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Arthritis and Rheumatism|December 1, 2011
A novel mutation of IL1RN in the deficiency of interleukin-1 receptor antagonist syndrome: description of two unrelated cases from BrazilAdriana A Jesus, Mazen Osman, Clovis A Silva, et al.Journal of the American College of Radiology : JACR|October 2, 2020
Mapping the Ultrasound Landscape to Define Point-of-Care Ultrasound and Diagnostic Ultrasound: A Proposal From the Society of Radiologists in Ultrasound and ACR Commission on UltrasoundMaitray D Patel, Mindy M Horrow, Aya Kamaya, et al.Bioorganic & Medicinal Chemistry Letters|October 10, 2002
A series of C-terminal amino alcohol dipeptide A beta inhibitorsAlbert W Garofalo, David W G Wone, Angela Phuc, et al.Proceedings of the National Academy of Sciences of the United States of America|April 12, 2011
Periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) is a disorder of innate immunity and Th1 activation responsive to IL-1 blockadeSilvia Stojanov, Sivia Lapidus, Puja Chitkara, et al.Frontiers in Psychology|September 20, 2021
The Frequent Stressor and Mental Health Monitoring-Paradigm: A Proposal for the Operationalization and Measurement of Resilience and the Identification of Resilience Processes in Longitudinal Observational StudiesRaffael Kalisch, Göran Köber, Harald Binder, et al.PDA Journal of Pharmaceutical Science and Technology|October 17, 2023
Best Practices for Microbial Challenge In-Use Studies to Evaluate the Microbial Growth Potential of Parenteral Biological Products; Industry and Regulatory ConsiderationsCamellia Zamiri, Danielle L Leiske, Patricia Hughes, et al.Molecular Genetics and Metabolism|July 26, 2017
Neonatal detection of Aicardi Goutières Syndrome by increased C26:0 lysophosphatidylcholine and interferon signature on newborn screening blood spotsThais Armangue, Joseph J Orsini, Asako Takanohashi, et al.Immunity|May 31, 2025
A CD4+ T cell-intrinsic complement C5aR2-prostacyclin-IL-1R2 axis orchestrates Th1 cell contractionJubayer Rahman, Jack A Bibby, Parul Singh, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 11, 2016
Phenotypic and Genotypic Characterization and Treatment of a Cohort With Familial Tumoral Calcinosis/Hyperostosis-Hyperphosphatemia SyndromeMary Scott Ramnitz, Pravitt Gourh, Raphaela Goldbach-Mansky, et al.Biorxiv : the Preprint Server for Biology|September 2, 2025
Proteasome mutations associated with CANDLE syndrome cause altered neuronal development by dysregulating polyamine synthesisClayton W Winkler, Benjamin Schwarz, Katie Williams, et al.Pageof 72