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Formulas for the Detection β-Thalassemia Carriers Are Affected by Changes in Red Cell Parameters.

作者信息

Aslan Deniz

机构信息

Section of Hematology, Department of Pediatrics, Faculty of Medicine, Gazi University, Ankara, Turkey.

出版信息

Mediterr J Hematol Infect Dis. 2018 Apr 20;10(1):e2018026. doi: 10.4084/MJHID.2018.026. eCollection 2018.

DOI:10.4084/MJHID.2018.026
PMID:29757336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5937978/
Abstract
摘要

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Detection of β-Thalassemia Carriers by Red Cell Parameters Obtained from Automatic Counters using Mathematical Formulas.使用数学公式通过自动血细胞计数器获得的红细胞参数检测β地中海贫血携带者
Mediterr J Hematol Infect Dis. 2018 Jan 1;10(1):e2018008. doi: 10.4084/MJHID.2018.008. eCollection 2018.
2
Reliability of Different RBC Indices and Formulas in Discriminating between β-Thalassemia Minor and other Microcytic Hypochromic Cases.不同红细胞指数及公式在鉴别轻型β地中海贫血与其他小细胞低色素性贫血病例中的可靠性
Mediterr J Hematol Infect Dis. 2015 Feb 20;7(1):e2015022. doi: 10.4084/MJHID.2015.022. eCollection 2015.
3
δβ-Thalassemia trait: how can we discriminate it from β-thalassemia trait and iron deficiency anemia?δβ-地中海贫血性状：如何将其与β-地中海贫血性状和缺铁性贫血区分开来？
Am J Clin Pathol. 2014 Oct;142(4):567-73. doi: 10.1309/AJCPPBQ8UB1WHXTS.
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KLF1 gene mutations cause borderline HbA(2).KLF1 基因突变导致边缘性 HbA(2)。
Blood. 2011 Oct 20;118(16):4454-8. doi: 10.1182/blood-2011-04-345736. Epub 2011 Aug 5.
5
Incidence of high erythrocyte count in infants and young children with iron deficiency anemia: re-evaluation of an old parameter.缺铁性贫血婴幼儿高红细胞计数的发生率：对一个旧参数的重新评估
J Pediatr Hematol Oncol. 2003 Apr;25(4):303-6. doi: 10.1097/00043426-200304000-00007.
6
Laboratory investigation of hemoglobinopathies and thalassemias: review and update.血红蛋白病和地中海贫血的实验室研究：综述与更新
Clin Chem. 2000 Aug;46(8 Pt 2):1284-90.
7
Molecular, haematological and clinical studies of the -101 C --> T substitution of the beta-globin gene promoter in 25 beta-thalassaemia intermedia patients and 45 heterozygotes.对25例中间型β地中海贫血患者和45例杂合子β珠蛋白基因启动子-101 C→T替换的分子、血液学及临床研究。
Br J Haematol. 1999 Dec;107(4):699-706. doi: 10.1046/j.1365-2141.1999.01788.x.
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Genetic analysis of beta-thalassemia intermedia in Israel: diversity of mechanisms and unpredictability of phenotype.以色列中间型β地中海贫血的基因分析：机制多样性与表型不可预测性
Am J Hematol. 1997 Jan;54(1):16-22. doi: 10.1002/(sici)1096-8652(199701)54:1<16::aid-ajh3>3.0.co;2-7.