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International Urology and Nephrology|September 25, 2022
Modified histopathological classification with age-related glomerulosclerosis for predicting kidney survival in ANCA-associated glomerulonephritisMehmet Fethullah Aydın, Abdülmecit Yıldız, Ayşegül Oruç, et al.Revista Brasileira De Reumatologia|November 28, 2017
Clinical outcomes and survival in AA amyloidosis patientsYavuz Ayar, Alparslan Ersoy, Mustafa Ferhat Oksuz, et al.Renal Failure|January 22, 2021
Morning blood pressure surge in early autosomal dominant polycystic kidney disease and its relation with left ventricular hypertrophyAbdülmecit Yildiz, Saim Sag, Cuma Bulent Gul, et al.Renal Failure|October 1, 2025
Evaluating gene variations in autosomal dominant polycystic kidney disease patients using whole exome sequencing and phenotype to genotype analysisHande Aypek, Rumeysa Fatma Balaban, Nuseybe Huriyet, et al.Journal of Nephrology|February 22, 2023
Propensity score-matched analysis of long-term outcomes for living kidney donation in alternative complement pathway diseases: a pilot studyYasar Caliskan, Seda Safak, Ozgur Akin Oto, et al.Iranian Journal of Kidney Diseases|November 2, 2014
Arterial dysfunction in early autosomal dominant polycystic kidney disease independent of fibroblast growth factor 23Abdulmecit Yildiz, Cuma Bulent Gul, Alparslan Ersoy, et al.American Journal of Nephrology|November 9, 2022
Long-Term Outcomes of Living-Related Kidney Donation for Alport Syndrome Spectrum: A Propensity Score-Matched AnalysisOzgur Akin Oto, Seda Safak, Safak Mirioglu, et al.Clinical Nephrology|July 22, 2024
Biopsy-proven BK virus nephropathy in renal transplant recipients: A multi-central study from Turkey (BK-TURK STUDY)Ozkan Gungor, Hamad Dheir, Mahmud Islam, et al.Pageof 5