Improved renal survival in Japanese children with IgA nephropathy

por Yata, Nahoko, Nakanishi, Koichi, Shima, Yuko, Togawa, Hiroko, Obana, Mina, Sako, Mayumi, Nozu, Kandai, Tanaka, Ryojiro, Iijima, Kazumoto, Yoshikawa, Norishige
Publicado 2008

Comprehensive genetic diagnosis of Japanese patients with severe proteinuria

por Nagano, China, Yamamura, Tomohiko, Horinouchi, Tomoko, Aoto, Yuya, Ishiko, Shinya, Sakakibara, Nana, Shima, Yuko, Nakanishi, Koichi, Nagase, Hiroaki, Iijima, Kazumoto, Nozu, Kandai
Publicado 2020

Study protocol: high-dose mizoribine with prednisolone therapy in short-term relapsing steroid-sensitive nephrotic syndrome to prevent frequent relapse (JSKDC05 trial)

por Hama, Taketsugu, Nakanishi, Koichi, Ishikura, Kenji, Ito, Shuichi, Nakamura, Hidefumi, Sako, Mayumi, Saito-Oba, Mari, Nozu, Kandai, Shima, Yuko, Iijima, Kazumoto, Yoshikawa, Norishige
Publicado 2018

Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6‐year clinical course

por Uraki, Shinsuke, Furuta, Hiroto, Miyawaki, Masakazu, Matsutani, Norihiko, Shima, Yuko, Iwamoto, Miki, Matsuno, Shohei, Morita, Shuhei, Furuta, Machi, Doi, Asako, Iwakura, Hiroshi, Ariyasu, Hiroyuki, Nishi, Masahiro, Suzuki, Hiroyuki, Akamizu, Takashi
Publicado 2019

A multicenter randomized trial indicates initial prednisolone treatment for childhood nephrotic syndrome for two months is not inferior to six-month treatment

por Yoshikawa, Norishige, Nakanishi, Koichi, Sako, Mayumi, Oba, Mari S, Mori, Rintaro, Ota, Erika, Ishikura, Kenji, Hataya, Hiroshi, Honda, Masataka, Ito, Shuichi, Shima, Yuko, Kaito, Hiroshi, Nozu, Kandai, Nakamura, Hidefumi, Igarashi, Takashi, Ohashi, Yasuo, Iijima, Kazumoto
Publicado 2015

Natural History and Genotype–Phenotype Correlation in Female X-Linked Alport Syndrome

por Yamamura, Tomohiko, Nozu, Kandai, Fu, Xue Jun, Nozu, Yoshimi, Ye, Ming Juan, Shono, Akemi, Yamanouchi, Satoko, Minamikawa, Shogo, Morisada, Naoya, Nakanishi, Koichi, Shima, Yuko, Yoshikawa, Norishige, Ninchoji, Takeshi, Morioka, Ichiro, Kaito, Hiroshi, Iijima, Kazumoto
Publicado 2017

Clinical and Genetic Characteristics in Patients With Gitelman Syndrome

por 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
Publicado 2018

Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay

por 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
Publicado 2019

Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing

por Aoto, Yuya, Horinouchi, Tomoko, Yamamura, Tomohiko, Kondo, Atsushi, Nagai, Sadayuki, Ishiko, Shinya, Okada, Eri, Rossanti, Rini, Sakakibara, Nana, Nagano, China, Awano, Hiroyuki, Nagase, Hiroaki, Shima, Yuko, Nakanishi, Koichi, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai
Publicado 2021

Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay

por 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
Publicado 2020

Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome

por 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
Publicado 2019

Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes

por Ishiko, Shinya, Morisada, Naoya, Kondo, Atsushi, Nagai, Sadayuki, Aoto, Yuya, Okada, Eri, Rossanti, Rini, Sakakibara, Nana, Nagano, China, Horinouchi, Tomoko, Yamamura, Tomohiko, Ninchoji, Takeshi, Kaito, Hiroshi, Hamada, Riku, Shima, Yuko, Nakanishi, Koichi, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai
Publicado 2021

Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases

por Kondo, Atsushi, Nagano, China, Ishiko, Shinya, Omori, Takashi, Aoto, Yuya, Rossanti, Rini, Sakakibara, Nana, Horinouchi, Tomoko, Yamamura, Tomohiko, Nagai, Sadayuki, Okada, Eri, Shima, Yuko, Nakanishi, Koichi, Ninchoji, Takeshi, Kaito, Hiroshi, Takeda, Hiroki, Nagase, Hiroaki, Morisada, Naoya, Iijima, Kazumoto, Nozu, Kandai
Publicado 2021

Systematic Review of Genotype-Phenotype Correlations in Frasier Syndrome

por Tsuji, Yurika, Yamamura, Tomohiko, Nagano, China, Horinouchi, Tomoko, Sakakibara, Nana, Ishiko, Shinya, Aoto, Yuya, Rossanti, Rini, Okada, Eri, Tanaka, Eriko, Tsugawa, Koji, Okamoto, Takayuki, Sawai, Toshihiro, Araki, Yoshinori, Shima, Yuko, Nakanishi, Koichi, Nagase, Hiroaki, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai
Publicado 2021

Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases

por Ishiko, Shinya, Horinouchi, Tomoko, Fujimaru, Rika, Shima, Yuko, Kaito, Hiroshi, Tanaka, Ryojiro, Ishimori, Shingo, Kondo, Atsushi, Nagai, Sadayuki, Aoto, Yuya, Sakakibara, Nana, Nagano, China, Yamamura, Tomohiko, Yoshimura, Momoka, Nakanishi, Koichi, Fujimura, Junya, Kamiyoshi, Naohiro, Nagase, Hiroaki, Yoshikawa, Norishige, Iijima, Kazumoto, Nozu, Kandai
Publicado 2020