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The New Zealand Medical Journal|June 21, 2022
Clinical outcomes of campylobacteriosis: a case series analysis of hospitalisations associated with the Havelock North Campylobacter outbreakBridget Wilson, Nicholas Jones, Tim Wood, et al.Health Promotion and Chronic Disease Prevention in Canada : Research, Policy and Practice|July 13, 2022
"I see beauty, I see art, I see design, I see love." Findings from a resident-driven, co-designed gardening program in a long-term care facilityShannon Freeman, Davina Banner, Meg Labron, et al.Clinical Chemistry|November 4, 2006
Tandem mass spectrometry for the direct assay of enzymes in dried blood spots: application to newborn screening for mucopolysaccharidosis II (Hunter disease)Ding Wang, Tim Wood, Martin Sadilek, et al.Molecular Genetics and Metabolism|February 9, 2010
Identification and characterization of a novel homozygous deletion in the alpha-N-acetylglucosaminidase gene in a patient with Sanfilippo type B syndrome (mucopolysaccharidosis IIIB)Kristen J Champion, Monica J Basehore, Tim Wood, et al.JIMD Reports|February 23, 2013
Primary Carnitine Deficiency Presents Atypically with Long QT Syndrome: A Case ReportIrene De Biase, Neena Lorenzana Champaigne, Richard Schroer, et al.Developmental Medicine and Child Neurology|November 6, 2007
Early onset alpha-mannosidosis with slow progression in three Hispanic malesMichael J Lyons, Tim Wood, Lesby Espinoza, et al.European Journal of Medical Genetics|October 12, 2021
3-Methylglutaconic aciduria in carriers of primary carnitine deficiencyCatherine A Ziats, William B Burns, Matt L Tedder, et al.Canadian Association of Radiologists Journal = Journal L'Association Canadienne Des Radiologistes|January 6, 2021
Diagnostic Radiology Residency Assessment Tools: A Scoping ReviewWendy Tu, Rebecca Hibbert, Mario Kontolemos, et al.Academic Medicine : Journal of the Association of American Medical Colleges|December 24, 2013
The etiology of diagnostic errors: a controlled trial of system 1 versus system 2 reasoningGeoffrey Norman, Jonathan Sherbino, Kelly Dore, et al.BMC Medical Genetics|May 3, 2013
Deletion Xq27.3q28 in female patient with global developmental delays and skewed X-inactivationLauren S Marshall, Julie Simon, Tim Wood, et al.Pageof 10