{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,22]],"date-time":"2026-10-22T22:59:08Z","timestamp":1792709948064,"version":"4.5.0"},"reference-count":57,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Blood Cells, Molecules, and Diseases"],"published-print":{"date-parts":[[2016,1]]},"DOI":"10.1016\/j.bcmd.2015.09.001","type":"journal-article","created":{"date-parts":[[2015,9,16]],"date-time":"2015-09-16T02:01:34Z","timestamp":1442368894000},"page":"9-22","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":136,"title":["Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer"],"prefix":"10.1016","volume":"56","author":[{"given":"Lydie","family":"Da Costa","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ludovic","family":"Suner","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Julie","family":"Galimand","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amandine","family":"Bonnel","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tiffany","family":"Pascreau","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nathalie","family":"Couque","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Odile","family":"Fenneteau","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Narla","family":"Mohandas","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.bcmd.2015.09.001_bb0005","doi-asserted-by":"crossref","first-page":"3939","DOI":"10.1182\/blood-2008-07-161166","article-title":"Red cell membrane: past, present, and future","volume":"112","author":"Mohandas","year":"2008","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0010","first-page":"225","article-title":"The influence of membrane skeleton on red cell deformability, membrane material properties, and shape","volume":"20","author":"Mohandas","year":"1983","journal-title":"Semin. Hematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0015","first-page":"171","article-title":"Red blood cell deformability, membrane material properties and shape: regulation by transmembrane, skeletal and cytosolic proteins and lipids","volume":"30","author":"Mohandas","year":"1993","journal-title":"Semin. Hematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0020","doi-asserted-by":"crossref","first-page":"787","DOI":"10.1146\/annurev.bb.23.060194.004035","article-title":"Mechanical properties of the red cell membrane in relation to molecular structure and genetic defects","volume":"23","author":"Mohandas","year":"1994","journal-title":"Annu. Rev. Biophys. Biomol. Struct."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0025","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1016\/j.tracli.2006.02.017","article-title":"New insights into function of red cell membrane proteins and their interaction with spectrin-based membrane skeleton","volume":"13","author":"Mohandas","year":"2006","journal-title":"Transfus. Clin. Biol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0030","article-title":"Red cell membrane disorders","volume":"13\u201318","author":"Gallagher","year":"2005","journal-title":"Hematol. Am. Soc. Hematol. Educ. Prog."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0035","doi-asserted-by":"crossref","first-page":"367","DOI":"10.1111\/j.1365-2141.2008.07091.x","article-title":"Disorders of red cell membrane","volume":"141","author":"An","year":"2008","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0040","first-page":"295","article-title":"Red cell membrane disorders in pediatrics","volume":"37","author":"Iolascon","year":"2008","journal-title":"Pediatr. Ann."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0045","first-page":"22","article-title":"Red blood cell membrane defects","volume":"7","author":"Iolascon","year":"2003","journal-title":"Rev. Clin. Exp. Hematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0050","doi-asserted-by":"crossref","first-page":"1411","DOI":"10.1016\/S0140-6736(08)61588-3","article-title":"Hereditary spherocytosis","volume":"372","author":"Perrotta","year":"2008","journal-title":"Lancet"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0055","doi-asserted-by":"crossref","first-page":"1190","DOI":"10.1111\/j.1365-2141.2000.02441.x","article-title":"A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis","volume":"111","author":"Gallagher","year":"2000","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0060","doi-asserted-by":"crossref","first-page":"689","DOI":"10.1046\/j.1365-2141.2001.02800.x","article-title":"Band 3 Cape Town (E90K) causes severe hereditary spherocytosis in combination with band 3 Prague III","volume":"113","author":"Bracher","year":"2001","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0065","doi-asserted-by":"crossref","first-page":"1062","DOI":"10.1182\/blood.V88.3.1062.1062","article-title":"Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas)","volume":"88","author":"Alloisio","year":"1996","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0070","doi-asserted-by":"crossref","first-page":"417","DOI":"10.1006\/bcmd.1997.0160","article-title":"Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis","volume":"23","author":"Gallagher","year":"1997","journal-title":"Blood Cells Mol. Dis."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0075","doi-asserted-by":"crossref","first-page":"2300","DOI":"10.1172\/JCI119041","article-title":"Combination of two mutant alpha spectrin alleles underlies a severe spherocytic hemolytic anemia","volume":"98","author":"Wichterle","year":"1996","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0080","doi-asserted-by":"crossref","first-page":"502","DOI":"10.1111\/j.1365-2141.1995.tb05330.x","article-title":"Beta spectrin PRAGUE: a truncated beta spectrin producing spectrin deficiency, defective spectrin heterodimer self-association and a phenotype of spherocytic elliptocytosis","volume":"91","author":"Jarolim","year":"1995","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0085","doi-asserted-by":"crossref","first-page":"118","DOI":"10.1111\/j.1365-2141.2004.05160.x","article-title":"Different impacts of alleles alphaLEPRA and alphaLELY as assessed versus a novel, virtually null allele of the SPTA1 gene in trans","volume":"127","author":"Delaunay","year":"2004","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0090","doi-asserted-by":"crossref","first-page":"4481","DOI":"10.1182\/blood.V92.11.4481","article-title":"Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosis","volume":"92","author":"Dhermy","year":"1998","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0095","doi-asserted-by":"crossref","first-page":"2091","DOI":"10.1172\/JCI116432","article-title":"Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V\/41 polymorphism) and intron 45 and with partial skipping of exon 46","volume":"91","author":"Wilmotte","year":"1993","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0100","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1002\/(SICI)1098-1004(1996)8:2<97::AID-HUMU1>3.0.CO;2-M","article-title":"Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis","volume":"8","author":"Maillet","year":"1996","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0105","doi-asserted-by":"crossref","first-page":"210","DOI":"10.1159\/000065657","article-title":"Molecular basis of red cell membrane disorders","volume":"108","author":"Delaunay","year":"2002","journal-title":"Acta Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0110","doi-asserted-by":"crossref","first-page":"266","DOI":"10.1182\/blood.V75.1.266.266","article-title":"Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis","volume":"75","author":"Warkentin","year":"1990","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0115","doi-asserted-by":"crossref","first-page":"110","DOI":"10.1002\/ajh.2830400207","article-title":"Splenic sequestration associated with sickle cell trait and hereditary spherocytosis","volume":"40","author":"Yang","year":"1992","journal-title":"Am. J. Hematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0120","doi-asserted-by":"crossref","first-page":"1385","DOI":"10.1182\/blood.V63.6.1385.1385","article-title":"Rigid membranes of Malayan ovalocytes: a likely genetic barrier against malaria","volume":"63","author":"Mohandas","year":"1984","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0125","doi-asserted-by":"crossref","DOI":"10.1007\/s00430-012-0272-z","article-title":"Malaria and human red blood cells","author":"Mohandas","year":"2012","journal-title":"Med. Microbiol. Immunol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0130","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pmed.1001305","article-title":"Reduced risk of Plasmodium vivax malaria in Papua New Guinean children with Southeast Asian Ovalocytosis in two cohorts and a case\u2013control study","volume":"9","author":"Rosanas-Urgell","year":"2012","journal-title":"PLoS Med."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0135","first-page":"993","article-title":"Twenty-seven base pair deletion in erythrocyte band 3 protein gene responsible for Southeast Asian ovalocytosis is not common among Southeast Asians","volume":"70","author":"Kimura","year":"1998","journal-title":"Hum. Biol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0140","doi-asserted-by":"crossref","first-page":"11022","DOI":"10.1073\/pnas.88.24.11022","article-title":"Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis","volume":"88","author":"Jarolim","year":"1991","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0145","doi-asserted-by":"crossref","first-page":"110","DOI":"10.1097\/00062752-199903000-00009","article-title":"Hereditary dehydrated and overhydrated stomatocytosis: recent advances","volume":"6","author":"Delaunay","year":"1999","journal-title":"Curr. Opin. Hematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0150","doi-asserted-by":"crossref","first-page":"165","DOI":"10.1053\/j.seminhematol.2004.02.005","article-title":"The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations","volume":"41","author":"Delaunay","year":"2004","journal-title":"Semin. Hematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0155","doi-asserted-by":"crossref","first-page":"1884","DOI":"10.1038\/ncomms2899","article-title":"Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels","volume":"4","author":"Albuisson","year":"2013","journal-title":"Nat. Commun."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0160","doi-asserted-by":"crossref","first-page":"3925","DOI":"10.1182\/blood-2013-02-482489","article-title":"Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1","volume":"121","author":"Andolfo","year":"2013","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0165","doi-asserted-by":"crossref","first-page":"1908","DOI":"10.1182\/blood-2012-04-422253","article-title":"Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis","volume":"120","author":"Zarychanski","year":"2012","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0170","doi-asserted-by":"crossref","first-page":"C419","DOI":"10.1152\/ajpcell.00092.2011","article-title":"Human RhAG ammonia channel is impaired by the Phe65Ser mutation in overhydrated stomatocytic red cells","volume":"302","author":"Genetet","year":"2012","journal-title":"Am. J. Physiol. Cell Physiol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0175","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1111\/j.1365-2141.2011.08921.x","article-title":"Guidelines for the diagnosis and management of hereditary spherocytosis\u20132011 update","volume":"156","author":"Bolton-Maggs","year":"2012","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0180","doi-asserted-by":"crossref","first-page":"516","DOI":"10.3324\/haematol.2011.052845","article-title":"Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics","volume":"97","author":"Bianchi","year":"2012","journal-title":"Haematologica"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0185","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1159\/000322253","article-title":"Reliability of EMA binding test in the diagnosis of hereditary spherocytosis in Italian patients","volume":"125","author":"D'Alcamo","year":"2011","journal-title":"Acta Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0190","doi-asserted-by":"crossref","first-page":"106","DOI":"10.1046\/j.1365-2141.2003.04730.x","article-title":"Eosin-5-maleimide binding to band 3 and Rh-related proteins forms the basis of a screening test for hereditary spherocytosis","volume":"124","author":"King","year":"2004","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0195","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1111\/j.1751-553X.2010.01270.x","article-title":"Detection of hereditary pyropoikilocytosis by the eosin-5-maleimide (EMA)-binding test is attributable to a marked reduction in EMA-reactive transmembrane proteins","volume":"33","author":"King","year":"2011","journal-title":"Int. J. Lab. Hematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0200","first-page":"924","article-title":"Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia","volume":"111","author":"King","year":"2000","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0205","doi-asserted-by":"crossref","first-page":"244","DOI":"10.1002\/cyto.b.20413","article-title":"Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis","volume":"74","author":"King","year":"2008","journal-title":"Cytometry B Clin. Cytom."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0210","doi-asserted-by":"crossref","first-page":"8","DOI":"10.1111\/j.1751-553X.2008.01098.x","article-title":"Evaluation of eosin-5-maleimide flow cytometric test in diagnosis of hereditary spherocytosis","volume":"32","author":"Kar","year":"2010","journal-title":"Int. J. Lab. Hematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0215","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1046\/j.0141-9854.2003.00557.x","article-title":"Experience with eosin-5\u2032-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders","volume":"25","author":"Kedar","year":"2003","journal-title":"Clin. Lab. Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0220","first-page":"570","article-title":"Rapid flow cytometric test using eosin-5-maleimide for diagnosis of red blood cell membrane disorders","volume":"40","author":"Tachavanich","year":"2009","journal-title":"Southeast Asian J. Trop. Med. Public Health"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0225","doi-asserted-by":"crossref","first-page":"625","DOI":"10.1007\/s00277-010-1112-0","volume":"90","author":"Crisp","year":"2011","journal-title":"Ann. Hematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0230","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1111\/j.1365-2141.2007.06944.x","article-title":"Usefulness of the eosin-5\u2032-maleimide cytometric method as a first-line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis","volume":"140","author":"Girodon","year":"2008","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0235","doi-asserted-by":"crossref","first-page":"2894","DOI":"10.1182\/blood.V98.10.2894","article-title":"Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia","volume":"98","author":"Da Costa","year":"2001","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0240","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1016\/S0022-2143(96)90027-X","article-title":"Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity","volume":"128","author":"Cynober","year":"1996","journal-title":"J. Lab. Clin. Med."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0245","doi-asserted-by":"crossref","first-page":"419","DOI":"10.1002\/bimj.200710415","article-title":"Youden Index and optimal cut-point estimated from observations affected by a lower limit of detection","volume":"50","author":"Ruopp","year":"2008","journal-title":"Biom. J."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0250","doi-asserted-by":"crossref","first-page":"e48","DOI":"10.3324\/haematol.2012.074070","article-title":"Testing for hereditary spherocytosis: a French experience","volume":"97","author":"Mayeur-Rousse","year":"2012","journal-title":"Haematologica"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0255","doi-asserted-by":"crossref","first-page":"2169","DOI":"10.1172\/JCI115250","article-title":"Sp alpha V\/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans","volume":"87","author":"Alloisio","year":"1991","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0260","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1042\/BJ20070615","article-title":"Dominant-negative effect of Southeast Asian ovalocytosis anion exchanger 1 in compound heterozygous distal renal tubular acidosis","volume":"410","author":"Kittanakom","year":"2008","journal-title":"Biochem. J."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0265","doi-asserted-by":"crossref","first-page":"425","DOI":"10.1042\/BJ20051076","article-title":"Trafficking defects of the Southeast Asian ovalocytosis deletion mutant of anion exchanger 1 membrane proteins","volume":"392","author":"Cheung","year":"2005","journal-title":"Biochem. J."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0270","doi-asserted-by":"crossref","first-page":"1464","DOI":"10.1016\/j.arcped.2008.04.023","article-title":"Hereditary spherocytosis: guidelines for the diagnosis and management in children","volume":"15","author":"Guitton","year":"2008","journal-title":"Arch. Pediatr."},{"key":"10.1016\/j.bcmd.2015.09.001_bb0275","doi-asserted-by":"crossref","first-page":"768","DOI":"10.1182\/blood.V59.4.768.768","article-title":"A technique to detect reduced mechanical stability of red cell membranes: relevance to elliptocytic disorders","volume":"59","author":"Mohandas","year":"1982","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0280","first-page":"329","article-title":"Ektacytometric analysis of factors regulating red cell deformability","volume":"6","author":"Mohandas","year":"1980","journal-title":"Blood Cells"},{"key":"10.1016\/j.bcmd.2015.09.001_bb0285","first-page":"62","article-title":"Comparison between a camera and a four quadrant detector, in the measurement of red blood cell deformability as a function of osmolality","volume":"2","author":"Finkelstein","year":"2013","journal-title":"J. Med. Biogr."}],"container-title":["Blood Cells, Molecules, and Diseases"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1079979615001679?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1079979615001679?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,21]],"date-time":"2025-10-21T12:31:10Z","timestamp":1761049870000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1079979615001679"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,1]]},"references-count":57,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2016,1]]}},"alternative-id":["S1079979615001679"],"URL":"https:\/\/doi.org\/10.1016\/j.bcmd.2015.09.001","relation":{},"ISSN":["1079-9796"],"issn-type":[{"value":"1079-9796","type":"print"}],"subject":[],"published":{"date-parts":[[2016,1]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer","name":"articletitle","label":"Article Title"},{"value":"Blood Cells, Molecules, and Diseases","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.bcmd.2015.09.001","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2015 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}