@article{oai:u-ryukyu.repo.nii.ac.jp:02015760,
 author = {上原, 正照 and 佐久川, 廣 and 川木, 忠仁 and 下地, 克佳 and 嘉手納, 啓三 and 金城, 福則 and 浦崎, 政仁 and 安座間, 聡 and 小張一峰 and Uehara, Masaaki and Sakugawa, Hiroshi and Kawaki, Tadahito and Shimoji, Katsuyoshi and Kadena, Keizo and Kinjo, Fukunori and Urasaki, Masahito and Azama, Satoshi and Kobari, Kazumine},
 issue = {1},
 journal = {琉球大学医学会雑誌 : 医学部紀要 = Ryukyu medical journal},
 month = {},
 note = {Sarcoidosis is a multisystem granulomatous disorder of unknown etiology involving various organs. Hilar adenopathy, pulmonary parenchymal infiltration and skin or eye lesions are the most common presentations, and also in liver granuloms are frequently found. However, usually no evidence of hepatic cellular dysfunction is observed in the beginning of the disease. In the paper it was reported that three cases of sarcoidosis revealed the clinical manifestation of liver dysfunction, ascites and other sings of portal hypertension, and these symtoms could be clues of the diagnosis of sarcoidosis., 論文},
 pages = {64--74},
 title = {[症例報告]肝サルコイドーシス3例についての検討},
 volume = {9},
 year = {1986}
}