Izawa Kazushi 井澤和司

… Alternative Names

Researcher Number	90634931
Other IDs
Affiliation (Current)	2020: 京都大学, 医学研究科, 助教
Affiliation (based on the past Project Information) *help	2016 – 2019: 京都大学, 医学研究科, 助教 2016: 京都大学, 大学院医学研究科発達小児科学, 助教 2012 – 2013: 京都大学, 医学(系)研究科(研究院), 医員
Review Section/Research Field	Principal Investigator Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related
Keywords	Principal Investigator 自己炎症性疾患 / サイトカイン / 炎症 / 遺伝子変異 / モザイク変異 / 分子バーコード / 遺伝子欠失 / 遺伝子重複 / 遺伝子 / 遺伝子診断 / 医療 / NLRP3 / NLRC4 … More Except Principal Investigator … More

Elucidation of molecular mechanism of TNF receptor-associated periodic syndrome by cell technology and multi-omics analysisOngoing
- Principal Investigator
  
  西小森隆太
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Kurume University
NLRP3、NLRC4疾患関連変異によるカスパーゼ1非依存性細胞死の機序解明Principal InvestigatorOngoing
- Principal Investigator
  
  井澤和司
- Project Period (FY)
  2019 – 2020
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Kyoto University
Detection of Low frequent mosaism in autoinflammatory diseases using molecular barcode methodPrincipal Investigator
- Principal Investigator
  
  Izawa Kazushi
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kyoto University
Establishing a platform for molecular analysis and drug innovation of auto-inflammatory disorders
- Principal Investigator
  
  Heike Toshio
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Pediatrics
- Research Institution
  Kyoto University
Elucidation of molecular mechanisms of NLRP3 mosaicismPrincipal Investigator
- Principal Investigator
  
  IZAWA Kazushi
- Project Period (FY)
  2012 – 2013
- Research Category
  
  Grant-in-Aid for Research Activity start-up
- Research Field
  
  Pediatrics
- Research Institution
  Kyoto University

All 2019 2018 2017 2015 2014 2013 2012 Other

All Journal Article Presentation Book

[Book] 【自己炎症性疾患における最近の展開】自己炎症性疾患の診療ガイドライン2019
- Author(s)
  井澤和司(京都大学大学院医学研究科発達小児科学), 西小森隆太
- Total Pages
  3
- Publisher
  先端医学社
- ISBN
- Data Source
  KAKENHI-PROJECT-16K19640
[Book] 【自己炎症性疾患-最新の基礎・臨床知見-】狭義の自己炎症性疾患　アデノシンデアミナーゼ-2(ADA2)欠損症2018
- Author(s)
  井澤和司(京都大学医学部附属病院小児科), 仁平寛士, 西小森隆太
- Total Pages
  5
- Publisher
  日本臨床社
- ISBN
- Data Source
  KAKENHI-PROJECT-16K19640
[Book] 【自己炎症性疾患-最新の基礎・臨床知見-】狭義の自己炎症性疾患　インターロイキンI受容体拮抗分子欠損症、NLRP12関連周期熱症候群、H症候群2018
- Author(s)
  柴田洋史(京都大学大学院医学研究科発達小児科学講座), 井澤和司, 西小森隆太
- Total Pages
  6
- Publisher
  日本臨床社
- ISBN
- Data Source
  KAKENHI-PROJECT-16K19640
[Book] 【小児疾患の診断治療基準】 (第2部)疾患　アレルギー性疾患、自己免疫・リウマチ性疾患(膠原病)　自己炎症症候群2018
- Author(s)
  西小森隆太(京都大学大学院医学研究科発達小児科学), 井澤和司
- Total Pages
  3
- Publisher
  東京医学社
- ISBN
- Data Source
  KAKENHI-PROJECT-16K19640
[Book] 【自己炎症性疾患-病態解明から診療体制の確立まで】病態解明・治療法確立にむけての新展開　アデノシンデアミナーゼ-2(ADA2)欠損症2018
- Author(s)
  井澤和司(京都大学医学部附属病院小児科), 仁平寛士, 西小森隆太
- Total Pages
  5
- Publisher
  医歯薬出版
- ISBN
- Data Source
  KAKENHI-PROJECT-16K19640
[Book] 【自己炎症性疾患-最新の基礎・臨床知見-】狭義の自己炎症性疾患　蕁麻疹様皮疹を伴う自己炎症性疾患　ホスホリパーゼCγ2関連抗体欠損・免疫異常症(PLAID)、Schnitzler症候群など2018
- Author(s)
  本田吉孝(京都大学大学院医学研究科発達小児科学), 井澤和司, 西小森隆太
- Total Pages
  6
- Publisher
  日本臨床社
- ISBN
- Data Source
  KAKENHI-PROJECT-16K19640
[Book] 自己炎症性疾患・自然免疫不全症とその近縁疾患（CAPSの項）2012
- Author(s)
  井澤和司
- Total Pages
  280
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-24890096
[Journal Article] Expanding clinical spectrum of autosomal dominant pyrin-associated autoinflammatory disorder caused by the heterozygous MEFV p.Thr577Asn variant.2019
- Author(s)
  Nakaseko H, Iwata N, Izawa K, Shibata H, Yasuoka R, Kohagura T, Abe N, Kawabe S, Nishikomori R.
- Journal Title
  
  Rheumatology (Oxford).
  
  Volume: 1;58(1) Pages: 182-184
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K19640
[Journal Article] Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency.2019
- Author(s)
  Boisson B, Honda Y, Ajiro M, Bustamante J, Bendavid M, Gennery AR, Kawasaki Y, Ichishima J, Osawa M, Nihira H, Shiba T, Tanaka T, Chrabieh M, Bigio B, Hur H, Itan Y, Liang Y, Okada S, Izawa K, Nishikomori R, Ohara O, Heike T, et al.
- Journal Title
  
  J Clin Invest.
  
  Volume: 1;129(2) Pages: 583-597
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K19640
[Journal Article] Characterization of a large UNC13D gene duplication in a patient with familial hemophagocytic lymphohistiocytosis type 3.2018
- Author(s)
  Hiejima E, Shibata H, Yasumi T, Shimodera S, Hori M, Izawa K, Kawai T, Matsuoka M, Kojima Y, Ohara A, Nishikomori R, Ohara O, Heike T.
- Journal Title
  
  Clin Immunol.
  
  Volume: 191 Pages: 63-66
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K19640
[Journal Article] Human CTL-based functional analysis shows the reliability of a munc13-4 protein expression assay for FHL3 diagnosis.2018
- Author(s)
  Shibata H, Yasumi T, Shimodera S, Hiejima E, Izawa K, Kawai T, Shirakawa R, Wada T, Nishikomori R, Horiuchi H, Ohara O, Ishii E, Heike T.
- Journal Title
  
  Blood.
  
  Volume: 3;131(18) Pages: 2016-2025
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K19640
[Journal Article] Comprehensive molecular diagnosis of Epstein-Barr virus-associated lymphoproliferative diseases using next-generation sequencing.2018
- Author(s)
  Ono S, Nakayama M, Kanegane H, Hoshino A, Shimodera S, Shibata H, Fujino H, Fujino T, Yunomae Y, Okano T, Yamashita M, Yasumi T, Izawa K, Takagi M, Imai K, Zhang K, Marsh R, Picard C, Latour S, Ohara O, Morio T.
- Journal Title
  
  Int J Hematol.
  
  Volume: 108(3) Pages: 319-328
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K19640
[Journal Article] Fever of unknown origin with rashes in early infancy is indicative of adenosine deaminase type 2 deficiency.2018
- Author(s)
  Nihira H、Nakagawa K、Izawa K、Kawai T、Yasumi T、Nishikomori R、Nambu M、Miyagawa-Hayashino A、Nomura T、Kabashima K、Ito M、Iwaki-Egawa S、Sasahara Y、Nakayama M、Heike T
- Journal Title
  
  Scand J Rheumatol
  
  Volume: 47 Pages: 170-172
- DOI
  10.1080/03009742.2017.1324912
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K19640, KAKENHI-PROJECT-15H04876
[Journal Article] Accurate clinical genetic testing for autoinflammatory diseases using the next-generation sequencing platform MiSeq.2017
- Author(s)
  Nakayama Manabu、Oda Hirotsugu、Nakagawa Kenji、Yasumi Takahiro、Kawai Tomoki、Izawa Kazushi、Nishikomori Ryuta、Heike Toshio、Ohara Osamu
- Journal Title
  
  Biochem Biophys Rep
  
  Volume: 9 Pages: 146-152
- DOI
  10.1016/j.bbrep.2016.12.002
- NAID
  120006355733
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K19640, KAKENHI-PROJECT-15H04876
[Journal Article] Enhanced chondrogenesis of iPS cells from neonatal-onset multisystem inflammatory disease occurs via the caspase-1-independent cAMP/PKA/CREB pathway2015
- Author(s)
  Yokoyama, K. Ikeya, M. Umeda, K. Oda, H. Nodomi, S. Nasu, A. Matsumoto, Y. Izawa, K. Horigome, K. Kusaka, T. Tanaka, T. Saito, M. K. Yasumi, T. Nishikomori, R. Ohara, O. Nakayama, N. Nakahata, T. Heike, T. Toguchida, J.
- Journal Title
  
  Arthritis Rheumatol.
  
  Volume: 67 Pages: 302-314
- DOI
  10.1002/art.38912
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24390263, KAKENHI-PROJECT-24390353, KAKENHI-PROJECT-24591507, KAKENHI-PROJECT-25461591, KAKENHI-PROJECT-26253062, KAKENHI-PROJECT-26670498, KAKENHI-PROJECT-15K15549
[Journal Article] Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes2015
- Author(s)
  Nakagawa K, Kawai T, Umebayashi H, Takei S, Kobayashi N, Yashiro M, Kubota T, Koike R, Akuta N, Shimoyama K, Iwata N, Saito MK, Ohara O, Kambe N, Yasumi T, Izawa K, Kawai T, Heike T, Yagüe J, Nishikomori R, Aróstegui JI et al.
- Journal Title
  
  Ann Rheum Di
  
  Volume: in press Pages: 603-610
- DOI
  10.1136/annrheumdis-2013-204361
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23249056, KAKENHI-PROJECT-24390263, KAKENHI-PROJECT-24590681, KAKENHI-PROJECT-25460838, KAKENHI-PROJECT-25461591, KAKENHI-PROJECT-26253062
[Journal Article] Real-time single-cell imaging of protein secretion2014
- Author(s)
  Yoshitaka Shirasaki, Mai Yamagishi, Nobutake Suzuki, Kazushi Izawa, Asahi Nakahara, Jun Mizuno, Shuichi Shoji, Toshio Heike, Yoshie Harada Ryuta Nishikomori, and Osamu Ohara
- Journal Title
  
  Scientific Reports
  
  Volume: 未定
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24890096
[Journal Article] Real-time single-cell imaging of protein secretion2014
- Author(s)
  Shirasaki Y, Yamagishi M, Suzuki N, Izawa K, Nakahara A, Mizuno J, Shoji S, Heike T, Harada Y, Nishikomori R, Ohara O
- Journal Title
  
  scientific reports
  
  Volume: 4 Pages: 4736-4736
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24890096
[Journal Article] Autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency caused by a novel NFKBIA mutation, p.Ser36Tyr, presents with mild ectodermal dysplasia and non-infectious systemic inflammation2013
- Author(s)
  Yoshioka T, Nishikomori R, Hara J, Okada K, Hashii Y, Okafuji I, Nodomi S, Kawai T, Izawa K, Ohnishi H, Yasumi T, Nakahata T, Heike T
- Journal Title
  
  J Clin Immunol.
  
  Volume: 33(7) Pages: 1165-74
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24890096
[Journal Article] Heterozygous TREX1 p.Asp18Asn mutation can cause variable neurological symptoms in a family with Aicardi-Goutieres syndrome/familial chilblain lupus2013
- Author(s)
  Abe J, Izawa K, Nishikomori R, Awaya T, Kawai T, Yasumi T, Hiragi N, Hiragi T, Ohshima Y, Heike T
- Journal Title
  
  Rheumatology (Oxford)
  
  Volume: 52(2) Pages: 406-408
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24890096
[Journal Article] A nationwide survey of Aicardi-Goutieres syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions : Japanese cohort study
- Author(s)
  Abe J, Nakamura K, Nishikomori R, Kato M, Mitsuiki N, Izawa K, Awaya T, Kawai T, Yasumi T, Toyoshima I, Hasegawa K, Ohshima Y, Hiragi T, Sasahara Y, Suzuki Y, Kikuchi M, Osaka H, Ohya T, Ninomiya S, Fujikawa S, Akasaka M, Iwata N, Kawakita A, Funatsuka M, Shintaku H, Ohara O, Ichinose H, Heike T
- Journal Title
  
  Rheumatology
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24890096
[Journal Article] Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes
- Author(s)
  Nakagawa K, Gonzalez-Roca E, Souto A, Kawai T, Umebayashi H, Campistol JM, Cañellas J, Takei S, Kobayashi N, Callejas-Rubio JL, Ortego-Centeno N, Ruiz-Ortiz E, Rius F, Anton J, Iglesias E, Jimenez-Treviño S, Vargas C, Fernandez-Martin J, Calvo I, Hernández-Rodríguez J, Mendez M, Dordal MT, Basagaña M, Bujan S, Yashiro M, Kubota T, Koike R, Akuta N, Shimoyama K, Iwata N, Saito MK, Ohara O, Kambe N, Yasumi T, Izawa K, Kawai T, Heike T, Yagüe J, Nishikomori R, Aróstegui JI
- Journal Title
  
  Ann Rheum Dis.
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24890096
[Presentation] 反復性高サイトカイン血症、慢性炎症を呈したKARS遺伝子異常症の1例2018
- Author(s)
  仁平寛士, 井澤和司, 伊佐真彦, 芝剛, 本田吉孝, 下寺佐栄子, 柴田洋史, 田中孝之, 八角高裕, 矢野直子, 舞鶴賀奈子, 吉田健司, 横山淳史, 村山圭, 小原収, 西小森隆太
- Organizer
  日本小児リウマチ学会総会・学術集会プログラム・抄録集28回 Page73(2018.10)
- Data Source
  KAKENHI-PROJECT-16K19640
[Presentation] 自己炎症症候群インフリキシマブが二次無効となったADA2欠損症の乳児例2018
- Author(s)
  山田早紀, 井澤和司, 西谷真彦, 仁平寛士, 柴田洋史, 田中孝之, 河合朋樹, 八角高裕, 西小森隆太
- Organizer
  日本リウマチ学会総会・学術集会プログラム・抄録集62回 Page461(2018.03)
- Data Source
  KAKENHI-PROJECT-16K19640
[Presentation] 本邦におけるAdenosine Deaminase 2欠損症の臨床的および遺伝学的解析2018
- Author(s)
  笹原洋二, 井澤和司, 梅林宏明, 中野直子, 金兼弘和, 森尾友宏, 平家俊男, 呉繁夫
- Organizer
  日本小児科学会雑誌(0001-6543)122巻2号 Page255(2018.02)
- Data Source
  KAKENHI-PROJECT-16K19640
[Presentation] 意義不明なMEFV遺伝子の変異/SNPが疾患発症に関連するかの評価系の検討2018
- Author(s)
  田中孝之, 芝剛, 西小森隆太, 井田弘明, 柴田洋史, 井澤和司, 八角高裕, 齋藤潤, 平家俊男
- Organizer
  日本小児リウマチ学会総会・学術集会プログラム・抄録集28回 Page86(2018.10)
- Data Source
  KAKENHI-PROJECT-16K19640
[Presentation] Self-limitedであったNLRC4の新規SNP変異を持つ女児例2018
- Author(s)
  楠田政輝, 井澤和司, 山崎雄一, 久保田知洋, 野中由希子, 嶽崎智子, 今中啓之, 武井修治, 山遠剛, 芝剛, 西小森隆太, 平家俊男, 河野嘉文
- Organizer
  日本小児リウマチ学会総会・学術集会プログラム・抄録集28回 Page71(2018.10)
- Data Source
  KAKENHI-PROJECT-16K19640
[Presentation] 患者由来iPS細胞を用いた家族性地中海熱の病態解明2018
- Author(s)
  田中孝之, 西小森隆太, 井田弘明, 柴田洋史, 井澤和司, 河合朋樹, 八角高裕, 齋藤潤, 平家俊男
- Organizer
  日本小児科学会雑誌(0001-6543)122巻2号 Page255(2018.02)
- Data Source
  KAKENHI-PROJECT-16K19640
[Presentation] Early Diagnosis of an Infant with DADA2-Japanese Cohort2018
- Author(s)
  Kazushi Izawa, Hiroshi Nihira, Takahiro Yasumi, Ryuta Nishikomori
- Organizer
  The Second International Conference on Deficiency of ADA2
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K19640
[Presentation] gene expression and signaling in the immune system2014
- Author(s)
  Yoshitaka Shirasaki, Mai Yamagishi, Kazushi Izawa Hirotsugu Oda, Toshio Heike, Ryuta Nishikomori, Osamu Ohara
- Place of Presentation
  New York
- Data Source
  KAKENHI-PROJECT-24890096
[Presentation] Real-time single-cell imaging of IL-1β secretion by Inflammasomes2014
- Author(s)
  Yoshitaka Shirasaki, Mai Yamagishi, Kazushi Izawa, Hirotsugu Oda, Toshio Heike, Ryuta Nishikomori, Osamu Ohara
- Organizer
  Gene Expression&Signaling in the Immune System meeting
- Place of Presentation
  New York
- Data Source
  KAKENHI-PROJECT-24890096
[Presentation] Muckle-Wells症候群におけるNLRP3体細胞モザイク変異の検討2013
- Author(s)
  中川権史, 西小森隆太, 井澤和司, 河合朋樹, 八角高裕, 河合利尚, 梅林宏明, 武井修治, 小林法元, 小原收, Eva Gonzalez-Roca, Juan I. Arostegui, 平家俊男
- Organizer
  第41回日本臨床免疫学会
- Place of Presentation
  下関
- Year and Date
  2013-11-27
- Data Source
  KAKENHI-PROJECT-24890096
[Presentation] Muckle-Wells症候群におけるNLRP3体細胞モザイク変異の検討2013
- Author(s)
  中川権史, 西小森隆太, 井澤和司, 河合朋樹, 八角高裕, 河合利尚, 梅林宏明, 武井修治, 小林法元, 小原收, Eva Gonzalez-Roca, Juan I. Arostegui, 平家俊男
- Organizer
  第23回日本小児リウマチ学会
- Place of Presentation
  埼玉
- Year and Date
  2013-10-12
- Data Source
  KAKENHI-PROJECT-24890096
[Presentation] CAPSに対するアナキンラ治療の有効性及び安全性の後方視的検討2013
- Author(s)
  中川権史, 井澤和司, 西小森隆太, 河合朋樹, 八角高裕, 津下充, 小林法元, 河島尚志, 谷口敦夫, 窪田哲朗, 松林正, 平家俊男
- Organizer
  第57回日本リウマチ学会
- Place of Presentation
  京都
- Year and Date
  2013-04-18
- Data Source
  KAKENHI-PROJECT-24890096

1. 西小森隆太 (70359800)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
2. Heike Toshio (90190173)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
3. 八角高裕 (00511891)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
4. 小原收 (20370926)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
5. 河合朋樹 (20631568)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
6. 斎藤潤 (90535486)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
7. IKEYA Makoto

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
8. NAKAGAWA Kenji

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
9. ODA Hirotsugu

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
10. KUBOTA Tetsuo

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
11. 戸田口淳也

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
12. 梅田雄嗣

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
13. 中畑龍俊

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
14. 神戸直智

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
15. 小池竜司

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Izawa Kazushi 井澤 和司

IZAWA Kazushi 井澤 和司

Research Projects

Research Products

Co-Researchers

Elucidation of molecular mechanism of TNF receptor-associated periodic syndrome by cell technology and multi-omics analysisOngoing

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NLRP3、NLRC4疾患関連変異によるカスパーゼ1非依存性細胞死の機序解明Principal InvestigatorOngoing

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Detection of Low frequent mosaism in autoinflammatory diseases using molecular barcode methodPrincipal Investigator

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Establishing a platform for molecular analysis and drug innovation of auto-inflammatory disorders

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Elucidation of molecular mechanisms of NLRP3 mosaicismPrincipal Investigator

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[Book] 【自己炎症性疾患における最近の展開】 自己炎症性疾患の診療ガイドライン2019

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[Book] 【自己炎症性疾患-最新の基礎・臨床知見-】 狭義の自己炎症性疾患 アデノシンデアミナーゼ-2(ADA2)欠損症2018

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[Book] 【自己炎症性疾患-最新の基礎・臨床知見-】 狭義の自己炎症性疾患 インターロイキンI受容体拮抗分子欠損症、NLRP12関連周期熱症候群、H症候群2018

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[Book] 【小児疾患の診断治療基準】 (第2部)疾患 アレルギー性疾患、自己免疫・リウマチ性疾患(膠原病) 自己炎症症候群2018

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[Book] 【自己炎症性疾患-病態解明から診療体制の確立まで】 病態解明・治療法確立にむけての新展開 アデノシンデアミナーゼ-2(ADA2)欠損症2018

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[Book] 【自己炎症性疾患-最新の基礎・臨床知見-】 狭義の自己炎症性疾患 蕁麻疹様皮疹を伴う自己炎症性疾患 ホスホリパーゼCγ2関連抗体欠損・免疫異常症(PLAID)、Schnitzler症候群など2018

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[Book] 自己炎症性疾患・自然免疫不全症とその近縁疾患（CAPSの項）2012

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[Journal Article] Expanding clinical spectrum of autosomal dominant pyrin-associated autoinflammatory disorder caused by the heterozygous MEFV p.Thr577Asn variant.2019

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Izawa Kazushi 井澤和司

IZAWA Kazushi 井澤和司

[Book] 【自己炎症性疾患における最近の展開】自己炎症性疾患の診療ガイドライン2019

[Book] 【自己炎症性疾患-最新の基礎・臨床知見-】狭義の自己炎症性疾患　アデノシンデアミナーゼ-2(ADA2)欠損症2018

[Book] 【自己炎症性疾患-最新の基礎・臨床知見-】狭義の自己炎症性疾患　インターロイキンI受容体拮抗分子欠損症、NLRP12関連周期熱症候群、H症候群2018

[Book] 【小児疾患の診断治療基準】 (第2部)疾患　アレルギー性疾患、自己免疫・リウマチ性疾患(膠原病)　自己炎症症候群2018

[Book] 【自己炎症性疾患-病態解明から診療体制の確立まで】病態解明・治療法確立にむけての新展開　アデノシンデアミナーゼ-2(ADA2)欠損症2018

[Book] 【自己炎症性疾患-最新の基礎・臨床知見-】狭義の自己炎症性疾患　蕁麻疹様皮疹を伴う自己炎症性疾患　ホスホリパーゼCγ2関連抗体欠損・免疫異常症(PLAID)、Schnitzler症候群など2018

[Presentation] 自己炎症症候群インフリキシマブが二次無効となったADA2欠損症の乳児例2018