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Kidney International Reports|October 8, 2021
Systematic Review of Genotype-Phenotype Correlations in Frasier SyndromeYurika Tsuji, Tomohiko Yamamura, China Nagano, et al.Journal of Human Genetics|February 21, 2018
Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent diseaseShogo Minamikawa, Kandai Nozu, Yoshimi Nozu, et al.Journal of Human Genetics|October 15, 2021
BCS1L mutations produce Fanconi syndrome with developmental disabilityKojima-Ishii Kanako, Nana Sakakibara, Kei Murayama, 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.Pediatric Nephrology (Berlin, Germany)|March 17, 2025
Differences in kidney prognosis between congenital and infantile nephrotic syndromeYuta Inoki, Tomoko Horinouchi, Shuhei Aoyama, et al.American Journal of Medical Genetics. Part A|April 22, 2021
Heterozygous missense variant in TRPC6 in a boy with rapidly progressive infantile nephrotic syndrome associated with diffuse mesangial sclerosisHiroaki Hanafusa, Yoshihiko Hidaka, Tomomi Yamaguchi, et al.Kidney360|May 18, 2022
Evaluation of Suspected Autosomal Alport Syndrome Synonymous VariantsRini Rossanti, Tomoko Horinouchi, Tomohiko Yamamura, et al.Clinical and Experimental Nephrology|July 11, 2026
Kidney outcomes of coenzyme Q10 supplementation in patients with genetically confirmed CoQ10 nephropathy in JapanChina Nagano, Katsumi Ushijima, Yuko Tezuka, et al.Pageof 12