Search Results - "喜田裕介"
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LOO1-42. 病理学的N0M0肺腺癌の予後規定因子の解析
Published in General Thoracic and Cardiovascular Surgery (2020)Get full text
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P19-10. 続発性気胸術後死亡症例の検討
Published in General Thoracic and Cardiovascular Surgery (2019)Get full text
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1P2肺P4-3. 当院での肺癌術後気管支断端瘻の発症リスクに関する検討
Published in General Thoracic and Cardiovascular Surgery (2018)Get full text
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4
PL-032 術式・アプローチの違いによる肺癌術後ドレーン管理の現状と成績
Published in General Thoracic and Cardiovascular Surgery (2017)Get full text
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5
PL-200 病理学的N1非小細胞肺癌切除例の臨床的検討
Published in General Thoracic and Cardiovascular Surgery (2017)Get full text
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1P1肺P1-5. 術前療法を施行したcN2 (8版) 非小細胞肺癌 (NSCLC) 切除例に対する検討
Published in General Thoracic and Cardiovascular Surgery (2018)Get full text
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PL-003 当科におけるsalvage operation症例の検討 ; 診断確定時手術非適応例の外科治療について
Published in General Thoracic and Cardiovascular Surgery (2016)Get full text
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PL-021 人工心肺下に左房合併切除を施行した左肺下葉転移性肺腫瘍の1例
Published in General Thoracic and Cardiovascular Surgery (2016)Get full text
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DL-12 赤外光胸腔鏡を用いた区域間面の切離法
Published in General Thoracic and Cardiovascular Surgery (2015)Get full text
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PL-087 胸腺上皮性腫瘍に対する治療成績と治療戦略
Published in General Thoracic and Cardiovascular Surgery (2015)Get full text
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VL-11 腫瘍浸潤により上大静脈症候群を合併した胸腺癌に対し, 術前導入療法後に血行再建を行わない上大静脈合併切除を施行した1例
Published in General Thoracic and Cardiovascular Surgery (2014)Get full text
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PL-088 肺葉別にみた術後難治性肺瘻の発生頻度についての検討
Published in General Thoracic and Cardiovascular Surgery (2014)Get full text
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VL-21 左主気管支腺様嚢胞癌に対してautograftを用いて気道再建を行ったsleeve pneumonectomyの一例
Published in General Thoracic and Cardiovascular Surgery (2014)Get full text
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14
OL10-06 残存肺全摘術の安全性に関する検討
Published in General Thoracic and Cardiovascular Surgery (10-09-2012)Get full text
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OL10-04 局所進行非小細胞肺癌に対する導入治療の効果を予測する, 循環腫瘍細胞を用いた新しい手法
Published in General Thoracic and Cardiovascular Surgery (10-09-2012)Get full text
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16
Inhibition of Cell-surface Molecular GPR87 With GPR87-suppressing Adenoviral Vector Disturb Tumor Proliferation in Lung Cancer Cells
Published in Anticancer research (01-02-2020)“…GPR87 is a member of the cell surface molecular G protein-coupled receptors (GPCR) family and suggested to contribute to the viability of human tumor cells…”
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