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Clinical Science (London, England : 1979)|October 25, 2007
Homocysteine, S-adenosylmethionine and S-adenosylhomocysteine are associated with retinal microvascular abnormalities: the Hoorn StudyManon V Van Hecke, Jacqueline M Dekker, Giel Nijpels, et al.Journal of Diabetes and Its Complications|July 22, 2014
Low-grade inflammation and endothelial dysfunction explain the association between retinopathy and left ventricular ejection fraction in men: an 8-year follow-up of the Hoorn StudyIris Walraven, Katja van den Hurk, Esther van 't Riet, et al.Diabetologia|April 26, 2014
Validation of a model to estimate personalised screening frequency to monitor diabetic retinopathyAmber A W A van der Heijden, Iris Walraven, Esther van 't Riet, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 1, 1992
Genetic amniocentesis in twin pregnancies: results of a multicenter study of 529 casesM R Pruggmayer, M G Jahoda, J G Van der Pol, et al.Nature Communications|December 8, 2015
Whole-genome sequencing reveals activation-induced cytidine deaminase signatures during indolent chronic lymphocytic leukaemia evolutionS Kasar, J Kim, R Improgo, et al.AJNR. American Journal of Neuroradiology|June 1, 2013
Effect of age on MRI phase behavior in the subcortical deep gray matter of healthy individualsJ Hagemeier, M G Dwyer, N Bergsland, et al.Journal of Clinical Microbiology|April 20, 2007
Molecular discrimination of atypical bovine spongiform encephalopathy strains from a geographical region spanning a wide area in EuropeJorg G Jacobs, Jan P M Langeveld, Anne-Gaëlle Biacabe, et al.Journal of Hypertension|August 4, 2015
Real-world evidence of suboptimal blood pressure control in patients with type 2 diabetesIris Walraven, M Ruth Mast, Trynke Hoekstra, et al.Acta Diabetologica|October 8, 2014
Distinct HbA1c trajectories in a type 2 diabetes cohortIris Walraven, M Ruth Mast, Trynke Hoekstra, et al.Nature Genetics|May 19, 2015
Genome-wide patterns and properties of de novo mutations in humansLaurent C Francioli, Paz P Polak, Amnon Koren, et al.Pageof 10