muramatu kazuhiro

FacultyPediatrics
Job titleAssociate ProfessorWeb site

Profile

Research Keywords

    Autophagy

Career

  • - School of Medicine
  • Aug.2009
    -
    Mar.2016
    群馬大学大学院医学系研究科小児科学分野, 助教
  • Apr.2011
    -
    Mar.2013
    Philipps University Marburg Germany, Neurology Research Fellow
  • Apr.2008
    -
    Jul.2009
    群馬大学医学部付属病院, 小児科医員
  • Apr.2005
    -
    Mar.2008
    日本学術振興会, 特別研究員
  • Apr.2004
    -
    Mar.2008
    群馬大学大学院医学系研究科, 博士課程
  • May2003
    -
    Mar.2004
    群馬大学医学部付属病院小児科, 医員
  • May1998
    -
    Apr.2003
    日本赤十字社医療センター小児科新生児科, レジデント

Research Activities

Papers(paper)

  • Demyelinating neuropathy in a 6-year-old girl with autism spectrum disorder
    Kamata A, Muramatsu K, Sawaura N, Makioka N, Ogata T, Kuwashima M, Arakawa H.
    Pediatrics International 59(8) 951-954 2017
  • Efficacy and tolerability of levetiracetam for pediatric refractory epilepsy.
    Muramatsu K, Sawaura N, Ogata T, Makioka N, Tomita K, Motojima T, Ida K, Hazama K, Arakawa H.
    Brain Dev. 39(3) 231-235 2017
  • Brainstem infarction associated with HHV-6 infection in an infant
    Wada A, Muramatsu K, Sunaga Y, Mizuno T, Takei M, Ogasawara S, Uchida M, Tsukida K, Tashiro M.
    Brain and Development 2017
  • Biallelic Mutations in the 3’ Exonuclease TOE1 Cause Pontocerebellar Hypoplasia and Uncover a Role in snRNA Processing.
    RM. Lardelli, AE. Schaffer, VR.C. Eggens, MS. Zaki, S Grainger, S Sathe, EL. V Nostrand, Z Schlachetzki, B Rosti, N Akizu, E Scott, LD Heckman, RO Rosti, E Dikoglu, A Gregor, A G-Gamboa, D Musaev, R Mande, A Widjaja, TL. Shaw, S Markmiller, I M-Valencia, JH.Davies, L de Meirleir, H Kayserili, U Altunoglu, ML Freckmann, L Warwick, D Chitayat, AO Çağlayan, K Bilguvar, H Per, C Fagerberg, M Kibaek, KA. Aldinger, D Manchester, N Matsumoto, K Muramatsu, H Saitsu, M Shiina, K Ogata, N Foulds, WB. Dobyns, N Chi, D Traver, L Spaccini, SM Bova, SB. Gabriel, M Gunel, EM Valente, EJ. Bennett, GW. Yeo, F Baas, J L-Andersen, JG. Gleeson.
    Nature Genetics. 49(3) 457-464 2017
  • NDUFAF3 variants that disrupt mitochondrial complex I assembly may associate with cavitating leukoencephalopathy
    Ishiyama A, Muramatsu K, Uchino S, Sakai C, Matsushima Y, Makioka N, Ogata T, Suzuki E, Komaki H, Sasaki M, Mimaki M, Goto Y.-I, Nishino I.
    Clinical Genetics 93(5) 1103-1106 2018
  • Molecular genetic analysis of 30 families with Joubert syndrome.
    Suzuki T, Miyake N, Tsurusaki Y, Okamoto N, Alkindy A, Inaba A, Sato M, Ito S, Muramatsu K, Kimura S, Ieda D, Saitoh S, Hiyane M, Suzumura H, Yagyu K, Shiraishi H, Nakajima M, Fueki N, Habata Y, Ueda Y, Komatsu Y, Yan K, Shimoda K, Shitara Y, Mizuno S, Ichinomiya K, Sameshima K, Tsuyusaki Y, Kurosawa K, Sakai Y, Haginoya K, Kobayashi Y, Yoshizawa C, Hisano M, Nakashima M, Saitsu H, Takeda S, Matsumoto N.
    Clin Genet. 90(6) 526-535 2016
  • De novo mutations in the autophagy gene WDR45 cause SENDA/BPAN
    Muramatsu K.
    No To Hattatsu 48(3) 177-183 2016
  • De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood.
    Saitsu H, Nishimura T, Muramatsu K (These authors contributed equally to this work.), Kodera H, Kumada S, Sugai K, Kasai-Yoshida E, Sawaura N, Nishida H, Hoshino A, Ryujin F, Yoshioka S, Nishiyama K, Kondo Y, Tsurusaki Y, Nakashima M, Miyake N, Arakawa H, Kato M, Mizushima N, Matsumoto N
    Nature genetics 45(4) 445-449 Apr. 2013
  • Uncovering genes required for neuronal morphology by morphology-based gene trap screening with a revertible retrovirus vector.
    Hashimoto Y, Muramatsu K,( These authors contributed equally to this work.) Kunii M, Yoshimura SI, Yamada M, Sato T, Ishida Y, Harada R, Harada A
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology 26(11) 4662-4674 Aug. 2012
  • Relation between psychological development and respiratory management in patients with congenital central hypoventilation syndrome in Japan
    Irahara K, Ogata T, Ozawa H, Otaki U, Yamamoto K, Ishizuka T, Arimoto K, Kimiya S, Arakawa K, Muramatsu K.
    No To Hattatsu 47(5) 343-347 2015
Display all
Papers(paper)close
  • Demyelinating neuropathy in a 6-year-old girl with autism spectrum disorder
    Kamata A, Muramatsu K, Sawaura N, Makioka N, Ogata T, Kuwashima M, Arakawa H.
    Pediatrics International 59(8) 951-954 2017
  • Efficacy and tolerability of levetiracetam for pediatric refractory epilepsy.
    Muramatsu K, Sawaura N, Ogata T, Makioka N, Tomita K, Motojima T, Ida K, Hazama K, Arakawa H.
    Brain Dev. 39(3) 231-235 2017
  • Brainstem infarction associated with HHV-6 infection in an infant
    Wada A, Muramatsu K, Sunaga Y, Mizuno T, Takei M, Ogasawara S, Uchida M, Tsukida K, Tashiro M.
    Brain and Development 2017
  • Biallelic Mutations in the 3’ Exonuclease TOE1 Cause Pontocerebellar Hypoplasia and Uncover a Role in snRNA Processing.
    RM. Lardelli, AE. Schaffer, VR.C. Eggens, MS. Zaki, S Grainger, S Sathe, EL. V Nostrand, Z Schlachetzki, B Rosti, N Akizu, E Scott, LD Heckman, RO Rosti, E Dikoglu, A Gregor, A G-Gamboa, D Musaev, R Mande, A Widjaja, TL. Shaw, S Markmiller, I M-Valencia, JH.Davies, L de Meirleir, H Kayserili, U Altunoglu, ML Freckmann, L Warwick, D Chitayat, AO Çağlayan, K Bilguvar, H Per, C Fagerberg, M Kibaek, KA. Aldinger, D Manchester, N Matsumoto, K Muramatsu, H Saitsu, M Shiina, K Ogata, N Foulds, WB. Dobyns, N Chi, D Traver, L Spaccini, SM Bova, SB. Gabriel, M Gunel, EM Valente, EJ. Bennett, GW. Yeo, F Baas, J L-Andersen, JG. Gleeson.
    Nature Genetics. 49(3) 457-464 2017
  • NDUFAF3 variants that disrupt mitochondrial complex I assembly may associate with cavitating leukoencephalopathy
    Ishiyama A, Muramatsu K, Uchino S, Sakai C, Matsushima Y, Makioka N, Ogata T, Suzuki E, Komaki H, Sasaki M, Mimaki M, Goto Y.-I, Nishino I.
    Clinical Genetics 93(5) 1103-1106 2018
  • Molecular genetic analysis of 30 families with Joubert syndrome.
    Suzuki T, Miyake N, Tsurusaki Y, Okamoto N, Alkindy A, Inaba A, Sato M, Ito S, Muramatsu K, Kimura S, Ieda D, Saitoh S, Hiyane M, Suzumura H, Yagyu K, Shiraishi H, Nakajima M, Fueki N, Habata Y, Ueda Y, Komatsu Y, Yan K, Shimoda K, Shitara Y, Mizuno S, Ichinomiya K, Sameshima K, Tsuyusaki Y, Kurosawa K, Sakai Y, Haginoya K, Kobayashi Y, Yoshizawa C, Hisano M, Nakashima M, Saitsu H, Takeda S, Matsumoto N.
    Clin Genet. 90(6) 526-535 2016
  • De novo mutations in the autophagy gene WDR45 cause SENDA/BPAN
    Muramatsu K.
    No To Hattatsu 48(3) 177-183 2016
  • De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood.
    Saitsu H, Nishimura T, Muramatsu K (These authors contributed equally to this work.), Kodera H, Kumada S, Sugai K, Kasai-Yoshida E, Sawaura N, Nishida H, Hoshino A, Ryujin F, Yoshioka S, Nishiyama K, Kondo Y, Tsurusaki Y, Nakashima M, Miyake N, Arakawa H, Kato M, Mizushima N, Matsumoto N
    Nature genetics 45(4) 445-449 Apr. 2013
  • Uncovering genes required for neuronal morphology by morphology-based gene trap screening with a revertible retrovirus vector.
    Hashimoto Y, Muramatsu K,( These authors contributed equally to this work.) Kunii M, Yoshimura SI, Yamada M, Sato T, Ishida Y, Harada R, Harada A
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology 26(11) 4662-4674 Aug. 2012
  • Relation between psychological development and respiratory management in patients with congenital central hypoventilation syndrome in Japan
    Irahara K, Ogata T, Ozawa H, Otaki U, Yamamoto K, Ishizuka T, Arimoto K, Kimiya S, Arakawa K, Muramatsu K.
    No To Hattatsu 47(5) 343-347 2015
  • Late delirious behavior with 2009 H1N1 influenza: mild autoimmune-mediated encephalitis?
    Takanashi J, Takahashi Y, Imamura A, Kodama K, Watanabe A, Tominaga K, Muramatsu K, Barkovich AJ
    Pediatrics 129(4) e1068-71 Apr. 2012
  • Differential regulation of eotaxin expression by dexamethasone in normal human lung fibroblasts.
    Suzuki T, Arakawa H, Mizuno T, Muramatsu K, Tadaki H, Takizawa T, Mochizuki H, Tokuyama K, Matsukura S, Morikawa A
    American journal of respiratory cell and molecular biology 38(6) 707-714 Jun. 2008
  • Neuron-specific and inducible recombination by Cre recombinase in the mouse.
    Hashimoto Y, Muramatsu K, Uemura T, Harada R, Sato T, Okamoto K, Harada A
    Neuroreport 19(6) 621-624 Apr. 2008
  • Neuron-specific recombination by Cre recombinase inserted into the murine tau locus.
    Muramatsu K, Hashimoto Y, Uemura T, Kunii M, Harada R, Sato T, Morikawa A, Harada A
    Biochemical and Biophysical Research Communications 370(3) 419-423 2008
  • 先天性中枢性肺胞低換気症候群の小児慢性特定疾患登録データによる疫学的動態の検討
    村松一洋, 村松礼子, 澤浦法子, 緒方朋実, 八木久子, 中嶋直樹, 萩原里実, 小山晴美, 荒川浩一
    日本小児呼吸器疾患学会雑誌 23(1) 8-14 Jun. 2012
  • Glucocorticoids inhibit MUC5AC production induced by transforming growth factor-α in human respiratory cells
    Takami S, Mizuno T, Oyanagi T, Tadaki H, Suzuki T, Muramatsu K, Takizawa T, Arakawa H.
    Allergology International 61(3) 451-459 2012
  • Low natural killer activity and central nervous system disease as a high-risk prognostic indicator in young patients with hemophagocytic lymphohistiocytosis.
    Imashuku S, Hyakuna N, Funabiki T, Ikuta K, Sako M, Iwai A, Fukushima T, Kataoka S, Yabe M, Muramatsu K, Kohdera U, Nakadate H, Kitazawa K, Toyoda Y, Ishii E
    Cancer 94(11) 3023-3031 Jun. 2002
  • 肺小動脈低形成による著明な肺高血圧を呈した左心低形成症候群
    村松一洋, 与田仁志, 川上義, 土屋恵司, 前田克英, 八巻重雄 
    日本周産期・新生児医学会雑誌 43(1) 135-139 2007
  • 第16回川崎病全国調査成績よりみた川崎病容疑例および4主要症状以下例の冠動脈拡大性病変出現頻度
    薗部友良, 村松一洋, 土屋恵司, 今田義夫, 麻生誠二郎, 清沢伸幸, 屋代真弓, 中村好一, 柳川洋
    小児科診療 67(5) 837-842 May 2004
  • ECMO設備を有さない施設における,ECMO適応基準到達例に対するNO吸入療法—その限界と有効性について—
    遠藤大一, 中島やよひ, 与田仁志, 山本和歌子, 増本健一, 春原大介, 村松一洋, 川上義
    日本未熟児新生児学会雑誌 16(1) 73-77 Feb. 2004

Papers(other)

  • Niemann-Pick disease type C presenting with fetal hepatosplenomegaly in a child: A case report
    内田亨, 内田亨, 緒方朋実, 五十嵐淑子, 牧岡西紀, 村松一洋, 村松一洋, 石毛崇, 澤浦法子, 浦野博央, 高橋勉, 衛藤義勝, 荒川浩一
    日本周産期・新生児医学会雑誌 54(3) 943‐947 Sep. 2018
  • Identification of CTLA4 Mutation in a Patient with Autoimmune Hemolytic Anemia
    岩脇史郎, 大和玄季, 柴徳生, 村松一洋, 川島淳, 小板橋実希子, 奥野はるな, 中舘尚也, 西村奈穂, 星野顕宏, 今井耕輔, 桑島信, 金兼弘和, 荒川浩一
    日本小児科学会雑誌 122(1) 55‐61 Jan. 2018
  • Development of consortium for the prevention of epilepsy
    兼子直, 岩城弘隆, 廣瀬伸一, 石井敦士, 山本達也, 矢野珠巨, 村松一洋, 池田昭夫, 人見健文, 曽良一郎, 渡辺雅子, 原広一郎, 猿渡淳二, 山田順子, 吉田秀一, 小島俊男, 金井数明
    てんかん治療研究振興財団研究年報 28 105‐112 Sep. 2017
  • 小児神経難病の緊急課題[第3報)鎮静薬の安全使用に向けて
    池田尚広, 村松一洋
    月刊難病と在宅ケア 23(5) 47‐51 Aug. 2017
  • A Pediatric Case of Miliary Tuberculosis with Multiple Central Nervous System Tuberculomas
    橋本真理, 橋本真理, 村松一洋, 神尾綾乃, 五十嵐恒雄, 荒川浩一
    日本小児科学会雑誌 121(8) 1376‐1381 Aug. 2017
  • A Cohort Study of L-carnitine Supplementation for Patients with Severe Physical and Mental Disabilities Who Also Have Hypocarnitinemia
    緒方朋実, 村松一洋, 田中宏子, 金子広司, 小和瀬貴律, 澤浦法子, 羽鳥麗子, 倉田加奈子, 大津義晃, 森川昭廣, 荒川浩一
    日本小児科学会雑誌 120(8) 1214‐1219 Aug. 2016
  • Inhaled NO treatment in facilities where ECMO treatment can not be possible
    ENDO Daiichi, NAKAJIMA Yayohi, YODA Hitoshi, YAMAMOTO Wakako, MASUMOTO Kenichi, SUNOHARA Daisuke, MURAMATU Kazuhiro, KAWAKAMI Tadashi
    16(1) 73-77 Feb. 2004
  • Imaging of Right Lung Agenesis (Severe Hypogenesis) : Autopsy Case and Alive Case
    MURAMATSU Kszuhiro, YODA Hitoshi, NAKAJIMA Yayohi, YAMAMOTO Wakako, ENDO Daiichi, KAWAKAMI Tadashi, TSUTIYA Keiji
    18(0) Apr. 2002
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Papers(other)close
  • Niemann-Pick disease type C presenting with fetal hepatosplenomegaly in a child: A case report
    内田亨, 内田亨, 緒方朋実, 五十嵐淑子, 牧岡西紀, 村松一洋, 村松一洋, 石毛崇, 澤浦法子, 浦野博央, 高橋勉, 衛藤義勝, 荒川浩一
    日本周産期・新生児医学会雑誌 54(3) 943‐947 Sep. 2018
  • Identification of CTLA4 Mutation in a Patient with Autoimmune Hemolytic Anemia
    岩脇史郎, 大和玄季, 柴徳生, 村松一洋, 川島淳, 小板橋実希子, 奥野はるな, 中舘尚也, 西村奈穂, 星野顕宏, 今井耕輔, 桑島信, 金兼弘和, 荒川浩一
    日本小児科学会雑誌 122(1) 55‐61 Jan. 2018
  • Development of consortium for the prevention of epilepsy
    兼子直, 岩城弘隆, 廣瀬伸一, 石井敦士, 山本達也, 矢野珠巨, 村松一洋, 池田昭夫, 人見健文, 曽良一郎, 渡辺雅子, 原広一郎, 猿渡淳二, 山田順子, 吉田秀一, 小島俊男, 金井数明
    てんかん治療研究振興財団研究年報 28 105‐112 Sep. 2017
  • 小児神経難病の緊急課題[第3報)鎮静薬の安全使用に向けて
    池田尚広, 村松一洋
    月刊難病と在宅ケア 23(5) 47‐51 Aug. 2017
  • A Pediatric Case of Miliary Tuberculosis with Multiple Central Nervous System Tuberculomas
    橋本真理, 橋本真理, 村松一洋, 神尾綾乃, 五十嵐恒雄, 荒川浩一
    日本小児科学会雑誌 121(8) 1376‐1381 Aug. 2017
  • A Cohort Study of L-carnitine Supplementation for Patients with Severe Physical and Mental Disabilities Who Also Have Hypocarnitinemia
    緒方朋実, 村松一洋, 田中宏子, 金子広司, 小和瀬貴律, 澤浦法子, 羽鳥麗子, 倉田加奈子, 大津義晃, 森川昭廣, 荒川浩一
    日本小児科学会雑誌 120(8) 1214‐1219 Aug. 2016
  • Inhaled NO treatment in facilities where ECMO treatment can not be possible
    ENDO Daiichi, NAKAJIMA Yayohi, YODA Hitoshi, YAMAMOTO Wakako, MASUMOTO Kenichi, SUNOHARA Daisuke, MURAMATU Kazuhiro, KAWAKAMI Tadashi
    16(1) 73-77 Feb. 2004
  • Imaging of Right Lung Agenesis (Severe Hypogenesis) : Autopsy Case and Alive Case
    MURAMATSU Kszuhiro, YODA Hitoshi, NAKAJIMA Yayohi, YAMAMOTO Wakako, ENDO Daiichi, KAWAKAMI Tadashi, TSUTIYA Keiji
    18(0) Apr. 2002

Prize

  • Jun. 2014 16thAnnual Meeting of the Infantile Seizure Society (ISS) Nihon-Koden Award, Infantile Seizure Society (ISS)
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Prizeclose
  • Jun. 2014 16thAnnual Meeting of the Infantile Seizure Society (ISS) Nihon-Koden Award, Infantile Seizure Society (ISS)

Industrial Property Rights

  • レトロウイルス産生用ベクター
    原田 彰宏, 佐藤 隆史, 村松 一洋, 橋本 由紀子, 植村 武文
    特願2007-075377 22 Mar. 2007
  • Crerecombinaseを神経細胞特異的に発現するマウス
    原田 彰宏, 村松 一洋
    特願2006-242026 06 Sep. 2006


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