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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.
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.
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