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Sickle cell disease: progress towards combination drug therapy

Published:2021-01-20 Issue:2 Volume:194 Page:240-251
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br. J. Haematol.

Author:

Pace Betty S.¹²^ORCID,Starlard‐Davenport Athena³^ORCID,Kutlar Abdullah⁴

Affiliation:

1. Department of Pediatrics Augusta University Augusta GAUSA

2. Department of Biochemistry and Molecular Biology Augusta University Augusta GAUSA

3. Department of Genetics, Genomics and Informatics University of Tennessee Health Science Center Memphis TN38163USA

4. Department of Medicine Center for Blood Disorders Augusta University Augusta GA USA

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.17312

Reference118 articles.

1. The cost of health care for children and adults with sickle cell disease

2. Sickle Hemoglobin (Hb S) Allele and Sickle Cell Disease: A HuGE Review

3. Improved survival of children and adolescents with sickle cell disease

4. Survival in adults with sickle cell disease in a high-income setting

5. How I treat the older adult with sickle cell disease

Cited by 23 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. Voxelotor (GBT440) in pediatric sickle cell disease: A review;Pediatric Hematology Oncology Journal;2024-12

2. Prevalence of metabolic syndrome in sickle cell disease patients: A cross‐sectional study at a tertiary hospital in Nepal;eJHaem;2024-08-05

3. The enigma of sickle cell hepatopathy: Pathophysiology, clinical manifestations and therapy;British Journal of Haematology;2024-07-08

4. Hydroxyurea in Sickle Cell Disease and Invasive Bacterial Infections: A Case–Control Study;Journal of the Pediatric Infectious Diseases Society;2024-07-06

5. Role of gene therapy in sickle cell disease;Disease-a-Month;2024-07

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