Severe autoimmune hemolytic anemia complicating hereditary spherocytosis treated successfully with glucocorticoids and cyclosporine: a case report-Reference-Cited by-同舟云学术

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Severe autoimmune hemolytic anemia complicating hereditary spherocytosis treated successfully with glucocorticoids and cyclosporine: a case report

Published:2023-07-28 Issue:1 Volume:28 Page:
ISSN:1607-8454
Container-title:Hematology
language:en
Short-container-title:Hematology

Author:

Wang Na¹,Lu Hongkai¹,Li Linzhang²,Gong Ming³,Cao Yongtong¹²

Affiliation:

1. Department of Blood Transfusion, China–Japan Friendship Hospital, Beijing, People’s Republic of China

2. Clinical Laboratory, China–Japan Friendship Hospital, Beijing, People’s Republic of China

3. Department of Hematology, China–Japan Friendship Hospital, Beijing, People’s Republic of China

Funder

Key Clinical Specialty Project of Beijing

Publisher

Informa UK Limited

Subject

Hematology,Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/16078454.2023.2235832

Reference33 articles.

1. Diagnosis and treatment of autoimmune hemolytic anemia in adults: Recommendations from the First International Consensus Meeting

2. Defining autoimmune hemolytic anemia: a systematic review of the terminology used for diagnosis and treatment

3. New Insights in the Pathogenesis of Autoimmune Hemolytic Anemia

4. Diagnosis and classification of autoimmune hemolytic anemia

5. Hemolytic anemia: evaluation and differential diagnosis;Phillips J;Am Fam Physician,2018

Cited by 1 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. Coexistence of hereditary spherocytosis with SPTB P.Trp1150 gene variant and Gilbert syndrome: A case report and literature review;Open Life Sciences;2024-01-01

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