Results
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Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. [electronic resource] by
- Hashimura, Yuya
- Nozu, Kandai
- Kanegane, Hirokazu
- Miyawaki, Toshio
- Hayakawa, Akira
- Yoshikawa, Norishige
- Nakanishi, Koichi
- Takemoto, Minoru
- Iijima, Kazumoto
- Matsuo, Masafumi
Producer: 20090914
In:
Pediatric nephrology (Berlin, Germany) vol. 24
Availability: No items available.
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Validity of the Oxford classification of IgA nephropathy in children. [electronic resource] by
- Shima, Yuko
- Nakanishi, Koichi
- Hama, Taketsugu
- Mukaiyama, Hironobu
- Togawa, Hiroko
- Hashimura, Yuya
- Kaito, Hiroshi
- Sako, Mayumi
- Iijima, Kazumoto
- Yoshikawa, Norishige
Producer: 20120724
In:
Pediatric nephrology (Berlin, Germany) vol. 27
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6.
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The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids. [electronic resource] by
- Kanda, Kyoko
- Nozu, Kandai
- Kaito, Hiroshi
- Iijima, Kazumoto
- Nakanishi, Koichi
- Yoshikawa, Norishige
- Ninchoji, Takeshi
- Hashimura, Yuya
- Matsuo, Masafumi
- Moritz, Michael L
Producer: 20110325
In:
Pediatric nephrology (Berlin, Germany) vol. 26
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Mitochondrial respiratory chain complex IV deficiency complicated with chronic intestinal pseudo-obstruction in a neonate. [electronic resource] by
- Hashimura, Yuya
- Morioka, Ichiro
- Hisamatsu, Chieko
- Yokoyama, Naoki
- Taniguchi-Ikeda, Mariko
- Yokozaki, Hiroshi
- Murayama, Kei
- Ohtake, Akira
- Itoh, Kyoko
- Takeshima, Yasuhiro
- Iijima, Kazumoto
Producer: 20170404
In:
Pediatrics international : official journal of the Japan Pediatric Society vol. 58
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Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients. [electronic resource] 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
Producer: 20090323
In:
Pediatric nephrology (Berlin, Germany) vol. 23
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Natural history of genetically proven autosomal recessive Alport syndrome. [electronic resource] by
- 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
Producer: 20150511
In:
Pediatric nephrology (Berlin, Germany) vol. 29
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In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation. [electronic resource] by
- Nozu, Kandai
- Iijima, Kazumoto
- Kawai, Kazuo
- Nozu, Yoshimi
- Nishida, Atsushi
- Takeshima, Yasuhiro
- Fu, Xue Jun
- Hashimura, Yuya
- Kaito, Hiroshi
- Nakanishi, Koichi
- Yoshikawa, Norishige
- Matsuo, Masafumi
Producer: 20091103
In:
Human genetics vol. 126
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11.
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Treatment strategies for Henoch-Schönlein purpura nephritis by histological and clinical severity. [electronic resource] by
- Ninchoji, Takeshi
- Kaito, Hiroshi
- Nozu, Kandai
- Hashimura, Yuya
- Kanda, Kyoko
- Kamioka, Ichiro
- Shima, Yuko
- Hamahira, Kiyoshi
- Nakanishi, Koichi
- Tanaka, Ryojiro
- Yoshikawa, Norishige
- Iijima, Kazumoto
- Matsuo, Masafumi
Producer: 20110617
In:
Pediatric nephrology (Berlin, Germany) vol. 26
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A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomy. [electronic resource] by
- Fu, Xue J
- Morisada, Naoya
- Hashimoto, Fusako
- Taniguchi-Ikeda, Mariko
- Hashimura, Yuya
- Ohtsubo, Hiromi
- Ninchoji, Takeshi
- Kaito, Hiroshi
- Nozu, Kandai
- Takahashi, Eihiko
- Nakanishi, Koichi
- Kurahashi, Hiroki
- Iijima, Kazumoto
Producer: 20160415
In:
Human genome variation vol. 1
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Metabolomics analysis of umbilical cord blood clarifies changes in saccharides associated with delivery method. [electronic resource] by
- Hashimoto, Fusako
- Nishiumi, Shin
- Miyake, Osamu
- Takeichi, Hitomi
- Chitose, Mari
- Ohtsubo, Hiromi
- Ishimori, Shingo
- Ninchoji, Takeshi
- Hashimura, Yuya
- Kaito, Hiroshi
- Morisada, Naoya
- Morioka, Ichiro
- Fukuoka, Hideoki
- Yoshida, Masaru
- Iijima, Kazumoto
Producer: 20131017
In:
Early human development vol. 89
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Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain. [electronic resource] by
- 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
Producer: 20150209
In:
Kidney international vol. 85
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15.
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X-linked Alport syndrome caused by splicing mutations in COL4A5. [electronic resource] by
- Nozu, Kandai
- Vorechovsky, Igor
- Kaito, Hiroshi
- Fu, Xue Jun
- Nakanishi, Koichi
- Hashimura, Yuya
- Hashimoto, Fusako
- Kamei, Koichi
- Ito, Shuichi
- Kaku, Yoshitsugu
- Imasawa, Toshiyuki
- Ushijima, Katsumi
- Shimizu, Junya
- Makita, Yoshio
- Konomoto, Takao
- Yoshikawa, Norishige
- Iijima, Kazumoto
Producer: 20150709
In:
Clinical journal of the American Society of Nephrology : CJASN vol. 9
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16.
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The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies. [electronic resource] by
- Nozu, Kandai
- Iijima, Kazumoto
- Kanda, Kyoko
- Nakanishi, Koichi
- Yoshikawa, Norishige
- Satomura, Kenichi
- Kaito, Hiroshi
- Hashimura, Yuya
- Ninchoji, Takeshi
- Komatsu, Hiroshi
- Kamei, Koichi
- Miyashita, Ritsuko
- Kugo, Masaaki
- Ohashi, Hiroshi
- Yamazaki, Hajime
- Mabe, Hiroyo
- Otsubo, Asa
- Igarashi, Takashi
- Matsuo, Masafumi
Producer: 20110114
In:
The Journal of clinical endocrinology and metabolism vol. 95
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17.
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Renal transplantations from parents to siblings with autosomal recessive Alport syndrome caused by a rearrangement in an intronic antisense Alu element in the COL4A3 gene led to different outcomes. [electronic resource] by
- Kaimori, Jun-Ya
- Ichimaru, Naotsugu
- Isaka, Yoshitaka
- Hashimoto, Fusako
- Fu, Xuejun
- Hashimura, Yuya
- Kaito, Hiroshi
- Iijima, Kazumoto
- Kyo, Masahiro
- Namba, Tomoko
- Obi, Yoshitsugu
- Hatanaka, Masaki
- Matsui, Isao
- Takabatake, Yoshitsugu
- Okumi, Masayoshi
- Yazawa, Koji
- Nonomura, Norio
- Rakugi, Hiromi
- Takahara, Shiro
Publication details: CEN case reports May 2013
In:
CEN case reports vol. 2
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18.
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Efficacy of primary treatment with immunoglobulin plus ciclosporin for prevention of coronary artery abnormalities in patients with Kawasaki disease predicted to be at increased risk of non-response to intravenous immunoglobulin (KAICA): a randomised controlled, open-label, blinded-endpoints, phase 3 trial. [electronic resource] by
- Hamada, Hiromichi
- Suzuki, Hiroyuki
- Onouchi, Yoshihiro
- Ebata, Ryota
- Terai, Masaru
- Fuse, Shigeto
- Okajima, Yoshitomo
- Kurotobi, Shunji
- Hirai, Katsuki
- Soga, Takashi
- Ishiguchi, Yukiko
- Okuma, Yoshiaki
- Takada, Nobuyuki
- Yanai, Masaaki
- Sato, Junichi
- Nakayashiro, Mami
- Ayusawa, Mamoru
- Yamamoto, Eiichi
- Nomura, Yuichi
- Hashimura, Yuya
- Ouchi, Kazunobu
- Masuda, Hiroshi
- Takatsuki, Shinichi
- Hirono, Keiichi
- Ariga, Tadashi
- Higaki, Takashi
- Otsuki, Akio
- Terauchi, Moe
- Aoyagi, Reiko
- Sato, Takatoshi
- Fujii, Yasuhisa
- Fujiwara, Tadami
- Hanaoka, Hideki
- Hata, Akira
Producer: 20190508
In:
Lancet (London, England) vol. 393
Availability: No items available.
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