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JMIR Human Factors|January 3, 2025
Improving Social Media-Based Support Groups for the Rare Disease Community: Interview Study With Patients and Parents of Children with Rare and Undiagnosed DiseasesTom A Doyle, Samantha L Vershaw, Erin Conboy, et al.Disability and Rehabilitation|April 17, 2023
Patients' strategies for numeric pain assessment: a qualitative interview study of individuals with hypermobile Ehlers-Danlos SyndromeColin M E Halverson, Tom A DoyleFrontiers in Medicine|January 2, 2023
Use of complementary and alternative medicine by patients with hypermobile Ehlers-Danlos Syndrome: A qualitative studyTom A Doyle, Colin M E HalversonAMA Journal of Ethics|October 1, 2025
What Are Ethical Merits and Drawbacks of Viewing "Medical Mysteries" as Human Subject Research?Tom A Doyle, Erin ConboyMolecular Genetics & Genomic Medicine|June 11, 2024
Social media use by patients with hypermobile Ehlers-Danlos syndromeColin M E Halverson, Tom A Doyle, Samantha VershawSSM. Mental Health|July 11, 2026
Painful subjects: the sociogenic processing of pain in individuals with Ehlers-Danlos syndromesTom A Doyle, Samantha L Vershaw, Colin M E HalversonOrphanet Journal of Rare Diseases|March 15, 2024
Patient interest in the development of a center for Ehlers-Danlos syndrome/hypermobility spectrum disorder in the Chicagoland regionWendy Wagner, Tom A Doyle, Clair A Francomano, et al.Perspectives in Biology and Medicine|September 12, 2022
Genetic Essentialism and Social WarrantingColin M E HalversonPatient Education and Counseling|August 2, 2023
Patient understanding of pharmacogenomic test results in clinical careTom A Doyle, Karen K Schmidt, Colin M E Halverson, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2012
Incidental findings of therapeutic misconception in biobank-based researchColin M E Halverson, Lainie Friedman RossPageof 7