Regional variation in the prevalence of sickle cell anemia (HBSS) across Africa.

Regional variation in the prevalence of sickle cell anemia (HBSS) across Africa.

<p>Map created by authors using shapefiles from GADM (Database of Global Administrative Areas, version 4.1, <a href="https://www.gadm.org" target="_blank">www.gadm.org</a>).</p>

Αποθηκεύτηκε σε:

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριος συγγραφέας:	Bwambale Jonani (21156747) (author)
Άλλοι συγγραφείς:	Emmanuel Charles Kasule (21156750) (author), Bwire Roman Herman (21168941) (author), Joel Fredrick Arturo (21156756) (author), Mwesigwa Calvin Mugambwa (22683322) (author), Ssebulime Stephen (21156771) (author), John Bosco Mundaka (20309196) (author), Richard Kwizera (606632) (author), Gerald Mboowa (770601) (author), Felix Bongomin (5081681) (author)
Έκδοση:	2025
Θέματα:	Biotechnology Science Policy Infectious Diseases Biological Sciences not elsewhere classified three decades despite systematically searched pubmed sickle cell anemia electrophoretic techniques predominated 21 %– 8 1994 &# 8211 improved diagnostic accessibility southern africa showed sensitivity analysis showed central africa showed 74 %; p significant genetic disorder including geographic region 08 %– 1 analysis </ p 2 </ sup males 2 diagnostic method xlink "> temporal variations systematic review subgroup analyses study variability study design specific interventions significantly moderated research output remained stable quality assurance quality assessments prediction interval marginally significant logit transformation google scholar fold increase findings highlight examine regional continued surveillance comprehensive data children exhibited cases ). care technologies base databases african populations 91 %. 88 %), 839 participants 694 ). 65 %) 6 %).
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