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UnknownPalliative care needs of people and/or their families with serious and/or chronic health conditions in low- or middle-income country (LMIC) humanitarian settings-a systematic scoping review protocol.
Not available
S-EPMC11007922 | biostudies-literature
UnknownIntensive care units follow-up: a scoping review protocol.
Not available
S-EPMC7643502 | biostudies-literature
UnknownDefining the gaps in transitional care to adulthood for patients in paediatric surgical specialties: a scoping review protocol.
Not available
S-EPMC11253754 | biostudies-literature
UnknownMethods to derive composite indicators used for quality and safety measurement and monitoring in healthcare: a scoping review protocol.
Not available
S-EPMC10351297 | biostudies-literature
UnknownGlobal image of countries in international wars: A scoping review of influencing factors.
Not available
S-EPMC12507244 | biostudies-literature
UnknownGlobal prevalence of insomnia symptoms in undergraduate university students: a systematic review and meta-analysis.
Not available
S-EPMC12687938 | biostudies-literature
UnknownService-level barriers to and facilitators of access to services for the treatment of alcohol use disorder and problematic alcohol use: protocol for a scoping review.
Not available
S-EPMC9680171 | biostudies-literature
MetabolomicsFeatures of acute COVID-19 associated with post-acute sequelae of SARS-CoV-2 phenotypes: results from the IMPACC study
Post-acute sequelae of SARS-CoV-2 (PASC) is a significant public health concern. We describe Patient Reported Outcomes (PROs) on 590 participants prospectively assessed from hospital admission for COVID-19 through one year after discharge. Modeling identified 4 PRO clusters based on reported deficit...
2024-01-12 | MTBLS850 | MetaboLights
Genomicsena-DATASET-GoT2D/T2D-GENES-09-07-2016-02:03:47:226-1135 - samples
The GoT2D study includes ~2800 samples, half T2D cases and half T2D controls, of Northern European ancestry sequenced over 3 three technologies: deep whole exome sequencing, low-pass (4x) whole genome sequencing, and OMNI 2.5M genotyping. Samples were ascertained to be phenotypically "extreme" (e.g....
EGAD00001002247 | EGA
GenomicsImputation analysis file
This data set includes the following summary level data file used for the imputation data: imputation.sv.assoc.txt: results from single variant association analysis in imputed samples
EGAD00010001184 | EGA
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