Advanced search
Publication Cover
Hematology Volume 19, 2014 - Issue 7
Submit an article Journal homepage
1,100
Views
13
CrossRef citations to date
0
Altmetric
Thalassemia

Values of mean cell volume and mean sphered cell volume can differentiate hereditary spherocytosis and thalassemia

Lin LiaoDepartment of Clinical LaboratoryThe First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China
,
Zeng-Fu DengDepartment of Clinical LaboratoryThe First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China
,
Yu-Ling QiuDepartment of Pediatric LaboratoryThe First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China
,
Ping ChenDepartment of Pediatric LaboratoryThe First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China
,
Wen-Qiang ChenDepartment of Pediatric LaboratoryThe First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China
&
Fa-Quan LinDepartment of Clinical LaboratoryThe First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, ChinaCorrespondence[email protected]
Pages 393-396 | Published online: 20 Jan 2014

Citations (13)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (1)

Min Chen, Yu-Ping Ye, Lin Liao, Xue-Lian Deng, Yu-Ling Qiu & Fa-Quan Lin. (2020) Hereditary spherocytosis overlooked for 7 years in a pediatric patient with β-thalassemia trait and novel compound heterozygous mutations of SPTA1 gene. Hematology 25:1, pages 438-445.
Read now

Articles from other publishers (12)

Adedamola Bello. 2023. The Misdiagnosis Casebook in Clinical Medicine. The Misdiagnosis Casebook in Clinical Medicine 275 282 .
Shiyue Ma, Lingjian Tang, Chaoli Wu, Hui Tang, Xue Pu & Jinhong Niu. (2022) Study on Management of Blood Transfusion Therapy in Patients with Hereditary Spherocytosis. Applied Bionics and Biomechanics 2022, pages 1-9.
Crossref
Yangyang Wu, Lin Liao & Faquan Lin. (2021) The diagnostic protocol for hereditary spherocytosis‐2021 update. Journal of Clinical Laboratory Analysis 35:12.
Crossref
Lin Liao, Yuchan Xu, Hongying Wei, Yuling Qiu, Wenqiang Chen, Jian Huang, Yifeng Tao, Xuelian Deng, Zengfu Deng, Hui Tao & Faquan Lin. (2019) Blood cell parameters for screening and diagnosis of hereditary spherocytosis. Journal of Clinical Laboratory Analysis 33:4, pages e22844.
Crossref
Manu Jamwal, Anu Aggarwal, Man Updesh Singh Sachdeva, Prashant Sharma, Pankaj Malhotra, Arindam Maitra & Reena Das. (2018) Overhydrated stomatocytosis associated with a complex RHAG genotype including a novel de novo mutation . Journal of Clinical Pathology 71:7, pages 648-652.
Crossref
Shiyue Ma, Jinqiu Qin, Aiqiu Wei, Xiaohong Li, Yuanyuan Qin, Lin Liao & Faquan Lin. (2018) Novel compound heterozygous SPTA1 mutations in a patient with hereditary elliptocytosis. Molecular Medicine Reports.
Crossref
Ben-Jin He, Lin Liao, Zeng-Fu Deng, Yi-Feng Tao, Yu-Chan Xu & Fa-Quan Lin. (2018) Molecular Genetic Mechanisms of Hereditary Spherocytosis: Current Perspectives. Acta Haematologica 139:1, pages 60-66.
Crossref
Xiaohong Li, Lin Liao, Xuelian Deng, Jian Huang, Zengfu Deng, Hongying Wei, Wuning Mo & Faquan Lin. (2017) α‑thalassaemia combined with hereditary spherocytosis in the same patient. Experimental and Therapeutic Medicine.
Crossref
Mariela Granero Farias. (2017) Advances in laboratory diagnosis of hereditary spherocytosis. Clinical Chemistry and Laboratory Medicine (CCLM) 55:7.
Crossref
Yuchan Xu, Wang Yang, Lin Liao, Zengfu Deng, Yuling Qiu, Wenqiang Chen & Faquan Lin. (2016) Mean reticulocyte volume: a specific parameter to screen for hereditary spherocytosis. European Journal of Haematology 96:2, pages 170-174.
Crossref
Thomas Pierre Lecompte & Michael Pierre Bernimoulin. (2015) Novel Parameters in Blood Cell Counters. Clinics in Laboratory Medicine 35:1, pages 209-224.
Crossref
Zengfu Deng, Lin Liao, Wang Yang & Faquan Lin. (2015) Misdiagnosis of two cases of hereditary spherocytosis in a family and review of published reports. Clinica Chimica Acta 441, pages 6-9.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.