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Clinical and Experimental Nephrology|July 16, 2020
Onset mechanism of a female patient with Dent disease 2Takayuki Okamoto, Nana Sakakibara, Kandai Nozu, et al.
Pediatric Nephrology (Berlin, Germany)|July 14, 2025
Clinical characteristics of patients with SALL1-related disorderYoshitaka Asagai, Yu Tanaka, Hiroaki Hanafusa, et al.
CEN Case Reports|June 28, 2020
Poststreptococcal acute glomerulonephritis can be a risk factor for accelerating kidney dysfunction in Alport syndrome: a case experienceYoshinori Araki, Azusa Kawaguchi, Nana Sakakibara, et al.
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.
CEN Case Reports|October 28, 2023
Familial focal segmental glomerulosclerosis with Alport-like glomerular basement changes caused by paired box protein 2 gene variantYuko Yamada, Hiroki Yokoyama, Ryo Kinoshita, et al.
Clinical Case Reports|February 18, 2021
Catheter-related blood stream infection caused by Mycobacterium chelonae in a child with myeloid leukemia associated with Down syndromeTomoko Fujikawa, Suguru Uemura, Yuya Aoto, 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.
BMJ Open|April 13, 2021
Multivariate analysis of the impact of weather and air pollution on emergency department visits for night-time headaches among children: retrospective, clinical observational studyHiroshi Yamaguchi, Kandai Nozu, Shinya Ishiko, et al.
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