Cerebral venous sinus thrombosis in the patient with multiple sclerosis associated with congenital antithrombin deficiency
Author:
Affiliation:
1. Department of Neurology, and Department of Radiology, Brain Attack Center Ota Memorial Hospital
2. Toyama University Hospital Clinical Laboratory
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/56/4/56_cn-000796/_pdf
Reference20 articles.
1. 1) Compston A, Coles A. Multiple sclerosis. Lancet 2008;372:1502-1517.
2. 2) Nylander A, Hafler DA. Multiple sclerosis. J Clin Invest 2012;122:1180-1188.
3. 3) Ciccarelli O, Barkhof F, Bodini B, et al. Pathogenesis of multiple sclerosis: insights from molecular and metabolic imaging. Lancet Neurol 2014;13:807-822.
4. 6) Nakahara Y, Tsuji H, Nakagawa K, et al. Genetic analysis in Japanese kindreds of congenital type 1 antithrombin deficiency causing thrombosis. Thromb Haemost 1997;77:616-619.
5. 7) Chowdhury V, Olds RJ, Lane DA, et al. Identification of nine novel mutations in type I antithrombin deficiency by heteroduplex screening. Br J Haematol 1993;84:656-661.
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2. Endovascular therapy for recurrent cerebral venous sinus thrombosis associated with congenital antithrombin deficiency;Japanese Journal of Stroke;2022
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