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Thalassemia

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

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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.
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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.
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Yangyang Wu, Lin Liao & Faquan Lin. (2021) The diagnostic protocol for hereditary spherocytosis‐2021 update. Journal of Clinical Laboratory Analysis 35:12.
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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.
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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.
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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.
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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.
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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.
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Mariela Granero Farias. (2017) Advances in laboratory diagnosis of hereditary spherocytosis. Clinical Chemistry and Laboratory Medicine (CCLM) 55:7.
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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.
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Thomas Pierre Lecompte & Michael Pierre Bernimoulin. (2015) Novel Parameters in Blood Cell Counters. Clinics in Laboratory Medicine 35:1, pages 209-224.
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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.
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