis. Br J Haematol. 1993;85:197-199.","journal-title":"Br J Haematol."},{"key":"E00013","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1046\/j.1365-2141.1998.00742.x","volume":"101","author":"O'Donnell, A","year":"1998","unstructured":"O'Donnell A, Allen SJ, Mgone CS, Martinson JJ, Clegg JB, Weatherall DJ. Red cell morphology and malaria anaemia in children with Southeast-Asian ovalocytosis band 3 in Papua New Guinea. Br J Haematol. 1998;101:407-412.","journal-title":"Br J Haematol."},{"key":"E00014","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1046\/j.1365-2141.1998.00742.x","volume":"101","author":"O'Donnell, A","year":"1998","unstructured":"Noparatana C, Noparatana C, Kanjanaopas S, Saechan V, Matsuo M. Southeast Asian ovalocytosis (SAO) in the south of Thailand. Paper presented at: PSU-ICMR Symposium; July 25-26, 1996; Songkla, Thailand (abstract 18).","journal-title":"Br J Haematol."},{"key":"E00015","first-page":"15","volume":"23","author":"Tanphaichitr, VS","year":"1987","unstructured":"Tanphaichitr VS, Pung-amritt P, Puchaiwatananon O, et al. Studies of hemoglobin Bart's and deletion of alpha-globin genes from cord blood in Thailand. Birth Defects Orig Artic Ser. 1987;23:15-21.","journal-title":"Birth Defects Orig Artic Ser."},{"key":"E00016","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1111\/j.1469-1809.1967.tb00546.x","volume":"31","author":"Pootrakul, S","year":"1967","unstructured":"Pootrakul S, Wasi P, Na-Nakorn S. Studies on haemoglobin Bart's in Thailand: the incidence and the mechanism of occurrence in cord blood. Ann Hum Genet. 1967;31:149.","journal-title":"Ann Hum Genet."},{"key":"E00017","first-page":"246","volume":"26","author":"Sae-Ung, N","year":"1995","unstructured":"Sae-Ung N, Fucharoen G, Fucharoen S. Expression of hemoglobin E in newborn. Southeast Asian J Trop Med Public Health. 1995; 26(suppl 1):246-248.","journal-title":"Southeast Asian J Trop Med Public Health."},{"key":"E00018","first-page":"97","volume":"30","author":"Pung-Amritt, P","year":"1999","unstructured":"Pung-Amritt P, Tanphaichitr VS, Tachavanich K, Suwantol L, Glomglao W. Prevalence of HbE from cord blood samples and after one year follow-up. Southeast Asian J Trop Med Public Health. 1999;30(suppl 2):97-99.","journal-title":"Southeast Asian J Trop Med Public Health."},{"key":"E00019","first-page":"601","volume":"67","author":"phosphate dehydrogenase, deficiency","year":"1989","unstructured":"Glucose-6-phosphate dehydrogenase deficiency. WHO Working Group. Bull World Health Organ. 1989;67:601-611.","journal-title":"Bull World Health Organ."},{"key":"E00020","doi-asserted-by":"crossref","first-page":"558","DOI":"10.1542\/peds.94.4.558","volume":"94","author":"management of hyperbilirubinemia in the healthy term, newborn","year":"1994","unstructured":"Practice parameter: management of hyperbilirubinemia in the healthy term newborn. American Academy of Pediatrics. Provisional Committee for Quality Improvement and Subcommittee on Hyperbilirubinemia. Pediatrics. 1994;94:558-565.","journal-title":"Pediatrics."},{"key":"E00021","doi-asserted-by":"crossref","first-page":"791","DOI":"10.1016\/S0022-3476(96)70331-1","volume":"128","author":"Kling, PJ","year":"1996","unstructured":"Kling PJ, Schmidt RL, Roberts RA, Widness JA. Serum erythropoietin levels during infancy: associations with erythropoiesis. J Pediatr. 1996;128:791-796.","journal-title":"J Pediatr."},{"key":"E00022","doi-asserted-by":"crossref","first-page":"427","DOI":"10.1046\/j.1442-200X.2002.01577.x","volume":"44","author":"Sutomo, R","year":"2002","unstructured":"Sutomo R, Laosombat V, Sadewa AH, et al. Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome. Pediatr Int. 2002;44:427-432.","journal-title":"Pediatr Int."}],"container-title":["International Journal of Hematology"],"original-title":[],"link":[{"URL":"http:\/\/www.springerlink.com\/index\/pdf\/10.1532\/IJH97.A20505","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,4]],"date-time":"2023-05-04T23:13:43Z","timestamp":1683242023000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1532\/IJH97.A20505"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2005,10,1]]},"references-count":22,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2005,10,1]]}},"alternative-id":["96935G922BQN61EN"],"URL":"https:\/\/doi.org\/10.1532\/ijh97.a20505","relation":{},"ISSN":["0925-5710"],"issn-type":[{"value":"0925-5710","type":"print"}],"subject":[],"published":{"date-parts":[[2005,10,1]]}}}