The effect of aldosterone blockade in patients with Alport syndrome by Kaito, Hiroshi, Nozu, Kandai, Iijima, Kazumoto, Nakanishi, Koichi, Yoshiya, Kunihiko, Kanda, Kyoko, Przybyslaw Krol, Rafal, Yoshikawa, Norishige, Matsuo, Masafumi

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A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism by Nozu, Kandai, Fu, Xue Jun, Kaito, Hiroshi, Kanda, Kyoko, Yokoyama, Naoki, Przybyslaw Krol, Rafal, Nakajima, Toshihiro, Kajiyama, Mizutaka, Iijima, Kazumoto, Matsuo, Masafumi

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Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients by Nozu, Kandai, Przybyslaw Krol, Rafal, Ohtsuka, Yasufumi, Nakanishi, Koichi, Yoshikawa, Norishige, Nozu, Yoshimi, Kaito, Hiroshi, Kanda, Kyoko, Hashimura, Yuya, Hamasaki, Yuhei, Iijima, Kazumoto, Matsuo, Masafumi

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A family with X-linked benign familial hematuria by Kaneko, Kazunari, Tanaka, Sachiyo, Hasui, Masafumi, Nozu, Kandai, Krol, Rafal Przybyslaw, Iijima, Kazumoto, Sugimoto, Keisuke, Takemura, Tsukasa

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Detection by multiplex ligation-dependent probe amplification of large deletion mutations in the COL4A5 gene in female patients with Alport syndrome by Nozu, Kandai, Krol, Rafal Przybyslaw, Nakanishi, Koichi, Yoshikawa, Norishige, Nozu, Yoshimi, Ohtsuka, Yasufumi, Iijima, Kazumoto, Matsuo, Masafumi

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Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome by Krol, Rafal Przybyslaw, Nozu, Kandai, Nakanishi, Koichi, Iijima, Kazumoto, Takeshima, Yasuhiro, Fu, Xue Jun, Nozu, Yoshimi, Kaito, Hiroshi, Kanda, Kyoko, Matsuo, Masafumi, Yoshikawa, Norishige

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