Results 251 to 260 of about 6,018,350 (361)
Error‐correction Mechanism Tests for Cointegration in a Single‐equation Framework
A. Banerjee, J. Dolado, R. Mestre
semanticscholar +1 more source
Glymphatic Dysfunction Reflects Post‐Concussion Symptoms: Changes Within 1 Month and After 3 Months
ABSTRACT Objective Mild traumatic brain injury (mTBI) may alter glymphatic function; however, its progression and variability remain obscure. This study examined glymphatic function following mTBI within 1 month and after 3 months post‐injury to determine whether variations in glymphatic function are associated with post‐traumatic symptom severity ...
Eunkyung Kim +3 more
wiley +1 more source
O16 A regional prison cleared of hepatitis C in less than 12 months
D.B. Russell +8 more
doaj +1 more source
The impact of data driven motion correction for clinical brain PET/MRI radiotracers. [PDF]
Bolin M, Falk Delgado A, Palmér E.
europepmc +1 more source
ABSTRACT Objective Accurate localization of epileptogenic tubers (ETs) in patients with tuberous sclerosis complex (TSC) is essential but challenging, as these tubers lack distinct pathological or genetic markers to differentiate them from other cortical tubers.
Tinghong Liu +11 more
wiley +1 more source
Correction: Effects of Capsular Polysaccharide amount on Pneumococcal-Host interactions. [PDF]
PLOS Pathogens Editors.
europepmc +1 more source
ABSTRACT Objective People with epilepsy (PWE) may experience cognitive deficits but fail to undergo formal evaluation. This study compares cognitive status between PWE and healthy controls in the West African Republic of Guinea. Methods A cross‐sectional, case–control study was conducted in sequential recruitment phases (July 2024–July 2025) at Ignace ...
Maya L. Mastick +14 more
wiley +1 more source
Correction: Exploratory analysis of gene aberrations and chemotherapy response: findings from a real-world database in Japan. [PDF]
Ishibashi N +5 more
europepmc +1 more source
Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron +5 more
wiley +1 more source

