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Annals of Internal Medicine|July 15, 1989
Persistent Cryptococcus neoformans infection of the prostate after successful treatment of meningitis. California Collaborative Treatment GroupR A Larsen, S Bozzette, J A McCutchan, et al.Brain : a Journal of Neurology|November 3, 2020
PET imaging of meningioma with 18F-FLT: a predictor of tumour progressionAsma Bashir, Mark B Vestergaard, Lisbeth Marner, et al.European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|April 25, 2016
Editor's Choice - High Heritability of Liability to Abdominal Aortic Aneurysms: A Population Based Twin StudyT M M Joergensen, K Christensen, J S Lindholt, et al.Biochemical Pharmacology|April 19, 2002
Developmental regulation of flavin-containing monooxygenase form 1 in the liver and kidney of fetal and neonatal rabbitsShelley A Larsen-Su, Sharon K Krueger, Mei Fei Yueh, et al.European Journal of Medical Genetics|November 28, 2017
A complex phenotype in a family with a pathogenic SOX3 missense variantAnne M Jelsig, Birgitte R Diness, Sven Kreiborg, et al.Sexually Transmitted Diseases|April 1, 1991
A population-based serosurveillance of syphilis in Costa RicaS A Larsen, M W Oberle, J M Sanchez-Braverman, et al.PLOS Global Public Health|January 10, 2024
Precision public health in schools enabled by wastewater surveillance: A case study of COVID-19 in an Upstate New York middle-high school campus during the 2021-2022 academic yearHaley Kappus-Kron, Dana Ahmad Chatila, Ainsley Mabel MacLachlan, et al.Journal of Molecular Biology|November 29, 2001
Structural basis for a disfavored elimination reaction in catalytic antibody 1D4N A Larsen, A Heine, L Crane, et al.Journal of School Choice|March 17, 2021
Comment on Asbury and Wai (2019), "Viewing education policy through a genetic lens," Journal of School ChoiceBrian Byrne, Callie W Little, Richard K Olson, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|March 25, 1999
A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndromeL A Larsen, P S Andersen, J K Kanters, et al.Pageof 105