YAMAGUCHI Hideki

写真a

Affiliation

Faculty of Medicine School of Medicine Department of Internal Medicine, Hematology, Diabetes, and Endocrinology

Title

Associate Professor

External Link

Related SDGs


Degree 【 display / non-display

  • 博士(医学) ( 1997.3   宮崎医科大学 )

  • 医学士 ( 1988.3   宮崎医科大学 )

Research Interests 【 display / non-display

  • Life science

Research Areas 【 display / non-display

  • Life Science / Metabolism and endocrinology  / bioactive peptide

Education 【 display / non-display

  • Miyazaki Medical College   Graduate School, Division of Medicine

    1993.4 - 1997.3

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    Country:Japan

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  • Miyazaki Medical College   Faculty of Medicine

    1982.4 - 1988.3

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    Country:Japan

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Campus Career 【 display / non-display

  • University of Miyazaki   Faculty of Medicine   School of Medicine   Department of Internal Medicine, Hematology, Diabetes, and Endocrinology   Associate Professor

    2021.10 - Now

  • University of Miyazaki   Faculty of Medicine   College Hospital   The third internal medicine department   Miyazaki University Hospital   Lecturer

    2010.03 - 2021.09

  • University of Miyazaki   Faculty of Medicine   School of Medicine   Internal medicine course nerve breath internal secretion metabolic study field   Assistant Professor

    2007.04 - 2010.02

  • University of Miyazaki   Faculty of Medicine   School of Medicine   Internal medicine course nerve breath internal secretion metabolic study field   Research Assistant

    1998.06 - 2007.03

  • 宮崎大学   旧組織   宮崎医科大学医学部附属病院   医員

    1998.04 - 1998.06

External Career 【 display / non-display

  • Baylor College of Medicine   Researcher

    1999.11 - 2001.10

Professional Memberships 【 display / non-display

  • 日本糖尿病協会

    2008.3

  • 日本甲状腺学会

    2002.4

  • 日本糖尿病学会

    1989.12

  • 日本内科学会

    1989.4

  • 日本内分泌学会

    1989.4

Qualification acquired 【 display / non-display

  • Doctor

 

Papers 【 display / non-display

  • Iliopsoas muscle to visceral fat ratio on CT predicts Cushing’s syndrome in elderly females with adrenal tumors Reviewed

    Uchida Taisuke, Yamaguchi Hideki, Arimura Yasuji, Nagayama Ayako, Moritaka Kanoko, Inoguchi Yukihiro, Ashida Kenji, Nomura Masatoshi, Nakazato Masamitsu, Shimoda Kazuya

    Endocrine Journal   advpub ( 0 )   825 - 832   2023.5

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    Authorship:Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:The Japan Endocrine Society  

    There is no computed tomography (CT)-based numerical index for predicting Cushing’s syndrome (CS) in patients with adrenal incidentalomas. We tested the hypothesis that the iliopsoas muscle (Ip-M) to visceral fat (V-fat) ratio (IVR) on CT may predict CS in elderly female patients with adrenal tumors. We examined the V-fat area, subcutaneous fat (S-fat) area, Ip-M area, V-fat/S-fat ratio, and IVR at the third lumbar vertebra (L3) level using abdominal CT in female patients aged ≥50 years with cortisol-producing adrenal tumor diagnosed with CS or non-functioning adrenal tumor (NFT) in the derivation cohort. We performed receiver operating characteristic (ROC) analysis to evaluate the diagnostic value of the V-fat/S-fat ratio and IVR for predicting CS. We assessed the usefulness of the IVR in a separate validation cohort. In the derivation cohort, the IVR was significantly lower in the 9 patients with CS than in the 15 patients with NFT (<i>p</i> < 0.001). In ROC analysis with a cut-off value of 0.067, the IVR showed a sensitivity of 100%, specificity of 80.0%, positive likelihood ratio (PLR) of 5.000, and negative likelihood ratio (NLR) of 0.000. The area under the curve was significantly higher for the IVR than for the V-fat/S-fat ratio (0.933 <i>vs.</i> 0.704, respectively, <i>p</i> = 0.036). In 23 patients in the validation cohort, the IVR demonstrated a PLR of 5.714 and an NLR of 0.327. The novel IVR index, based on single-slice CT at the L3 level, predicted CS in elderly female patients with adrenal tumors.

    DOI: 10.1507/endocrj.EJ23-0053

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  • Elevated levels of circulating fibroblast growth factor 23 with hypercalcemia following discontinuation of denosumab Reviewed

    Uchida Taisuke, Yamaguchi Hideki, Kushima Chinami, Yonekawa Tadato, Nakazato Masamitsu

    Endocrine Journal   67 ( 1 )   31 - 35   2019.9

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:The Japan Endocrine Society  

    <p>We report a case of a 47-year-old woman with hypercalcemia 6 months after discontinuation of denosumab. She underwent right mastectomy for breast cancer and had received aromatase inhibitor and denosumab therapy for 5 years. Thirst, appetite loss, and bilateral ankle pain began few months after cessation of denosumab. She was admitted to the hospital for hypercalcemia and hyperthyroidism 6 months after the last dose of denosumab. Laboratory investigations revealed hypercalcemia, normophosphatemia, normal renal function, and elevated levels of fibroblast growth factor 23 (FGF-23). Serum tartrate-resistant acid phosphatase 5b and urine N-terminal cross-linked telopeptide of type I collagen were both elevated, and bone scintigraphy revealed increase of whole bone uptake. Radiological examinations showed no recurrence of breast cancer or tumors that secrete intact PTH or FGF-23. Hypercalcemia, which lasted for 1 month, was refractory to discontinuation of the aromatase inhibitor, normalization of thyroid hormone levels, saline hydration, and calcitonin administration, but was effectively treated with zoledronic acid. Abnormal uptake on bone scintigraphy and ankle pain both resolved a few months after treatment, and hypercalcemia has not recurred in the ensuing 2 years. In conclusion, we found elevated levels of circulating FGF-23 with hypercalcemia following the discontinuation of denosumab. FGF-23 might be a surrogate marker for massive bone resorption triggered by discontinuation of long-term denosumab treatment.</p>

    DOI: 10.1507/endocrj.EJ19-0198

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  • TYK2 is essential for the therapeutic effect of IFN-α in Jak2V617F-induced murine myeloproliferative neoplasms Reviewed

    幣 光太郎, 亀田 拓郎, 内田 泰介, 上運天 綾子, 秋月 渓一, 久冨木 庸子, 池田 良磨, 宇都 倫史, 深谷 知宏, 三苫 修也, 佐藤 克明, 上平 雄大, 上野 浩晶, 山口 秀樹, 下田 和哉

    Blood Neoplasia   2 ( 3 )   100087   2025.8

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:Elsevier BV  

    Interferon-α (IFN-α) exhibits antiviral and antiproliferative effects on normal and neoplastic cells. Intracellular signaling of IFN-α is mediated by tyrosine kinase 2 (TYK2) and janus kinase 1 (JAK1), followed by signal transducers and activators of transcription (STATs). TYK2 is redundant for the antiviral effect of IFN-α; however, the requirements for antiproliferative effects are unknown. We assessed the role of TYK2 in the effects of IFN-α in myeloproliferative neoplasm (MPN) model mice. Jak2V617F transgenic mice develop MPNs resembling human primary myelofibrosis, and ropeginterferon-α-2b ameliorated their features. However, these IFN-α effects were absent in Jak2V617F;Tyk2−/− mice. In mixed wild-type (WT)/Jak2V617F chimeric mice, IFN-α treatment induces Jak2V617F hematopoietic stem cells (HSCs) to enter the cell cycle and skew their differentiation into the megakaryocyte lineage, decreasing the number of Jak2V617F HSCs. The effects of IFN-α on Jak2V617F HSCs were not observed in mixed WT/Jak2V617F;Tyk2−/− mice, indicating that TYK2 is essential for the effects of IFN-α on both Jak2V617F progenitors and HSCs. The mechanism of IFN-α in Jak2V617F HSCs and progenitors differed: genes regulating the cell cycle were enriched in IFN-α–stimulated Jak2V617F HSCs, but not in Jak2V617F progenitors; genes regulating antiproliferation were enriched in IFN-α–stimulated Jak2V617F progenitors but not in Jak2V617F HSCs. The major IFN-α signaling molecule activated by JAKs is STAT1, which is essential for the antiviral effect. Most effects of IFN-α on Jak2V617F cells were preserved in Jak2V617F;Stat1−/− mice but to a moderate degree compared with Jak2V617F mice. Our study reveals essential roles of TYK2 for the preferential suppressive effect of IFN-α on Jak2V617F progenitors and HSCs.

    DOI: 10.1016/j.bneo.2025.100087

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  • Effects of tucidinostat in adult T-cell leukemia/lymphoma in clinical practice Reviewed

    Kamiunten A., Kameda T., Sekine M., Kawano H., Toyama T., Akizuki K., Kawano N., Maeda K., Sato S., Takeuchi M., Ishizaki J., Nagamine K., Kuroki A., Ikeda R., Matsumoto K., Karasawa M., Tahira Y., Uchida T., Shimoda H., Hidaka T., Yamashita K., Yamaguchi H., Kubuki Y., Shimoda K., Shide K.

    International Journal of Hematology   122 ( 1 )   83 - 92   2025.6

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:International Journal of Hematology  

    Adult T-cell leukemia/lymphoma (ATL) is a peripheral T-cell malignancy with a poor prognosis. We conducted a retrospective study across six institutions in Miyazaki Prefecture, Japan, to assess the efficacy of tucidinostat in patients with relapsed/refractory ATL who had not undergone transplantation. Between October 2021 and July 2023, 24 patients aged 41 to 88 years (median, 73.4 years) who had undergone prior therapies, including intensive chemotherapy (79.2%) and mogamulizumab immunotherapy (79.2%), received tucidinostat. Objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), and overall survival (OS) were evaluated as key outcomes. ORR and DCR reached 54.2% and 91.7%, respectively. The median PFS was 3.95 months, and OS was 8.04 months, which were not inferior to the results of a phase IIb study. The influential factors for PFS were age ≥ 75 years and high soluble IL-2 receptor (sIL-2R) levels above 5000 U/mL at the start of treatment. Favorable patients without these factors achieved a PFS of 11.4 months. Treatment-related adverse events were mainly hematologic but were managed over the course of treatment. Our findings indicate that tucidinostat provides survival benefits in patients with relapsed/refractory ATL in clinical practice and highlight key clinical factors for better outcomes.

    DOI: 10.1007/s12185-025-03963-9

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  • Spindle epithelial tumor with thymus-like elements (SETTLE): a surgical case diagnosed preoperatively using fine-needle aspiration cytology Reviewed

    河野 文彰, 千代反田 顕, 中目 和彦, 明利 聡瑠, 福島 剛, 佐藤 勇一郎, 山口 秀樹, 池ノ上 実, 宗像 駿, 樋口 和宏, 武野 慎祐, 七島 篤志

    Endocrinology Diabetes and Metabolism Case Reports   2025 ( 2 )   2025.5

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

    Summary
    Spindle epithelial tumor with thymic-like elements (SETTLE) is an extremely rare tumor that occurs primarily in the thyroid gland. Histologically, SETTLE is characterized by the presence of spindle-shaped epithelial cells and glandular structures. However, it is known that diagnosis via fine-needle aspiration cytology can be challenging. SETTLE predominantly occurs in younger individuals and has a less favorable prognosis compared to differentiated thyroid carcinoma. Therefore, ensuring accurate diagnosis and appropriate treatment is crucial. We encountered a case of spindle epithelial tumor with thymus-like differentiation in a 10-year-old patient for whom the preoperative diagnosis was successfully established through fine-needle aspiration cytology, which facilitated appropriate surgical resection. Comprehensive histopathological examination and immunohistochemical analysis are essential to ensure appropriate management and surveillance of SETTLE.

    Learning points
    A rare thyroid tumor, spindle epithelial tumor with thymic-like elements (SETTLE), was diagnosed preoperatively and treated surgically.

    SETTLE presents with characteristic histological features that must be recognized for accurate diagnosis. In addition, diagnosis through cytology is often challenging.

    The primary treatment for SETTLE is surgical intervention as radiotherapy and pharmacological treatments are generally not expected to be highly effective.

    Radical resection is the only effective treatment, making the selection of the surgical procedure according to the stage of the disease essential.

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Books 【 display / non-display

  • 褐色細胞腫『救急・集中治療』 31巻3号 特集「ICU治療指針」 II

    上平 雄大, 山口秀樹( Role: Contributor)

    総合医学社  2919.12 

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    Total pages:770-1277   Responsible for pages:1066-1068   Language:Japanese Book type:Textbook, survey, introduction

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  • 副甲状腺機能低下症(偽性機能低下症を含む)

    内田 泰介, 山口秀樹( Role: Contributor)

    総合医学社  2019.12 

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    Total pages:1011-1277   Responsible for pages:1047-1049   Language:Japanese Book type:Textbook, survey, introduction

  • 慢性副腎不全(ステロイド補充療法を含む)

    古郷 芙未子, 山口秀樹( Role: Contributor)

    総合医学社  2019.12 

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    Total pages:770-1277   Responsible for pages:1053-1055   Language:Japanese Book type:Textbook, survey, introduction

  • 『病気がみえるvol.3』

    山口秀樹( Role: Supervisor (editorial))

    メディックメディア  2019.10 

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    Total pages:339   Responsible for pages:276-322   Language:Japanese Book type:Textbook, survey, introduction

  • Guide book of endocrine and metabolic diaease, anterior pituitary hormones

    ( Role: Contributor)

    Shindan to Chiryousya  2018.5 

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    Total pages:761   Responsible for pages:198-202   Language:Japanese Book type:Textbook, survey, introduction

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MISC 【 display / non-display

  • A Response to Letter to the Editor: Can Imeglimin Improve the Systolic Time Intervals in Diabetes Mellitus?

    Uchida T., Ueno H., Konagata A., Taniguchi N., Kogo F., Nagatomo Y., Shimizu K., Yamaguchi H., Shimoda K.

    Diabetes Therapy   14 ( 6 )   1075 - 1076   2023.6

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    Language:English   Publishing type:Rapid communication, short report, research note, etc. (scientific journal)   Publisher:Diabetes Therapy  

    DOI: 10.1007/s13300-023-01409-1

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  • Periodic Blood Pressure Fluctuations in Undiagnosed Pheochromocytoma Reviewed

    Uehira Yudai, Yamaguchi Hideki, Matsumoto Nobuhiro, Nakazato Masamitsu

    Internal Medicine   60 ( 3 )   491 - 492   2021.2

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    Authorship:Corresponding author   Language:Japanese   Publishing type:Rapid communication, short report, research note, etc. (scientific journal)   Publisher:The Japanese Society of Internal Medicine  

    DOI: 10.2169/INTERNALMEDICINE.5034-20

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  • 頭蓋咽頭腫術後による汎下垂体機能低下症ながら副腎皮質ホルモンの補充なしで16年間にわたり日常生活可能であった1症例. Invited

    米川忠人、山口秀樹、平野秀治、中里雅光

    ACTH RELATED PEPTIDES   29   7 - 9   2018

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    Language:Japanese   Publishing type:Article, review, commentary, editorial, etc. (scientific journal)  

  • キスペプチン受容体変異と思春期遅発症 Invited

    山口秀樹、米川忠人、清水浩一郎、中里雅光

    内分泌・糖尿病・代謝内科   44 ( 1 )   50 - 56   2017.1

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    Language:Japanese   Publishing type:Article, review, commentary, editorial, etc. (scientific journal)  

  • Basedow病治療中に糖尿病性ケトアシドーシスを呈した多腺性自己免疫症候群3型の1例

    中里浩子,米川忠人,野田智穂,迫田秀之,上野浩晶,山口秀樹,中里雅光

    宮崎県医師会医学会誌   39 ( 1 )   75 - 79   2015.3

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    Language:Japanese   Publishing type:Article, review, commentary, editorial, etc. (scientific journal)   Publisher:宮崎県医師会?  

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Presentations 【 display / non-display

  • Peptidomic identification and biological validation of neuroendocrine regulatory peptide-1 and -2. International conference

    Yamaguchi H, Sasaki K, Satomi Y, Shimbara T, Kageyama H, Mondal MS, Toshinai K, Date Y, González LJ, Shioda S, Takao T, Nakazato M, Minamino N

    The Endocrine Society’s 90th Annual Meeting  (San Francisco.)  The Endocrine Society’s

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    Event date: 2008.6.15 - 2008.6.18

    Language:English   Presentation type:Oral presentation (general)  

    Venue:San Francisco.  

  • Characterization and localization of novel neuroendocrine regulatory peptides, NERP-1 and -2, in the human plasma and the hypothalamus.  International conference

    Matsuo T, Yamaguchi H, Kageyama H, Mondal MS, Sasaki K, Shioda S, Minamino N, Nakazato M

    The Endocrine Society’s 90th Annual Meeting  (San Francisco.)  The Endocrine Society’s

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    Event date: 2008.6.15 - 2008.6.18

    Language:English   Presentation type:Oral presentation (general)  

    Venue:San Francisco.  

  • 双生児を無事出産した未治療先端巨大症の一例

    松尾 崇, 山口秀樹, 土持若葉, 米川忠人, 中里雅光

    第280回日本内科学会九州地方会  (福岡)  日本内科学会九州地方会

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    Event date: 2008.1.26

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:福岡  

  • 大量デキサメサゾンで抑制されず下垂体微小腫瘤の同定が困難なクッシング病と考えられる一例.

    松尾 崇, 山口秀樹, 米川忠人, 中里雅光

    第19回間脳・下垂体副腎研究会  (東京)  間脳下・垂体副腎研究会

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    Event date: 2008.3.29

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:東京  

  • メチラポンにて二次性糖尿病が軽快した腫瘤の同定困難なクッシング病疑いの一例.

    松尾 崇, 山口秀樹, 土持若葉, 米川忠人, 中里雅光

    第81回日本内分泌学会総会  (青森)  日本内分泌学会

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    Event date: 2008.5.16 - 2008.5.18

    Language:Japanese   Presentation type:Poster presentation  

    Venue:青森  

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Awards 【 display / non-display

  • 第1回日本心血管内分泌代謝学会 若手研究奨励賞

    1997.12   日本心血管内分泌代謝学会  

    山口 秀樹

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    Award type:Award from Japanese society, conference, symposium, etc.  Country:Japan

Grant-in-Aid for Scientific Research 【 display / non-display

  • 新規グラニン由来ペプチドNERP-4の摂食エネルギー・糖代謝機能の検討

    Grant number:15K09439  2015.04 - 2018.03

    科学研究費補助金  基盤研究(C)

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    Authorship:Principal investigator 

    新規に同定したグラニン由来ペプチドNERP-4の摂食エネルギー・糖代謝機能の検討を行う

  • 新規ペプチドNERPおよび新規グラニン由来ペプチドのインスリン分泌制御機能の探索

    Grant number:23591358  2011.05 - 2014.03

    科学研究費補助金  基盤研究(C)

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    Authorship:Principal investigator 

    分泌性ペプチドの網羅的解析にて新たな生理活性ペプチドNERP (NeuroEndocrine Regulatory Peptide, J Biol Chem, 2007)の同定に成功した。中枢での機能解析で、NERP-1とNERP-2がともにバソプレシン分泌を抑制すること、NERP-2のみが摂食を亢進させることを明らかにし、5つの英文誌に報告した。末梢組織においてNERPは膵β細胞でインスリンと共存すること、MIN6細胞やマウス摘出下垂体を用いた予備実験でインスリン分泌促進作用を有することが明らかとなった(未投稿)。NERPの膵作用機構の解明と、網羅的ペプチド解析時に同定したNERP以外のグラニン由来候補ペプチドのインスリン分泌促進活性の探索を行い、生体内分子を利用した新たな糖尿病治療法の開発研究を実施する。

 

Committee Memberships 【 display / non-display

  • 日本内分泌学会   教育責任者  

    2010.12   

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    Committee type:学協会

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  • 日本内分泌学会   評議員  

    2005.9   

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    Committee type:学協会

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Social Activities 【 display / non-display

  • 糖尿病フェスティバル ボランティア

    Role(s): Appearance

    2025.11.2

  • 糖尿病週間での無料検診

    2005.11 - Now

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    糖尿病週間での宮崎県無料検診に参加している。

  • 糖尿病サマーキャンプへの参加

    2003.7 - 2008.7

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    小中高生の糖尿病患者さんを対象としたサマーキャンプにボランティアで参加している。