Results 191 to 200 of about 347,172 (240)

Molecular and Transcriptional Signatures of Gray Matter Volume Alterations Associated With Depressive Symptoms in Mild Cognitive Impairment

open access: yesHuman Brain Mapping, Volume 47, Issue 2, February 1, 2026.
Morphological alterations related to depressive symptoms in mild cognitive impairment were primarily involved in emotion and affective processing, showing strong correspondence with serotonergic, dopaminergic, and GABAergic systems and enrichment of genes associated with synaptic function and excitatory neurons.
Hu Xu   +9 more
wiley   +1 more source

Feasibility of the Modified Telephone Interview for Cognitive Status (M‐TICS) in the peri‐operative environment

open access: yesAnaesthesia, Volume 81, Issue 2, Page 240-247, February 2026.
Summary Introduction Peri‐operative neurocognitive disorders are common among older adults presenting for surgery and anaesthesia. Cognitive screening is recommended to identify patients at risk for adverse neurocognitive outcomes, though the most appropriate peri‐operative tool remains debated.
Kelly J. Atkins   +6 more
wiley   +1 more source

Systematic Review and Meta‐Analysis of the Association Between Subjective and Objective Cognitive Function in Mood Disorders

open access: yesBipolar Disorders, Volume 28, Issue 1, February 2026.
ABSTRACT Introduction The association between subjective and objective cognitive function in mood disorders is hotly debated, particularly in the choice of outcomes to measure pro‐cognitive effects of interventions. We systematically reviewed the evidence regarding this association, including analysis of predicting or moderating factors.
Kate Eggleston   +4 more
wiley   +1 more source

RNA Analysis Uncovers Pathogenic PARN Variant in Dyskeratosis Congenita

open access: yesClinical Genetics, Volume 109, Issue 2, Page 346-351, February 2026.
Using WGS and RNA analysis, we identified a branch point‐disrupting variant in the PARN gene and elucidated its pathogenic molecular mechanism in a child with atypical dyskeratosis congenita presentation. ABSTRACT Dyskeratosis congenita (DC) is a rare genetic disorder caused by impaired telomere maintenance, leading to diverse clinical manifestations ...
Daria Akimova   +3 more
wiley   +1 more source

Psychomotor therapy for posttraumatic stress disorder

open access: hybrid
Minke M. van de Kamp   +5 more
openalex   +1 more source

Home - About - Disclaimer - Privacy