Results 271 to 280 of about 2,671,893 (362)
American Journal of Community Psychology, EarlyView.Abstract Although peer support is central to the social model approach emphasized in sober living houses (SLHs), no longitudinal studies have examined helping among SLH residents. This longitudinal study examined benefits of helping in three contexts among SLH residents. Data were from 205 participants entering 28 SLHs across 2021–2023. Interviews were
Sarah E. Zemore +4 more
wiley +1 more source
Promoting caring communities through collective action
American Journal of Community Psychology, EarlyView.Abstract Current times call for the promotion of caring communities through collective action. In caring communities, we feel connected, experience a sense of belonging, and deeply care about each other's health and well‐being. Seymour Sarason's notion of social change as the creation of settings may have anticipated the art and practice of creating ...
Yolanda Suarez‐Balcazar
wiley +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Costello syndrome (CS) is a rare dominant HRAS RASopathy characterized by curly hair, cardiac abnormalities, craniofacial anomalies, and developmental delay. HRAS codon 58, 59, and 60 variants are associated with milder phenotypes. We describe a three‐generation family with a previously unreported heterozygous HRAS variant c.175G>A (p.Ala59Thr)
Nikole Rautiainen +10 more
wiley +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim +9 more
wiley +1 more source
LEGAL STATUS OF CRYPTOCURRENCY
International scientific journal "Internauka". Series: "Juridical Sciences", 2018 Karina Katsiuba +2 more
openaire +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The FGFR2 gene, encoding the FGFR2 protein, plays a crucial role in embryonic cell development, particularly in bone tissue. Bent Bone Dysplasia (BBD), FGFR2‐related (MIM# 614592), is a rare severe skeletal dysplasia characterized by craniofacial differences, reduced bone mineral density, and bowed long bones.
Cheyenne Bates +6 more
wiley +1 more source
Undocumented and Unwell: Legal Status and Health among Mexican Migrants. [PDF]
Int Migr Rev, 2019 Cheong AR, Massey DS.
europepmc +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Spinal muscular atrophy with congenital bone fractures 2 is a rare and severe autosomal recessive neuromuscular disorder caused by pathogenic variants in ASCC1. This condition characterized by prenatal onset of severe hypotonia with fetal hypokinesia and congenital contractures results in arthrogryposis multiplex congenita, and increased ...
A. Civit +16 more
wiley +1 more source
Legal regulation of the embryo legal status
States and Regions. Series: Public Administration, 2019 openaire +1 more source