“Maximum tolerated dose” vs “fixed low‐dose” hydroxyurea for treatment of adults with sickle cell anemia-Reference-Cited by-同舟云学术

“Maximum tolerated dose” vs “fixed low‐dose” hydroxyurea for treatment of adults with sickle cell anemia

Published:2019-02-06 Issue:4 Volume:94 Page:
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am J Hematol

Author:

Akingbola Titilola S.¹,Tayo Bamidele O.²^ORCID,Ezekekwu Chinedu A.¹,Sonubi Omowunmi¹,Zhang Xu³,Saraf Santosh L.³^ORCID,Molokie Robert³⁴,Hsu Lewis L.⁵^ORCID,Han Jin⁶^ORCID,Cooper Richard S.²,Gordeuk Victor R.³^ORCID

Affiliation:

1. Department of Hematology, University of Ibadan College of Medicine, University College Hospital Ibadan Nigeria

2. Department of Public Health Sciences Loyola University Chicago Stritch School of Medicine Maywood Illinois

3. Division of Hematology & Oncology, Department of Medicine University of Illinois at Chicago Chicago Illinois

4. Jesse Brown VA Chicago Illinois

5. Division of Pediatric Hematology‐Oncology, Department of Pediatrics University of Illinois at Chicago Chicago Illinois

6. Department of Pharmacy Practice University of Illinois at Chicago Chicago Illinois

Funder

Doris Duke Charitable Foundation

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.25412

Reference15 articles.

1. Proportion of Adults With Sickle Cell Anemia and Pain Crises Receiving Hydroxyurea

2. Fixed low-dose hydroxyurea for the treatment of adults with sickle cell anemia in Nigeria

3. Hydroxyurea and Sickle Cell Anemia Clinical Utility of a Myelosuppressive “Switching” Agent

4. Effect of Hydroxyurea on the Frequency of Painful Crises in Sickle Cell Anemia

5. Hydroxyurea for the Treatment of Sickle Cell Anemia

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1. Hydroxyurea at escalated dose versus fixed low‐dose hydroxyurea in adults with sickle cell disease;European Journal of Haematology;2023-11-29

2. Design of an adaptive randomized clinical trial of intravenous citrulline for sickle cell pain crisis in the emergency department;Contemporary Clinical Trials Communications;2023-04

3. Transcranial Doppler screening in Nigerian children with sickle cell disease: A 10‐year longitudinal study on the SPPIBA cohort;Pediatric Blood & Cancer;2021-02

4. The Worst Things in Life are Free: The Role of Free Heme in Sickle Cell Disease;Frontiers in Immunology;2021-01-27

5. Hydroxycarbamide exposure and ovarian reserve in women with sickle cell disease in the Multicenter Study of Hydroxycarbamide;British Journal of Haematology;2020-07-26