Rchr
J-GLOBAL ID：200901001488654220
Update date: Apr. 08, 2024
Nakamura Kimitoshi
ナカムラ キミトシ | Nakamura Kimitoshi
Affiliation and department：
Job title：
Associate Professor
Research field (1)：
Fetal medicine/Pediatrics
Research theme for competitive and other funds (15)：
- 2020 - 2023 濾紙血中のSMNタンパク測定による脊髄性筋萎縮症の新生児スクリーニング
- 2017 - 2020 Newborn Screening for Hypophosphatasia
- 2017 - 2020 Development of novel medicine using iPS cells derived from Gaucher disease type II patients
- 2015 - 2019 Newborn screening and high risk screening for Pompe disease in Japan
- 2015 - 2018 Prediction of DiabetesMellitus by using with iPS cell technology
- 2011 - 2016 The effect of the Asian-specific polymorphisms on newborn screening of Pompe disease and new diagnostic approaches for the disease.
- 2011 - 2013 Role of calcium signaling on the endodermal stem cells in the metabolic syndrom from childhood.
- 2010 - 2012 Evaluation system for regenerative medicine of genetic disorders by using cloned pigs established from endoderm somatic stem cells
- 2008 - 2010 Role of calcium signaling on the hepatic and pancreatic stem cells in the animal model of metabolic syndrome during childhood.
- 2006 - 2007 The Role of Calcium Signaling in the Metabolic Syndrome during Childhood Onset
- 2005 - 2006 Roles and regulation of endoderm stem cells in hereditary liver disease
- 2004 - 2005 Role of calcium signals for metabolic syndromes in children.
- 2003 - 2004 A Role of somatic stem cells in pathogenesis and treatments of hereditary hepatic disorders.
- 2002 - 2003 小児心疾患におけるカルシウムシグナルの役割
- 2001 - 2002 Studies on mechanisms for apoptosis and carcinogenessis, and stam cell transplantation in hereditary liver diseases.
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Papers (270)：
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Kanako Higashi, Yuri Sonoda, Noriyuki Kaku, Fumihiko Fujii, Fumiya Yamashita, Sooyoung Lee, Vlad Tocan, Go Ebihara, Wakato Matsuoka, Kenichi Tetsuhara, et al. Rapid and long-lasting efficacy of high-dose ambroxol therapy for neuronopathic Gaucher disease: A case report and literature review. Molecular genetics & genomic medicine. 2024. 12. 4. e2427
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Keishiro Furuie, Shohei Kuraoka, Hideki Ban, Yuko Hidaka, Hiroko Nagata, Hiroshi Tamura, Koji Nagano, Tomoyasu Kawano, Akio Furuse, Hitoshi Nakazato, et al. Ongoing impacts of childhood-onset glomerular diseases during young adulthood. Pediatric nephrology (Berlin, Germany). 2023
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Mika Ogata, Takanobu Yoshida, Jun Kido, Natsuko Nishi, Sachiko Shimomura, Nami Hirai, Masaaki Yanai, Tomoyuki Mizukami, Kimitoshi Nakamura. Safety of Oral Food Challenge for Individuals with Low Egg White and Ovomucoid-Specific IgE Antibodies. International Archives of Allergy and Immunology. 2023. 185. 1. 33-42
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Jun Kido, Johannes Häberle, Toju Tanaka, Masayoshi Nagao, Yoichi Wada, Chikahiko Numakura, Ryosuke Bo, Hiromi Nyuzuki, Sumito Dateki, Shinsuke Maruyama, et al. Improved sensitivity and specificity for citrin deficiency using selected amino acids and acylcarnitines in the newborn screening. Journal of Inherited Metabolic Disease. 2023
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長谷川 真成, 時高 留依, 木村 献, 白石 昌弘, 清水 美保, 佐世 正勝, 澤田 貴彰, 中村 公俊. 当院におけるファブリー病の新生児スクリーニング. 日本小児科学会雑誌. 2023. 127. 9. 1215-1216
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MISC (238)：
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岡田真人, 藤井裕子, 武谷一徹, 酒見菖平, 淀川弘章, 丸山大地, 塩手仁也, 平井貴彦, 小川厚, 廣瀬伸一, et al. A Neonatal Case of Spinal Muscular Atrophy Treated Early by Cooperation with Obstetrics and Infection Control. 日本小児科学会雑誌. 2024. 128. 2
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西村円香, 水上智之, 澤田貴彰, 吉田真一郎, 中村公俊. TREC based newborn screening for severe combined immunodeficiency in Kumamoto: results of the first three years. 日本小児科学会雑誌. 2023. 127. 2
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吉田真一郎, 伊藤和美, 山本千尋, 大坂間遥香, 徳永美知代, 澤田貴彰, 水上智之, 遠藤文夫, 中村公俊. 熊本における新生児SCID,SMAスクリーニング経過報告. 日本先天代謝異常学会雑誌. 2023. 39
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山本晶子, 小松なぎさ, 橘秀和, 澤田貴彰, 中村公俊. Infant with traffic hydrocephalus presenting with rapid weight gain and developmental delay. 日本小児内分泌学会学術集会プログラム・抄録集. 2023. 56th
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Takaaki Sawada, Jun Kido, Keishin Sugawara, Shinichiro Yoshida, Shirou Matsumoto, Tomoyuki Shimazu, Yuki Matsushita, Takahito Inoue, Shinichi Hirose, Fumio Endo, et al. Newborn screening for Gaucher disease in Japan. Molecular Genetics and Metabolism Reports. 2022. 31
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Books (3)：
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最新小児・周産期遺伝医学研究と遺伝カウンセリング
メディカルドゥ 2019 ISBN:9784909508034
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厚生労働科学研究費補助金難治性疾患克服研究事業高チロシン血症を示す新生児における最終診断への診断プロトコールと治療指針の作成に関する研究研究報告書
[中村公俊] 2010
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Calreticulin, cardiac development and congenital heart block in children.
In Signal transduction and cardiac hypertrophy. (Dhalla, N.S., Hryschko, L., Kardami, E. and Singal, P.K., eds.). Kluwer Academic Publishers. 2003
Works (8)：
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小児期発症メタボリックシンドロームにおけるカルシウムシグナルの役割
2006 - 2008
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遺伝性肝疾患における内胚葉幹細胞の役割とその制御
2005 - 2007
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小児生活習慣病におけるカルシウムシグナルの役割
2004 - 2006
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遺伝性肝疾患の病態と治療における成体幹細胞の意義
2003 - 2005
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内胚葉性体制幹細胞の分離と再生治療への応用
2003 - 2004
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Education (4)：
- - 1996 Kumamoto University
- - 1996 Kumamoto University Graduate School, Division of Medicine
- - 1990 Kumamoto University School of Medicine School of Medicine
- - 1990 Kumamoto University Faculty of Medicine
Professional career (1)：
- PhD (Kumamoto University)
Work history (7)：
- 2017/09 - 現在 Kumamoto University Faculty of Life Sciences
- 2014 - 2017/08 Kumamoto University Faculty of Life Sciences
- 2009 - 2014 Kumamoto University University Hospital
- 2009 - 2014 Lecturer, ,University Hospital ,Kumamoto University
- 2014 - Associate Professor, ,University Hospital ,Kumamoto University
- 2001 - 2007 Kumamoto University University Hospital
- 2001 - 2007 Research Associate,
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