{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,9,30]],"date-time":"2023-09-30T06:41:04Z","timestamp":1696056064127},"reference-count":12,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2014,6,3]],"date-time":"2014-06-03T00:00:00Z","timestamp":1401753600000},"content-version":"vor","delay-in-days":2,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatrics International"],"published-print":{"date-parts":[[2014,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We describe three cases of hereditary spherocytosis (<jats:styled-content style=\"fixed-case\">HS<\/jats:styled-content>) diagnosed using the eosin\u20105\u2032\u2010maleimide (<jats:styled-content style=\"fixed-case\">EMA<\/jats:styled-content>) binding test and discuss the relevance of the <jats:styled-content style=\"fixed-case\">EMA<\/jats:styled-content> binding test. In <jats:styled-content style=\"fixed-case\">J<\/jats:styled-content>apan, this test is not widely used because the prevalence of <jats:styled-content style=\"fixed-case\">HS<\/jats:styled-content> is low. This test is a valuable screening test for the diagnosis of <jats:styled-content style=\"fixed-case\">HS<\/jats:styled-content>.<\/jats:p>","DOI":"10.1111\/ped.12293","type":"journal-article","created":{"date-parts":[[2014,6,4]],"date-time":"2014-06-04T03:19:16Z","timestamp":1401851956000},"page":"427-429","source":"Crossref","is-referenced-by-count":1,"title":["Hereditary spherocytosis diagnosed with the eosin\u20105\u2032\u2010maleimide binding test"],"prefix":"10.1111","volume":"56","author":[{"given":"Toru","family":"Watanabe","sequence":"first","affiliation":[{"name":"Department of Pediatrics Iwata City Hospital  Iwata Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hiroyuki","family":"Ono","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Iwata City Hospital  Iwata Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Iwao","family":"Tajima","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Iwata City Hospital  Iwata Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hidetoshi","family":"Ishigaki","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Iwata City Hospital  Iwata Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Akio","family":"Hakamata","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Iwata City Hospital  Iwata Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masami","family":"Shirai","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Iwata City Hospital  Iwata Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Akira","family":"Endoh","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Iwata City Hospital  Iwata Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Teruaki","family":"Hongo","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Iwata City Hospital  Iwata Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2014,6,3]]},"reference":[{"key":"e_1_2_5_2_1","first-page":"321","article-title":"Congenital hemolytic anemia","volume":"2","author":"Shibuya A","year":"2009","journal-title":"Shonika Rinsho"},{"key":"e_1_2_5_3_1","volume-title":"UpToDate","author":"Recht M","year":"2013"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(08)61588-3"},{"key":"e_1_2_5_5_1","first-page":"118","article-title":"Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population","volume":"71","author":"Yawata Y","year":"2000","journal-title":"Int. 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