Possible Risk Factors for Severe Anemia in Hospitalized Sickle Cell Patients at Muhimbili National Hospital, Tanzania: Protocol for a Cross-Sectional Study-Reference-Cited by-同舟云学术

Possible Risk Factors for Severe Anemia in Hospitalized Sickle Cell Patients at Muhimbili National Hospital, Tanzania: Protocol for a Cross-Sectional Study

Published:2018-02-28 Issue:2 Volume:7 Page:e46
ISSN:1929-0748
Container-title:JMIR Research Protocols
language:en
Short-container-title:JMIR Res Protoc

Author:

Tluway Furahini^ORCID,Urio Florence^ORCID,Mmbando Bruno^ORCID,Sangeda Raphael Zozimus^ORCID,Makubi Abel^ORCID,Makani Julie^ORCID

Publisher

JMIR Publications Inc.

Subject

General Medicine

Reference31 articles.

1. Definitions of the phenotypic manifestations of sickle cell disease

2. Global epidemiology of haemoglobin disorders and derived service indicators

3. The inherited diseases of hemoglobin are an emerging global health burden

4. World Health Organization2017-01-16https://www.scribd.com/document/142734837/WHO-Haemoglobin-Level-for-Anemia-2011

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1. Evaluation of Current Clinical Research Spectrum of Sickle Cell Anemia to Approach New Innovative Developmental Techniques for Enhancing Sudanese Health Systems;2022-10-03

2. Patterns and patient factors associated with loss to follow-up in the Muhimbili sickle cell cohort, Tanzania;BMC Health Services Research;2020-12

3. Epidemiological Characterization of a Directed and Weighted Disease Network Using Data From a Cohort of One Million Patients: Network Analysis;Journal of Medical Internet Research;2020-04-09

4. Sickling-suppressive effects of chrysin may be associated with sequestration of deoxy-haemoglobin, 2,3-bisphosphoglycerate mutase, alteration of redox homeostasis and functional chemistry of sickle erythrocytes;Human & Experimental Toxicology;2019-12-26

5. PREVALENCE AND FACTORS ASSOCIATED WITH HUMAN PARVOVIRUS B19 INFECTION IN SICKLE CELL PATIENTS HOSPITALIZED IN TANZANIA;Mediterranean Journal of Hematology and Infectious Diseases;2019-08-29