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Pediatric Nephrology (Berlin, Germany)|January 11, 2022
Use of renin-angiotensin system inhibitors as initial therapy in children with Henoch-Schönlein purpura nephritis of moderate severitySadayuki Nagai, Tomoko Horinouchi, Takeshi Ninchoji, et al.
Kidney360|April 14, 2022
Clear Evidence of <i>LAMA5</i> Gene Biallelic Truncating Variants Causing Infantile Nephrotic SyndromeYukimasa Taniguchi, China Nagano, Kiyotoshi Sekiguchi, et al.
Kidney International Reports|August 13, 2021
Genotype-Phenotype Correlation in <i>WT1</i> Exon 8 to 9 Missense VariantsChina Nagano, Yutaka Takaoka, Koichi Kamei, et al.
Scientific Reports|August 10, 2021
Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databasesAtsushi Kondo, China Nagano, Shinya Ishiko, et al.
Kidney International|July 27, 2020
Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndromeTomohiko Yamamura, Tomoko Horinouchi, China Nagano, et al.
Kidney International Reports|October 8, 2021
Systematic Review of Genotype-Phenotype Correlations in Frasier SyndromeYurika Tsuji, Tomohiko Yamamura, China Nagano, et al.
Clinical and Experimental Nephrology|March 20, 2021
Utility of glomerular Gd-IgA1 staining for indistinguishable cases of IgA nephropathy or Alport syndromeShinya Ishiko, Akihito Tanaka, Asami Takeda, et al.
Clinical and Experimental Nephrology|February 9, 2022
Efficacy of combination therapy for childhood complicated focal IgA nephropathyYuya Aoto, Takeshi Ninchoji, Hiroshi Kaito, et al.
Scientific Reports|August 22, 2020
Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseasesShinya Ishiko, Tomoko Horinouchi, Rika Fujimaru, et al.
Kidney360|May 18, 2022
Evaluation of Suspected Autosomal Alport Syndrome Synonymous VariantsRini Rossanti, Tomoko Horinouchi, Tomohiko Yamamura, et al.
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