This paper is in the following e-collection/theme issue:

Non-Randomized Study Protocols and Methods (Non-eHealth) (571)

Published on in Vol 7, No 2 (2018): February

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/7349, first published .
Possible Risk Factors for Severe Anemia in Hospitalized Sickle Cell Patients at Muhimbili National Hospital, Tanzania: Protocol for a Cross-Sectional Study

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

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

Authors of this article:

Furahini Tluway1 Author Orcid Image ;   Florence Urio2 Author Orcid Image ;   Bruno Mmbando3 Author Orcid Image ;   Raphael Zozimus Sangeda4 Author Orcid Image ;   Abel Makubi5 Author Orcid Image ;   Julie Makani1 Author Orcid Image
Article Authors Cited by (4) Tweetations (8) Metrics

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  2. Muhammad A, Waziri A, Forcados G, Sanusi B, Sani H, Malami I, Abubakar I, Muhammad A, Muhammad R, Mohammed H. 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 2020;39(4):537 View
  3. Ko K, Lee C, Nam S, Ahn S, Bae J, Ban C, Yoo J, Park J, Han H. 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;22(4):e15196 View
  4. Makani J, Masamu U, Tluway F, Sangeda R, Soka D, Osati E, Kindole C, Cox S, Mgaya J, Shayo S, Makubi A, Balandya E, Mmbando B. The epidemiology of very severe anaemia in sickle cell disease in Tanzania: a prospective cohort study. eClinicalMedicine 2024;76:102839 View