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European Urology Open Science|October 3, 2022
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary TractChen-Han Wilfred Wu, Tze Y Lim, Chunyan Wang, et al.Physical Review Letters|February 3, 2004
Semihard scattering unraveled from collective dynamics by two-pion azimuthal correlations in 158A GeV/c Pb+Au collisionsG Agakichiev, H Appelshäuser, R Baur, et al.Kidney International|September 13, 2017
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosisAnkana Daga, Amar J Majmundar, Daniela A Braun, et al.The Lancet. Oncology|December 3, 2014
Tumour genomic and microenvironmental heterogeneity for integrated prediction of 5-year biochemical recurrence of prostate cancer: a retrospective cohort studyEmilie Lalonde, Adrian S Ishkanian, Jenna Sykes, et al.SN Comprehensive Clinical Medicine|May 17, 2021
International Scientific Collaboration Is Needed to Bridge Science to Society: USERN2020 Consensus StatementSara Momtazmanesh, Amene Saghazadeh, Juan Carlos Aldave Becerra, et al.Frontiers in Human Neuroscience|March 12, 2025
Proceedings of the 12th annual deep brain stimulation think tank: cutting edge technology meets novel applicationsAlfonso Enrique Martinez-Nunez, Christopher J Rozell, Simon Little, et al.Frontiers in Human Neuroscience|May 21, 2025
Corrigendum: Proceedings of the 12th annual deep brain stimulation think tank: cutting edge technology meets novel applicationsAlfonso Enrique Martinez-Nunez, Christopher J Rozell, Simon Little, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 19, 2019
Treatment and long-term outcome in primary distal renal tubular acidosisSergio Camilo Lopez-Garcia, Francesco Emma, Stephen B Walsh, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 3, 2022
Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaireSarah C Grünert, Terry G J Derks, Katarina Adrian, et al.Journal of the American Society of Nephrology : JASN|August 26, 2018
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary TractAmelie T van der Ven, Dervla M Connaughton, Hadas Ityel, et al.Pageof 196