RED BLOOD CELL INDEXES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS AND β-THALASSEMIA COMBINATION-Reference-Cited by-同舟云学术

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RED BLOOD CELL INDEXES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS AND β-THALASSEMIA COMBINATION

Published:2002-01 Issue:8 Volume:19 Page:569-573
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Akar Nejat,Gökçe Hafize

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.1080/08880010290097431

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hereditary spherocytosis: review of cases and discussion of hematologic characteristics and updated diagnostic testing;Journal of Advanced Pediatrics and Child Health;2023-03-13

2. Hereditary spherocytosis overlooked for 7 years in a pediatric patient with β-thalassemia trait and novel compound heterozygous mutations of SPTA1 gene;Hematology;2020-01-01

3. Combined Hereditary Spherocytosis and β-thalassemia trait: A Rare Co-existence;JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH;2018

4. α‑thalassaemia combined with hereditary spherocytosis in the same patient;Experimental and Therapeutic Medicine;2017-11-28

5. Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases;Clinica Chimica Acta;2016-07

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