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Clinical and Experimental Nephrology|September 19, 2025
Investigation of clinical and genetic characteristics of Alport syndrome using a national registry in Japan (JP-ALPS)Yusuke Okuda, Naoaki Mikami, Riku Hamada, et al.Journal of the American Society of Nephrology : JASN|July 1, 2018
Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport SyndromeTomoko Horinouchi, Kandai Nozu, Tomohiko Yamamura, et al.Journal of Clinical Medicine|November 11, 2022
Cystic Kidney Diseases That Require a Differential Diagnosis from Autosomal Dominant Polycystic Kidney Disease (ADPKD)Akinari Sekine, Sumi Hidaka, Tomofumi Moriyama, et al.Clinical and Experimental Nephrology|May 11, 2024
Protocol for the nationwide registry of patients with polycystic kidney disease: japanese national registry of PKD (JRP)Shinya Nakatani, Haruna Kawano, Mai Sato, et al.Clinical and Experimental Nephrology|June 27, 2023
Public support for patients with intractable diseases in Japan: impact on clinical indicators from nationwide registries in patients with autosomal dominant polycystic kidney diseaseHiroshi Kataoka, Yosuke Shimada, Tomonori Kimura, et al.Pageof 2