Updated on 2026/03/24

写真a

 
YAMASHITA Yuta
 
Organization
Nagoya University Hospital Dermatology Assistant Professor of Hospital
Title
Assistant Professor of Hospital

Research History 5

  1. Nagoya University Hospital   Dermatology   Clinical assistant professor

    2025.4

  2. 名古屋大学医学部附属病院   皮膚科

    2020.7

  3. 豊橋市民病院   皮膚科

    2018.4 - 2020.6

  4. 名古屋大学医学部附属病院   皮膚科

    2017.4 - 2018.3

  5. 岐阜県立多治見病院   初期研修医

    2015.4 - 2017.3

To the head of Research History.▲

Education 1

  1. 名古屋大学大学院医学系研究科博士課程

    2019.4 - 2022.3

To the head of Education.▲

Professional Memberships 3

  1. 日本リウマチ学会

  2. 日本皮膚科学会

  3. 日本研究皮膚科学会

To the head of Professional Memberships.▲
 

Papers 81

  1. Anti-polymyositis/scleroderma antibody-positive myositis exhibits greater cutaneous T cell activation than anti-ARS antibody-positive myositis Open Access

    Akashi, N; Ogawa-Momohara, M; Muro, Y; Yokoyama, T; Kamiya, S; Yamashita, Y; Koizumi, H; Takeichi, T; Akiyama, M

    JAAD INTERNATIONAL   Vol. 25   page： 95 - 97   2026.4

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  2. Inter-institutional variability in kidney dosimetry during <SUP>177</SUP>Lu-DOTATATE therapy in Japan

    Miyaji, N; Miwa, K; Yamashita, K; Yamashita, Y; Ukon, N; Ogawa, M; Konishi, T; Kojima, H; Sato, T; Akiya, N; Wachi, K; Komatsu, A; Kimura, S; Yamao, T; Masubuchi, M; Maeda, Y; Morimoto, M; Oishi, A; Norikane, T; Yamamoto, Y; Nishiyama, Y; Ohashi, S; Hotta, M; Yagihashi, T; Murai, T; Nakanishi, K; Kamitaka, Y; Nishii, R

    RADIOLOGICAL PHYSICS AND TECHNOLOGY   Vol. 19 ( 1 ) page： 165 - 175   2026.3

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  3. 特集 脱毛症治療 臨床例 フルコナゾール内服が著効した乳児ケルスス禿瘡の双生児例

    本田 直, 笹本 桃子, 山下 雄太, 秋山 真志

    皮膚病診療   Vol. 48 ( 2 ) page： 128 - 131   2026.2

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    Publisher：協和企画  

    DOI： 10.24733/pd.0000004506

    CiNii Research

  4. Novel serum autoantibodies against alpha thalassemia/mental retardation syndrome X-linked, a component of promyelocytic leukaemia nuclear bodies, in dermatomyositis. International journal

    Yuta Yamashita, Hiroyuki Kanoh, Yoshinao Muro, Satoshi Kamiya, Eori Noda, Norika Akashi, Haruka Koizumi, Mariko Ogawa-Momohara, Takuya Takeichi, Masashi Akiyama

    Rheumatology (Oxford, England)   Vol. 65 ( 2 )   2026.2

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    Language：English   Publishing type：Research paper (scientific journal)  

    DOI： 10.1093/rheumatology/keaf596

    Web of Science

    PubMed

  5. Assessment of the impacts of anthropogenic ozone precursors on domestic and transboundary ozone concentrations using a high-resolution global chemistry model Open Access

    Goto, D; Yashiro, H; Yamashita, Y; Takigawa, M; Sudo, K; Uchida, J; Yumimoto, K; Takemura, T

    PROGRESS IN EARTH AND PLANETARY SCIENCE   Vol. 13 ( 1 )   2026.1

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  6. Anti-Ki/SL Antibody-Positive Deep Morphea Patient Also Positive for Anti-PL-12 and Anti-Ro60 Antibodies

    Ikumi Hattori, Haruka Koizumi, Eori Noda, Satoshi Kamiya, Norika Akashi, Yuta Yamashita, Mariko Ogawa-Momohara, Takuya Takeichi, Yoshinao Muro, Masashi Akiyama

    JOURNAL OF DERMATOLOGY   Vol. 52 ( 12 ) page： e1073 - e1074   2025.12

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  7. 症例報告 リツキシマブが有効であった尋常性天疱瘡と落葉状天疱瘡の4例

    藤井 靖子, 桃原 真理子, 神谷 怜志, 明石 憲佳, 小泉 遼, 山下 雄太, 武市 拓也, 室 慶直, 秋山 真志

    臨床皮膚科   Vol. 79 ( 12 ) page： 917 - 923   2025.11

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    Publisher：株式会社医学書院  

    DOI： 10.11477/mf.002149730790120917

    CiNii Research

  8. A prehistoric Japanese building constructed with wooden pillars that have an age range spanning 700 years Open Access

    Sano, M; Hakozaki, M; Yamashita, Y; Li, Z; Nakatsuka, T; Chiba, T; Arakawa, T; Sakamoto, M

    JOURNAL OF ARCHAEOLOGICAL SCIENCE-REPORTS   Vol. 67   2025.11

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  9. リツキシマブが有効であった尋常性天疱瘡と落葉状天疱瘡の4例

    藤井 靖子, 桃原 真理子, 神谷 怜志, 明石 憲佳, 小泉 遼, 山下 雄太, 武市 拓也, 室 慶直, 秋山 真志

    臨床皮膚科   Vol. 79 ( 12 ) page： 917 - 923   2025.11

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    Language：Japanese   Publisher：(株)医学書院  

  10. A Case of Rituximab Successfully Controlling SSc Vascular and Other Symptoms in a Pregnant Patient, Leading to a Safe Pregnancy and Delivery. International journal

    Norika Akashi, Mariko Ogawa-Momohara, Satoshi Kamiya, Yuta Yamashita, Haruka Koizumi, Rina Inami, Takafumi Ushida, Takuya Takeichi, Yoshinao Muro, Masashi Akiyama

    The Journal of dermatology   Vol. 52 ( 10 ) page： e919 - e920   2025.10

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  11. Prevalence of FOXA1 and ERBB2 activating mutations in extramammary Paget's disease: A retrospective multicenter analysis of 99 cases from Japanese and Taiwanese cohorts. International journal Open Access

    Michiya Omi, Takuya Takeichi, Yusuke Okuno, Chao-Kai Hsu, Cheng-Lin Wu, Yi-Han Chang, Shoichiro Mori, Yuta Yamashita, Akira Miyazaki, Takaya Taira, Teruki Yanagi, Keitaro Fukuda, Tatsuhiro Noda, Yuika Suzuki, Yoshinao Muro, Masashi Akiyama

    Journal of dermatological science   Vol. 120 ( 1 ) page： 32 - 38   2025.10

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    Language：English   Publishing type：Research paper (scientific journal)  

    BACKGROUND: Extramammary Paget's disease (EMPD) occurs in areas where apocrine glands are abundant. EMPD is associated with the known somatic hotspot mutation g.chr14:38064406 G>A in the promoter region of FOXA1 and S310F in ERBB2. Whether EMPD patients in non-Japanese populations have FOXA1 driver mutations remains undetermined, and the relationship between the clinical characteristics of EMPD patients and the presence of somatic FOXA1 driver mutations has yet to be investigated. OBJECTIVE: To assess the prevalence and clinical significance of the FOXA1 and ERBB2 hotspot somatic mutations. METHODS: Surgical specimens from 99 EMPD patients who underwent surgery from January 2013 to March 2024 were collected from five facilities in Japan and Taiwan. To detect the somatic mutations, amplicon sequencing was performed for FOXA1, and ddPCR was conducted for ERBB2. Immunohistochemical analysis for FOXA1 was performed on 38 samples. RESULTS: The frequencies of the FOXA1 (g.chr14:38064406 G>A) mutation and the ERBB2 S310F mutation were 8/93 (8.6 %) and 37/93 (40.0 %), respectively, among the non-fresh-frozen specimens. FOXA1 somatic hotspot mutation-positive cases were found at all five medical institutions. Regardless of the mutational status of the FOXA1 promoter mutation, all examined cases immunohistochemically exhibited strong FOXA1 expression in the Paget cell nuclei. No significant correlation was found between the FOXA1 somatic mutation or the ERBB2 somatic mutation and any clinical parameter. CONCLUSION: The FOXA1 somatic hotspot mutation was found in both Japanese and Taiwanese EMPD patients. We cannot rule out the possibility that FOXA1 might be a potential target for EMPD therapies in Japan and Taiwan.

    DOI： 10.1016/j.jdermsci.2025.08.001

    Open Access

    Web of Science

    Scopus

    PubMed

  12. Immune Checkpoint Inhibitor-Induced IgA Vasculitis With Abundant IgA Anti-Endothelial Cell Antibodies. International journal

    Eori Noda, Mariko Ogawa-Momohara, Satoshi Kamiya, Norika Akashi, Yuta Yamashita, Haruka Koizumi, Takuya Takeichi, Yoshinao Muro, Masashi Akiyama

    The Journal of dermatology   Vol. 52 ( 10 ) page： e938 - e939   2025.10

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  13. Development of an enzyme-linked immunosorbent assay for the efficient detection of autoantibodies against nuclear valosin-containing protein-like protein (NVL) 2 using its manipulated cDNA. International journal

    Yuta Yamashita, Yasuhiko Yamano, Yoshinao Muro, Haruka Koizumi, Mariko Ogawa-Momohara, Satoshi Kamiya, Norika Akashi, Takuya Takeichi, Yasuhiro Kondoh, Masashi Akiyama

    RMD open   Vol. 11 ( 3 )   2025.8

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    Language：English   Publishing type：Research paper (scientific journal)  

    PURPOSE: Antinuclear valosin-containing protein-like protein (NVL) antibodies have been detected only in systemic sclerosis (SSc) patients, and diverse comorbidities have been reported in anti-NVL antibody-positive SSc patients. Any relationship between antibodies against NVL1, a minor isoform of NVL, and the clinical symptoms also remains unclear. To clarify the clinical features of anti-NVL2 antibody-positive patients, we developed an ELISA for measuring antibodies against NVL2, a major target of autoantibodies against NVL. METHODS: Sera from 1676 patients with various conditions were included. 167 anti-nucleolar antibody (ANoA)-positive sera, 120 ANoA-negative sera and 17 healthy control sera were examined by an ELISA that uses the recombinant protein of NVL2 derived from its gene-manipulated complementary DNA clone (modified NVL2 (mNVL2)). RESULTS: 18 ANoA-positive sera subjected to indirect immunofluorescence (IIF) were positive for anti-mNVL2 ELISA. Although one ANoA-negative serum was judged false positive in our anti-mNVL2 ELISA, the above 18 anti-mNVL2 ELISA-positive sera were confirmed to be positive for anti-NVL2 antibodies by immunoprecipitation-Western blotting. Anti-NVL2 antibodies were detected in 17.0% of homogeneous nucleolar (AC-8) patterns in IIF. Six SSc patients had anti-NVL2 antibodies, whereas five with idiopathic interstitial pneumonia and seven with other diseases had anti-NVL2 antibodies. Anti-mNVL2 ELISA titres were significantly higher in the anti-NVL2 antibody-positive SSc patients than in the anti-NVL2 antibody-positive non-SSc patients (p<0.042). CONCLUSIONS: We found more anti-NVL2 antibody-positive cases than any previous study, as far as we know. Our ELISA, which showed an association between titres of these antibodies and SSc diagnosis, promises to expand knowledge about anti-NVL2 antibodies.

    DOI： 10.1136/rmdopen-2025-005679

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  14. Expanding the relevance of anti-Ki/SL beyond systemic lupus erythematosus to systemic sclerosis and dermatomyositis in in-house enzyme-linked immunosorbent assay analyses. International journal

    Haruka Koizumi, Yoshinao Muro, Yuta Yamashita, Mariko Ogawa-Momohara, Satoshi Kamiya, Norika Akashi, Eori Noda, Takuya Takeichi, Masashi Akiyama

    Clinical and experimental dermatology   Vol. 50 ( 8 ) page： 1679 - 1682   2025.8

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    Language：English   Publishing type：Research paper (scientific journal)  

    DOI： 10.1093/ced/llaf166

    Web of Science

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  15. Occurrence of bullous pemphigoid during long-term maintenance treatment for pemphigus vulgaris in remission. International journal

    Ayane Goto, Takuya Takeichi, Norito Ishii, Yuta Yamashita, Mariko Ogawa-Momohara, Yoshinao Muro, Masashi Akiyama

    The Journal of dermatology   Vol. 52 ( 6 ) page： e548 - e550   2025.6

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  16. Concurrent wild-type transthyretin amyloidosis and psoriasis vulgaris in an elderly man. International journal Open Access

    Yasuko Fujii, Takuya Takeichi, Yuta Yamashita, Takahiro Okumura, Ayako Sakakibara, Yoshinao Muro, Masashi Akiyama

    The Journal of dermatology   Vol. 52 ( 6 ) page： e546 - e547   2025.6

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  17. Alopecia universalis and type 1 diabetes mellitus both successfully controlled with baricitinib in a patient with autoimmune polyglandular syndrome type 3A. International journal

    Ayane Goto, Yuta Yamashita, Jun Yuasa, Satoshi Kamiya, Norika Akashi, Haruka Koizumi, Mariko Ogawa-Momohara, Takuya Takeichi, Yoshinao Muro, Masashi Akiyama

    The Journal of dermatology   Vol. 52 ( 6 ) page： e575 - e577   2025.6

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  18. リツキシマブが有効であった尋常性天疱瘡と落葉状天疱瘡の4症例

    藤井 靖子, 桃原 真理子, 神谷 怜志, 明石 憲佳, 小泉 遼, 山下 雄太, 武市 拓也, 室 慶直, 秋山 真志

    日本皮膚科学会雑誌   Vol. 135 ( 6 ) page： 1620 - 1620   2025.5

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    Language：Japanese   Publisher：(公社)日本皮膚科学会  

  19. 寛解導入後に再燃した,原発性シェーグレン病に伴う肺動脈性肺高血圧症の1例

    野田 絵織, 桃原 真理子, 中野 嘉久, 神谷 怜志, 明石 憲佳, 小泉 遼, 山下 雄太, 武市 拓也, 室 慶直, 秋山 真志

    日本皮膚科学会雑誌   Vol. 135 ( 5 ) page： 1364 - 1365   2025.5

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    Language：Japanese   Publisher：(公社)日本皮膚科学会  

  20. 外傷後の瘢痕部位から生じた抗LAD-1IgG抗体陽性のDPP-4阻害薬関連水疱性類天疱瘡の1例

    笹本 桃子, 桃原 真理子, 神谷 怜志, 明石 憲佳, 小泉 遼, 山下 雄太, 武市 拓也, 室 慶直, 秋山 真志, 石井 文人

    日本皮膚科学会雑誌   Vol. 135 ( 6 ) page： 1617 - 1617   2025.5

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    Language：Japanese   Publisher：(公社)日本皮膚科学会  

  21. 全身性野生型トランスサイレチン型アミロイドーシスを発症した尋常性乾癬の1例

    藤井 靖子, 武市 拓也, 山下 雄太, 室 慶直, 秋山 真志, 奥村 貴裕, 榊原 綾子

    日本皮膚科学会雑誌   Vol. 135 ( 6 ) page： 1617 - 1617   2025.5

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    Language：Japanese   Publisher：(公社)日本皮膚科学会  

  22. 特集 手こずる皮膚病とありふれた皮膚病 臨床例 足底の過角化を呈した抗PM/Scl抗体陽性の全身性強皮症

    野田 絵織, 山下 雄太, 桃原 真理子, 室 慶直, 吉田 祥啓, 秋山 真志

    皮膚病診療   Vol. 47 ( 4 ) page： 326 - 331   2025.4

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    Publisher：協和企画  

    DOI： 10.24733/pd.0000004129

    CiNii Research

  23. Predictive Value of Anti-SMN Complex Antibodies for Monitoring Cardiopulmonary Complications in MCTD: Insights From an ELISA Study Using Recombinant Gemin4 and an Anti-Nuclear Antibody Test. International journal

    Haruka Koizumi, Yoshinao Muro, Satoshi Kamiya, Norika Akashi, Yuta Yamashita, Mariko Ogawa-Momohara, Takuya Takeichi, Masashi Akiyama

    International journal of rheumatic diseases   Vol. 28 ( 1 ) page： e70089   2025.1

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    Language：English  

    DOI： 10.1111/1756-185X.70089

    PubMed

  24. Anti-SS-B antibody seroconversion occurring simultaneously with exacerbation of pulmonary arterial hypertension in a patient with primary Sjögren's syndrome in long-term remission. International journal

    Eori Noda, Mariko Ogawa-Momohara, Yoshihisa Nakano, Yuta Yamashita, Norika Akashi, Satoshi Kamiya, Haruka Koizumi, Takuya Takeichi, Yoshinao Muro, Masashi Akiyama

    European journal of dermatology : EJD   Vol. 35 ( 1 ) page： 61 - 63   2025.1

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    Language：English   Publishing type：Research paper (scientific journal)  

    DOI： 10.1684/ejd.2025.4837

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  25. Pitfalls in the detection of anti-Nucleolar Organizer Region 90 (NOR90) antibodies. International journal

    Satoshi Kamiya, Yoshinao Muro, Yuta Yamashita, Mariko Ogawa-Momohara, Masashi Akiyama

    European journal of internal medicine   Vol. 127   page： 157 - 160   2024.9

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  26. Correlation of serum allergen-specific IgE with total serum IgE and IgE specific to other allergens in Atopic dermatitis patients. International journal

    Norika Akashi, Mariko Ogawa-Momohara, Tomoki Taki, Ryo Fukaura, Keiko Wakahara, Satoshi Kamiya, Yuta Yamashita, Haruka Koizumi, Takuya Takeichi, Yoshinao Muro, Masashi Akiyama

    Journal of the European Academy of Dermatology and Venereology : JEADV   Vol. 38 ( 9 ) page： e761 - e763   2024.9

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  27. Comment on: Longitudinal study of patients with anti-SAE antibody-positive dermatomyositis: a multicenter cohort study in China. International journal

    Yuta Yamashita, Yoshinao Muro, Haruka Koizumi, Satoshi Kamiya, Norika Akashi, Mariko Ogawa-Momohara, Takuya Takeichi, Masashi Akiyama

    Rheumatology (Oxford, England)   Vol. 64 ( 3 ) page： 1565 - 1567   2024.8

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    Language：English   Publishing type：Research paper (scientific journal)  

    DOI： 10.1093/rheumatology/keae405

    Web of Science

    Scopus

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  28. アレルゲン特異的IgG4抗体の脱感作における機能解析と新規治療法の開発

    滝 奉樹, 桃原 真理子, 室 慶直, 村瀬 千晶, 棚橋 華奈, 山下 雄太, 小泉 遼, 深浦 遼, 武市 拓也, 秋山 真志

    アレルギー   Vol. 73 ( 6-7 ) page： 734 - 734   2024.8

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    Language：Japanese   Publisher：(一社)日本アレルギー学会  

  29. A case of anti-Th/To antibody-positive interstitial lung disease and pulmonary arterial hypertension that does not meet the classification criteria of systemic sclerosis. Comment on the article by Moschetti et al. International journal

    Eri Sakaida, Yuta Yamashita, Yoshinao Muro, Mirai Sawa, Teruyuki Mitsuma, Masashi Akiyama

    Clinical and experimental rheumatology   Vol. 42 ( 8 ) page： 1701 - 1702   2024.8

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  30. Panniculitis on the trunk as a possible characteristic feature of anti-SAE1/2 antibody-positive dermatomyositis: A possible cutaneous manifestation of treatment resistance. International journal Open Access

    Mahori Tago, Haruka Koizumi, Satoshi Kamiya, Norika Akashi, Akira Miyazaki, Yuta Yamashita, Mariko Ogawa-Momohara, Takuya Takeichi, Yoshinao Muro, Masashi Akiyama

    The Journal of dermatology   Vol. 51 ( 7 ) page： e227 - e228   2024.7

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  31. 特集 環状の紅斑と環状紅斑 臨床例 annular erythema of infancy

    山下 雄太, 室 慶直, 秋山 真志

    皮膚病診療   Vol. 46 ( 6 ) page： 524 - 527   2024.6

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    Publisher：協和企画  

    DOI： 10.24733/pd.0000003834

    CiNii Research

  32. Avacopan単剤治療により皮膚症状が改善した顕微鏡的多発血管炎の1例

    神谷 怜志, 小泉 遼, 明石 憲佳, 今井 聡子, 山下 雄太, 桃原 真理子, 武市 拓也, 室 慶直, 安田 和史, 秋山 真志

    西日本皮膚科   Vol. 86 ( 3 ) page： 326 - 326   2024.6

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    Language：Japanese   Publisher：日本皮膚科学会-西部支部  

  33. Combined oral lichen planus and oral lichenoid contact hypersensitivity reaction in a patient with Hashimoto's thyroiditis Open Access

    Suzuki S., Yamashita Y., Fujio M., Hanai Y., Koizumi H., Ogawa-Momohara M., Takeichi T., Muro Y., Akiyama M.

    Oral Oncology Reports   Vol. 10   2024.6

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    Publisher：Oral Oncology Reports  

    DOI： 10.1016/j.oor.2024.100356

    Open Access

    Scopus

  34. ELISA detection of anti-eIF2B antibodies in Japanese patients with systemic sclerosis. International journal

    Haruka Koizumi, Yasuhiko Yamano, Yoshinao Muro, Ryo Fukaura, Yuta Yamashita, Satoshi Kamiya, Norika Akashi, Mariko Ogawa-Momohara, Takuya Takeichi, Yasuhiro Kondoh, Masashi Akiyama

    Rheumatology (Oxford, England)   Vol. 63 ( 6 ) page： e164 - e165   2024.5

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    Language：English   Publishing type：Research paper (scientific journal)  

    DOI： 10.1093/rheumatology/kead649

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  35. 顆粒球単球吸着除去療法とビメキズマブの併用で救命し得た汎発性膿疱性乾癬の1例

    宿院 梨衣, 小泉 遼, 江畑 葵, 鈴木 由以佳, 山下 雄太, 桃原 真理子, 武市 拓也, 室 慶直, 秋山 真志, 高見 徳人

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 809 - 809   2024.4

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    Language：Japanese   Publisher：(公社)日本皮膚科学会  

  36. 血漿交換とステロイド,アニフロルマブが奏効した全身性エリテマトーデスの1例

    佐橋 祐子, 今井 聡子, 横山 多可志, 小泉 遼, 山下 雄太, 桃原 真理子, 武市 拓也, 室 慶直, 秋山 真志, 立枩 良崇

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 807 - 807   2024.4

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    Language：Japanese   Publisher：(公社)日本皮膚科学会  

  37. 足底の過角化を呈した抗PM/Scl抗体陽性の全身性強皮症の1例

    吉田 祥啓, 山下 雄太, 桃原 真理子, 小泉 遼, 武市 拓也, 室 慶直, 秋山 真志, 杉浦 一充

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 806 - 806   2024.4

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    Language：Japanese   Publisher：(公社)日本皮膚科学会  

  38. 橋本病に合併した口腔扁平苔癬の1例

    鈴木 須真子, 山下 雄太, 小泉 遼, 武市 拓也, 室 慶直, 秋山 真志, 藤井 正人, 花井 有里子

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 801 - 801   2024.4

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    Language：Japanese   Publisher：(公社)日本皮膚科学会  

  39. COVID-19にレムデシベルを投与した全身性強皮症の2例

    多湖 真帆里, 小泉 遼, 山下 雄太, 桃原 真理子, 武市 拓也, 室 慶直, 秋山 真志

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 820 - 820   2024.4

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    Language：Japanese   Publisher：(公社)日本皮膚科学会  

  40. ELISA法で抗TIF1-γ抗体が偽陰性を呈した若年性無筋症性皮膚筋炎の1例

    神谷 怜志, 小泉 遼, 明石 憲佳, 今井 聡子, 山下 雄太, 桃原 真理子, 武市 拓也, 室 慶直, 秋山 真志, 村上 めぐみ, 満間 照之

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 812 - 812   2024.4

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    Language：Japanese   Publisher：(公社)日本皮膚科学会  

  41. アニフロルマブを投与した全身性エリテマトーデス5例のまとめ

    近藤 あきほ, 小泉 遼, 森川 いくみ, 山下 雄太, 桃原 真理子, 武市 拓也, 室 慶直, 秋山 真志

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 818 - 818   2024.4

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  42. ゴットロン徴候様皮疹を認めた蕁麻疹様血管炎の1例

    鈴木 須真子, 桃原 真理子, 小泉 遼, 山下 雄太, 室 慶直, 秋山 真志, 近藤 猛

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 808 - 808   2024.4

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  43. 分節型白斑に合併したtwenty-nail dystrophy疑いの1例

    鈴木 友惟香, 小泉 遼, 室 慶直, 山下 雄太, 武市 拓也, 秋山 真志, 花井 有里子, 満間 照之

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 789 - 790   2024.4

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  44. 多発性皮膚線維腫を合併した皮膚筋炎・アトピー性皮膚炎の1例

    宿院 梨衣, 室 慶直, 小泉 遼, 山下 雄太, 桃原 真理子, 武市 拓也, 秋山 真志

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 814 - 814   2024.4

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  45. 抗TIF-1γ抗体陽性皮膚筋炎の寛解後に胆嚢管癌を認めた1例

    堀崎 健, 室 慶直, 桃原 真理子, 山下 雄太, 小泉 遼, 武市 拓也, 秋山 真志

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 801 - 802   2024.4

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  46. 抗TIF1-a及びγ抗体と抗セントロメア抗体が陽性となった皮膚筋炎の1例

    服部 いくみ, 小泉 遼, 山下 雄太, 桃原 真理子, 武市 拓也, 室 慶直, 秋山 真志

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 824 - 824   2024.4

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  47. 有棘細胞癌様の臨床像を呈したメトトレキサート関連リンパ増殖異常症の1例

    岩田 真衣, 山田 元人, 松井 健一郎, 中根 啓允, 藤城 里香, 滝 奉樹, 山下 雄太, 藤原 慎二

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 787 - 787   2024.4

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  48. 横行結腸癌の合併を認めた抗SAE抗体陽性の皮膚筋炎の1例

    豊田 紗麗, 山下 雄太, 神谷 怜志, 小泉 遼, 桃原 真理子, 武市 拓也, 室 慶直, 秋山 真志

    日本皮膚科学会雑誌   Vol. 134 ( 4 ) page： 818 - 818   2024.4

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  49. Increased JAK activation in cutaneous vasculitis. International journal

    Aoi Ebata, Mariko Ogawa-Momohara, Ryo Fukaura, Yuta Yamashita, Haruka Koizumi, Takuya Takeichi, Yoshinao Muro, Masashi Akiyama

    Journal of the American Academy of Dermatology   Vol. 90 ( 3 ) page： 627 - 629   2024.3

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    Language：English   Publishing type：Research paper (scientific journal)  

    DOI： 10.1016/j.jaad.2023.10.056

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  50. 自己免疫性多内分泌腺症候群3A型に併発した円形脱毛症をバリシチニブにて治療した1例

    後藤 文音, 山下 雄太, 小泉 遼, 桃原 真理子, 武市 拓也, 室 慶直, 秋山 真志, 湯浅 淳

    日本皮膚科学会雑誌   Vol. 134 ( 2 ) page： 350 - 350   2024.2

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  51. 早期治療介入が間質性肺炎に著効した抗PM/Scl抗体陽性皮膚筋炎の1例

    加藤 史織, 桃原 真理子, 山下 雄太, 小泉 遼, 武市 拓也, 室 慶直, 秋山 真志, 星野 慶

    日本皮膚科学会雑誌   Vol. 134 ( 2 ) page： 345 - 346   2024.2

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  52. 早期治療介入が間質性肺炎に著効した抗PM/Scl抗体陽性皮膚筋炎の1例

    加藤 史織, 桃原 真理子, 山下 雄太, 小泉 遼, 武市 拓也, 室 慶直, 秋山 真志, 星野 慶

    日本皮膚科学会雑誌   Vol. 134 ( 2 ) page： 345 - 346   2024.2

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  53. デュピルマブの長期使用によるアトピー性皮膚炎におけるアレルゲン特異的IgG4の増加

    桃原 真理子, 室 慶直, 村瀬 千晶, 滝 奉樹, 棚橋 華奈, 山下 雄太, 小泉 遼, 深浦 遼, 武市 拓也, 秋山 真志

    日本皮膚免疫アレルギー学会総会学術大会プログラム・抄録集   Vol. 53回   page： 203 - 203   2023.12

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  54. デュピルマブの長期使用によるアトピー性皮膚炎におけるアレルゲン特異的IgG4の増加

    桃原 真理子, 室 慶直, 村瀬 千晶, 滝 奉樹, 棚橋 華奈, 山下 雄太, 小泉 遼, 深浦 遼, 武市 拓也, 秋山 真志

    日本皮膚免疫アレルギー学会総会学術大会プログラム・抄録集   Vol. 53回   page： 203 - 203   2023.12

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  55. 特集 psoriatic disease～全身疾患へのアプローチ～ 臨床例 SAPHO症候群に併発した汎発性膿疱性乾癬

    江畑 葵, 小泉 遼, 滝 奉樹, 山下 雄太, 秋山 真志

    皮膚病診療   Vol. 45 ( 10 ) page： 916 - 920   2023.10

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    Publisher：協和企画  

    DOI： 10.24733/pd.0000003525

    CiNii Research

  56. 【psoriatic disease～全身疾患へのアプローチ～】SAPHO症候群に併発した汎発性膿疱性乾癬

    江畑 葵, 小泉 遼, 滝 奉樹, 山下 雄太, 秋山 真志

    皮膚病診療   Vol. 45 ( 10 ) page： 916 - 920   2023.10

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  57. Allergen-specific IgG4 increase in atopic dermatitis with long-term dupilumab use. International journal Open Access

    Mariko Ogawa-Momohara, Yoshinao Muro, Chiaki Murase, Tomoki Taki, Kana Tanahashi, Yuta Yamashita, Haruka Koizumi, Ryo Fukaura, Takuya Takeichi, Masashi Akiyama

    The British journal of dermatology   Vol. 189 ( 4 ) page： 472 - 474   2023.9

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    Language：English   Publishing type：Research paper (scientific journal)  

    DOI： 10.1093/bjd/ljad207

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  58. Comment on: Successful treatment of rapid progressive interstitial lung disease in a case of anti-Zo antibody positive anti-synthetase syndrome. International journal Open Access

    Haruka Koizumi, Yoshinao Muro, Satoshi Kamiya, Norika Akashi, Satoko Imai, Yuta Yamashita, Mariko Ogawa-Momohara, Takuya Takeichi, Masashi Akiyama

    International journal of rheumatic diseases   Vol. 26 ( 9 ) page： 1872 - 1873   2023.9

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  59. Anti-KIF20B autoantibodies in systemic autoimmune rheumatic diseases: Their high prevalence in systemic lupus erythematosus. International journal Open Access

    Haruka Koizumi, Yoshinao Muro, Yuta Yamashita, Takuya Takeichi, Marvin J Fritzler, Masashi Akiyama

    The Journal of dermatology   Vol. 50 ( 8 ) page： 990 - 998   2023.8

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    The kinesin superfamily protein 20B (KIF20B), also known as M-phase phosphoprotein-1, is a plus-end-directed motor enzyme for cytokinesis. Anti-KIF20B antibodies have been reported in idiopathic ataxia, but no previous studies have examined anti-KIF20B antibodies in systemic autoimmune rheumatic diseases (SARDs). We aimed to establish methods for detecting anti-KIF20B antibodies and to investigate the clinical significance of these antibodies in SARDs. Serum samples from 597 patients with various SARDs and 46 healthy controls (HCs) were included. Fifty-nine samples that had been examined by immunoprecipitation using the recombinant KIF20B protein produced by in vitro transcription/translation were used for establishing the ELISA cutoff with the same recombinant protein for measuring the anti-KIF20B antibodies. The ELISA performed well, showing close agreement with the immunoprecipitation results (Cohen's κ >0.8). The ELISA results for 643 samples showed the prevalence of anti-KIF20B to be higher in the systemic lupus erythematosus (SLE) patients than in the HCs (18/89 vs. 3/46, P = 0.045). Since no SARD other than SLE had higher frequencies of anti-KIF20B antibodies than those of the HCs, we investigated the clinical characteristics of anti-KIF20B antibody-positive cases in SLE. The score on the SLE Disease Activity Index-2000 (SLEDAI-2K) was significantly higher for the anti-KIF20B-positive SLE patients than for the anti-KIF20B-negative SLE patients (P = 0.013). In a multivariate regression analysis of the anti-single-stranded deoxyribonucleic acid, anti-double-stranded deoxyribonucleic acid, and anti-KIF20B antibodies, the presence of anti-KIF20B antibody was significantly associated with high SLEDAI-2K scores (P = 0.003). Anti-KIF20B antibodies were found in ~20% of patients with SLE and were associated with high SLEDAI-2K scores. Much larger cohort and longitudinal studies are needed to confirm the association between anti-KIF20B antibodies and SLE.

    DOI： 10.1111/1346-8138.16813

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  60. Cutaneous manifestations of microscopic polyangiitis successfully controlled with avacopan alone. International journal

    Satoshi Kamiya, Haruka Koizumi, Yuika Suzuki, Satoko Imai, Yuta Yamashita, Mariko Ogawa-Momohara, Takuya Takeichi, Yoshinao Muro, Kazushi Yasuda, Masashi Akiyama

    The Journal of dermatology   Vol. 50 ( 7 ) page： E206 - E207   2023.7

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  61. Successful combination therapy of bimekizumab and granulocyte monocyte adsorption apheresis for generalized pustular psoriasis complicated with microscopic polyangiitis. International journal Open Access

    Rie Shukuin, Haruka Koizumi, Aoi Ebata, Satoko Imai, Yuta Yamashita, Mariko Ogawa-Momohara, Takuya Takeichi, Yoshinao Muro, Norito Takami, Masashi Akiyama

    The Journal of dermatology   Vol. 50 ( 6 ) page： E181 - E182   2023.6

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  62. 特集 皮膚筋炎とその周辺 臨床 筋炎自己抗体の最近の知見

    山下 雄太, 室 慶直

    皮膚科   Vol. 3 ( 1 ) page： 19 - 25   2023.1

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    Publisher：(有)科学評論社  

    DOI： 10.69337/j07608.2023088264

    CiNii Research

  63. Occurrence of cholangiocarcinoma, three years after negative seroconversion of anti-TIF1γ antibody, in a dermatomyositis patient. International journal Open Access

    Ken Horisaki, Yoshinao Muro, Mariko Ogawa-Momohara, Yuta Yamashita, Haruka Koizumi, Takuya Takeichi, Masashi Akiyama

    European journal of dermatology : EJD   Vol. 33 ( 1 ) page： 48 - 49   2023.1

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    Language：English   Publishing type：Research paper (scientific journal)  

    DOI： 10.1684/ejd.2023.4414

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  64. A case of juvenile amyopathic dermatomyositis with anti-transcription intermediary factor 1-α antibody showing negative anti-TIF1-γ ELISA results: Comment on "Case of pembrolizumab-induced dermatomyositis with anti-transcription intermediary factor 1-γ antibody". International journal

    Haruka Koizumi, Yoshinao Muro, Satoko Imai, Yuta Yamashita, Mariko Ogawa-Momohara, Takuya Takeichi, Megumi Murakami, Teruyuki Mitsuma, Masashi Akiyama

    The Journal of dermatology   Vol. 50 ( 1 ) page： E39 - E40   2023.1

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  65. Comment on: Disease evolution in a long-term follow-up of 104 undifferentiated connective tissue disease patients. International journal Open Access

    Yuta Yamashita, Yoshinao Muro, Haruka Koizumi, Mariko Ogawa-Momohara, Takuya Takeichi, Masashi Akiyama

    Clinical and experimental rheumatology   Vol. 41 ( 1 ) page： 195 - 196   2023.1

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  66. Appropriate immunoassay systems are needed to evaluate various anticentromere antibodies as biomarkers for disease progression in systemic sclerosis. International journal Open Access

    Yoshinao Muro, Yuta Yamashita, Haruka Koizumi, Mariko Ogawa-Momohara, Takuya Takeichi, Masashi Akiyama

    Journal of immunological methods   Vol. 512   page： 113400 - 113400   2023.1

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  67. 当科における好酸球性多発血管炎性肉芽腫症に対するメポリズマブの使用経験と有効性の検討

    山下 雄太, 室 慶直, 小泉 遼, 桃原 真理子, 武市 拓也, 秋山 真志

    日本皮膚免疫アレルギー学会総会学術大会プログラム・抄録集   Vol. 52回   page： 217 - 217   2022.12

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  68. Two novel anti-aminoacyl tRNA synthetase antibodies: Autoantibodies against cysteinyl-tRNA synthetase and valyl-tRNA synthetase. International journal Open Access

    Yoshinao Muro, Yuta Yamashita, Haruka Koizumi, Mariko Ogawa-Momohara, Takuya Takeichi, Teruyuki Mitsuma, Masashi Akiyama

    Autoimmunity reviews   Vol. 21 ( 12 ) page： 103204 - 103204   2022.12

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    Anti-aminoacyl-tRNA synthetase (anti-ARS) antibodies are useful for identifying a clinical subset of patients with inflammatory myopathies. Since the myositis of anti-ARS-positive patients is characterized by a unique set of non-myopathic manifestations, including interstitial lung disease, mechanic's hands, and arthralgia, the patients are classified as having anti-synthetase syndrome. Autoantibodies have been identified to eight kinds of ARSs. Of the other 12 ARSs, eight are components of the "OJ" multi-synthetase complex. Autoantibodies to the four remaining ARSs (CysARS, ValARS, SerARS, and TrpARS) have not been reported to be present in patients with inflammatory myopathies. In this study, we first screened samples from more than 300 Japanese patients majorly consisting of those with dermatomyositis (DM) by our established in-house ELISA to find autoantibodies against the four ARSs described above. Since sera from two DM patients specifically reacted to CysARS or ValARS, we determined their reactivities by immunoprecipitation (IP) with the corresponding recombinant proteins and IP-Western blotting with cellular extract. One patient had several features found in anti-synthetase syndrome, but the other did not. The clinical differences among the various anti-ARS antibodies should be explored in a future work.

    DOI： 10.1016/j.autrev.2022.103204

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  69. Clinical characteristics of systemic sclerosis patients with anti-NOR90 antibodies

    Yamashita, Y; Muro, Y; Koizumi, H; Ogawa-Momohara, M; Takeichi, T; Akiyama, M

    JOURNAL OF INVESTIGATIVE DERMATOLOGY   Vol. 142 ( 12 ) page： S204 - S204   2022.12

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  70. Comment on: Favourable complete remission of anti-OJ antibody-positive myositis after lung cancer resection. International journal

    Yoshinao Muro, Kazuki Nishida, Yuta Yamashita, Haruka Koizumi, Takuya Takeichi, Minoru Satoh, Masashi Akiyama

    Rheumatology (Oxford, England)   Vol. 61 ( 8 ) page： E232 - E234   2022.8

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  71. Eosinophilic granulomatosis with polyangiitis complicated with idiopathic thrombocytopenic purpura and sclerosing cholangitis showing eosinophilic infiltration. International journal

    Yuta Yamashita, Takuya Takeichi, Yoji Ishizu, Nobuaki Suzuki, Takashi Tsuboi, Kentaro Matsuura, Haruka Koizumi, Yoshinao Muro, Masashi Akiyama

    The Journal of dermatology   Vol. 49 ( 8 ) page： E270 - E271   2022.8

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  72. Clinical significance of anti-NOR90 antibodies in systemic sclerosis and idiopathic interstitial pneumonia. International journal Open Access

    Yuta Yamashita, Yasuhiko Yamano, Yoshinao Muro, Mariko Ogawa-Momohara, Takuya Takeichi, Yasuhiro Kondoh, Masashi Akiyama

    Rheumatology (Oxford, England)   Vol. 61 ( 4 ) page： 1709 - 1716   2022.4

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    OBJECTIVE: Anti-NOR90 antibodies are usually found in patients with SSc; however, their clinical relevance remains obscure. We developed an ELISA for measuring them to investigate the clinical features of patients with anti-NOR90 antibodies. METHODS: Serum samples from 1252 patients with various conditions from Nagoya University Hospital and 244 patients with idiopathic interstitial pneumonia (IIP) from Tosei General Hospital were included. Anti-NOR90 antibodies were assayed by an ELISA using the recombinant protein produced by in vitro transcription/translation. RESULTS: Five (0.4%) patients in the Nagoya University Hospital cohort had anti-NOR90 antibodies. One patient with diffuse cutaneous SSc, three with limited cutaneous SSc, and one with Raynaud's disease were positive for anti-NOR90 antibodies. Anti-NOR90 antibodies were found more frequently in patients with systemic scleroderma-spectrum disorders (SSDs) than without SSDs (5/316 vs 0/936, P <0.00101) and were found more frequently in patients with SSc than without SSc (4/249 vs 0/528, P <0.0104) in the systemic autoimmune rheumatic diseases cohort. Three of the four anti-NOR90-positive SSc patients had interstitial lung disease (ILD), and two of those four had cancer. Three (1.2%) patients in the Tosei General Hospital cohort had anti-NOR90 antibodies. All three of the anti-NOR90-positive IIP patients had gastrointestinal tract involvement, and two of those three had cancer or skin lesions observed in SSc. CONCLUSIONS: Although anti-NOR90 antibodies are rarely found in clinics, our ELISA is useful for their detection. Further studies are needed to confirm the association of anti-NOR90 antibodies with ILD and cancer in SSc and IIP patients.

    DOI： 10.1093/rheumatology/keab575

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  73. 新生児エリテマトーデス、小児シェーグレン症候群と鑑別を要したannular erythema of infancyの1例

    山下 雄太, 室 慶直, 武市 拓也, 秋山 真志

    日本皮膚科学会雑誌   Vol. 132 ( 3 ) page： 522 - 522   2022.3

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  74. Long-term risk of cancer development among anti-Th/To antibody-positive systemic sclerosis patients: comment on the article by Mecoli et al. International journal Open Access

    Yuta Yamashita, Yoshinao Muro, Haruka Koizumi, Takuya Takeichi, Yasuhiko Yamano, Yasuhiro Kondoh, Masashi Akiyama

    Arthritis & rheumatology (Hoboken, N.J.)   Vol. 74 ( 2 ) page： 368 - 369   2022.2

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  75. 特集 診断に苦慮した症例 臨床例 診断に苦慮したメトトレキサート関連リンパ増殖異常症

    岩田 真衣, 山田 元人, 藤原 慎二, 滝 奉樹, 山下 雄太, 藤城 里香

    皮膚病診療   Vol. 44 ( 1 ) page： 72 - 75   2022.1

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    DOI： 10.24733/pd.0000002813

    CiNii Research

  76. Pitfalls in establishing mouse model of female infertility by immunization with human centromere protein. International journal Open Access

    Yoshinao Muro, Yuta Yamashita, Haruka Koizumi, Takuya Takeichi, Masashi Akiyama

    Immunology letters   Vol. 239   page： 20 - 22   2021.11

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  77. Subcutaneous giant trichoblastoma in the abdomen. International journal

    Katsunobu Goto, Michihiro Kono, Toru Urata, Yoshie Hasegawa-Murakami, Takaaki Matsumoto, Yuta Yamashita, Kenji Yokota, Masashi Akiyama

    The Journal of dermatology   Vol. 48 ( 8 ) page： E393 - E394   2021.8

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  78. Cutaneous malignant melanoma in an elderly patient with intermediate junctional epidermolysis bullosa. International journal Open Access

    Yuta Yamashita, Tomoki Taki, Takuya Takeichi, Mao Okumura, Shoichiro Mori, Yasutoshi Ito, Tomoo Ogi, Motohito Yamada, Masashi Akiyama

    The Journal of dermatology   Vol. 48 ( 8 ) page： E384 - E385   2021.8

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  79. 全身性強皮症との鑑別を要したPalmar fasciitis and polyarthritis syndromeの1例

    山下 雄太, 室 慶直, 福澤 沙麗, 桃原 真理子, 武市 拓也, 秋山 真志

    日本皮膚科学会雑誌   Vol. 131 ( 5 ) page： 1402 - 1402   2021.5

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  80. Odontogenic keratocysts are an important clue for diagnosing basal cell nevus syndrome. Open Access

    Kaori Kaibuchi-Ando, Takuya Takeichi, Yasutoshi Ito, So Takeuchi, Yuta Yamashita, Motohito Yamada, Yoshinao Muro, Tomoo Ogi, Masashi Akiyama

    Nagoya journal of medical science   Vol. 83 ( 2 ) page： 393 - 396   2021.5

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    Basal cell nevus syndrome (BCNS) is an autosomal dominant skin disorder characterized by multiple basal cell nevi. Patients with BCNS tend to develop basal cell carcinoma (BCC) and frequently show skeletal abnormalities. Most cases of BCNS are caused by mutations in patched 1 (PTCH1). PTCH1 encodes a transmembrane receptor protein for the secreted molecule sonic hedgehog, which plays a key role in the development of animals ranging from insects to mammals. We analyzed two Japanese BCNS patients from two independent families. Both of our patients had multiple jaw keratocysts. In one patient, these were the key to noticing his BCNS, as he had no skin tumors. The early detection of PTCH1 mutations would enable BCNS patients to be carefully followed up for the occurrence of BCC. The diagnosis of BCC at the early stage leads to prompt surgical treatments, resulting in a good prognosis. The present cases suggest that keratocysts of the jaw might be an important clue for diagnosing BCNS.

    DOI： 10.18999/nagjms.83.2.393

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  81. Late-Onset Fulminant Myocarditis With Immune Checkpoint Inhibitor Nivolumab. International journal

    Shogo Yamaguchi, Ryota Morimoto, Takahiro Okumura, Yuta Yamashita, Tomoaki Haga, Tasuku Kuwayama, Tsuyoshi Yokoi, Hiroaki Hiraiwa, Toru Kondo, Yuki Sugiura, Naoki Watanabe, Naoaki Kano, Kei Kohno, Kenji Fukaya, Akinori Sawamura, Kenji Yokota, Hideki Ishii, Masato Nakaguro, Masashi Akiyama, Toyoaki Murohara

    The Canadian journal of cardiology   Vol. 34 ( 6 ) page： 812.e1-812.e3 - 812.e3   2018.6

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    Language：English   Publishing type：Research paper (scientific journal)  

    A 60-year-old man was diagnosed with melanoma. After receiving 13 infusions of nivolumab, he had fulminant myocarditis. The myocardial biopsy specimen revealed extensive lymphocytic infiltration, interstitial edema, and myocardial necrosis, with predominant CD4+, CD8+, CD20-, and programmed death-1- markers. Programmed death-1 ligand 1 (PD-L1) was predominantly expressed on the surface of the damaged myocardium. Although it is reported that myocarditis induced by the human anti-programmed death-1 inhibitor nivolumab therapy rarely occurred at > 2 months use in clinical trials, this case showed that even if at a late phase, long-term use of immune checkpoint inhibitors might to lead immune-related adverse events including myocarditis.

    DOI： 10.1016/j.cjca.2018.03.007

    Web of Science

    Scopus

    PubMed

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MISC 8

  1. 自己免疫性多内分泌腺症候群3A型に併発した円形脱毛症をバリシチニブにて治療した1例

    後藤文音, 山下雄太, 小泉遼, 桃原真理子, 武市拓也, 室慶直, 秋山真志, 湯浅淳

    日本皮膚科学会雑誌   Vol. 134 ( 2 )   2024

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  2. 血清抗BP180抗体が陽性であった疱疹状膿痂疹の1例

    服部いくみ, 小泉遼, 神谷怜志, 明石憲佳, 野田達弘, 山下雄太, 桃原真理子, 武市拓也, 室慶直, 秋山真志

    日本皮膚科学会雑誌   Vol. 134 ( 5 )   2024

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  3. ゴットロン徴候様皮疹を認めた蕁麻疹様血管炎の1例

    鈴木須真子, 桃原真理子, 小泉遼, 山下雄太, 室慶直, 秋山真志, 近藤猛

    日本皮膚科学会雑誌   Vol. 134 ( 4 )   2024

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  4. 特発性血小板減少性紫斑病、好酸球浸潤を呈した硬化性胆管炎を合併し、メポリズマブが奏功した好酸球性多発血管炎性肉芽腫症の1例

    山下 雄太, 武市 拓也, 石津 洋二, 鈴木 伸明, 坪井 崇, 松浦 健太郎, 小泉 遼, 室 慶直, 秋山 真志

    中部リウマチ   Vol. 52 ( 1 ) page： 28 - 28   2023.3

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    Language：Japanese   Publisher：中部リウマチ学会  

  5. 当科における好酸球性多発血管炎性肉芽腫症に対するメポリズマブの使用経験と有効性の検討

    山下 雄太, 室 慶直, 小泉 遼, 桃原 真理子, 武市 拓也, 秋山 真志

    日本皮膚免疫アレルギー学会総会学術大会プログラム・抄録集   Vol. 52回   page： 217 - 217   2022.12

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    Language：Japanese   Publisher：(一社)日本皮膚免疫アレルギー学会  

  6. 【診断に苦慮した症例】診断に苦慮したメトトレキサート関連リンパ増殖異常症

    岩田 真衣, 山田 元人, 藤原 慎二, 滝 奉樹, 山下 雄太, 藤城 里香

    皮膚病診療   Vol. 44 ( 1 ) page： 72 - 75   2022.1

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    Language：Japanese   Publisher：(株)協和企画  

  7. 【診断に苦慮した症例】診断に苦慮したメトトレキサート関連リンパ増殖異常症

    岩田 真衣, 山田 元人, 藤原 慎二, 滝 奉樹, 山下 雄太, 藤城 里香

    皮膚病診療   Vol. 44 ( 1 ) page： 72 - 75   2022.1

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    Language：Japanese   Publisher：(株)協和企画  

  8. 全身性強皮症との鑑別を要したPalmar fasciitis and polyarthritis syndromeの1例

    山下 雄太, 室 慶直, 福澤 沙麗, 桃原 真理子, 武市 拓也, 秋山 真志

    日本皮膚科学会雑誌   Vol. 131 ( 5 ) page： 1402 - 1402   2021.5

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    Language：Japanese   Publisher：(公社)日本皮膚科学会  

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To the head of MISC.▲

KAKENHI (Grants-in-Aid for Scientific Research) 1

  1. Identification of immune checkpoint inhibitor-related antibodies and establishment of biomarkers using proteomics

    Grant number：24K19167  2024.4 - 2026.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Early-Career Scientists

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    Authorship：Principal investigator 

    Grant amount：\4680000 （ Direct Cost: \3600000 、 Indirect Cost：\1080000 ）

To the head of KAKENHI (Grants-in-Aid for Scientific Research).▲