Results 191 to 200 of about 363,740 (285)
ABSTRACT Background Healthcare decision‐making for individuals with rare genetic neurodevelopmental disorders (RGNDs) associated with intellectual disabilities (ID) can be complex due to the intersection of lifelong care needs, limited medical expertise and communication barriers.
Mirthe J. Klein Haneveld +6 more
wiley +1 more source
ABSTRACT The visit to Bogotá of a fééeneminaa (Muinane) friend, Célimo Nejedeka Jifichíu, and in particular, his work in researching and transmitting traditional health knowledge, offer the pretext to navigate the relationship between elements that at first glance seem distant from each other: indigenous imaginaries about otherness, their visions of ...
Giovanna Micarelli
wiley +1 more source
Educational attainment is associated with reduced functional decline in Puerto Ricans with elevated pTau181. [PDF]
Dorfsman DA +34 more
europepmc +1 more source
ABSTRACT Introduction Point‐of‐care ultrasound has become an essential tool in critical care medicine. The provision of adequate ultrasound training is one of the most significant barriers to point‐of‐care ultrasound adoption. Sonographers are a valuable resource for ultrasound training but often lack support and formal recognition of their role as ...
Carolynne Cormack +15 more
wiley +1 more source
Perceived physical literacy instruments for sports club coaches: further differentiated validation. [PDF]
Fu J, Zhang W, Cao B, Yu H, Li H.
europepmc +1 more source
X‐Linked Anhidrotic Ectodermal Dysplasia in A 19‐Year‐Old Male: A Classic Phenotype
ABSTRACT X‐linked anhidrotic/hypohidrotic ectodermal dysplasia (XLHED), also known as Christ‐Siemens‐Touraine syndrome, is a rare genetic disorder characterized by the abnormal development of ectodermal structures, primarily affecting sweat glands, hair, and teeth. It results from mutations in the Ectodysplasin A (EDA) gene.
Laxman Chapagain +4 more
wiley +1 more source
The Insistence of Possibles Towards a Speculative Pragmatism
Isabelle Stengers
doaj

