Yersinia pseudotuberculosis infection in Kawasaki disease and its clinical characteristics

di Horinouchi, Tomoko, Nozu, Kandai, Hamahira, Kiyoshi, Inaguma, Yosuke, Abe, Jun, Nakajima, Hiroshi, Kugo, Masaaki, Iijima, Kazumoto
Pubblicato in BMC Pediatr (2015)

An extremely mild clinical course in a case with LAMB2-associated nephritis diagnosed with next-generation sequencing

di Sakuraya, Koji, Nozu, Kandai, Murakami, Hitohiko, Nagano, China, Horinouchi, Tomoko, Fujinaga, Shuichiro, Iijima, Kazumoto, Ohtomo, Yoshiyuki
Pubblicato in CEN Case Rep (2021)

Study protocol: mycophenolate mofetil as maintenance therapy after rituximab treatment for childhood-onset, complicated, frequently-relapsing nephrotic syndrome or steroid-dependen...

di Horinouchi, Tomoko, Sako, Mayumi, Nakanishi, Koichi, Ishikura, Kenji, Ito, Shuichi, Nakamura, Hidefumi, Oba, Mari Saito, Nozu, Kandai, Iijima, Kazumoto
Pubblicato in BMC Nephrol (2018)

Poststreptococcal acute glomerulonephritis can be a risk factor for accelerating kidney dysfunction in Alport syndrome: a case experience

di Araki, Yoshinori, Kawaguchi, Azusa, Sakakibara, Nana, Nagaoka, Yoshinobu, Yamamura, Tomohiko, Horinouchi, Tomoko, Nagano, China, Morisada, Naoya, Iijima, Kazumoto, Nozu, Kandai
Pubblicato in CEN Case Rep (2020)

FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child

di Rossanti, Rini, Watanabe, Toshio, Nagano, China, Hara, Shigeo, Horinouchi, Tomoko, Yamamura, Tomohiko, Sakakibara, Nana, Ninchoji, Takeshi, Iijima, Kazumoto, Nozu, Kandai
Pubblicato in CEN Case Rep (2020)

Comprehensive genetic diagnosis of Japanese patients with severe proteinuria

di Nagano, China, Yamamura, Tomohiko, Horinouchi, Tomoko, Aoto, Yuya, Ishiko, Shinya, Sakakibara, Nana, Shima, Yuko, Nakanishi, Koichi, Nagase, Hiroaki, Iijima, Kazumoto, Nozu, Kandai
Pubblicato in Sci Rep (2020)

Genetic background, recent advances in molecular biology, and development of novel therapy in Alport syndrome

di Nozu, Kandai, Takaoka, Yutaka, Kai, Hirofumi, Takasato, Minoru, Yabuuchi, Kensuke, Yamamura, Tomohiko, Horinouchi, Tomoko, Sakakibara, Nana, Ninchoji, Takeshi, Nagano, China, Iijima, Kazumoto
Pubblicato in Kidney Res Clin Pract (2020)

A case with somatic and germline mosaicism in COL4A5 detected by multiplex ligation-dependent probe amplification in X-linked Alport syndrome

di Aoto, Yuya, Kise, Tomoo, Nakanishi, Koichi, Nagano, China, Horinouchi, Tomoko, Yamamura, Tomohiko, Ishiko, Shinya, Sakakibara, Nana, Shima, Yuko, Morisada, Naoya, Iijima, Kazumoto, Nozu, Kandai
Pubblicato in CEN Case Rep (2020)

Three Severe Cases of Viral Infections with Post-Kidney Transplantation Successfully Confirmed by Polymerase Chain Reaction and Flow Cytometry

di Nakanishi, Keita, Kaito, Hiroshi, Ogi, Miki, Takai, Denshi, Fujimura, Junya, Horinouchi, Tomoko, Yamamura, Tomohiko, Minamikawa, Shogo, Ninchoji, Takeshi, Nozu, Kandai, Imadome, Ken-Ichi, Iijima, Kazumoto
Pubblicato in Case Rep Nephrol Dial (2018)

TGFBI-associated corneal dystrophy and nephropathy: a novel syndrome?

di Nagano, China, Nozu, Kandai, Yamamura, Tomohiko, Minamikawa, Shogo, Fujimura, Junya, Sakakibara, Nana, Nakanishi, Keita, Horinouchi, Tomoko, Iwafuchi, Yoichi, Kusuhara, Sentaro, Matsumiya, Wataru, Yoshikawa, Norishige, Iijima, Kazumoto
Pubblicato in CEN Case Rep (2018)

Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1

di Inoue, Tomohiko, Nagano, China, Matsuo, Masafumi, Yamamura, Tomohiko, Sakakibara, Nana, Horinouchi, Tomoko, Shibagaki, Yugo, Ichikawa, Daisuke, Aoto, Yuya, Ishiko, Shinya, Ishimori, Shingo, Rossanti, Rini, Iijima, Kazumoto, Nozu, Kandai
Pubblicato in Clin Exp Nephrol (2020)

Correction to: Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1

di Inoue, Tomohiko, Nagano, China, Matsuo, Masafumi, Yamamura, Tomohiko, Sakakibara, Nana, Horinouchi, Tomoko, Shibagaki, Yugo, Ichikawa, Daisuke, Aoto, Yuya, Ishiko, Shinya, Ishimori, Shingo, Rossanti, Rini, Iijima, Kazumoto, Nozu, Kandai
Pubblicato in Clin Exp Nephrol (2021)

The utility of urinary CD80 as a diagnostic marker in patients with renal diseases

di Minamikawa, Shogo, Nozu, Kandai, Maeta, Shingo, Yamamura, Tomohiko, Nakanishi, Keita, Fujimura, Junya, Horinouchi, Tomoko, Nagano, China, Sakakibara, Nana, Nagase, Hiroaki, Shima, Hideaki, Noda, Kenta, Ninchoji, Takeshi, Kaito, Hiroshi, Iijima, Kazumoto
Pubblicato in Sci Rep (2018)

An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis

di Yamamura, Tomohiko, Nozu, Kandai, Miyoshi, Yuya, Nakanishi, Keita, Fujimura, Junya, Horinouchi, Tomoko, Minamikawa, Shogo, Mori, Nobuo, Fujimaru, Rika, Nakanishi, Koichi, Ninchoji, Takeshi, Kaito, Hiroshi, Mariko, Taniguchi-Ikeda, Morioka, Ichiro, Matsuo, Masafumi, Iijima, Kazumoto
Pubblicato in BMC Nephrol (2017)

Clinical and Genetic Characteristics in Patients With Gitelman Syndrome

di 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
Pubblicato in Kidney Int Rep (2018)

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

di 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
Pubblicato in Sci Rep (2019)

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

di 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
Pubblicato in Mol Genet Genomic Med (2020)

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

di 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
Pubblicato in Mol Genet Genomic Med (2019)

A review of clinical characteristics and genetic backgrounds in Alport syndrome

di Nozu, Kandai, Nakanishi, Koichi, Abe, Yoshifusa, Udagawa, Tomohiro, Okada, Shinichi, Okamoto, Takayuki, Kaito, Hiroshi, Kanemoto, Katsuyoshi, Kobayashi, Anna, Tanaka, Eriko, Tanaka, Kazuki, Hama, Taketsugu, Fujimaru, Rika, Miwa, Saori, Yamamura, Tomohiko, Yamamura, Natsusmi, Horinouchi, Tomoko, Minamikawa, Shogo, Nagata, Michio, Iijima, Kazumoto
Pubblicato in Clin Exp Nephrol (2018)

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

di 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
Pubblicato in Sci Rep (2020)