@article{oai:niigata-u.repo.nii.ac.jp:00022184,
 author = {根本, 啓一 and 本間, 慶一 and 大西, 義久 and 小池, 正 and 柴田, 昭},
 issue = {7},
 journal = {新潟医学会雑誌, 新潟医学会雑誌},
 month = {Jul},
 note = {Clinical and morphological findings are described in 44 patients with myelofibrosis. Idiopathic myelofibrosis was subclassified into three types: acute, chronic and intermediate type. Acute myelofibrosis (AMF) presented with the following clinical characteristics: pancytopenia, fibrotic bone marrow, abscence of a splenomegaly and rapidly fatal course. However, we concluded that it was heterogenous disorder including myelodysplastic syndrome, acute megakaryoblastic leukemia, erythroleukemia, strict case of AMF and so on. Association between megakaryocytic proliferation and myelofibrosis was suggested in several cases.},
 pages = {605--613},
 title = {骨髄線維症の臨床と病理（第20回新潟造血器腫瘍研究会十周年記念シンポジウム : 造血器腫瘍十年の歩み）},
 volume = {104},
 year = {1990}
}