Results from a narrative review published in the Journal of Medical Ethics suggest broad yet conditional support for data sharing among patients and the general public, with many studies citing concerns about confidentiality, privacy, data security, risk management, and accountability.
Patients with ASS often present with a psoriasiform tissue reaction in the hand lesions and fasciitis-dominant myopathy; the relatives of patients with ASS are at high risk for collagen diseases.
Cutaneous comorbidity is frequent in those with atopic dermatitis, suggesting the need for comprehensive, dermatologically guided diagnostics.
The development of pulmonary arterial hypertension in patients with SLE is a poor prognostic factor, but systemic hypertension may be a predictive factor for PAH in the SLE population.
In an application process more focused on applicant characteristics than proposal content, women achieved significantly less success than men.
A large-scale bibliometric analysis underscores a lack of sex-related reporting in biomedical research, despite efforts to include more women in health-based studies.
The AMA Code of Medical Ethics offers guidance on how physicians and healthcare systems can best support undocumented and lawfully present immigrants to promote the best possible care for all who need it.
This commentary examines physician options for documenting immigration status considering ethical, legal, and historical circumstances when caring for stigmatized populations during changing political landscapes.
