Background: Fibrodysplasia ossificans progressiva is a rare autosomal dominant connective tissue disorder with a prevalence of 2 per million individuals.Activating mutation of ACVR1, a bone morphogenetic protein receptor causes ossification of extra-skeletal structures like ligaments, tendons, and aponeurosis.The BAGS characteristic findings are bi
Health worker perspectives of Smart Triage, a digital triaging platform for quality improvement at a referral hospital in Uganda: a qualitative analysis
Abstract Background Effective triage at hospitals can improve outcomes for children globally by helping identify and prioritize care for those most at-risk of death.Paper-based pediatric triage guidelines have been developed to support frontline health workers in low-resource settings, but these guidelines can be challenging to implement.Smart Tria
Ascl1 is a required downstream effector of Gsx gene function in the embryonic mouse telencephalon
Abstract Background The homeobox gene Gsx2 (formerly Gsh2) is known to regulate patterning in the lateral ganglionic eminence (LGE) of the embryonic telencephalon.In its absence, the closely related gene Gsx1 (previously known as Gsh1) can partially compensate in the patterning and differentiation of ventral telencephalic structures, such as the st