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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.Kidney360|April 14, 2022
Clear Evidence of LAMA5 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 WT1 Exon 8 to 9 Missense VariantsChina Nagano, Yutaka Takaoka, Koichi Kamei, et al.Clinical and Experimental Nephrology|January 27, 2018
Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseasesChina Nagano, Kandai Nozu, Naoya Morisada, 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.Pageof 12