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稲葉 雄二  イナバ ユウジ

教員組織電話番号
教育組織医学部 小児環境保健疫学研究センターFAX番号
職名特任教授メールアドレス
住所〒390-8621 松本市旭3-1-1ホームページURL

更新日:2021/07/19

プロフィール

兼担研究科・学部
医学部附属病院 小児科
研究分野
小児神経学
神経免疫学
発達小児科学
現在の研究課題
中枢神経の炎症性疾患におけるサイトカインの動態

実験的脳炎モデルにおける病態と治療

重症筋無力症における免疫学的基盤の検討

小児のてんかん

発達障害の基礎的研究

発達障害医療の社会基盤の研究

先天性サイトメガロウイルス感染症の中枢神経病変の解析

所属学会
所属学会
日本小児科学会
日本小児神経学会
日本重症心身障害学会
日本神経免疫学会
日本小児神経精神学会
日本てんかん学会
日本小児保健学会

所属学会役職担当
日本小児神経学会 , 評議員
日本小児科学会 , 代議員
学歴
出身学校・専攻等(大学院を除く)
1991 , 信州大学 , 医学部

取得学位
医学博士

免許・資格等
2011 , 小児精神神経学会認定医
2007 , 小児神経科専門医
1997 , 小児科専門医
研究職歴等
研究職歴
2017- , 信州大学医学部 特任教授
2012-2017 , 信州大学医学部 准教授
2007-2011 , 信州大学(医学部附属病院) 講師
2001-2005 , 信州大学(医学部) 助手
1999-2001 , 信州大学(医学部加齢適応研究センター) 研究員
1994-1996 , 帝京大学(医学部) 助手

留学歴
2003-2005 , McGill大学Montreal Neurological Institute

研究活動業績

研究業績(著書・
発表論文等)
書籍等出版物
中枢神経疾患と管理 小児の急性脳症., ICU治療指針 I 31 , 281-6
2019
Author:本林光雄、稲葉雄二


中枢神経疾患と管理 小児の細菌性髄膜炎, ICU治療指針 I 31 , 273-6
2019
Author:佐藤公則、稲葉雄二


中枢神経疾患と管理 小児の急性脳炎., ICU治療指針 I 31 , 277-280
2019
Author:稲葉雄二、本林光雄


Gullain-Barré症候群、Fisher症候群、慢性炎症性脱髄性多発ニューロパチー、Bell麻痺, 最新ガイドライン準拠 小児科診断・治療指針
2017
Author:稲葉雄二


Gullain-Barré症候群、Fisher症候群、慢性炎症性脱髄性多発ニューロパチー、Bell麻痺, 小児科診断・治療指針
2016
Author:稲葉雄二


重症筋無力症, 小児疾患診療のための病態生理
2016
Author:稲葉雄二


Guillain-Barré症候群, 慢性炎症性脱髄性多発ニュ-ロパチ-, 今日の小児治療指針 16
医学書院 2015
Author:稲葉雄二;水口 雅, 他総編


末梢の病態 GBS、CIDP、MGの理解と実践, 小児神経学の進歩 48 , 41-55
Author:稲葉雄二


『ルーマニアの遺棄された子どもたちの発達への影響と回復への取り組み ‐施設養護児への里親養育による早期介入研究(BEIP)からの警鐘』
Author:著者:チャールズ・A・ネルソン、ネイサン・A・フォックス、チャールズ・H・ジーナー監訳:上鹿渡和宏、青木豊、稲葉雄二、本田秀夫、高橋恵里子、御園生直美訳:門脇陽子、森田由美


論文
Usefulness of Continuous Glucose Monitoring for Prevention and Early Detection of Hypoglycemia Caused by a Ketogenic Diet and Late Dumping Syndrome.
Pediatr Neurol,105:65-66 2020
Author:Morikawa, M., Hara, Y., Nakazawa, Y., Inaba, Y. and Motobayashi, M.


発達障害専門外来の利用状況の推移
長野県立こども病院医学雑誌,2(1):30-36 2019
Author:中嶋 英子, 稲葉 雄二, 山内 翔子, 渥美 香奈, 竹内 史穂子, 本林 光雄, 三澤 由佳, 日詰 恵里子, 平林 伸一


Alcohol Consumption During Pregnancy and Risk of Placental Abnormality: The Japan Environment and Children's Study.
Sci Rep,9(1):10259 2019
Author:Ohira, S., Motoki, N., Shibazaki, T., Misawa, Y., Inaba, Y., Kanai, M., Kurita, H., Shiozawa, T., Nakazawa, Y., Tsukahara, T., Nomiyama, T., Japan, Environment and Children's Study, Group


Maternal Exposure to Housing Renovation During Pregnancy and Risk of Offspring with Congenital Malformation: The Japan Environment and Children's Study.
Sci Rep,9(1):11564 2019
Author:Motoki, N., Inaba, Y., Shibazaki, T., Misawa, Y., Ohira, S., Kanai, M., Kurita, H., Nakazawa, Y., Tsukahara, T., Nomiyama, T., Japan, Environment and Children's Study, Group


A novel PAK3 pathogenic variant identified in two siblings from a Japanese family with X-linked intellectual disability: case report and review of the literature.
Cold Spring Harb Mol Case Stud ,5(6) 2019
Author:Iida, A., Takano, K., Takeshita, E., Abe-Hatano, C., Hirabayashi, S., Inaba, Y., Kosugi, S., Kamatani, Y., Momozawa, Y., Kubo, M., Nakagawa, E., Inoue, K. and Goto, Y. I.


Concentrations of various forms of vitamin B6 in ginkgo seed poisoning.
Brain Dev.,41(3):292-5 2019
Author:Sado T, Nakata S, Tsuno T, Sato M, Misawa Y, Yamauchi S, Inaba Y, Kobayashi D, Wada K.


PIEZO2 deficiency is a recognizable arthrogryposis syndrome: A new case and literature review.
Am J Med Genet A. ,179(6):948-57 2019
Author:Yamaguchi T, Takano K, Inaba Y, Morikawa M, Motobayashi M, Kawamura R, Wakui K, Nishi E, Hirabayashi SI, Fukushima Y, Kato H, Takahashi J, Kosho T.


Examining the Validity of Efforts of the Muscular Dystrophy Medical Network in Nagano : A Questionnaire Study
信州医学雑誌,66(3):205-212 2018(Jun.)
Author:Nishizawa H, Takahashi H, Aoki K, Kosho T, Inaba Y, Nakamura A


A Pediatric Case of Relapsing-Remitting Multiple Sclerosis Onset following Varicella Zoster Ophthalmicus with Optic Neuritis.
Case Rep Pediatr. 2018
Author:Shiba N, Inaba Y, Motobayashi M, Nishioka M, Kawasaki Y, Noda S, Matsuura H, Kobayashi N, Matsuoka T, Nakamura A, Nakazawa Y.


A rational approach to identifying newborns with hearing loss caused by congenital cytomegalovirus infection by dried blood spot screening.
Acta Otolaryngol. ,138(8):708-12 2018
Author:Moteki H, Isaka Y, Inaba Y, Motobayashi M, Nishio SY, Ohira S, Yano T, Iwasaki S, Shiozawa T, Koike K, Usami SI.


Postencephalitic epilepsy secondary to cytomegalovirus encephalitis.
Pediatr Int. ,60(8):758-60 2018
Author:Nasuno M, Shigemura T, Nakazawa Y, Inaba Y, Motobayashi M.


A pediatric case with peripheral facial nerve palsy caused by a granulomatous lesion associated with cat scratch disease.
Brain Dev. ,40(2):159-62 2018
Author:Nakamura C, Inaba Y, Tsukahara K, Mochizuki M, Sawanobori E, Nakazawa Y, Aoyama K.


An infant case of diffuse cerebrospinal lesions and cardiomyopathy caused by a BOLA3 mutation.
Brain Dev. ,40(6):484-8 2018
Author:Nishioka M, Inaba Y, Motobayashi M, Hara Y, Numata R, Amano Y, Shingu K, Yamamoto Y, Murayama K, Ohtake A, Nakazawa Y.


Early prognostic factors for acute encephalopathy with reduced subcortical diffusion.
Brain Dev. ,40(8):707-13 2018
Author:Fukuyama T, Yamauchi S, Amagasa S, Hattori Y, Sasaki T, Nakajima H, Takei Y, Okuno J, Misawa Y, Fueki N, Kitamura M, Matsui H, Inaba Y, Hirabayashi S.


Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome.
J Hum Genet. ,63(5):647-65 2018
Author: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.


Nationwide survey on cerebrotendinous xanthomatosis in Japan.
J Hum Genet. ,63(3):271-280 2018
Author:Sekijima Y, Koyama S, Yoshinaga T, Koinuma M, Inaba Y.


Comparison of the phenotypes of patients harboring in-frame deletions starting at exon 45 in the Duchenne muscular dystrophy gene indicates potential for the development of exon skipping therapy
Journal of Human Genetics 2016
Author:Akinori Nakamura, Naoko Shiba, Daigo Miyazaki, Hitomi Nishizawa, Yuji Inaba, Noboru Fueki, Rika Maruyama, Yusuke Echigoya, and Toshifumi Yokota


Usefulness of Circulating B-cell-Activating Factor Serial Monitoring in Childhood-Onset Ocular Myasthenia Gravis.
2016
Author:Motobayashi M, Nishimura T, Inaba Y.


Viral load and ganciclovir concentration in cerebrospinal fluid of patients successfully treated with ganciclovir or valganciclovir for human herpesvirus 6 encephalitis/myelitis following umbilical cord blood transplantation
Transplant Infectious Disease 2016
Author:Morita D, Hirabayashi K, Katsuyama K, Morokawa H, Motobayashi M, Kurata T, Shigemura T, Tanaka M, Inaba Y, Koike K, Nakazaw Y.


Successful Treatment of Arrhythmia-Induced Cardiomyopathy in an Infant with Tuberous Sclerosis Complex.
BMC Pediatrics 2016
Author:Motoki N, Inaba Y, Matsuzaki S, Akazawa Y, Nishimura T, Fukuyama T and Koike K.


発達障害児への上手な対応
小児科診療 2016
Author:稲葉雄二


Cross-sectional Observation of the Relationship of Depressive Symptoms with Lifestyles and Parents' Status among Japanese Junior High School Students.
Environmental Health and Preventive Medicine 2016
Author:Hyakutake A, Kamijo , Misawa Y, Washizuka S, Inaba Y Tsukahara M, Nomiyama T.


Correlation between white matter lesions and intelligence quotient in patients with congenital cytomegalovirus infection.
Pediatric Neurology. 2016
Author:Inaba Y, Motobayashi M, Nishioka M,et al


Cytomegalovirus encephalitis in a patient with severe combined immunodeficiency
J Clin Immunol 2015
Author:Motobayashi M, Shigemura T, Kurata T, Nakazawa Y, Inaba Y, Koike K.


先天性サイトメガロウイルス感染症をめぐる各科の取り組み~小児神経領域における知見と当科での取り組み
小児耳鼻咽喉科学会誌 2015
Author:稲葉雄二


An increase in circulating B-cell activating factor in childhood-onset ocular myasthenia gravis.
Pediatric Neurology,52(4):404-409 2015
Author:Motobayashi M, Inaba Y, Nishimura T, Kobayashi N, Nakazawa Y, Koike K.


Reduction in peripheral regulatory T cell population in childhood ocular type myasthenia gravis.
Brain & Development,37(8):808-816 2015
Author:Nishimura T, Inaba Y, Nakazawa Y, Omata T, Akasaka M, Shirai I, Ichikawa M.


Differential roles of MMP-9 in early and late stages of dystrophic muscles in a mouse model of Duchenne muscular dystrophy.
Biochim Biophys Acta 2015
Author:Shiba N, Miyazaki D, Yoshizawa T, Fukushima K, Shiba Y, Inaba Y, Imamura M,Takeda S, Koike K, Nakamura A


Elevation of neuron specific enolase and brain iron deposition on susceptibility-weighted imaging as diagnostic clues for beta-propeller protein-associated neurodegeneration in early childhood: Additional case report and review of the literature.
,Am J Med Genet A 2015
Author:Takano K, Shiba N, Wakui K, Yamaguchi T, Aida N, Inaba Y, Fukushima Y, Kosho T


Dimethyl fumarate suppresses Theiler's murine encephalomyelitis virus-induced demyelinating disease by modifying the Nrf2-Keap1 pathway.
Int Immunol,27(7):333-344 2015
Author:Kobayashi K, Tomiki H, Inaba Y, Ichikawa M, Kim BS, Koh CS


Reversible Cerebral Vasoconstriction Syndrome and Posterior Reversible Encephalopathy Syndrome in a Boy with Loeys-Dietz Syndrome.
Am J Med Genet A 2015
Author:Akazawa Y, Inaba Y*, Hachiya A, Motoki N, Matsuzaki S, Minatoya K, Morisaki T, Morisaki H, Kosaki K, Kosho T*, Koike K.


Blockade of in vitro ictogenesis by low frequency stimulation coincedes with increased epileptiform response latency.
J Neurophysiol,114(1):21-28 2015
Author:Toshiyuki Kano, Yuji Inaba, Margherita D'Antuono, Giuseppe Biagini, Maxime Levésque, Massimo Avoli


2013年に流行した手足口病の疫学的・臨床的特徴
日本小児科学会雑誌,119(8):1219-1225 2015
Author:松岡高史, 松岡明子, 松岡伊津夫, 稲葉雄二


てんかん診療の進歩と長野県における課題
信州医学雑誌,63(3):133-143 2015
Author:福山哲広,稲葉雄二


頭蓋骨幹端骨異形成症でのカルシトリオール経口パルス療法中の骨代謝マーカーの推移
小児科学会雑誌 2014
Author:竹内勇介、稲葉雄二*、松浦宏樹、倉田研児、三澤由佳、本林光雄、新美妙美、西村貴文、柴直子、小池健一


ctivity-dependent changes in excitability of perirhinal cortex networks in vitro
Pflugers Arch, Eur J Physiol 2014
Author:Biagini G, D'Antuono M, Inaba Y, Kano T, Ragsdale D, Avoli M


Successful treatment of fulminant Wilson’s disease without liver transplantation
Int Pediatr 2014
Author:Motobayashi M, Fukuyama T, Nakayama Y, Sano k, Noda S, Hidaka Y, Amano Y, Ikeda S, Koike K, Inaba Y


ytokine production profiles in chronic relapsing-remitting experimental autoimmune encephalomyelitis: IFN-γ and TNF-α are important participants in the first attack but not in the relapse
J Neurol Sci,340:117-122 2014
Author:Yoshihiko Hidaka, Yuji Inaba, Kazuyuki Matsuda, Makoto Itoh, Tomoki Kaneyama, Yozo Nakazawa, Chang-Sung Koh, Motoki Ichikawa


ヒブワクチン・小児用肺炎球菌ワクチン普及前の小児細菌性髄膜炎の発生頻度
日本小児科学会雑誌,118:17-22 2014
Author:内海雅史、天野芳郎、諸橋文雄、樋口司、牛久英雄、長沼邦明、野見山哲生、稲葉雄二、小池健一


Successful treatment for West syndrome with severe combined immunodeficiency
Brain Dev 2014
Author:Motobayashi M, Inaba Y, Fukuyama T, Kurata T, Niimi T, Saito S, Shiba N, Nishimura T, Shigemura T, Nakazawa Y, Kobayashi N, Sakashita K, Agematsu K, Ichikawa M, Koike K


Analysis of Phosphorylated Neurofilament H Levels in a Low Birth Weight Infant with Posthemorrhagic Hydrocephalus: A Case Report
Pediatrics & Therapeutics 2014
Author:Motobayashi M, Inaba Y*, et al.


TIM-3 pathway ameliorates Theiler’s murine encephalomyelitis virus-induced demyelinating diseaseee
Int Immunol 2014
Author:Kaneyama T, Tomiki H, Tsugane S, Inaba Y, Ichikawa M, Akiba H, Yagita H, Kim BS, Koh CS


Therapeutic effect of anti-αv integrin mAb on Theiler's murine encephalomyelitis virus-induced demyelinating disease
J Neuroimmunol 2014
Author:Tomiki H, Kaneyama T, Kobayashi K, Inaba Y, Ichikawa M, Yagita H, Kim BS, Koh CS


A case of Bardet-Biedl syndrome complicated
Brain Dev,36:721-724 2014
Author:Saida K, Inaba Y, Hirano M, Satake W, Toda T, Suzuki Y, Sudo A, Noda S, Hidaka Y, Hirabayashi K, Imai H, Kurokawa T, Koike K


Availability of DMD mRNA transcripts analysis in a patients with dystrophinopathy having a nonsense mutation
Journal of Neurology & Translational Neuroscience,1(4) 2013
Author:Narumi Y, Fueki N, Hayashi Y, Shiba N, Nishino I, Inaba Y, Kosho T, Fukushima Y, Nakamura A


Evaluation of Behavior and Cognitive Function in Children with Myoclonic Astatic Epilepsy
Pediatrics & Therapeutics,3(3) 2013
Author:Niimi T, Inaba Y, Fukuyama T, Higuchi T, Motobayashi M, Nishimura T, Shiba N and Koike K


駒ヶ根市における5歳児健診と就学前リハビリテーションの有用性
認知リハ学会誌,18:91-95 2013
Author:上村智彦,稲葉 雄二,本田哲三,坂本 虎雄,西村 貴文


てんかん発症における細胞性免疫制御機構の関与に関する研究
てんかん治療研究振興財団 研究年報,24:71-78 2013
Author:稲葉雄二,本林光雄,西村貴文,新美妙美,柴 直子,小池健一


5歳児健診における視覚認知課題の有用性
脳と発達,45(5):355-359 2013
Author:稲葉雄二,新美妙美,西村貴文,三澤由佳,福山哲広,樋口 司,滝 芳樹


急性脳症後,後天性読字障害を呈した6歳女児例
脳と発達,44(6):482-486 2012
Author:永春幸子,稲葉雄二,本林光雄,三澤由佳,福山哲広,樋口 司,原田真知子


環境要因、特に汚染物質の曝露によるDNAメチル化変化と小児の健康への影響
信州医学雑誌,60(5):241-248 2012
Author:堺 温哉,稲葉雄二


上伊那地域における「こどもの健康と環境に関する全国調査」
信州公衆衛生雑誌,6(2):101-106 2012
Author:堺 温哉,津田洋子,塚原照臣,日高義彦,稲葉雄二,金井 誠,福嶋義光,野見山哲生


ギラン・バレー症候群 神経疾患のケアポイント
こどもケア,6(6):61-65 2012
Author:稲葉雄二


Recessive RYR1 mutations in a patient with severe congenital nemaline myopathy with ophthalomoplegia identified through massively parallel sequencing.
Am J Med Genet A,158A(77):772-8 2012
Author:Kondo E, Nishimura T, Kosho T, Inaba Y, Mitsuhashi S, Ishida T, Baba A, Koike K, Nishino I, Nonaka I, Furukawa T, Saito K.


 Neurodevelopmental features in 2q23.1 microdeletion syndrome: Report of a new patient with intractable seizures and review of literature.
Am J Med Genet A,158A:861-8 2012
Author:Motobayashi M, Nishimura-Tadaki A, Inaba Y, Kosho T, Miyatake S, Niimi T, Nishimura T, Wakui K, Fukushima Y, Matsumoto N, Koike K.


Reflex seizures induced by micturition and defecation, successfully treated with clobazam and phenytoin.
Epileptic Disord. 2011 Jun;13(2):166-71.,13(2):166-71 2011
Author:Higuchi T, Fukuyama T, Misawa Y, Inaba Y, Ichikawa M, Koike K.


Prophylactic treatment for hypertension and seizure in a case of allogeneic hematopoietic stem cell transplantation after posterior reversible encephalopathy syndrome.
Pediatr Transplant 2010
Author:Fukuyama T, Tanaka M, Nakazawa Y, Motoki N, Inaba Y, Higuchi T, Koike K


軽度発達障害児の支援を目的とした学校へのoutreach clinic の実践
脳と発達,42(4):267-272 2010
Author:稲葉雄二,新美妙美,石田修一


Diminished presynaptic GABA(B) receptor function in the neocortex of a genetic model of absence epilepsy
Neurosignals.,17(2):121-31 2009
Author:Inaba Y, D'Antuono M, Bertazzoni G, Biagini G, Avoli M


Network hyperexcitability within the deep layers of the pilocarpine-treated rat entorhinal cortex
J Physiol.,586(7):1867-83 2008
Author:de Guzman P, Inaba Y, Baldelli E, de Curtis M, Biagini G, Avoli M


Reduced GABA(B) receptor subunit expression and paired-pulse depression in a genetic model of absence seizures.
Neurobiol Dis. 2007
Author:Merlo D, Mollinari C, Inaba Y, Cardinale A, Rinaldi AM, D'Antuono M, D'Arcangelo G, Tancredi V, Ragsdale D, Avoli M


The H current blocker ZD7288 decreases epileptiform hyperexcitability in the rat neocortex by depressing synaptic transmission.
Neuropharmacology,51(3):681-91 2006
Author:Inaba Y, Biagini G, Avoli M


NMDA receptor-mediated transmission contributes to network 'hyperexcitability' in the rat insular cortex
Eur J Neurosci,23:1071-6 2006
Author:Inaba Y, de Guzman P, Avoli M


Synaptic hyperexcitability of deep layer neocortical cells in a genetic model of absence seizures.
Genes Brain Behav,5:73-84 2006
Author:D'Antuono M, Inaba Y, Biagini G, D'Arcangelo G, Tancredi V, Avoli M


Subiculum network excitability is increased in a rodent model of temporal lobe epilepsy.
Hippocampus,16(10):843-60 2006
Author:de Guzman P, Inaba Y, Biagini G, Baldelli E, Mollinari C, Merlo D, Avoli M


Volume-conducted epileptiform events between adjacent necortical slices in an interface tissue chamber.
J Neurosci Methods,151(2):287-90 2006
Author:Inaba Y, Avoli M


Periodic oscillatory activity in parahippocampal slices maintained in vitro.
Neuroscience,130(4):1041-53 2005
Author:Kano T, Inaba Y, Avoli M


Brain-specific potential guanine nucleotide exchange factor for Arf,synArfGEF(Po),is localized to postsynaptic density
J Neurochem,89:1347-1357 2004
Author:Inaba Y, Tian QB, Okano A, Zhang JP, Sakagami H, Miyazawa S, Li W, Komiyama A, Inokuchi K, Kondo H, Suzuki T


重症心身障害児・者における栄養と微量元素
輸液・栄養ジャーナル,25:69-75 2003
Author:朴 成愛,稲葉雄二,河野千夏,原 洋治,山崎宗廣,塚田昌滋,小宮山 淳


経管栄養管理下の重症心身障害児・者におけるセレン欠乏症の実態-栄養形態による差異と心電図変化-
脳と発達,34:37-42 2002
Author:朴成愛,稲葉雄二,関 千夏,原 洋治,山崎宗廣,塚田昌滋


Plasma thrombin-antithrombin III complex is associated with the severity of experimental autoimmune encephalomyelitis
JOURNAL OF THE NEUROLOGICAL SCIENCES,185(2):89-93 2001
Author:Inaba Y, Ichikawa M, Inoue A, 他6名


Anti-IL-12 antibody prevents the development and progression of multiple sclerosis-like relapsing-remitting demyelinating disease in NOD mice induced with myelin oligodendrocyte glycoprotein peptide.
JOURNAL OF NEUROIMMUNOLOGY,102(1):56-66 2000
Author:Ichikawa M, Koh C -S, Inoue A, Tsuyusaki J, Yamazaki M, Inaba Y, 他4名


IgG subclass switching is associated with the severity of experimental autoimmune encephalomyelitis induced with myelin oligodendrocyte glycoprotein peptide in NOD mice
CELLULAR IMMUNOLOGY,191(2):97-104 1999
Author:Ichikawa, M; Koh, CS; Inaba, Y; Seki, C; Inoue, A; Itoh, M; Ishihara, Y; Bernard, CCA; Komiyama, A


Suppression of experimental autoimmune encephalomyelitis by dermatan sulfate
CELLULAR IMMUNOLOGY,198(2):96-102 1999
Author:Inaba Y, Ichikawa M, Koh C -S, 他4名


The production of IL-8 in cerebrospinal fluid in aseptic meningitis of children
CLINICAL AND EXPERIMENTAL IMMUNOLOGY,109(3):426-430 1997
Author:Ishiguro, A; Suzuki, Y; Inaba, Y; Fukushima, K; Komiyama, A; Koeffler, HP; Shimbo, T


The production of macrophage inflammatory protein-1alfa in the cerebrospinal fluid at the initial stage of meningitis in children
Pediatr Res,42:788-793 1997
Author:Inaba Y, Ishiguro A, Shimbo T


Production of interleukin-10 in the cerebrospinal fluid in aseptic meningitis of children
PEDIATRIC RESEARCH,40(4):610-614 1996
Author:Ishiguro, A; Suzuki, Y; Inaba, Y; Komiyama, A; Koeffler, HP; Shimbo, T

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2002 , 小児科学
2002 , 小児神経学