2017 - 2020 Elucidation of pathogenesis and identification of novel causative gene of primary immunodeficiency due to PIP3-related molecular abnormality.
2016 - 2020 Neurotoxicity of deoxyadenosine and neuroprotective effects of adenosine deaminase
2016 - 2020 The role of neutrophil extracellular traps in the pathogenesis of Kawasaki disease
2010 - 2012 Research for developing of a screening method for the congenital immunodeficiency by KREC/TREC to apply the method to the pathologic analysis
2010 - 2011 自己識別機構の破綻をきたす免疫不全症の病態解明と原因遺伝子同定
2009 - 2010 Development of easy and cost-effective mass-screening of severe combined immunodeficiency using neonatal guthrie cards.
2008 - 原発性免疫不全症候群に関する調査研究
2002 - 2003 Analysis of the new molecules associated with Wiskott-Aldrich syndrome protein.
2001 - 2002 MOLECULAR PATHOLOGY IN DISEASES WITH DNA STRAND BREAKS AND REPAIR DEFECTS.
2000 - 2002 B細胞シグナル伝達系におけるKuの役割に関する研究
2001 - 2001 毛細血管拡張性運動失調症の酵母による大規模スクリーニング法の開発とその応用
2000 - 2001 Study on the Molecule That Plays Critical Role in Allergic Response.
1999 - 2001 Roles of CD40/CD40 ligand molecules in human immunological disorders
Takahiro Kido, Sho Hosaka, Kazuo Imagawa, Hiroko Fukushima, Tomohiro Morio, Shigeaki Nonoyama, Hidetoshi Takada. Initial manifestations in Patients with Inborn Errors of Immunity Based on Onset Age: a Study from a Nationwide Survey in Japan. Journal of clinical immunology. 2023. 43. 4. 747-755
松本浩, 植松賢司, 座波清誉, 野々山恵章. Prediction of acute encephalopathy with febrile status epilepticus. 日本小児科学会雑誌. 2021. 125. 2. 271-271
小島涼, 川口裕之, 井上翔太, 仁紙千尋, 澁川尚幸, 関中佳奈子, 関中悠仁, 野々山恵章. A case of Philadelphia chromosome-positive Acute Lymphoblastic Leukemia with BCR-ABL fusion gene detected in neutrophils. 日本小児科学会雑誌. 2021. 125. 2. 311-311
井上翔太, 川口裕之, 小島涼, 仁紙千尋, 澁川尚幸, 關中佳奈子, 關中悠仁, 野々山恵章. A case of Early T cell Precursor Acute Lymphoblastic Leukemia with deficiency in protein S. 日本小児科学会雑誌. 2021. 125. 2. 333-333
In vitro cell differentiation analysis of induced pluripotent stem (iPS) cells from Leigh-like encephalopathy patient with DNM1L mutation into neuronal and muscular cells
(19th International Symposium on Severe Infantile epilepsies (ISSET2018). Rome, Italy. 2018)
Infantile spasms in a patient with mosaic monocentric and duplicated supernumerary marker chromosome 15
(19th International Symposium on Severe Infantile epilepsies (ISSET2018). Rome, Italy. 2018)
Common variable immunodeficiency caused by FANC mutations.
(ESID 2016. Barcelona, Spain. 2016)
2009 - Dream Maker Award (Jeffrey Modell Foundation, USA)
2009 - Dream Maker Award(Jeffrey Modell Foundation, USA)
1994 - 第8回お茶の水医科同窓会研究奨励賞
Association Membership(s) (9):
European Society for Primary Immunodeficiencies
, International Union of Immunological Societies(IUIS)
, 日本血液学会
, 日本小児感染症学会
, 日本小児血液学会
, 日本小児科学会
, American Association of Immunologists
, 日本アレルギ-学会
, 日本免疫学会