{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,6,29]],"date-time":"2024-06-29T03:40:08Z","timestamp":1719632408564},"reference-count":23,"publisher":"Spandidos Publications","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Exp Ther Med"],"DOI":"10.3892\/etm.2017.5579","type":"journal-article","created":{"date-parts":[[2017,11,28]],"date-time":"2017-11-28T08:01:42Z","timestamp":1511856102000},"source":"Crossref","is-referenced-by-count":0,"title":["\u03b1\u2011thalassaemia combined with hereditary spherocytosis in the same patient"],"prefix":"10.3892","author":[{"given":"Xiaohong","family":"Li","sequence":"first","affiliation":[{"name":"Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lin","family":"Liao","sequence":"additional","affiliation":[{"name":"Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xuelian","family":"Deng","sequence":"additional","affiliation":[{"name":"Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jian","family":"Huang","sequence":"additional","affiliation":[{"name":"Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zengfu","family":"Deng","sequence":"additional","affiliation":[{"name":"Department of Clinical Laboratory, First Affiliated Hospital of Guangxi University of Traditional Chinese Medicine, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hongying","family":"Wei","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wuning","family":"Mo","sequence":"additional","affiliation":[{"name":"Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Faquan","family":"Lin","sequence":"additional","affiliation":[{"name":"Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"2249","published-online":{"date-parts":[[2017,11,28]]},"reference":[{"key":"key20200713143451_b1-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"419","DOI":"10.1111\/j.1399-0004.2007.00791.x","article-title":"Current status of thalassemia in minority populations in Guangxi, China","volume":"71","author":"Pan","year":"2007","journal-title":"Clin Genet"},{"key":"key20200713143451_b2-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"28","DOI":"10.3109\/03630269.2010.547429","article-title":"Molecular spectrum of \u03b1- and \u03b2-globin gene mutations detected in the population of Guangxi Zhuang Autonomous Region, People's Republic of China","volume":"35","author":"Zheng","year":"2011","journal-title":"Hemoglobin"},{"key":"key20200713143451_b3-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"139","DOI":"10.1111\/j.1399-0004.2010.01430.x","article-title":"Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China","volume":"78","author":"Xiong","year":"2010","journal-title":"Clin Genet"},{"key":"key20200713143451_b4-etm-0-0-5579","first-page":"204","article-title":"Compound heterozygote factor and clinical significance of hemolysis system analysis in the diagnosis of congenital hemolytic anemia: Etiological analysis of 506 cases of anemia and jaundice","volume":"18","author":"Li","year":"2005","journal-title":"J Clin Hematol"},{"key":"key20200713143451_b5-etm-0-0-5579","doi-asserted-by":"publisher","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":"key20200713143451_b6-etm-0-0-5579","volume-title":"National Guide to Clinical Laboratory Procedures","author":"Shang","year":"2014","edition":"4th"},{"key":"key20200713143451_b7-etm-0-0-5579","volume-title":"Guidelines for Thalassemia Prevention and Control Programme","author":"Xu","year":"2011"},{"key":"key20200713143451_b8-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"373","DOI":"10.1016\/S0140-6736(11)60283-3","article-title":"Thalassaemia","volume":"379","author":"Higgs","year":"2012","journal-title":"Lancet"},{"key":"key20200713143451_b9-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"13","DOI":"10.1186\/1750-1172-5-13","article-title":"Alpha-thalassaemia","volume":"5","author":"Harteveld","year":"2010","journal-title":"Orphanet J Rare Dis"},{"key":"key20200713143451_b10-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"1908","DOI":"10.1056\/NEJMra1404415","article-title":"The \u03b1-thalassemias","volume":"371","author":"Piel","year":"2014","journal-title":"N Engl J Med"},{"key":"key20200713143451_b11-etm-0-0-5579","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":"key20200713143451_b12-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"37","DOI":"10.1111\/j.1365-2141.2011.08921.x","article-title":"Guidelines for the diagnosis and management of hereditary spherocytosis-2011 update","volume":"156","author":"Bolton-Maggs","year":"2012","journal-title":"Br J Haematol"},{"key":"key20200713143451_b13-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"373","DOI":"10.1111\/j.1600-0609.2009.01289.x","article-title":"The use of real-time PCR technique in the detection of novel protein 4.2 gene mutations that coexist with thalassaemia alpha in a single patient","volume":"83","author":"Maciag","year":"2009","journal-title":"Eur J Haematol"},{"key":"key20200713143451_b14-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"271","DOI":"10.3109\/08880019809028796","article-title":"Alpha-Thalassemia and hereditary spherocytosis in the same patient: The interaction of two diseases","volume":"15","author":"Uysal","year":"1998","journal-title":"Pediatr Hematol Oncol"},{"key":"key20200713143451_b15-etm-0-0-5579","first-page":"137","article-title":"Homozygous \u00df-thalassemia (FCS8-AA) and hereditary spherocytosis in the same patient","volume":"18","author":"Uysal","year":"2001","journal-title":"Turk J Haematol"},{"key":"key20200713143451_b16-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"569","DOI":"10.1080\/08880010290097431","article-title":"Red blood cell indexes in patients in patients with hereditary spherocytosis and beta-thalassemia combination","volume":"19","author":"Akar","year":"2002","journal-title":"Pediatr Hematol Oncol"},{"key":"key20200713143451_b17-etm-0-0-5579","first-page":"225","article-title":"Differential diagnosis of hereditary spherocytosis associated with beta thalassemia","volume":"9","author":"Li","year":"2010","journal-title":"J Diagnos Concepts Pract"},{"key":"key20200713143451_b18-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"519","DOI":"10.1111\/j.1751-553X.2009.01216.x","article-title":"Evaluation of mean sphered corpuscular volume for predicting hereditary spherocytosis","volume":"32","author":"Bros\u00e9us","year":"2010","journal-title":"Int J Lab Hematol"},{"key":"key20200713143451_b19-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"393","DOI":"10.1179\/1607845413Y.0000000149","article-title":"Values of mean cell volume and mean sphered cell volume can differentiate hereditary spherocytosis and thalassemia","volume":"19","author":"Liao","year":"2014","journal-title":"Hematology"},{"key":"key20200713143451_b20-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"170","DOI":"10.1111\/ejh.12563","article-title":"Mean reticulocyte volume: A specific parameter to screen for hereditary spherocytosis","volume":"96","author":"Xu","year":"2016","journal-title":"Eur J Haematol"},{"key":"key20200713143451_b21-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"337","DOI":"10.1007\/s00277-006-0083-7","article-title":"(AC)n microsatellite polymorphism and 14-nucleotide deletion in exon 42 ankyrin-1 gene in several families with hereditary spherocytosis in a population of South-Western Poland","volume":"85","author":"Bogus\u0142awska","year":"2006","journal-title":"Ann Hematol"},{"key":"key20200713143451_b22-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"669","DOI":"10.1046\/j.1365-2141.2003.04479.x","article-title":"Simultaneous (AC)n microsatellite polymorphism analysis and single-stranded conformation polymorphism screening is an efficient strategy for detecting ankyrin-1 mutations in dominant hereditary spherocytosis","volume":"122","author":"Ozcan","year":"2003","journal-title":"Br J Haematol"},{"key":"key20200713143451_b23-etm-0-0-5579","doi-asserted-by":"publisher","first-page":"5491","DOI":"10.1182\/blood-2006-09-046573","article-title":"A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis","volume":"109","author":"Edelman","year":"2007","journal-title":"Blood"}],"container-title":["Experimental and Therapeutic Medicine"],"original-title":[],"deposited":{"date-parts":[[2024,6,29]],"date-time":"2024-06-29T03:24:31Z","timestamp":1719631471000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.spandidos-publications.com\/10.3892\/etm.2017.5579"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,11,28]]},"references-count":23,"URL":"https:\/\/doi.org\/10.3892\/etm.2017.5579","relation":{},"ISSN":["1792-0981","1792-1015"],"issn-type":[{"value":"1792-0981","type":"print"},{"value":"1792-1015","type":"electronic"}],"subject":[],"published":{"date-parts":[[2017,11,28]]}}}