@article{oai:kanazawa-u.repo.nii.ac.jp:00031022,
 author = {Mabuchi, Kazunori and Yoshikawa, Hiroaki and Takamori, Masaharu and Yokoji, Hidehiro and Takahira, Masayuki},
 issue = {4},
 journal = {Journal of Neurology Neurosurgery and Psychiatry},
 month = {Oct},
 note = {A pseudo-Argyll Robertson pupil is a neurological sign indicating a normal near reflex but the absence of a light reflex (light-near dissociation), a lack of miosis, and pupil irregularity. It has been reported in patients with diabetes mellitus, multiple sclerosis, Wernicke's encephalopathy, sarcoidosis, tumours, and haemorrhage.1 Although the appearance of pseudo-Argyll Robertson pupil is very similar to Holmes-Adie pupil, the first is distinguishable from the second by the location of lesions and pharmacological response. The responsible lesion in pseudo-Argyll Robertson pupil is in the central region, whereas that of Holmes-Adie pupil is peripheral. Dilute pilocarpine constricts the pupils of patients with Holmes-Adie pupil, but it is not effective in patients with pseudo-Argyll Robertson pupil. We present a patient with spinocerebellar ataxia type 1 (SCA1) and her asymptomatic younger brother who both exhibited pseudo-Argyll Robertson pupil., 金沢大学保健管理センター},
 pages = {612--613},
 title = {Pseudo-Argyll Robertson pupil of patients with spinocerebellar ataxia type 1 (SCA1)},
 volume = {65},
 year = {1998}
}