Results 201 to 210 of about 489,431 (300)

Abnormal temporal prediction relates to psychomotor retardation in major depressive disorder [PDF]

open access: green
Jianfeng Zhang   +8 more
openalex   +1 more source

Isolated absence epilepsy associated with a de novo FBXW7 missense variant in the F‐box domain

open access: yesEpilepsia Open, Volume 11, Issue 2, Page 643-651, April 2026.
Abstract The FBXW7 gene encodes a substrate‐recognition component of the Skp1‐Cul1‐F‐box (SCF) E3 ubiquitin ligase complex, which targets key regulatory proteins for proteasomal degradation. Recently, loss‐of‐function FBXW7 variants have been associated with a novel neurodevelopmental disorder characterized by heterogeneous clinical features.
Anees Muhammad   +10 more
wiley   +1 more source

Psychometric Analysis of Scores on a Mexican Dialect Spanish Version of the PHQ‐9 With Mexican Earthquake Survivors

open access: yesJournal of Counseling &Development, Volume 104, Issue 2, Page 167-179, April 2026.
ABSTRACT This study explored the psychometric characteristics of the PHQ‐9 scores in a sample of 289 Spanish‐speaking participants who endured the 2017 Mw7.1 earthquake, which impacted the Mexican states of Puebla and Morelos, as well as the Greater Mexico City area.
Khalid Stetkevych   +3 more
wiley   +1 more source

The Association Between Contentment and Depressive Symptoms: Results From Three Panel Studies

open access: yesJournal of Clinical Psychology, Volume 82, Issue 4, Page 513-520, April 2026.
ABSTRACT We examined whether contentment was associated with depressive symptoms at both between‐ and within‐person levels, both concurrently and prospectively. We examined our hypotheses using random‐intercept cross‐lagged panel models (RI‐CLPM) that computed the associations between contentment and depressive symptoms, treating tranquility and cheer ...
Shuo Yan   +2 more
wiley   +1 more source

Early‐Onset Hyperkinetic Movement Disorders Define the Most Severe Presentation of the ATP8A2‐Related Phenotypic Spectrum

open access: yesInternational Journal of Developmental Neuroscience, Volume 86, Issue 2, April 2026.
Our short communication establishes that the most severe, early‐onset presentation of ATP8A2 deficiency is a congenital encephalopathy hallmarked by prominent, nonprogressive hyperkinetic movement disorders. Moving beyond the historical CAMRQ4 ataxia classification is essential for the accurate diagnosis of this profound extrapyramidal phenotype ...
Fabio Bruschi   +5 more
wiley   +1 more source

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