Results 121 to 130 of about 600,648 (272)

Women online: A study of Common Service Centres in India using a capability approach

open access: yesAsia &the Pacific Policy Studies, Volume 9, Issue 3, Page 268-287, September 2022., 2022
Abstract Income‐generating activities by women are an effective means of reducing gender‐based deprivation and disparities. In the constrained familial and community settings of developing economies, online platforms can be an appropriate means for women to carry out economic activities. In this context, important initiatives taken by the Government of
Meenakshi Rajeev, Supriya Bhandarkar
wiley   +1 more source

Study Protocol: Pegasus: psychotherapy incorporating horses for ‘therapy-resistant’ adolescents with autism spectrum disorders, a study with series of randomised, baseline controlled n-of-1 trials

open access: yesBMC Psychiatry
Background For people with autism spectrum disorder (ASD), daily life can be highly stressful with many unpredictable events that can evoke emotion dysregulation (ED): a strong difficulty with appropriately negative affect regulation.
Jenny C. den Boer   +10 more
doaj   +1 more source

A Pilot Study to Evaluate Neurodevelopmental Outcomes in a Pediatric Cohort With Genodermatoses

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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

Endostructural and periosteal growth of the human humerus

open access: yesThe Anatomical Record, Volume 306, Issue 1, Page 60-78, January 2023., 2023
Abstract The growth and development of long bones are of considerable interests in the fields of comparative anatomy and palaeoanthropology, as evolutionary changes and adaptations to specific physical activity patterns are expected to be revealed during bone ontogeny.
Thomas George O'Mahoney   +3 more
wiley   +1 more source

Natural History of NAA15‐Related Neurodevelopmental Disorder Through Adolescence

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The NatA N‐terminal acetyltransferase complex is composed of the NAA10 catalytic subunit and the auxiliary subunits NAA15 and HYPK. While those with variants in the enzymatic subunit develop Ogden Syndrome, individuals with variants in the NAA15 coding region develop NAA15‐related neurodevelopmental syndrome, which presents with a wide array ...
Rikhil Makwana   +5 more
wiley   +1 more source

Adverse maternal environment alters Oprl1 variant expression in mouse hippocampus

open access: yesThe Anatomical Record, Volume 306, Issue 1, Page 162-175, January 2023., 2023
Abstract An adverse maternal environment (AME) and Western diet (WD) in early life predispose offspring toward cognitive impairment in humans and mice. Cognitive impairment associates with hippocampal dysfunction. An important regulator of hippocampal function is the hippocampal Nociceptin/Orphanin FQ (N/OFQ) system. Previous studies find links between
Xingrao Ke   +5 more
wiley   +1 more source

Reflexão Crítica sobre Saúde Mental na Infância e na Adolescência, em Portugal

open access: yesGazeta Médica
A saúde mental da infância e da adolescência é uma área clínica em crescente procura de cuidados, traduzindo-se no aumento das necessidades cuja resposta não foi acompanhada por financiamento proporcional na área, em Portugal.
Tânia B. Cavaco, Filipa Martins Silva
doaj   +2 more sources

MTSS2‐Related Disorder: Refining the Phenotype in Four New Cases and Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT MTSS2 encodes a protein highly expressed in the central nervous system, with a crucial role in neurodevelopment. The de novo recurrent variant c.2011C>T (p.Arg671Trp) was first identified in 2022 as cause of Intellectual Developmental Disorder with ocular anomalies and distinctive facial features (OMIM#620086).
Angela De Dominicis   +12 more
wiley   +1 more source

Beyond the Extra X and Y Chromosome: The Contribution of Familial Risk for Psychopathology to the Neurodevelopmental Phenotype of Children With Sex Chromosome Trisomy

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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

Home - About - Disclaimer - Privacy