Results 21 to 30 of about 350,349 (330)

Cultural aspects in social anxiety and social anxiety disorder [PDF]

open access: yesDepression and Anxiety, 2010
To examine cultural aspects in social anxiety and social anxiety disorder (SAD), we reviewed the literature on the prevalence rates, expressions, and treatments of social anxiety/SAD as they relate to culture, race, and ethnicity. We further reviewed factors that contribute to the differences in social anxiety/SAD between different cultures, including ...
Anu Asnaani   +2 more
openaire   +3 more sources

Patterns of community violence exposure among urban adolescents and their associations with adjustment

open access: yesAmerican Journal of Community Psychology, Volume 70, Issue 3-4, Page 265-277, December 2022., 2022
Abstract Community violence exposure is prevalent among urban and marginalized adolescents. Although there is strong evidence that community violence exposure is associated with negative consequences, prior studies and theories suggest that these associations may differ as a function of specific characteristics of exposure.
Sarah K. Pittman, Albert D. Farrell
wiley   +1 more source

Facilitating connection to enhance college student well‐being: Evaluation of an experiential group program

open access: yesAmerican Journal of Community Psychology, Volume 70, Issue 3-4, Page 314-326, December 2022., 2022
Abstract This randomized controlled trial examined the impact of The Connection Project, an experiential, relationship‐focused intervention designed to improve school belongingness and decrease symptoms of depression and loneliness among new college students.
Meghan A. Costello   +6 more
wiley   +1 more source

The Social Costs of Anxiety Disorders

open access: yesBritish Journal of Psychiatry, 1995
Background. The social costs of anxiety disorders, which afflict a substantial proportion of the general population in the United States, are considered.Method. Data from the National Institute of Mental Health (NIMH) Epidemiological Catchment Area Program were analysed.Results.
Leon, Andrew C   +2 more
openaire   +5 more sources

Familial Bainbridge‐Ropers syndrome: Report of familial ASXL3 inheritance and a milder phenotype

open access: yesAmerican Journal of Medical Genetics Part A, Volume 191, Issue 1, Page 29-36, January 2023., 2023
Abstract De novo truncating and splicing pathogenic variants in the Additional Sex Combs‐Like 3 (ASXL3) gene are known to cause neurodevelopmental delay, intellectual disability, behavioral difficulties, hypotonia, feeding problems and characteristic facial features.
Schaida Schirwani   +10 more
wiley   +1 more source

Refractory social anxiety disorder [PDF]

open access: yesJournal of Psychiatry & Neuroscience, 2017
When first seen, our patient was 27 years old and had severe social and performance anxiety dating back to elementary school. She dropped out in grade 11 and was unable work owing to severe social anxiety. She was housebound unless accompanied, and she avoided speaking with authority figures,
Van Ameringen M, Beth Patterson
openaire   +3 more sources

Teaching perspectives on the communication of difficult news of genetic conditions to medical students

open access: yesAmerican Journal of Medical Genetics Part A, Volume 191, Issue 1, Page 299-305, January 2023., 2023
Abstract Informing parents that their child has a diagnosis of Down syndrome (DS) is a common example of the delivery of unexpected or difficult news. Expectations and life planning will change, and if detected prenatally, discussions might include the option of pregnancy termination.
Ashley M. Vanasse   +8 more
wiley   +1 more source

Comorbidity of Social Anxiety Disorder and Attention Deficit Hyperactivity Disorder

open access: yesPsikiyatride Güncel Yaklaşımlar, 2014
Despite high rates of reported comorbidity in patients with social anxiety disorder, attention deficit hyperactivity disorder comorbidity was not evaluated in these studies.
Ahmet Koyuncu, Zerrin Binbay
doaj   +1 more source

Biallelic GTF2IRD1 variants in brothers with profound neurodevelopmental disorder: A possible novel disorder involving a critical gene for Williams syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 191, Issue 2, Page 332-337, February 2023., 2023
Abstract GTF2IRD1, a gene on chromosome 7 which encodes a transcription factor, is of significant clinical interest due to its heterozygous loss as part of the classical deletion associated with Williams–Beuren syndrome (WBS). However, biallelic variants in GTF2IRD1 alone as part of an autosomal recessive disease have not been previously reported. Here,
Christopher Thomas Cummings   +1 more
wiley   +1 more source

The developmental trajectories of the behavioral phenotype and neuropsychiatric functioning in Cornelia de Lange and Rubinstein Taybi syndromes: A longitudinal study

open access: yesAmerican Journal of Medical Genetics Part A, Volume 191, Issue 2, Page 424-436, February 2023., 2023
Abstract Several changes in the behavioral phenotype arise with the growth of children affected by Cornelia de Lange Syndrome (CdLS) and Rubinstein‐Taybi Syndrome (RSTS). However, previous research relied on a cross‐sectional study design turning into age‐related comparisons of different syndromic cohorts to explore age‐dependent changes.
Paola Francesca Ajmone   +11 more
wiley   +1 more source

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