@article{oai:u-ryukyu.repo.nii.ac.jp:02016283,
 author = {大浦, 孝 and 河上, 好秀 and 本多, 幸博 and 竹田, 亮祐 and Oura, Takashi and Kawakami, Yoshihide and Honda, Yukihiro and Takeda, Ryoyu},
 issue = {1},
 journal = {琉球大学保健学医学雑誌＝Ryukyu University Journal of Health Sciences and Medicine},
 note = {We reported a typical case of Neuro-Behcet Syndrome whose clinical course was relatively slow extending over about 15 years. The patient, a 39-year-old male, showed the initial symptom of a mucocutaneous lesion. He complained of visual disturbances after one year and then became blind. This case presented a great variety of symptomes and signs of the central nervous system such as facial paralysis, pyramidal tract-involvement, cerebellar signs, pseudobulbar palsy, euphoria and the inability to learn. These symptoms and signs suggested lesions extending widely from the cerebrum to the brain stem. Laboratory data were not particular except ESR acceleration, but the cell count and the protein volume showed a slight increase in the cerebrospinal fuild., 論文},
 pages = {75--80},
 title = {[原著]Neuro-Behcet 症候群の1例},
 volume = {4}
}