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Pediatric Transplantation|June 28, 2023
Heart transplantation in neonatal Marfan syndrome: Saving life in a rare and fatal conditionJessica A Laks, Aine Lynch, Osami Honjo, et al.The Journal of Urology|June 5, 2020
Does the Visibility of Grade Group 1 Prostate Cancer on Baseline Multiparametric Magnetic Resonance Imaging Impact Clinical Outcomes?Dominik Deniffel, Emmanuel Salinas, Marc Ientilucci, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 7, 2006
Variants of the hK2 protein gene (KLK2) are associated with serum hK2 levels and predict the presence of prostate cancer at biopsyRobert K Nam, William W Zhang, Laurence H Klotz, et al.Urology|September 19, 2013
Obesity is associated with larger prostate volume but not with worse urinary symptoms: analysis of a large multiethnic cohortBimal Bhindi, David Margel, Greg Trottier, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|December 25, 2003
Comprehensive assessment of candidate genes and serological markers for the detection of prostate cancerRobert K Nam, William W Zhang, John Trachtenberg, et al.American Journal of Medical Genetics. Part A|April 9, 2023
Biallelic variants in TUBGCP6 result in microcephaly and chorioretinopathy 1: Report of four cases and a literature reviewAmanda Thomas-Wilson, John P Schacht, David Chitayat, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 19, 2009
Utility of incorporating genetic variants for the early detection of prostate cancerRobert K Nam, William W Zhang, John Trachtenberg, et al.BJU International|April 22, 2011
Comparison of risk calculators from the Prostate Cancer Prevention Trial and the European Randomized Study of Screening for Prostate Cancer in a contemporary Canadian cohortGreg Trottier, Monique J Roobol, Nathan Lawrentschuk, et al.PEC Innovation|May 22, 2023
Development of a storytelling communication facilitation tool (SCFT) to facilitate discussion of complex genetic diagnoses between parents and their children: A pilot study using 22q11.2 deletion syndrome as a model conditionSimina Bogatan, Andrea Shugar, Syed Wasim, et al.Journal of Clinical Medicine|October 6, 2018
Fetal Renal Echogenicity Associated with Maternal Focal Segmental Glomerulosclerosis: The Effect of Transplacental Transmission of Permeability Factor suPARShirley Shuster, Ghada Ankawi, Christoph Licht, et al.Pageof 53