Results 191 to 200 of about 8,071,853 (298)
Scoping review protocol of interventions for widening access to healthcare services in people living with rare diseases in Africa. [PDF]
Seheri M +5 more
europepmc +1 more source
Abstract Evaluations of community‐engaged research (CEnR) typically emphasize health outcomes rather than the partnership processes that contribute to intervention effectiveness. This scoping review synthesized community partner‐identified strategies for successful community‐academic health research partnerships with Black American communities and ...
Kaylyn A. Garcia +6 more
wiley +1 more source
Broiler Farming in Africa vs. the EU: Divergent Systems, Shared Challenges, and Future Directions-A Review. [PDF]
Ludwiczak A, Temitope A.
europepmc +1 more source
ABSTRACT Although circulating nucleated red blood cells (cNRBCs) have previously been detected in patients with sickle cell disease (SCD), their prevalence and clinical significance during steady‐state disease have not been established. We retrospectively analyzed 270 adults with an SS or Sβ0‐thalassemia genotype.
Ugo Boccadifuoco +7 more
wiley +1 more source
The status, or conspicuous absence, of regulation of proprietary or locally manufactured African traditional medicines in South Africa: a constitutional injustice. [PDF]
Gambo A, Gqaleni N, Lebina L.
europepmc +1 more source
ABSTRACT Microdeletions impacting 15q11.2 breakpoint (BP) 1 to BP2, adjacent to the Prader–Willi critical region, have previously described neuropsychiatric associations, with potential low penetrance presentations of congenital heart disease (CHD) also identified.
Morgan B. Wright +10 more
wiley +1 more source
Vaccine equity in Africa: a rapid review of policy, legal and governance frameworks to improve research and development. [PDF]
Ataguba JE +11 more
europepmc +1 more source
Mobilities and Cosmopolitanisms in African and Afrodiasporic Literatures (Anna-Leena Toivanen)
Polo B. Moji
doaj
Genetic Variation in ADHD‐Related Risk Genes in an Indigenous Population of the Amazon
ABSTRACT Attention‐Deficit/Hyperactivity Disorder (ADHD) is a highly heritable neurodevelopmental disorder; however, its genetic architecture remains poorly explored in Indigenous populations. This study aimed to analyze and characterize genetic variation in 11 genes (ADGRL3, CDH8, DCC, DUSP6, FOXP1, FOXP2, MEF2C, PCDH7, SEMA6D, SORCS3, and ST3GAL3 ...
Hirlesson Paixão de Matos +11 more
wiley +1 more source

