Results 181 to 190 of about 3,598,771 (321)
Immigration enforcement in hospitals: a framework for health systems. [PDF]
Sakran JV +3 more
europepmc +1 more source
Validity and reliability of a questionnaire assessing Brazilian adolescents' experiences in orthodontic treatment. [PDF]
Freitas TEDVS +3 more
europepmc +1 more source
ABSTRACT Bardet–Biedl syndrome (BBS) is a rare genetic condition with a broad phenotypic spectrum. Knowledge about quality of life, executive functioning, and eating behavior in adults with BBS remains limited. This study aimed to assess health‐related quality of life (HRQoL), everyday executive functioning, and eating behavior in adults with BBS and ...
Cecilie Fremstad Rustad +6 more
wiley +1 more source
Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy +16 more
wiley +1 more source
Development and Psychometric Properties of an Effective Evacuation Preparedness Checklist for Hospitals in Disasters: A Methodological Study. [PDF]
Taheri F, Salehi M, Dowlati M.
europepmc +1 more source
ABSTRACT Smith–Magenis syndrome (SMS) results from either a recurrent 17p11.2 deletion or pathogenic variants in the retinoic acid induced 1 gene (RAI1). While neurodevelopmental impairment and behavioral dysregulation are well recognized, systematic genotype‐stratified analyses across psychiatric domains remain limited.
Albin Blanc +7 more
wiley +1 more source
With qualitative research, the risks of data sharing can outweigh the rewards. [PDF]
Calarco J.
europepmc +1 more source
Expanding the Utility of Exome Sequencing in Preventive and Population Genetics
ABSTRACT Carrier screening is a long‐standing genetic testing process offered to at‐risk couples, with or without a family history, who might have pregnancies affected by an autosomal recessive (AR) or X‐linked (XL) disorder. A total of 276 unrelated individuals, initially referred for rare disorder screening by clinicians, were enrolled in this study ...
Charilaos Kostoulas +6 more
wiley +1 more source
Bridging the Gap in Chinese Legal Conflict Review: A Dataset, Benchmark Tasks, and Framework. [PDF]
Zhao S +9 more
europepmc +1 more source
Legal validation and recommendations
This deliverable will contain a legal assessment of the general privacy enabling tools and technologies, as well as the specific e-Health and Financial Services scenarios that have been developed in the WITDOM project and will furthermore include draft recommendations on privacy enabling tools and technologies to ensure legally compliant systems ...
openaire +1 more source

