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Molecular Genetics & Genomic Medicine|August 1, 2019
Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndromeTomohiko Yamamura, Kandai Nozu, Shogo Minamikawa, et al.Journal of Human Genetics|November 8, 2018
Clinical spectrum of male patients with OFD1 mutationsNana Sakakibara, Naoya Morisada, Kandai Nozu, et al.Clinical and Experimental Nephrology|September 18, 2021
Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypesShinya Ishiko, Naoya Morisada, Atsushi Kondo, et al.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.Pediatric Nephrology (Berlin, Germany)|April 25, 2024
Clinical characteristics and outcomes of immune-complex membranoproliferative glomerulonephritis and C3 glomerulopathy in Japanese childrenChika Ueda, Tomoko Horinouchi, Yuta Inoki, 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.Pediatric Nephrology (Berlin, Germany)|June 28, 2023
Long-term outcome of combination therapy with corticosteroids, mizoribine and RAS inhibitors as initial therapy for severe childhood IgA vasculitis with nephritisSadayuki Nagai, Tomoko Horinouchi, Takeshi Ninchoji, et al.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.Pageof 8