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Clinical and Experimental Nephrology|July 25, 2025
Prolonged hypokalemia long after causative factor elimination in pseudo-Bartter/Gitelman syndromeAtsushi Kondo, Tomoko Horinouchi, Yuta Inoki, 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)|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.
Pediatric Nephrology (Berlin, Germany)|January 25, 2024
Feasibility of discontinuing immunosuppression in children with idiopathic nephrotic syndromeYoko Sobue, Kentaro Nishi, Koichi Kamei, et al.
Clinical and Experimental Nephrology|June 14, 2024
Evaluation of pathogenicity of WT1 intron variants by in vitro splicing analysisSeiya Inoue, Atsushi Kondo, Yuta Inoki, et al.
Pediatric Nephrology (Berlin, Germany)|November 25, 2024
Saline versus balanced crystalloids for hydration post-kidney biopsyYu Tanaka, Tomoko Horinouchi, Yuta Inoki, et al.
The Journal of Pediatrics|October 12, 2022
Changes in Patterns of Infection Associated with Pediatric Idiopathic Nephrotic Syndrome: A Single-Center Experience in JapanHiroyuki Takao, Kentaro Nishi, Takanori Funaki, et al.
Kidney International Reports|December 22, 2025
Impact of Age-3 Urine Screening on Diagnosis and Treatment Timing in Alport SyndromeHideaki Kitakado, Shingo Ishimori, Shuhei Aoyama, et al.
Clinical and Experimental Nephrology|June 10, 2025
Potential involvement of abnormal splicing in severe WT1-related disordersChina Nagano, Masafumi Matuso, Yuta Inoki, et al.
Clinical and Experimental Nephrology|April 17, 2025
Clinical use of the VNtyper-Kestrel pipeline for MUC1 variant detection in autosomal-dominant tubulointerstitial kidney diseaseChina Nagano, Naoya Morisada, Yuta Inoki, et al.
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