Results 231 to 240 of about 232,303 (307)

Prevalence of poor sleep quality among critical care unit nurses: a systematic review and meta-analysis. [PDF]

BMC Nurs
Sanaie N, Sarmadi S, Zare-Kaseb A.
europepmc   +1 more source

Guidance for umbrella reviews of observational studies: A scoping review

JCPP Advances, Volume 6, Issue 1, March 2026.
This review examined existing guidance on conducting and reporting umbrella reviews of observational studies on epidemiological associations, aiming to help develop a formal reporting guideline. The search identified 4491 records, with eight documents providing limited guidance across seven topic areas.
Carl Zhou, Nicholas Fabiano, Arnav Gupta, Stanley Wong, Kelly D. Cobey, David Moher, Sanam Ebrahimzadeh, Jeremy Y. Ng, Elena Dragioti, Jae Il Shin, Joaquim Radua, Samuele Cortese, Beverley Shea, Nicola Veronese, Lisa Hartling, Michelle Pollock, Stefania Papatheodorou, John P. A. Ioannidis, Marco Solmi   +18 more
wiley   +1 more source

CNS Myelin Sheath Lengths Locally Scale to Axon Diameter via Piezo1

Young AR, Lewis RW, Cash M, Polis B, Zalusky M, Reyngoudt J, Datta A, Bechler ME.   +7 more
europepmc   +1 more source

A comparison of acceptability of contraceptive vaginal rings, pills, and injectables among cisgender women in Kenya and Zimbabwe: protocol for a mixed-methods study. [PDF]

Gates Open Res
Polis CB, Obare FO, Bruce IV, Banda C, Haddad LB, Heyns A, Isaakidis P, Kamupira M, Kufakunesu T, Kwena ZA, Machinga F, Magore RF, Mapangire A, Marimirofa M, Mathipa M, Mathur S, Mudavanhu M, Mujuru TP, Mutero P, Njoroge B, Nyatsambo C, Okumu S, Omondi L, Omondi T, Plagianos MG, Rota G, Sithole S, Variano B, Burnett-Zieman JB, Musara P, Odwe G, Hangaika G, Gitome S, Bukusi EA, Kuwenyi K.   +34 more
europepmc   +1 more source

A Meta‐Analysis to Unveil the Diagnostic Gaps in Anderson–Fabry Disease in Women

Journal of Inherited Metabolic Disease, Volume 49, Issue 2, March 2026.
ABSTRACT Anderson–Fabry disease (AFD) is an X‐linked lysosomal storage disorder caused by mutations in the GLA gene, leading to deficient α‐galactosidase A activity. Although historically considered a male disease, it is now recognized that heterozygous women can present with a wide range of symptoms. However, diagnosis in women remains challenging, as
L. Lenzini, G. Pintus, G. Gugelmo, A. P. Burlina, G. P. Fadini, A. B. Burlina, N. Vitturi   +6 more
wiley   +1 more source

Images of Extremely Rare Cantrell Phenomenon. [PDF]

Diagnostics (Basel)
Fabijan A, Korabiewska-Pluta S, Puzio T, Polis B, Moszura T.   +4 more
europepmc   +1 more source

Scoring Criteria for Autoimmune Bullous Diseases: Utility, Merits, and Demerits. [PDF]

Indian Dermatol Online J
Tseng H, Stone C, Murrell DF.
europepmc   +1 more source