Results 271 to 280 of about 2,904,902 (351)
Dataset for assessing the professional ethics of teaching by medical teachers from the perspective of students in Kermanshah University of Medical Sciences, Iran (2017). [PDF]
Safari Y, Yoosefpour N.
europepmc +1 more source
ABSTRACT Background Prior work has linked work stressors to asthma. However, research related to gender‐specific associations remains sparse and yielded mixed results. We aimed to address this gap. Methods We drew on cross‐sectional data from the 2015 National Health Interview Survey (individual‐level response rate = 79.7%).
Adrian Loerbroks+5 more
wiley +1 more source
Component Associations of the Healthy Worker Survivor Bias in Medical Radiation Workers
ABSTRACT Background The healthy worker survivor bias may vary by sex. This study investigated three component associations necessary for this bias to determine the origins of sex differences in this bias among male and female workers. Methods We analyzed a data set of 93,918 South Korean diagnostic medical radiation workers registered in the National ...
Won Jin Lee, Jaeho Jeong, Young Min Kim
wiley +1 more source
Professional practice and ethics in the context of healthcare policies
Heloísa Wey Berti Mendes+1 more
openalex
Professional Ethics in Occupational Health-Western European Perspectivesa
Peter Westerholm
openalex +2 more sources
ABSTRACT Schinzel‐Giedion Syndrome (SGS) is an ultra‐rare, multisystem, genetic developmental disorder caused by gain‐of‐function pathogenic variants in the SETBP1 gene. No standard of care (SoC) recommendations currently exist. To assess expert opinion on SoC for individuals with SGS using a modified Delphi method.
Jessica Duis+16 more
wiley +1 more source
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
ABSTRACT The scarcity of clinical information surrounding rare chromosome disorders poses challenges for parents and clinicians. To bridge this gap for chromosome 6 disorders, the Chromosome 6 Project collects detailed genotype and phenotype data, aiming to provide aberration‐specific phenotype information to parents via an interactive website.
Eleana Rraku+6 more
wiley +1 more source