参考文献/References:
[1] Fang BY,McKeon A,Hinson SR,et al.Autoimmune glial fibrillary acidic protein astrocytopathy: a novel meningoencephalomyelitis[J].JAMA Neurol,2016,73(11):1297-1307.
[2] Flanagan EP,Hinson SR,Lennon VA,et al.Glial fibrillary acidic protein immunoglobulin G as biomarker of autoimmune astrocytopathy: analysis of 102 patients[J].Ann Neurol,2017,81(2):298-309.
[3] Iorio R,Damato V,Evoli A,et al.Clinical and immunological characteristics of the spectrum of GFAP autoimmunity: a case series of 22 patients[J].J Neurol Neurosurg Psychiatry,2018,89(2):138-146.
[4] Long Y,Liang J,Xu H,et al.Autoimmune glial fibrillary acidic protein astrocytopathy in Chinese patients: a retrospective study[J].Eur J Neurol,2018,25(3):477-483.
[5] Dubey D,Hinson SR,Jolliffe EA,et al.Autoimmune GFAP astrocytopathy: prospective evaluation of 90 patients in 1 year[J].J Neuroimmunol,2018,321:157-163.
[6] Kimura A,Takekoshi A,Yoshikura N,et al.Clinical characteristics of autoimmune GFAP astrocytopathy[J].J Neuroimmunol,2019,332:91-98.
[7] Luessi F,Engel S,Spreer A,et al.GFAPα IgG-associated encephalitis upon daclizumab treatment of MS[J].Neurol Neuroimmunol Neuroinflamm,2018,5(5):e481.
[8] Oger V,Bost C,Salah L,et al.Mild encephalitis/encephalopathy with reversible splenial lesion syndrome: an unusual presentation of anti-GFAP astrocytopathy[J].Eur J Paediatr Neurol,2020,26:89-91.
[9] Li XL,Han JM,Zhao HT,et al.Autoimmune glial fibrillary acidic protein astrocytopathy with lesions distributed predominantly in the entire spinal cord[J].Ther Adv Neurol Disord,2020,13:1756286420909973.
[10] Héraud C,Capet N,Levraut M,et al.Glial fibrillary acidic protein(GFAP)astrocytopathy presenting as mild encephalopathy with reversible splenium lesion[J].Neurology and Therapy,2022,11(1):499-505.
[11] Gao X,Tang Y,Yang GD,et al.Autoimmune glial fibrillary acidic protein astrocytopathy associated with area postrema syndrome: a case report[J].Front Neurol,2021,12:803116.
[12] Fang HJ,Hu WJ,Jiang Z,et al.Autoimmune glial fibrillary acidic protein astrocytopathy in children: a retrospective analysis of 35 cases[J].Front Immunol,2021,12:761354.
[13] Handoko M,Hong W,Espineli E,et al.Autoimmune glial fibrillary acidic protein astrocytopathy following herpes simplex virus encephalitis in a pediatric patient[J].Pediatr Neurol,2019,98:85-86.
[14] Yang X,Zhang CY,Zhang J,et al.Autoimmune glial fibrillary acidic protein astrocytopathy mimics infectious meningitis: Two case reports[J].Mult Scler Relat Disord,2020,45:102350.
[15] Ip B,Lam C,Ip V,et al.Autoimmune glial fibillary acidic protein astrocytopathy associated meningoencephalomyelitis and bilateral sensorineuronal deafness[J].Mult Scler Relat Disord,2020,40:101922.
[16] Wang H,Chin JH,Fang BY,et al.Autoimmune glial fibrillary acidic protein astrocytopathy manifesting as subacute meningoencephalitis with descending myelitis: a case report[J].BMC Neurol,2020,20(1):443.
[17] Lin H,Huang YH,Zeng HZ,et al.Overlapping clinical syndromes in patients with glial fibrillary acidic protein IgG[J].Neuroimmunomodulation,2020,27(1):69-74.
[18] 梁奇明,许峰,张萍,等.自身免疫性胶质纤维酸性蛋白星形细胞病的临床特征分析[J].华中科技大学学报(医学版),2021,50(5):620-625.
[19] Equiza J,Rodríguez-Antigüedad J,Campo-Caballero D,et al.Autoimmune GFAP astrocytopathy presenting with remarkable CNS hyperexcitability and oculogyric crises[J].J Neuroimmunol,2021,359:577695.
[20] Sava �瘙 塂 M,Tzartos J,Küçükali CI,et al.Glial fibrillary acidic protein(GFAP)-antibody in children with focal seizures of undetermined cause[J].Acta Neurol Belg,2021,121(5):1275-1280.
[21] Wickel J,Chung HY,Kirchhof K,et al.Encephalitis with radial perivascular emphasis: not necessarily associated with GFAP antibodies[J].Neurol Neuroimmunol Neuroinflamm,2020,7(2):e670.
[22] Huang HX,Bai K,Fu YQ,et al.Glial fibrillary acidic protein astrocytopathy in pediatric patients: a retrospective study[J].Front Pediatr,2020,8:626564.
[23] Sechi E,Flanagan EP.Area postrema syndrome in autoimmune GFAP astrocytopathy[J].Mult Scler,2020,26(2):255-256.
[24] Papa A,Tzartos JS,Sakoutis G,et al.Black holes and high levels of neurofilaments in glial fibrillary acidic protein - astrocytopathy: a case report[J].Eur J Neurol,2020,27(11):2381-2384.
[25] Zhou ZH,Yu QY,Hong MF.Autoimmune glial fibrillary acidic protein astrocytopathy with the detection of Anti-GM3 and Anti-GM4 IgG antibodies, masquerading as Brown-Sequared syndrome[J].JAMA Neurol,2021,78(1):115-116.
[26] Luo Y,Yan W,Zhou ZY,et al.Elevated levels of NLRP3 in cerebrospinal fluid of patients with autoimmune GFAP astrocytopathy[J].Front Neurol,2019,10:1019.
[27] Kudo T,Kimura A,Higashida K,et al.Autoimmune glial fibrillary acidic protein astrocytopathy presenting with slowly progressive myelitis and longitudinally extensive spinal cord lesions[J].Intern Med,2020,59(21):2777-2781.
[28] Kimura A,Takemura M,Yamamoto Y,et al.Cytokines and biological markers in autoimmune GFAP astrocytopathy: the potential role for pathogenesis and therapeutic implications[J].J Neuroimmunol,2019,334:576999.
[29] Tanaka R,Nukui TKM,Haryuni RD,et al.Radial linear perivascular emphasis in coronavirus disease 2019-associated acute disseminated encephalomyelitis[J].Clin Exp Neuroimmunol,2021,12(4):281-282.
[30] Shu YQ,Long YM,Chang YY,et al.Brain immunohistopathology in a patient with autoimmune glial fibrillary acidic protein astrocytopathy[J].Neuroimmunomodulation,2018,25(1):1-6.
[31] Tokimura R,Matsuda N,Kobayashi S,et al.Abnormal evoked potentials in autoimmune glial fibrillary acidic protein astrocytopathy[J].eNeurologicalSci,2020,18:100229.
[32] 叶锦龙,张伟劲,龙友明,等.以中枢系统炎症为主要表现的14例自身免疫性胶质纤维酸性蛋白星形细胞病患者的临床特征分析[J].中风与神经疾病杂志,2020,37(12):1101-1104.
[33] 袁泉,谭淑慧.胶质纤维酸性蛋白星型细胞病的病例特点[J].中风与神经疾病杂志,2021,38(6):501-504.
[34] 李小晶,彭炳蔚,侯池,等.以脑膜炎起病的儿童自身免疫性胶质纤维酸性蛋白星形胶质细胞病一例[J].中华儿科杂志,2019,57(11):882-884.
[35] 徐辉明,黄清梅,肖小玉,等.自身免疫性胶质纤维酸性蛋白星形细胞病患者脊髓磁共振成像及临床特征分析[J].中华神经科杂志,2019,52(2):92-97.
[36] 郭昆典,洪桢.4例自身免疫性胶质纤维酸性蛋白星形胶质细胞病的临床特征分析[J].中国神经免疫学和神经病学杂志,2021,28(3):204-208.
[37] 王华.儿童自身免疫性胶质纤维酸性蛋白星形细胞病[J].中国小儿急救医学,2021,28(6):458-461.
[38] Li XJ,Peng BW,Hou C,et al.A child of autoimmune glial fibrillary acidic protein astrocytopathy who had onset with meningitis[J].Zhonghua Er Ke Za Zhi,2019,57(11):882-884.
[39] Yang XG,Liang JY,Huang QM,et al.Treatment of autoimmune glial fibrillary acidic protein astrocytopathy: follow-Up in 7 cases[J].Neuroimmunomodulation,2017,24(2):113-119.
[40] Di H,Yin Y,Chen RX,et al.Uncommon manifestations of a rare disease: a case of autoimmune GFAP astrocytopathy[J].BMC Neurol,2021,21(1):37.
[41] Ji SQ,Liu CC,Bi ZJ,et al.Overlapping syndrome mimicking infectious meningoencephalitis in a patient with MOG and GFAP IgG[J].BMC Neurol,2021,21(1):348.
[42] Tomczak A,Su E,Tugizova M,et al. A case of GFAP-astroglial autoimmunity presenting with reversible parkinsonism[Z], 2019: 101900.
[43] Kunchok A,Zekeridou A,McKeon A.Autoimmune glial fibrillary acidic protein astrocytopathy[J].Curr Opin Neurol,2019,32(3):452-458.
[44] Ding JQ,Ren KX,Wu J,et al.Overlapping syndrome of MOG-IgG-associated disease and autoimmune GFAP astrocytopathy[J].J Neurol,2020,267(9):2589-2593.
[45] Huang QM,Yang HC,Liu TN,et al.Patients with suspected benign tumors and glial fibrillary acidic protein autoantibody: an analysis of five cases[J].Int J Neurosci,2019,129(12):1183-1188.