[1] 邵冰,楚兰,徐竹,等.极后区综合征在视神经脊髓炎谱系疾病中的研究进展[J].临床神经病学杂志,2017,(5):385-388.
[2] WINGERCHUK D M, BANWELL B, BENNETT J L, et al. International consensus diagnostic criteria for neuromyelitis optica spectrum disorders[J]. Neurology, 2015, 85(2):177-189.
[3] PITTOCK S J, LUCCHINETTI C F. Neuromyelitis optica and the evolving spectrum of autoimmune aquaporin-4 channelopathies: a decade later[J]. Ann N Y Acad Sci, 2016, 1366(1):20-39.
[4] 中国免疫学会神经免疫学分会.中国视神经脊髓炎谱系疾病诊断与治疗指南[J].中国神经免疫学和神经病学杂志,2016,23(3):155-166.
[5] APIWATTANAKUL M , POPESCU B F,MATIELLO M, et al. Intractable vomiting as the initial presentation of neuromyelitis optica[J]. Ann Neurol, 2010, 68(5):757-761.
[6] PRICE C J, HOVDA T D, FERGUSON A V. The Area Postrema: A Brain Monitor and Integrator of Systemic Autonomic State[J]. Neuroscientist, 2008, 14(2):182-94.
[7] IORIO R, PLANTONE D, DAMATO V, et al. Anorexia Heralding the Onset of Neuromyelitis Optica[J]. Intern Med, 2013, 52(4):489-91.
[8] KREMER L, MEALY M, JACOB A, et al. Brainstem manifestations in neuromyelitis optica: a multicenter study of 258 patients[J]. Mult Scler, 201, 20(7):843-847.
[9] 马文巧,杨丽娜,赵宁,等.以最后区综合征为首发症状的视神经脊髓炎谱系疾病8例临床分析[J].中国神经免疫学和神经病学杂志,2016,23(3):71-73.
[10] WINGERCHUK D M , WEINSHENKER B G . The emerging relationship between neuromyelitis optica and systemic rheumatologic autoimmune disease[J]. Multiple Sclerosis, 2012, 18(1):5-10.
[11] WU L, HUANG D, YANG Y, et al. Combined screening for serum anti-nuclear and anti-aquaporin-4 antibodies improves diagnostic accuracy for distinguishing neuromyelitis optica from multiple sclerosis.[J]. European Neurology, 2014, 72(1-2):103-108.
[12] HONGYANG L , YAN Z , ZUOHUIZI Y , et al. Frequency of Autoantibodies and Connective Tissue Diseases in Chinese Patients with Optic Neuritis[J]. PLoS ONE, 2014, 9(6):e99323. |
