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Items for Author "Nagase, Hiroaki"
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| Clinical and Genetic Characteristics in Patients With Gitelman Syndrome | Fujimura, Junya; Nozu, Kandai; Yamamura, Tomohiko; Minamikawa, Shogo; Nakanishi, Keita; Horinouchi, Tomoko; Nagano, China; Sakakibara, Nana; Nakanishi, Koichi; Shima, Yuko; Miyako, Kenichi; Nozu, Yoshimi; Morisada, Naoya; Nagase, Hiroaki; Ninchoji, Takeshi; Kaito, Hiroshi; Iijima, Kazumoto | Jan-2019 |
| Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome | Yamamura, Tomohiko; Nozu, Kandai; Minamikawa, Shogo; Horinouchi, Tomoko; Sakakibara, Nana; Nagano, China; Aoto, Yuya; Ishiko, Shinya; Nakanishi, Koichi; Shima, Yuko; Nagase, Hiroaki; Rossanti, Rini; Ye, Ming J.; Nozu, Yoshimi; Ishimori, Shingo; Morisada, Naoya; Kaito, Hiroshi; Iijima, Kazumoto | Sep-2019 |
| Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay | Horinouchi, Tomoko; Nozu, Kandai; Yamamura, Tomohiko; Minamikawa, Shogo; Nagano, China; Sakakibara, Nana; Nakanishi, Koichi; Shima, Yuko; Morisada, Naoya; Ishiko, Shinya; Aoto, Yuya; Nagase, Hiroaki; Takeda, Hiroki; Rossanti, Rini; Kaito, Hiroshi; Matsuo, Masafumi; Iijima, Kazumoto | 3-Sep-2019 |
| Pathogenic evaluation of synonymous COL4A5 variants in X-linked Alport syndrome using a minigene assay | Horinouchi, Tomoko; Yamamura, Tomohiko; Minamikawa, Shogo; Nagano, China; Sakakibara, Nana; Nakanishi, Koichi; Shima, Yuko; Morisada, Naoya; Ishiko, Shinya; Aoto, Yuya; Nagase, Hiroaki; Takeda, Hiroki; Rossanti, Rini; Ishimori, Shingo; Kaito, Hiroshi; Matsuo, Masafumi; Iijima, Kazumoto; Nozu, Kandai | 2020 |
| Comprehensive genetic diagnosis of Japanese patients with severe proteinuria | Nagano, China; Yamamura, Tomohiko; Horinouchi, Tomoko; Aoto, Yuya; Ishiko, Shinya; Sakakibara, Nana; Shima, Yuko; Nakanishi, Koichi; Nagase, Hiroaki; Iijima, Kazumoto; Nozu, Kandai | 14-Jan-2020 |
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