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European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 1, 2016
Safety and effectiveness of the Bonebridge transcutaneous active direct-drive bone-conduction hearing implant at 1-year device useSébastien Schmerber, O Deguine, M Marx, et al.Viruses|May 28, 2022
Effect of Relative Humidity on Transfer of Aerosol-Deposited Artificial and Human Saliva from Surfaces to Artificial Finger-PadsMaurice D Walker, Jack C Vincent, Lee Benson, et al.Human Molecular Genetics|March 21, 1998
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1S Abdelhak, V Kalatzis, R Heilig, et al.Annals of the Rheumatic Diseases|November 18, 2004
Rheumatoid factor and anticitrullinated protein antibodies in rheumatoid arthritis: diagnostic value, associations with radiological progression rate, and extra-articular manifestationsL De Rycke, I Peene, I E A Hoffman, et al.BMJ Military Health|November 13, 2021
Management of a large outbreak of COVID-19 at a British Army training centre: lessons for the futureMatthew Routledge, J Lyon, C Vincent, et al.Biorxiv : the Preprint Server for Biology|April 10, 2026
Bile acid dependent attenuation of toxin mediated disease is independent of colonization resistance against C. difficileSamantha C Kisthardt, C E Perkins, Abigail S Gancz, et al.Journal of Immunology (Baltimore, Md. : 1950)|November 8, 2001
Immature human dendritic cells express asialoglycoprotein receptor isoforms for efficient receptor-mediated endocytosisJ Valladeau, V Duvert-Frances, J J Pin, et al.International Journal of Pharmaceutics: X|December 5, 2022
Long term behavior of dexamethasone-loaded cochlear implants: In vitro & in vivoT Rongthong, A Qnouch, M Maue Gehrke, et al.Human Molecular Genetics|September 26, 1997
Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular CenterJ Laporte, C Guiraud-Chaumeil, M C Vincent, et al.Clinical Genetics|October 19, 2010
The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated malesD Germanaud, M Rossi, G Bussy, et al.Pageof 83