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Genome Medicine|January 8, 2026
DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defectsGregor Dombrowsky, Liselot van der Laan, Ananília Silva, et al.
Pain Medicine (Malden, Mass.)|November 30, 2025
Consensus practice guidelines on sacroiliac joint complex pain from a multispecialty, international working groupZachary L McCormick, Robert W Hurley, Magdalena Anitescu, et al.
JAMA Network Open|November 27, 2024
Social Vulnerability, Intervention Utilization, and Outcomes in US Adults Hospitalized With InfluenzaKatherine Adams, Kimberly Yousey-Hindes, Catherine H Bozio, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2025
Mainstreaming of clinical genetic testing: A conceptual frameworkMichael P Mackley, Julie Richer, Andrea Guerin, et al.
American Journal of Human Genetics|September 3, 2025
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 22, 2024
Timing of Influenza Antiviral Therapy and Risk of Death in Adults Hospitalized With Influenza-Associated Pneumonia, Influenza Hospitalization Surveillance Network (FluSurv-NET), 2012-2019Mark W Tenforde, Kameela P Noah, Alissa C O'Halloran, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|May 20, 2022
Comparison of Influenza and Coronavirus Disease 2019-Associated Hospitalizations Among Children Younger Than 18 Years Old in the United States: FluSurv-NET (October-April 2017-2021) and COVID-NET (October 2020-September 2021)Miranda J Delahoy, Dawud Ujamaa, Christopher A Taylor, et al.
The Journal of Infectious Diseases|April 27, 2026
Effects of age and birth cohort on influenza A virus subtype-specific hospitalization rates, United States 2010-2025Alissa O'Halloran, Nicole Hood, Dawud Ujamaa, et al.
American Journal of Human Genetics|September 23, 2025
Heterozygous pathogenic variants in the splicing factor SF1 lead to a large spectrum of neurodevelopmental disordersJohnny Bou-Rouphael, Auriane Cospain, Thomas Courtin, et al.
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