ABSTRACT Background Prior work has linked work stressors to asthma. However, research related to gender‐specific associations remains sparse and yielded mixed results. We aimed to address this gap. Methods We drew on cross‐sectional data from the 2015 National Health Interview Survey (individual‐level response rate = 79.7%).
Adrian Loerbroks+5 more
wiley +1 more source
Advancing the diagnosis of major depressive disorder: Integrating neuroimaging and machine learning. [PDF]
Yin SQ, Li YH.
europepmc +1 more source
The association between traumatic temporomandibular joint bony ankylosis and depressive disorder in growing rats. [PDF]
Deng T+11 more
europepmc +1 more source
Autonomous Neurobiological Pathways to Late-Life Major Depressive Disorder Clinical and Pathophysiological Implications [PDF]
Anand Kumar+3 more
openalex +1 more source
Autobiographical memory specificity and the course of major depressive disorder [PDF]
Frenk Peeters+3 more
openalex +1 more source
Social capital and major depressive disorder among youth in Iran. [PDF]
Savari E+10 more
europepmc +1 more source
Brain connectivity and transcriptional changes induced by rTMS in first-episode major depressive disorder. [PDF]
Guan M+6 more
europepmc +1 more source
A Pilot Study to Evaluate Neurodevelopmental Outcomes in a Pediatric Cohort With Genodermatoses
ABSTRACT Our study aimed to evaluate cognitive function in individuals with genetic skin disorders involving neuroectoderm (n = 8) compared to individuals with only ectoderm or mesoderm (n = 16) involvement. We hypothesized that neuroectodermal involvement would result in poorer neurocognitive performance.
Sneha A. Rangu+10 more
wiley +1 more source
ABSTRACT Individuals with an extra X or Y chromosome (sex chromosome trisomy or SCT) have an increased risk for symptoms of psychopathology and neurocognitive dysfunction. In this study, we evaluated the contribution of family history (FH) of neuropsychiatric or neurocognitive disorders to the phenotype of SCT. One hundred and six children with SCT and
Sophie van Rijn+2 more
wiley +1 more source
Extended Growth Curves for the Wolf‐Hirschhorn Syndrome (4p‐)
ABSTRACT Wolf‐Hirschhorn syndrome (WHS) is a rare, highly variable contiguous gene deletion syndrome caused by deletions of the distal portion of the short arm of chromosome 4. Individuals with this disorder have prenatal onset of poor growth of all dimensions, along with neurological manifestations, developmental disability, and distinctive facial ...
Amy R. U. L. Calhoun+3 more
wiley +1 more source