Results 201 to 210 of about 874,138 (343)

Portable Low‐Field Magnetic Resonance Imaging in People With Human Immunodeficiency Virus

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective The aging population of people with HIV (PWH) raises heightened concerns regarding accelerated aging and dementia. Portable, low‐field MRI (LF‐MRI) is an innovative technology that could enhance access and facilitate routine monitoring of PWH.
Annabel Sorby‐Adams   +14 more
wiley   +1 more source

Targeting TM4SF1 exhibits therapeutic potential via inhibition of cancer stem cells

open access: yesSignal Transduction and Targeted Therapy, 2022
Guang Chen   +7 more
doaj   +1 more source

Meteorological factors, air pollution, and hospitalization rates of intestinal diseases. [PDF]

open access: yesMedicine (Baltimore)
Wang J   +8 more
europepmc   +1 more source

High Concordance of CT Colonography and Colonoscopy Allows for the Distinguishing and Diagnosing of Intestinal Diseases. [PDF]

open access: yesLife (Basel), 2023
Chervenkov L   +7 more
europepmc   +1 more source

Fibrinogen Changes Before and After Intravenous Thrombolysis as Predictors of Cerebral Injury and Clinical Outcomes in Acute Ischemic Stroke: A Multicenter Prospective Cohort Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Plasma fibrinogen is essential in thrombosis and fibrinolysis, yet its dynamic changes pre‐ and post‐intravenous thrombolysis (IVT) for predicting brain injury severity and prognosis in acute ischemic stroke (AIS) patients remain unclear.
Wenhai Zhai   +28 more
wiley   +1 more source

Lipocalin-2 and intestinal diseases. [PDF]

open access: yesWorld J Gastroenterol
Zhang ZX, Peng J, Ding WW.
europepmc   +1 more source

The emerging roles of bacterial proteases in intestinal diseases. [PDF]

open access: yesGut Microbes, 2023
Caminero A   +3 more
europepmc   +1 more source

Exploratory Analysis of ELP1 Expression in Whole Blood From Patients With Familial Dysautonomia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Familial dysautonomia (FD) is a hereditary neurodevelopmental disorder caused by aberrant splicing of the ELP1 gene, leading to a tissue‐specific reduction in ELP1 protein expression. Preclinical models indicate that increasing ELP1 levels can mitigate disease manifestations.
Alejandra González‐Duarte   +13 more
wiley   +1 more source

Home - About - Disclaimer - Privacy