MORISADA NAOYA

J-GLOBAL         Last updated: Jun 14, 2019 at 16:26
 
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Name
MORISADA NAOYA
Affiliation
Kobe University
Section
Graduate School of Medicine Faculty of Medical Sciences
Job title
Associate Professor

Research Areas

 
 

Awards & Honors

 
Jun 2014
神戸こども初期急病センターを受診した血糖値異常症例の検討, 日本小児救急医学会 最優秀論文賞, 日本小児救急医学会
Winner: Morisada Naoya
 

Published Papers

 
Inaguma Y, Kaito H, Morisada N, Iijima K, Tanaka R
Pediatrics international : official journal of the Japan Pediatric Society   61(2) 210-212   Feb 2019   [Refereed]
Sakakibara N, Morisada N, Nozu K, Nagatani K, Ohta T, Shimizu J, Wada T, Shima Y, Yamamura T, Minamikawa S, Fujimura J, Horinouchi T, Nagano C, Shono A, Ye MJ, Nozu Y, Nakanishi K, Iijima K
Journal of human genetics   64(1) 3-9   Jan 2019   [Refereed]
Fujimura J, Nozu K, Yamamura T, Minamikawa S, Nakanishi K, Horinouchi T, Nagano C, Sakakibara N, Nakanishi K, Shima Y, Miyako K, Nozu Y, Morisada N, Nagase H, Ninchoji T, Kaito H, Iijima K
Kidney international reports   4(1) 119-125   Jan 2019   [Refereed]
Ohara Y, Okada Y, Yamada T, Sugawara K, Kanatani M, Fukuoka H, Hirota Y, Maeda T, Morisada N, Iijima K, Ogawa W
Journal of diabetes investigation      Jan 2019   [Refereed]
Nagano C, Nozu K, Morisada N, Yazawa M, Ichikawa D, Numasawa K, Kourakata H, Matsumura C, Tazoe S, Tanaka R, Yamamura T, Minamikawa S, Horinouchi T, Nakanishi K, Fujimura J, Sakakibara N, Nozu Y, Ye MJ, Kaito H, Iijima K
Clinical and experimental nephrology   22(4) 881-888   Aug 2018   [Refereed]
Horinouchi T, Nozu K, Yamamura T, Minamikawa S, Omori T, Nakanishi K, Fujimura J, Ashida A, Kitamura M, Kawano M, Shimabukuro W, Kitabayashi C, Imafuku A, Tamagaki K, Kamei K, Okamoto K, Fujinaga S, Oka M, Igarashi T, Miyazono A, Sawanobori E, Fujimaru R, Nakanishi K, Shima Y, Matsuo M, Ye MJ, Nozu Y, Morisada N, Kaito H, Iijima K
Journal of the American Society of Nephrology : JASN   29(8) 2244-2254   Aug 2018   [Refereed]
Matsunoshita N, Nozu K, Yoshikane M, Kawaguchi A, Fujita N, Morisada N, Ishimori S, Yamamura T, Minamikawa S, Horinouchi T, Nakanishi K, Fujimura J, Ninchoji T, Morioka I, Nagase H, Taniguchi-Ikeda M, Kaito H, Iijima K
Journal of human genetics   63(8) 887-892   Jul 2018   [Refereed]
Ninchoji T, Iwatani S, Nishiyama M, Kamiyoshi N, Nakagawa T, Taniguchi-Ikeda M, Morisada N, Ishibashi K, Iijima K, Ishida A, Morioka I
Minerva pediatrica   70(3) 212-216   Jun 2018   [Refereed]
Minamikawa S, Nozu K, Nozu Y, Yamamura T, Taniguchi-Ikeda M, Nakanishi K, Fujimura J, Horinouchi T, Shima Y, Nakanishi K, Hattori M, Kanda K, Tanaka R, Morisada N, Nagano C, Sakakibara N, Nagase H, Morioka I, Kaito H, Iijima K
Journal of human genetics   63(5) 589-595   May 2018   [Refereed]
Unzaki A, Morisada N, Nozu K, Ye MJ, Ito S, Matsunaga T, Ishikura K, Ina S, Nagatani K, Okamoto T, Inaba Y, Ito N, Igarashi T, Kanda S, Ito K, Omune K, Iwaki T, Ueno K, Yahata M, Ohtsuka Y, Nishi E, Takahashi N, Ishikawa T, Goto S, Okamoto N, Iijima K
Journal of human genetics   63(5) 647-656   May 2018   [Refereed]
Morisada Naoya, Nozu Kandai, Iijima Kazumoto
Pediatr Int   56(5) e75-8   Oct 2014   [Refereed]
Ninchoji T, Iwatani S, Nishiyama M, Kamiyoshi N, Taniguchi-Ikeda M, Morisada N, Ishibashi K, Iijima K, Ishida A, Morioka I
Pediatric emergency care   34(4) e64-e67   Apr 2018   [Refereed]
Nozu Kandai, Kaito Hiroshi, Morisada Naoya, Iijima Kazumoto
Pediatr Nephrol   29(9) 1535-44   Sep 2014   [Refereed]
Yoshioka M, Morisada N, Toyoshima D, Yoshimura H, Nishio H, Iijima K, Takeshima Y, Uehara T, Kosaki K
Brain & development   40(4) 343-347   Apr 2018   [Refereed]
Ikeda Mariko, Morisada Naoya, Iijima Kazumoto,
Mol Cytogenet   7 55   Aug 2014   [Refereed]
Tsuji Y, Nozu K, Sofue T, Hara S, Nakanishi K, Yamamura T, Minamikawa S, Nozu Y, Kaito H, Fujimura J, Horinouchi T, Morisada N, Morioka I, Taniguchi-Ikeda M, Matsuo M, Iijima K
Nephron   138(2) 166-171   2018   [Refereed]
Morisada Naoya, Nozu Kandai, Iijima Kazumoto
Pediatr Int   56(3) 309-14   Jun 2014   [Refereed]
Nakanishi K, Nozu K, Hiramoto R, Minamikawa S, Yamamura T, Fujimura J, Horinouchi T, Ninchoji T, Kaito H, Morisada N, Ishimori S, Nakanishi K, Morioka I, Awano H, Matsuo M, Iijima K
European journal of medical genetics   60(12) 631-634   Dec 2017   [Refereed]
Ar Rochmah M, Awano H, Awaya T, Harahap NIF, Morisada N, Bouike Y, Saito T, Kubo Y, Saito K, Lai PS, Morioka I, Iijima K, Nishio H, Shinohara M
Brain & development   39(10) 851-860   Nov 2017   [Refereed]
Sasaki M, Ishii A, Morisada Naoya, Iijima Kazumoto, Takada S, Araki A, Tanabe Y, Arai H, Yamashita S, Ohashi T, Oda Y,
Neurology   82(6) 482-90   Feb 2014   [Refereed]
Yokota K, Nozu K, Minamikawa S, Yamamura T, Nakanishi K, Kaneda H, Hamada R, Nozu Y, Shono A, Ninchoji T, Morisada N, Ishimori S, Fujimura J, Horinouchi T, Kaito H, Nakanishi K, Morioka I, Taniguchi-Ikeda M, Iijima K
Clinical and experimental nephrology   21(5) 877-883   Oct 2017   [Refereed]
Nozu Kandai, Kaito Hiroshi, Ninchoji Takeshi, Morisada Naoya, Iijima Kazumoto
Kidney Int   85(5) 1208-1213   Dec 2013   [Refereed]
Gender Effects on the Clinical Phenotype in Japanese Patients with Spinal Muscular Atrophy.
Ar Rochmah M, Shima A, Harahap NIF, Niba ETE, Morisada N, Yanagisawa S, Saito T, Kaneko K, Saito K, Morioka I, Iijima K, Lai PS, Bouike Y, Nishio H, Shinohara M
The Kobe journal of medical sciences   63(2) E41-E44   Oct 2017   [Refereed]
Yamamura T, Nozu K, Fu XJ, Nozu Y, Ye MJ, Shono A, Yamanouchi S, Minamikawa S, Morisada N, Nakanishi K, Shima Y, Yoshikawa N, Ninchoji T, Morioka I, Kaito H, Iijima K
Kidney international reports   2(5) 850-855   Sep 2017   [Refereed]
Nishiumi Shin, Ninchoji Takeshi, Kaito Hiroshi, Morisada Naoya, Morioka Ichiro, Yoshida Masaru, Iijima Kazumoto
Early Hum Dev   89(5) 315-20   May 2013   [Refereed]
Nozu K, Minamikawa S, Yamada S, Oka M, Yanagita M, Morisada N, Fujinaga S, Nagano C, Gotoh Y, Takahashi E, Morishita T, Yamamura T, Ninchoji T, Kaito H, Morioka I, Nakanishi K, Vorechovsky I, Iijima K
Journal of human genetics   62(7) 733-735   Jul 2017   [Refereed]
SLC26A3 gene analysis in patients with Bartter and Gitelman syndromes and the clinical characteristics of patients with unidentified mutations
Kaito Hiroshi, Ninchoji Takeshi, Nozu Kandai, Morisada Naoya, Iijima Kazumoto
Kobe J Med Sci   59(2) E36-43   Apr 2013   [Refereed]
Yoshikawa T, Kamei K, Nagata H, Saida K, Sato M, Ogura M, Ito S, Miyazaki O, Urushihara M, Kondo S, Sugawara N, Ishizuka K, Hamasaki Y, Shishido S, Morisada N, Iijima K, Nagata M, Yoshioka T, Ogata K, Ishikura K
Nephrology (Carlton, Vic.)   22(7) 566-571   Jul 2017   [Refereed]
Yamamura T, Morisada N, Nozu K, Minamikawa S, Ishimori S, Toyoshima D, Ninchoji T, Yasui M, Taniguchi-Ikeda M, Morioka I, Nakanishi K, Nishio H, Iijima K
Clinical and experimental nephrology   21(1) 136-142   Feb 2017   [Refereed]
Nozu K, Nozu Y, Nakanishi K, Konomoto T, Horinouchi T, Shono A, Morisada N, Minamikawa S, Yamamura T, Fujimura J, Nakanishi K, Ninchoji T, Kaito H, Morioka I, Taniguchi-Ikeda M, Vorechovsky I, Iijima K
Journal of human genetics   62(2) 335-337   Feb 2017   [Refereed]
Hanafusa H, Morisada N, Ishida Y, Sakata R, Morita K, Miura S, Ye MJ, Yamamoto T, Okamoto N, Nozu K, Iijima K
Human genome variation   4 17050   2017   [Refereed]
Fu XJ, Nozu K, Eguchi A, Nozu Y, Morisada N, Shono A, Taniguchi-Ikeda M, Shima Y, Nakanishi K, Vorechovsky I, Iijima K
Clinical and experimental nephrology   20(5) 699-702   Oct 2016   [Refereed]
Iijima T, Hoshino J, Mise K, Sumida K, Suwabe T, Hayami N, Ueno T, Takaichi K, Fujii T, Ohashi K, Morisada N, Iijima K, Ubara Y
Human pathology   55 24-29   Sep 2016   [Refereed]
Kamiyoshi N, Nozu K, Fu XJ, Morisada N, Nozu Y, Ye MJ, Imafuku A, Miura K, Yamamura T, Minamikawa S, Shono A, Ninchoji T, Morioka I, Nakanishi K, Yoshikawa N, Kaito H, Iijima K
Clinical journal of the American Society of Nephrology : CJASN   11(8) 1441-1449   Aug 2016   [Refereed]
Kanda S, Morisada N, Kaneko N, Yabuuchi T, Nawashiro Y, Tada N, Nishiyama K, Miyai T, Sugawara N, Ishizuka K, Chikamoto H, Akioka Y, Iijima K, Hattori M
Pediatric transplantation   20(3) 467-471   May 2016   [Refereed]
Noguchi Y, Onishi A, Nakamachi Y, Hayashi N, Harahap NI, Rochmah MA, Shima A, Yanagisawa S, Morisada N, Nakagawa T, Iijima K, Kasagi S, Saegusa J, Kawano S, Shinohara M, Tairaku S, Saito T, Kubo Y, Saito K, Nishio H
Pediatric neurology   58 83-89   May 2016   [Refereed]
[A woman with beta-propeller protein-associated neurodegeneration identified by the WDR45 mutation presenting as Rett-like syndrome in childhood].
Morisada N, Tsuneishi S, Taguchi K, Yagi R, Nishiyama M, Toyoshima D, Nakagawa T, Takeshima Y, Takada S, Iijima K
No to hattatsu = Brain and development   48(3) 209-212   May 2016   [Refereed]
Kamiyoshi N, Nozu K, Urahama Y, Matsunoshita N, Yamamura T, Minamikawa S, Ninchoji T, Morisada N, Nakanishi K, Kaito H, Iijima K
Clinical and experimental nephrology   20(2) 253-257   Apr 2016   [Refereed]
Fu XJ, Nozu K, Kaito H, Ninchoji T, Morisada N, Nakanishi K, Yoshikawa N, Ohtsubo H, Matsunoshita N, Kamiyoshi N, Matsumura C, Takagi N, Maekawa K, Taniguchi-Ikeda M, Iijima K
European journal of human genetics : EJHG   24(3) 387-391   Mar 2016   [Refereed]
Toyoshima D, Morisada N, Takami Y, Kidokoro H, Nishiyama M, Nakagawa T, Ninchoji T, Nozu K, Takeshima Y, Takada S, Nishio H, Iijima K
Brain & development   38(3) 346-349   Mar 2016   [Refereed]
Matsunoshita N, Nozu K, Shono A, Nozu Y, Fu XJ, Morisada N, Kamiyoshi N, Ohtsubo H, Ninchoji T, Minamikawa S, Yamamura T, Nakanishi K, Yoshikawa N, Shima Y, Kaito H, Iijima K
Genetics in medicine : official journal of the American College of Medical Genetics   18(2) 180-188   Feb 2016   [Refereed]
Nakagawa T, Taniguchi-Ikeda M, Murakami Y, Nakamura S, Motooka D, Emoto T, Satake W, Nishiyama M, Toyoshima D, Morisada N, Takada S, Tairaku S, Okamoto N, Morioka I, Kurahashi H, Toda T, Kinoshita T, Iijima K
American journal of medical genetics. Part A   170A(1) 183-188   Jan 2016   [Refereed]
[A girl with recurrent febrile seizures and developmental delay].
Morisada N
No to hattatsu = Brain and development   48(1) 3-4   Jan 2016   [Refereed]
Iwafuchi Y, Morioka T, Morita T, Yanagihara T, Oyama Y, Morisada N, Iijima K, Narita I
Case reports in nephrology and dialysis   6(1) 61-69   Jan 2016   [Refereed]
Morisada N, Ioroi T, Taniguchi-Ikeda M, Juan Ye M, Okamoto N, Yamamoto T, Iijima K
Human genome variation   3 16029   2016   [Refereed]
Yoshimoto S, Harahap NI, Hamamura Y, Ar Rochmah M, Shima A, Morisada N, Shinohara M, Saito T, Saito K, Lai PS, Matsuo M, Awano H, Morioka I, Iijima K, Nishio H
Human genome variation   3 16040   2016   [Refereed]
Harahap NIF, Nurputra DK, Ar Rochmah M, Shima A, Morisada N, Takarada T, Takeuchi A, Tohyama Y, Yanagisawa S, Nishio H
Biochemistry and biophysics reports   4 351-356   Dec 2015   [Refereed]
Kato T, Morisada N, Nagase H, Nishiyama M, Toyoshima D, Nakagawa T, Maruyama A, Fu XJ, Nozu K, Wada H, Takada S, Iijima K
Brain & development   37(9) 911-915   Oct 2015   [Refereed]
Nishiyama M, Nagase H, Tanaka T, Fujita K, Maruyama A, Toyoshima D, Nakagawa T, Taniguchi-Ikeda M, Morioka I, Morisada N, Takada S, Iijima K
Pediatric neurology   52(5) 499-503   May 2015   [Refereed]
Kuma A, Tamura M, Ishimatsu N, Miyamoto T, Serino R, Ishimori S, Morisada N, Iijima K, Yamada S, Takeuchi M, Abe H, Otsuji Y
Internal medicine (Tokyo, Japan)   54(6) 631-635   2015   [Refereed]
ヒトCAKUTの原因遺伝子解析
Morisada Naoya, Nozu Kandai, Iijima Kazumoto
発達腎研究会誌   22(1号) 27-29   Apr 2014   [Refereed]
Fu XJ, Morisada N, Hashimoto F, Taniguchi-Ikeda M, Hashimura Y, Ohtsubo H, Ninchoji T, Kaito H, Nozu K, Takahashi E, Nakanishi K, Kurahashi H, Iijima K
Human genome variation   1 14006   2014   [Refereed]
神戸こども初期急病センターを受診した血糖値異常症例の検討
Morisada Naoya, Hiroyuki Awano, Ikeda Mariko,
日本小児救急医学会雑誌   12(3号) 375-379   Oct 2013   [Refereed]
小児ステロイド感受性ネフローゼ症候群患者の成人期における現状と問題点
Ishimori Shingo, Kaito Hiroshi, Ninchoji Takeshi, Hashimura Yuya, Morisada Naoya, Iijima Kazumoto
日本小児科学会雑誌   117(1号) 90-96   Jan 2013   [Refereed]
Ogawa A, Kitamura S, Nakayama K, Sugiyama H, Morisada N, Iijima K, Makino H
Kidney international   82(9) 1037   Nov 2012   [Refereed]
Ohtsubo H, Morisada N, Kaito H, Nagatani K, Nakanishi K, Iijima K
Pediatric nephrology (Berlin, Germany)   27(7) 1189-1192   Jul 2012   [Refereed]
腎移植後の副甲状腺機能亢進症に対して副甲状腺摘出術を行った1症例
Hashimura Yuya, Ishimori Shingo, Ninchoji Takeshi, Kaito Hiroshi, Morisada Naoya, Kadoguchi Hiraku, Nishi Shinichi, Iijima Kazumoto
日本小児腎不全学会雑誌   32 108-110   Jul 2012   [Refereed]
Furuno Y, Morishita T, Toyohira Y, Yamada S, Ueno S, Morisada N, Sugita K, Noguchi K, Sakanashi M, Miyata H, Tanimoto A, Sasaguri Y, Shimokawa H, Otsuji Y, Yanagihara N, Tamura M, Tsutsui M
Nitric oxide : biology and chemistry   25(3) 350-359   Oct 2011   [Refereed]
Spontaneous development of left ventricular hypertrophy and diastolic dysfunction in mice lacking all nitric oxide synthases.
Shibata K, Yatera Y, Furuno Y, Sabanai K, Morisada N, Nakata S, Morishita T, Yamazaki F, Tanimoto A, Sasaguri Y, Tasaki H, Nakashima Y, Shimokawa H, Yanagihara N, Otsuji Y, Tsutsui M
Circulation journal : official journal of the Japanese Circulation Society   74(12) 2681-2692   Nov 2010   [Refereed]
Yatera Y, Shibata K, Furuno Y, Sabanai K, Morisada N, Nakata S, Morishita T, Toyohira Y, Wang KY, Tanimoto A, Sasaguri Y, Tasaki H, Nakashima Y, Shimokawa H, Yanagihara N, Otsuji Y, Tsutsui M
Cardiovascular research   87(4) 675-682   Sep 2010   [Refereed]
Morisada N, Rendtorff ND, Nozu K, Morishita T, Miyakawa T, Matsumoto T, Hisano S, Iijima K, Tranebjaerg L, Shirahata A, Matsuo M, Kusuhara K
Pediatric nephrology (Berlin, Germany)   25(7) 1343-1348   Jul 2010   [Refereed]
Complete disruption of all nitric oxide synthase genes causes markedly accelerated renal lesion formation following unilateral ureteral obstruction in mice in vivo.
Morisada N, Nomura M, Nishii H, Furuno Y, Sakanashi M, Sabanai K, Toyohira Y, Ueno S, Watanabe S, Tamura M, Matsumoto T, Tanimoto A, Sasaguri Y, Shimokawa H, Kusuhara K, Yanagihara N, Shirahata A, Tsutsui M
Journal of pharmacological sciences   114(4) 379-389   2010   [Refereed]
Morisada N, Okita S, Sato T, Miyaji R, Kamizono J, Shimono M, Osajima A, Kaizu K, Asayama K, Shirahata A
Pediatrics international : official journal of the Japan Pediatric Society   46(4) 480-483   Aug 2004   [Refereed]
Stimulation of catecholamine synthesis by orexin-A in bovine adrenal medullary cells through orexin receptor 1.
Kawada Y, Ueno S, Asayama K, Tsutsui M, Utsunomiya K, Toyohira Y, Morisada N, Tanaka K, Shirahata A, Yanagihara N
Biochemical pharmacology   66(1) 141-147   Jul 2003   [Refereed]

Misc

 
【広く嚢胞性腎疾患を捉える】 腎嚢胞性疾患と原因遺伝子
Morisada Naoya, Iijima Kazumoto
腎と透析   77(5号) 711-715   Nov 2014   [Refereed]
【神経症候群(第2版)-その他の神経疾患を含めて-】 先天異常/先天奇形 染色体異常・先天奇形症候群 Branchio-oto-renal(BOR)症候群
Morisada Naoya, Iijima Kazumoto
日本臨床   (別冊神経症候群IV) 505-508   Sep 2014   [Invited]
【よくわかる遺伝子】 単一遺伝子異常と疾患 顎顔面奇形
Morisada Naoya, Iijima Kazumoto
JOHNS   30(6号) 723-725   Jun 2014   [Invited]
【クローズアップ 新しい子どもの病気】 水・電解質疾患 原因が解明された既存疾患 先天性腎尿路奇形の遺伝子変異
Morisada Naoya,
小児内科   45(6号) 1077-1078   Jun 2013   [Invited]
多腺性自己免疫症候群を合併した微小変化型ネフローゼ症候群の1例
Kaito Hiroshi, Hiroyuki Awano, Ishimori Shingo, Ninchoji Takeshi, Hashimura Yuya, Morisada Naoya, Iijima Kazumoto, Fukunaga Atsushi, Nishigori Chikako
日本小児腎臓病学会雑誌   25(2号) 201   Nov 2012

Conference Activities & Talks

 
Demographics and outcomes of pediatric febrile convulsive status epilepticus. [Invited]
Nishiyama Masahiro, Toyoshima Daisaku, Nakagawa Taku, Ikeda Mariko, Morioka Ichiro, Morisada Naoya, Takada Satoshi, Iijima Kazumoto
American Epilepsy Society 68th Annual Meeting   Dec 2014   
染色体構造異常によるsyndromic CAKUT の原因遺伝子についての検討 [Invited]
Morisada Naoya, Nozu Kandai, Iijima Kazumoto
第59回日本人類遺伝学会   Nov 2014   
てんかん発作にビタミンB6製剤が著効した先天性GPI欠損症の一男児例 [Invited]
Nakagawa Taku, Nishiyama Masahiro, Toyoshima Daisaku, Morisada Naoya, Ikeda Mariko, Takada Satoshi, Iijima Kazumoto
第48回日本てんかん学会学術集会   Oct 2014   
The comprehensive genetic analysis of congenital anomalies of kidney and urinary tract (CAKUT) in Japan. [Invited]
Morisada Naoya, Ikeda Mariko, Nozu Kandai, Iijima Kazumoto
The American Society of Human Genetics   Oct 2014   
X-linked Alport syndrome patients caused by atypical splicing mutations in COL4A5. [Invited]
Nozu Kandai, Morisada Naoya, Kaito Hiroshi, Ninchoji Takeshi, Iijima Kazumoto
47th Annual Scientific Meeting of the European Society for Pediatric Nephrology   Sep 2014   

Research Grants & Projects

 
Pediatric nephrology
Project Year: 2000   
branshio-oto-renal syndrome