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Sensors (Basel, Switzerland)|September 9, 2023
Deep Learning in the Recognition of Activities of Daily Living Using Smartwatch DataAriany F Cavalcante, Victor H de L Kunst, Thiago de M Chaves, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 4, 2008
Clinical and molecular responses in lung cancer patients receiving RomidepsinDavid S Schrump, Maria R Fischette, Dao M Nguyen, et al.
Journal of Epidemiology and Community Health|April 16, 2005
Trends in smoking behaviour between 1985 and 2000 in nine European countries by educationK Giskes, A E Kunst, J Benach, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|March 3, 2021
TB management in the European Union/European Economic Area: a multi-centre surveyG Sotgiu, S Rosales-Klintz, R Centis, et al.
Pharmacoeconomics|February 27, 2026
Ten Recommendations for Modelling Cost Effectiveness of Screening: Perspectives of an International Stakeholder GroupOlena Mandrik, Chloe Thomas, Alice Bessey, et al.
Bioorganic & Medicinal Chemistry Letters|March 20, 2003
Discovery of 4'-[(imidazol-1-yl)methyl]biphenyl-2-sulfonamides as dual endothelin/angiotensin II receptor antagonistsJohn E Tellew, Rose Ann F Baska, Sophie M Beyer, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 15, 2001
Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCHS J Bom, E M De Leenheer, F X Lemaire, et al.
Journal of Clinical Pathology|March 31, 2012
Prolonged sampling of spontaneous sputum improves sensitivity of hypermethylation analysis for lung cancerA Jasmijn Hubers, Daniëlle A M Heideman, Gerarda J M Herder, et al.
BMC Medical Genetics|April 17, 2009
The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patientsJean-Pierre Bayley, Anneliese E M Grimbergen, Patrick A van Bunderen, et al.
Human Molecular Genetics|November 16, 2001
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing lossI N Bespalova, G Van Camp, S J Bom, et al.
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