Results 241 to 250 of about 5,438,043 (393)

Genotype–Phenotype Correlations, Mortality, and Clinical Insights in Keratitis–Ichthyosis–Deafness Syndrome: A Comprehensive Review and Case Report

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero, Marco Antonio Hernández Lepe, José de Jesús Manríquez Torres, Diego Daniel Aguirre‐Gómez, Natsuo Hayashi‐Mercado, Genaro Rodríguez Uribe, Tadeo Cerón, María Ruiz‐Gamboa, Jesús Alonso Gándara‐Mireles, Ismael Lares‐Asseff, Verónica Loera‐Castañeda, Jorge Alvelais‐Palacios, Lucrecia Arzamendi‐Cepeda, Lidia Magdalena Castañeda‐González, Adolfo García‐Barrón, Francisco Yamal Quiroz Herrera, Francisco González‐Salazar, Horacio Almanza‐Reyes   +17 more
wiley   +1 more source

Context, implementation and mechanisms of impact of a stepped-care WHO psychological intervention for migrants with psychological distress. [PDF]

Glob Ment Health (Camb)
Compri B, Turrini G, Purgato M, Bryant R, Cristobal P, Haro JM, Kalisch R, Lorant V, McDaid D, McGreevy KR, Mediavilla R, Nosè M, Park AL, Petri-Romão P, Roversi A, Sijbrandij M, Tortelli A, Witteveen A, Barbui C.   +18 more
europepmc   +1 more source

The service for Monitoring and Early Intervention against psychoLogical and mEntal suffering in young people (SMILE) at the University of L'Aquila: first year experience [PDF]

, 2007
R. Pollice, E. Di Giovambattista, Donatella Ussorio, A. Di Pucchio, A. Tomassini, Monica Mazza, Rita Roncone, M Casacchia   +7 more
openalex   +1 more source

A review of the effectiveness of a brief (8 session) Cognitive Analytic Therapy (CAT) for clients with anger problems [PDF]

This report represents evaluative data from 12 months of psychotherapeutic intervention using Cognitive Analytic Therapy at Winn Gardens and some reflections on the subsequent development of the project into Burngreave. The focus of the intervention was
Mackintosh, Paula, Turner, James
core  

Depression Symptom Trajectories in Mothers With the FMR1 Premutation Vary by CGG Repeat Length: A Longitudinal Study of 73 Women Spanning 20–75 Years of Age

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Women with the FMR1 premutation (FXpm) are at heightened genetic vulnerability for depression, with risk compounded by the stressors of parenting a disabled child. Although risk factors persist as FXpm women age, depression in FXpm mothers during midlife and old age is poorly characterized. This study used an accelerated longitudinal design to
Jessica Klusek, Lauren Jenner, Abigail L. Hogan, Laura Friedman, Elizabeth Berry‐Kravis, Flora Tassone, Tatyana Adayev, Amanda J. Fairchild, Jane E. Roberts   +8 more
wiley   +1 more source

The acquired dyad inclination and decreased interpersonal brain communication in the pursuit of collective benefit

NeuroImage
People perform better collectively than individually, a phenomenon known as the collective benefit. To pursue the benefit, they may learn from previous behaviors, come to know whose initial opinion should be valued, and develop the inclination to take it
Shuyi Li, Linwei Yu, Xiaorong Gan, Yingying Hou, Yafeng Pan, Yi Luo, Yi Hu   +6 more
doaj  

Effect of psychological intervention on the quality of life and mental health of leukemia patients: a meta-analysis. [PDF]

Front Psychol
Yin B, Liu X, Mao Y, Han Y.
europepmc   +1 more source

Psychological features of patients reaction on the stress connected with laparoscopic by intervention

, 2005
А. N. Tayts
openalex   +2 more sources

Psychologic Interventions and Lifestyle Modifications for Arthritis Pain Management [PDF]

, 2008
Francis J. Keefe, Tamara J. Somers, Lynn M. Martire   +2 more
openalex   +1 more source

Genome Sequencing Uncovers Additional Findings in Phelan‐McDermid Syndrome

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Phelan‐McDermid syndrome (PMS) is a genetic condition caused by deletions of chromosome 22q13.3 or pathogenic variants in the SHANK3 gene. Neurologic features typically include intellectual disability, autism spectrum disorder, hypotonia, and absent speech, though there is considerable variability even among individuals with the same molecular
Rachel Gore Moses, Morgan Similuk, Alexandra Hehn, Rylee Duncan, Margaret Pekar, Eliza Gordon‐Lipkin, Maria T. Acosta, Deena Zeltser, Nadjalisse Reynolds‐Lallement, Latha Soorya, Mustafa Sahin, Tess Levy, Alexander Kolevzon, Joseph D. Buxbaum, Elizabeth Berry‐Kravis, Craig M. Powell, Jonathan A. Bernstein, Mari Tokita, Bryce A. Seifert, Rajarshi Ghosh, Magdalena A. Walkiewicz, Audrey Thurm   +21 more
wiley   +1 more source