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78 results for Kaito,+Hiroshi

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A review of clinical characteristics and genetic backgrounds in Alport syndrome
Author / Creator: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
Publisher:Tokyo: Springer Nature B.V
Journal title:Clinical and experimental nephrology, 2019-02, Vol.23 (2), p.158-168
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Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial
Author / Creator:Iijima, Kazumoto, Prof ; Sako, Mayumi, MD ; Nozu, Kandai, MD ; Mori, Rintaro, MD ; Tuchida, Nao, MD ; Kamei, Koichi, MD ; Miura, Kenichiro, MD ; Aya, Kunihiko, MD ; Nakanishi, Koichi, MD ; Ohtomo, Yoshiyuki, MD ; Takahashi, Shori, Prof ; Tanaka, Ryojiro, MD ; Kaito, Hiroshi, MD ; Nakamura, Hidefumi, MD ; Ishikura, Kenji, MD ; Ito, Shuichi, MD ; Ohashi, Yasuo, Prof
Publisher:Kidlington: Elsevier Ltd
Journal title:The Lancet (British edition), 2014-10, Vol.384 (9950), p.1273-1281
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Clinicopathological significance of glomerular capillary IgA deposition in childhood IgA nephropathy
Author / Creator:Shima, Yuko ; Nakanishi, Koichi ; Mukaiyama, Hironobu ; Tanaka, Yu ; Wada, Takuzo ; Tanaka, Ryojiro ; Kaito, Hiroshi ; Nozu, Kandai ; Sako, Mayumi ; Iijima, Kazumoto ; Yoshikawa, Norishige
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2021-04, Vol.36 (4), p.899-908
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Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases
Author / Creator: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
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2021-08, Vol.11 (1), p.16099-7, Article 16099
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Factors related to recurrence of proteinuria in childhood IgA nephropathy
Author / Creator:Shima, Yuko ; Mukaiyama, Hironobu ; Tanaka, Yu ; Shimabukuro, Wataru ; Nozu, Kandai ; Kaito, Hiroshi ; Tanaka, Ryojiro ; Sako, Mayumi ; Iijima, Kazumoto ; Tokuhara, Daisuke ; Yoshikawa, Norishige ; Nakanishi, Koichi
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2024-02, Vol.39 (2), p.463-471
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Clinical and genetic variability of PAX2-related disorder in the Japanese population
Author / Creator:Rini, Rossanti ; Morisada Naoya ; Nozu Kandai ; Kamei Koichi ; Horinouchi Tomoko ; Yamamura Tomohiko ; Minamikawa Shogo ; Fujimura Junya ; Nagano China ; Sakakibara Nana ; Ninchoji Takeshi ; Kaito Hiroshi ; Ito Shuichi ; Tanaka Ryojiro ; Iijima Kazumoto
Publisher:London: Nature Publishing Group
Journal title:Journal of human genetics, 2020-06, Vol.65 (6), p.541-549
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An “old and new” complication in a child with nephrotic syndrome: Answers
Author / Creator:Inaguma, Yosuke ; Kaito, Hiroshi ; Horinouchi, Tomoko ; Ogawa, Yoshiharu ; Yoshida, Makiko ; Yoshikawa, Norishige ; Tanaka, Ryojiro
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2021-07, Vol.36 (7), p.1955-1958
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An “old and new” complication in a child with nephrotic syndrome: Questions
Author / Creator:Inaguma, Yosuke ; Kaito, Hiroshi ; Horinouchi, Tomoko ; Ogawa, Yoshiharu ; Yoshida, Makiko ; Yoshikawa, Norishige ; Tanaka, Ryojiro
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2021-07, Vol.36 (7), p.1953-1954
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Crescentic IgA nephropathy in children
Author / Creator:Shima, Yuko ; Nakanishi, Koichi ; Hama, Taketsugu ; Mukaiyama, Hironobu ; Sato, Masashi ; Tanaka, Yu ; Tanaka, Ryojiro ; Kaito, Hiroshi ; Nozu, Kandai ; Sako, Mayumi ; Iijima, Kazumoto ; Yoshikawa, Norishige
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2020-06, Vol.35 (6), p.1005-1014
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Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo–Bartter/Gitelman syndrome based on clinical characteristics
Author / Creator:Matsunoshita, Natsuki ; Nozu, Kandai ; Shono, Akemi ; Nozu, Yoshimi ; Fu, Xue Jun ; Morisada, Naoya ; Kamiyoshi, Naohiro ; Ohtsubo, Hiromi ; Ninchoji, Takeshi ; Minamikawa, Shogo ; Yamamura, Tomohiko ; Nakanishi, Koichi ; Yoshikawa, Norishige ; Shima, Yuko ; Kaito, Hiroshi ; Iijima, Kazumoto
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2016-02, Vol.18 (2), p.180-188
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Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain
Author / Creator:Hashimura, Yuya ; Nozu, Kandai ; Kaito, Hiroshi ; Nakanishi, Koichi ; Fu, Xue Jun ; Ohtsubo, Hiromi ; Hashimoto, Fusako ; Oka, Masafumi ; Ninchoji, Takeshi ; Ishimori, Shingo ; Morisada, Naoya ; Matsunoshita, Natsuki ; Kamiyoshi, Naohiro ; Yoshikawa, Norishige ; Iijima, Kazumoto
Publisher:United States: Elsevier Inc
Journal title:Kidney international, 2014-05, Vol.85 (5), p.1208-1213
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Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis
Author / Creator:Nozu, Kandai ; Minamikawa, Shogo ; Yamada, Shiro ; Oka, Masafumi ; Yanagita, Motoko ; Morisada, Naoya ; Fujinaga, Shuichiro ; Nagano, China ; Gotoh, Yoshimitsu ; Takahashi, Eihiko ; Morishita, Takahiro ; Yamamura, Tomohiko ; Ninchoji, Takeshi ; Kaito, Hiroshi ; Morioka, Ichiro ; Nakanishi, Koichi ; Vorechovsky, Igor ; Iijima, Kazumoto
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2017-07, Vol.62 (7), p.733-735
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Long-term outcome of childhood-onset complicated nephrotic syndrome after a multicenter, double-blind, randomized, placebo-controlled trial of rituximab
Author / Creator:Kamei, Koichi ; Ishikura, Kenji ; Sako, Mayumi ; Aya, Kunihiko ; Tanaka, Ryojiro ; Nozu, Kandai ; Kaito, Hiroshi ; Nakanishi, Koichi ; Ohtomo, Yoshiyuki ; Miura, Kenichiro ; Takahashi, Shori ; Morimoto, Tetsuji ; Kubota, Wataru ; Ito, Shuichi ; Nakamura, Hidefumi ; Iijima, Kazumoto
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2017-11, Vol.32 (11), p.2071-2078
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Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases
Author / Creator: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
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2020-08, Vol.10 (1), p.14026-6, Article 14026
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Validity of the Oxford classification of IgA nephropathy in children
Author / Creator:Shima, Yuko ; Nakanishi, Koichi ; Hama, Taketsugu ; Mukaiyama, Hironobu ; Togawa, Hiroko ; Hashimura, Yuya ; Kaito, Hiroshi ; Sako, Mayumi ; Iijima, Kazumoto ; Yoshikawa, Norishige
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Pediatric nephrology (Berlin, West), 2012-05, Vol.27 (5), p.783-792
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Cryptic exon activation in SLC12A3 in Gitelman syndrome
Author / Creator:Nozu, Kandai ; Nozu, Yoshimi ; Nakanishi, Keita ; Konomoto, Takao ; Horinouchi, Tomoko ; Shono, Akemi ; Morisada, Naoya ; Minamikawa, Shogo ; Yamamura, Tomohiko ; Fujimura, Junya ; Nakanishi, Koichi ; Ninchoji, Takeshi ; Kaito, Hiroshi ; Morioka, Ichiro ; Taniguchi-Ikeda, Mariko ; Vorechovsky, Igor ; Iijima, Kazumoto
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2017-02, Vol.62 (2), p.335-337
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Natural history of genetically proven autosomal recessive Alport syndrome
Author / Creator:Oka, Masafumi ; Nozu, Kandai ; Kaito, Hiroshi ; Fu, Xue Jun ; Nakanishi, Koichi ; Hashimura, Yuya ; Morisada, Naoya ; Yan, Kunimasa ; Matsuo, Masafumi ; Yoshikawa, Norishige ; Vorechovsky, Igor ; Iijima, Kazumoto
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2014-09, Vol.29 (9), p.1535-1544
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Lisinopril versus lisinopril and losartan for mild childhood IgA nephropathy: a randomized controlled trial (JSKDC01 study)
Author / Creator:Shima, Yuko ; Nakanishi, Koichi ; Sako, Mayumi ; Saito-Oba, Mari ; Hamasaki, Yuko ; Hataya, Hiroshi ; Honda, Masataka ; Kamei, Koichi ; Ishikura, Kenji ; Ito, Shuichi ; Kaito, Hiroshi ; Tanaka, Ryojiro ; Nozu, Kandai ; Nakamura, Hidefumi ; Ohashi, Yasuo ; Iijima, Kazumoto ; Yoshikawa, Norishige
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2019-05, Vol.34 (5), p.837-846
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Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome
Author / Creator:Rossanti, Rini ; Shono, Akemi ; Miura, Kenichiro ; Hattori, Motoshi ; Yamamura, Tomohiko ; Nakanishi, Keita ; Minamikawa, Shogo ; Fujimura, Junya ; Horinouchi, Tomoko ; Nagano, China ; Sakakibara, Nana ; Kaito, Hiroshi ; Nagase, Hiroaki ; Morisada, Naoya ; Asanuma, Katsuhiko ; Matsuo, Masafumi ; Nozu, Kandai ; Iijima, Kazumoto
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2019-07, Vol.64 (7), p.673-679
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Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes
Author / Creator:Ishiko Shinya ; Morisada Naoya ; Kondo Atsushi ; Nagai Sadayuki ; Aoto Yuya ; Okada Eri ; Rini, Rossanti ; Sakakibara Nana ; Nagano China ; Horinouchi Tomoko ; Yamamura Tomohiko ; Ninchoji Takeshi ; Kaito Hiroshi ; Hamada Riku ; Shima Yuko ; Nakanishi Koichi ; Matsuo Masafumi ; Iijima Kazumoto ; Nozu Kandai
Publisher:Tokyo: Springer Nature B.V
Journal title:Clinical and experimental nephrology, 2022-02, Vol.26 (2), p.140-153
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Showing 1 to 20 of 78 results

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A review of clinical characteristics and genetic backgrounds in Alport syndrome

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Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial

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Clinicopathological significance of glomerular capillary IgA deposition in childhood IgA nephropathy

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

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Factors related to recurrence of proteinuria in childhood IgA nephropathy

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Clinical and genetic variability of PAX2-related disorder in the Japanese population

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An “old and new” complication in a child with nephrotic syndrome: Answers

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An “old and new” complication in a child with nephrotic syndrome: Questions

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Crescentic IgA nephropathy in children

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Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo–Bartter/Gitelman syndrome based on clinical characteristics

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Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain

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Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis

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Long-term outcome of childhood-onset complicated nephrotic syndrome after a multicenter, double-blind, randomized, placebo-controlled trial of rituximab

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

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Validity of the Oxford classification of IgA nephropathy in children

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Cryptic exon activation in SLC12A3 in Gitelman syndrome

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Natural history of genetically proven autosomal recessive Alport syndrome

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Lisinopril versus lisinopril and losartan for mild childhood IgA nephropathy: a randomized controlled trial (JSKDC01 study)

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Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome

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

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