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Pediatric Nephrology (Berlin, Germany)|September 4, 2012
Spontaneous remission in children with IgA nephropathyYuko Shima, Koichi Nakanishi, Taketsugu Hama, et al.
BMC Nephrology|September 12, 2018
Study protocol: high-dose mizoribine with prednisolone therapy in short-term relapsing steroid-sensitive nephrotic syndrome to prevent frequent relapse (JSKDC05 trial)Taketsugu Hama, Koichi Nakanishi, Kenji Ishikura, et al.
Pediatric Nephrology (Berlin, Germany)|August 28, 2014
Renal biopsy criterion in idiopathic nephrotic syndrome with microscopic hematuria at onsetTaketsugu Hama, Koichi Nakanishi, Yuko Shima, et al.
Pediatric Nephrology (Berlin, Germany)|August 18, 2023
Factors related to recurrence of proteinuria in childhood IgA nephropathyYuko Shima, Hironobu Mukaiyama, Yu Tanaka, 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.
Kidney International Reports|December 18, 2023
Clinical Practice Patterns in IgA Nephropathy: A Global Questionnaire-Based SurveyBhavik Bansal, Amritesh Grewal, Boon Wee Teo, et al.
Pediatric Nephrology (Berlin, Germany)|July 11, 2018
Combination therapy with or without warfarin and dipyridamole for severe childhood IgA nephropathy: an RCTYuko Shima, Koichi Nakanishi, Yoshitsugu Kaku, et al.
CEN Case Reports|July 5, 2020
A case with somatic and germline mosaicism in COL4A5 detected by multiplex ligation-dependent probe amplification in X-linked Alport syndromeYuya Aoto, Tomoo Kise, Koichi Nakanishi, et al.
Kidney360|April 4, 2022
Heterozygous Urinary Abnormality-Causing Variants of <i>COL4A3</i> and <i>COL4A4</i> Affect Severity of Autosomal Recessive Alport SyndromeTomoko Horinouchi, Tomohiko Yamamura, China Nagano, et al.
Pediatric Nephrology (Berlin, Germany)|August 5, 2015
Long-term outcome of childhood IgA nephropathy with minimal proteinuriaAsumi Higa, Yuko Shima, Taketsugu Hama, et al.
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