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CEN Case Reports|September 9, 2020
FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a childRini Rossanti, Toshio Watanabe, China Nagano, et al.
Kidney Research and Clinical Practice|November 20, 2020
Genetic background, recent advances in molecular biology, and development of novel therapy in Alport syndromeKandai Nozu, Yutaka Takaoka, Hirofumi Kai, et al.
Scientific Reports|January 16, 2020
Comprehensive genetic diagnosis of Japanese patients with severe proteinuriaChina Nagano, Tomohiko Yamamura, Tomoko Horinouchi, et al.
Clinical and Experimental Nephrology|May 26, 2026
Clinical and functional evaluation of non-missense MYH9 variants in MYH9-related diseaseSeiya Inoue, China Nagano, Masafumi Matsuo, et al.
Pediatric Nephrology (Berlin, Germany)|November 30, 2022
Is influenza vaccination associated with nephrotic syndrome relapse in children? A multicenter prospective studyShingo Ishimori, Tomoko Horinouchi, Junya Fujimura, et al.
Pediatric Nephrology (Berlin, Germany)|July 20, 2020
Comparison of clinical and genetic characteristics between Dent disease 1 and Dent disease 2Nana Sakakibara, China Nagano, Shinya Ishiko, et al.
Pediatric Nephrology (Berlin, Germany)|August 2, 2024
In steroid-resistant nephrotic syndrome that meets the strict definition, monogenic variants are less common than expectedYuta Ichikawa, Nana Sakakibara, China Nagano, et al.
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