A case of neuromyelitis optica presenting marked pleocytosis and hypoglycorrhachia
Author:
Affiliation:
1. Section of Neurology, Sapporo Kosei General Hospital
2. Department of Neurology, Sapporo Medical University School of Medicine
Publisher
Societas Neurologica Japonica
Subject
Clinical Neurology
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/56/8/56_cn-000753/_pdf
Reference5 articles.
1. 1) Brettschneider J, Claus A, Kassubek J, et al. Isolated blood-cerebrospinal fluid barrier dysfunction: prevalence and associated diseases. J Neurol 2005;252:1067-1073.
2. 2) Lepur D, Peterkovìć V, Kalabrić-Lepur N. Neuromyelitis optica with CSF examination mimicking bacterial meningomyelitis. Neurol Sci 2009;30:51-54.
3. 3) Meireles M, Martel F, Araújo J, et al. Characterization and modulation of glucose uptake in a human blood-brain barrier model. J Membrane Biol 2013;246:669-677.
4. 4) Maher F, Vannucci SJ, Simpson IA. Glucose transporter proteins in brain. FASEB J 1994;8:1003-1011.
5. 6) Cayrol R, Saikali P, Vincent T. Effector functions of antiaquaporin-4 autoantibodies in neuromyelitis optica. Ann N Y Acad Sci 2009;1173:478-486.
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