藤村 博信 ふじむら ひろのぶ 先生

来歴等

略歴

1988年 大阪大学医学部 卒業
1998年 医学博士 取得
2006年 市立豊中病院 心臓血管外科 部長

論文

• The incidence of activated protein C resistance among patients with deep vein thrombosis and health subjects in Osaka. Thromb Res 79, 227-9, 1995

  Kambayashi J, Fujimura H, Kawasaki T, Sakon M, Monden M, Suehisa E, Amino N

• Coagulation factor V Leiden mutation may have a racial background. Thromb Haemost 74, 859-60, 1995

  Fujimura H, Kambayashi J, Monden M, Kato H, Miyata T

• Genetic characterization of protein C deficiency in Japanese subjects using a rapid and nonradioactive method for single-strand conformational polymorphism analysis and a model building. Thromb Haemost 76, 302-11, 1996

  Miyata T, Sakata T, Zheng YZ, Tsukamoto H, Umeyama H, Uchiyama S, Ikusaka M, Yoshioka A, Imanaka Y, Fujimura H, Kambayashi J, Kato H

• Diagnositic value of plasma thrombin-antithrombin III complex and D-dimer concentration in patients with varicose veins for exclusion of deep-vein thrombosis. Thromb Res 91, 101-4, 1998

  Kawasaki T, Shinoki N, Iwamoto S, Fujimura H, Yoshikawa N, Ohta Y, Ikeda M, Ariyoshi H, Shibuya T, Monden M

• C-399T polymorphism in the promoter region of human tissue factor pathway inhibitor(TFPI) gene does not change the plasma TFPI antigen level and does not cause venous thrombosis. Thromb Haemost 80, 345-6, 1998

  Miyata T, Sakata T, Kumeda K, Uchida K, Tsushima M, Fujimura H, Kawasaki T, Kato H

• The prothrombin gene G20210A mutation is not found among Japanese patients with deep vein thrombosis and healthy individuals. Blood Coagul Fibrinolysis 9, 451-2, 1998.

  Miyata T, Kawasaki T, Fujimura H, Uchida K, Tsushima M, Kato H

• Platelet glycoprotein IIIa Pl(A) polymorphism and Japanese patients with venous thrombosis. Blood Coagul Fibrinolysis 9, 449-50, 1998.

  Fujimura H, Kawasaki T, Kambayashi J, Kato H, Monden M, Miyata T

• Three novel missense mutations in unrelated Japanese patients with type I and type II protein S deficiency and venous thrombosis. Thromb Res 89, 151-60, 1998.

  Fujimura H, Kambayashi J, Kato H, Sakon M, Kawasaki T, Ariyoshi H, Suehisa E, Monden M, Miyata T

• Is there a role for genetic polymorphism of C677T methylenetetrahydrofolate reductase(MTHFR) in burger’s disease? Thromb Haemost 84, 736-37, 2000.

  Kawasaki T, Fujimura H, Kakinori E, Uemichi A, Miyata T

• Common C677T methylenetetrahydrofolate reductase gene increases the risk for deep vein thrombosis in patients with predisposition of thrombophilia. Thrombos Res 98, 1-18, 2000.

  Fujimura H, Kawasaki T, Sakata T, Ariyoshi H, Kato H, Monden M, Miyata T

• Vascular endotheial cells synthesize and secrete brain-derived neurotropic factor. FEBS Lett 24, 113-7, 2000

  Nakahashi T, Fujimura H, Altar CA, Li J, Kambayashi J, Tandon NN

• 遺伝子欠損と血栓症．血液アゴラ　7，96-102，2000．

  宮田敏行、加藤久雄、阪田敏幸、片山善章、川崎富夫、藤村博信

• Brain-derived neurotrophic factor is stored in human platelets and released by agonist stimulation. Thromb Haemost 87, 728-734, 2002

  Fujimura H, Altar CA, Chen R, Nakamura T, Nakahashi T, Kambayashi J, Sun B, Tandon NN

• ワーファリン投与中止後の凝固能異常と心臓血管外科手術時の出血．血栓止血誌　13, 87-88, 2002．

  藤村博信

• Mobilization of the posterior leaflet of the mitral valve for resection of a left ventricular tumor producing carbohydrate antigen 19-9. Jpn J Thorac Cardiovasc Surg 51, 466-68, 2003．

  Yamauchi T, Sakakibara T, Takano H, Fujimura H, and Suhara H

• 閉塞性動脈硬化症患者における併存冠動脈疾患とその治療に関する検討．診療と新薬　42，49-50，2005．

  藤村博信、正井崇史、永井義幸、笹子佳門

• 人工膝関節置換術後リハビリ中に発症した膝窩動脈仮性動脈瘤破裂の1例．日本血管外科学会雑誌18巻4号495-498．

  藤村博信、黒瀬公啓、只腰雅夫．

• Klippel-Trenaunay症候群に対して外側辺縁静脈の結紮切除術を行った1例．臨床外科64巻7号1003-1005．

  藤村博信、黒瀬公啓．

• Radiation arteritisと考えられる放射線照射後に発症した腸骨動脈閉塞に対する血行再建の経験．日本血管外科学会雑誌18巻6号641-645．

  藤村博信、黒瀬公啓．

• さまざまな症状にて発症した膝窩動脈瘤6例7肢の治療経験．日本血管外科学会雑誌2010；19：573-577

  藤村博信、黒瀬公啓

• 下肢静脈瘤として紹介された血管平滑筋腫の1治験例．静脈学2010；21：277-280

  黒瀬公啓、藤村博信

• Opera MasterTM(HOGY Medical®)を用いた下肢静脈瘤手術に対する収支計算．静脈学　2011；22：315-319

  藤村博信、黒瀬公啓