重症肌无力
上QQ阅读APP看书,第一时间看更新

参考文献

吴卫平.重症肌无力//蒲传强,吴卫平,郎森阳.神经系统感染免疫学.北京:科学出版社,2003:449-452.
许贤豪.重症肌无力//匡培根.神经系统疾病药物治疗学.北京:人民卫生出版社,2008:877-892.
刘卫彬,夏强,门丽娜,等.以声带麻痹为突出表现的重症肌无力7例.中华医学杂志,2006,86(25):1778-1780.
刘卫彬,门丽娜,何雪桃,等.我国南方1520例重症肌无力患者的临床特点.中国神经免疫学和神经病学杂志,2006,13(6):326-330.
刘卫彬,丰岩清,曾樱,等.伴耳鸣和听力下降的重症肌无力:附7例报告.中国神经精神疾病杂志,2006,32(5):461-463.
刘卫彬,门丽娜,夏强,等.疑难病例析评第91例味觉丧失-排便困难-复视-呼吸困难.中华医学杂志,2005,85(46):3301-3303.
欧昶毅,刘卫彬,冯慧宇,等.重症肌无力伴发特发性甲状旁腺功能减退症二例.中国神经免疫学和神经病学杂志,2011,18(5):377-378.
邱力刘卫彬.眼睑下垂-吞咽困难-肢体震颤--行走困难(疑难病例析评).中华医学杂志,2013,93(27):2170-2173.
Aragonés,JM,Bolíbar I,Bonfill X,et al.Myasthenia Gravis.A higher than expected incidence in the elderly.Neurology,2003,60:1024-1026.
Barnett C,Katzberg H,NabaVi M,et al.The quantitative myasthenia Gravis score:comparison with clinical,electrophysiological,and laboratory markers.J Clin Neuromuscul Dis,2012,13(4):201-205.
Chan KH,Cheung RT,Mak W,et al.Nonthymoma early-onset-and late-onset-generalized myasthenia Gravis--a retrospective hospital-based study.Clin Neurol Neurosurg,2007,109(8):686-691.
Christensen PB.Associated autoimmune disease in myasthenia Gravis.A population-based study.Acta Neurol Scand,1995,91:192-195.
EVoli A,Minisci C,Di Schino C,et al.Thymoma in patients with MG:characteristics and longterm outcome.Neurology,2002,59:1844-1850.
Ropper AH,Samuels MA.Other somatic sensation.//Ropper AH,Samuels MA.Adams and Victor’s Principles of Neurology.9th ed.New York:McGraw-Hill Medical,2009.
Grob D,Brunner N,Namba T,et al.Lifetime course of myasthenia Gravis.Muscle Nerve,2008,37:141-149.
Huang X,Liu WB,Men LN,et al.Clinical features of myasthenia gravis in southern China:a retrospective review of 2,154cases over 22years.Neurol Sci,2013,34(6):911-917.
Kuks J B.M.Clinical Presentation and Epidemiology of Myasthenia Gravis.Current Clinical Neurology,Myasthenia Gravis and Related Disorders,79-94.Kaminski HJ,Humana Press,New York,2009.
Kabasawa C,Shimizu Y,Suzuki S,et al.Taste disorders in myasthenia Gravis:a multicenter cooperative study.Eur J Neurol,2012,31:1468
Masuda T,Motomura M,Utsugisawa K,et al.Antibodies against the main immunogenic region of the acetylcholine receptor correlate with disease severity in myasthenia gravis. Journal of Neurology,Neurosurgery &Psychiatry,2012,83(9):935-940.
McGrogan A,Sneddon S,de Vries CS.The incidence of myasthenia Gravis:a systematic literature review.Neuroepidemiology,2010,34(3):171-183.
Meriggioli MN,Sanders DB.Autoimmune myasthenia Gravis:emerging clinical and biological heterogeneity.Lancet Neurol,2009,8(5):475-490.
Mygland A,Aarli JA,Matre R,et al.Ryanodine receptor antibodies related to severity of thymoma associated myasthenia Gravis.J Neurol Neurosurg Psychiatry,1994,57(7):843-846.
Niks EH,Kuks JBM,Verschuuren JJGM.Epidemiology of myasthenia Gravis with anti-muscle specific kinase antibodies in the Netherlands.J Neurol Neurosurg Psychiatry,2007,78(4):417-418.
Osserman KE.Myasthenia Gravis.New York:Grune &Stratton,1958.
Osserman KE,Genkins G.Studies in myasthenia Gravis:review of a twenty year experience in over 1200patients.Mt Sinai J Med,1971,34:497-537.
Oosterhuis HJ.The natural course of myasthenia Gravis:a long term follow up study.J Neurol Neurosurg Psychiatry,1989,52:1121-1127.
Potagas C,Dellatotas G,Tavernarakis A,et al.Myasthenia Gravis:changes observed in a 30-years retrospective clinical study of a hospital-based population.J Neurol,2004,251(1):116-117.
Pasutharnchat N,Wacharapluesadee S,Hemachudha T.Clinical manifestations of acetylcholine receptor antibody positive and negative myasthenia Gravis.J Med Assoc Thai,2012,95(3):313-319.
Rotstein DL,Bril V.A family with myasthenia Gravis with and without thymoma.Can J Neurol Sci,2012,39(4):539-540
Romi F,Skeie GO,Gilhis NE,et al.Striational antibodies in myasthenia Gravis.Arch Neurol,2005,62:442-446.
Romi F,Skeie GO,Aarli JA,et al.The severity of myasthenia Gravis correlates with the serum concentration of titin and ryanodine receptor antibodies.Arch Neurol,2000,57:1596-1600.
Romi F,Aarli JA,Gilhus NE.Myasthenia Gravis patients with ryanodine receptor antibodies have distinctive clinical features.Eur J Neurol,2007,14:617-620.
Romi F,Gilhus NE,Varhaug JE,et al.Disease severity and outcome in thymoma myasthenia:a long-term observational study.Eur J Neurol,2003,10:701-706.
Somnier FE.Increasing incidence of late-onset anti-AChR antibody-seropositive myasthenia Gravis.Neurology,2005,65:928-930.
Skeie GO,Romi F.Paraneoplastic myasthenia Gravis:immunological and clinical aspects.Eur J Neurol,2008,15:1029-1033.
Sanders DB,Juel VC.MuSK-antibody positive myasthenia Gravis:questions from the clinic.J Neuroimmunol,2008,201-202:85-89..
Task Force of the Medical Scientific Advisory Board of the Myasthenia Gravis Foundation of America,Jartezki A,Barohn RJ,et al.Myasthenia Gravis.Recommendations for clinical research standards.Neurology,2000,55:16-23
Tola MR,Caniatti LM,Casetta I,et al.Immunogenetic heterogeneity and associated autoimmune disorders in myasthenia Gravis:apopulation based survey in the province of Ferrara,northern Italy.Acta Neurol Scand,1994,90:318-323.
Zhang X,Yang M,Xu J,et al.Clinical and serological study of myasthenia Gravis in HuBei Province,China.J Neurol Neurosurg Psychiatry,2007,78:386-390.
Zivkovi SA,Clemens PR,Lacomis D.Characteristics of late-onset myasthenia Gravis.J Neurol,2012,259(10):2167-2171.