²Î¿¼ÎÄÏ×/References:
[1] Spring J,Spies M.Myasthenia gravis: options and timing of immunomodulatory treatment[J].BioDrugs,2001,15(3):173-183.
[2] Sathasivam Sivakumar.Steroids and immunosuppressant drugs in myasthenia gravis[J].Nat Clin Pract Neurol,2008,4(6):317-327.
[3] ÖлªÒ½Ñ§»áÉñ¾²¡Ñ§·Ö»áÉñ¾ÃâÒßѧ×é.ÖйúÃâÒßѧ»áÉñ¾ÃâÒßѧ·Ö»á.ÖйúÖØÖ¢¼¡ÎÞÁ¦Õï¶ÏºÍÖÎÁÆÖ¸ÄÏ[J].ÖлªÉñ¾¿ÆÔÓÖ¾,2015,3(2):934.
[4] ÀîÖùÒ»,ÕÅκ.ÖйúÖØÖ¢¼¡ÎÞÁ¦Õï¶ÏºÍÖÎÁÆר¼Ò¹²Ê¶[J].ÖйúÉñ¾ÃâÒßѧºÍÉñ¾²¡Ñ§ÔÓÖ¾,2011,18(5):368-372.
[5] ÐíÏͺÀ.¼¡ÎÞÁ¦¡ªÁÙ´²Óë»ù´¡[M].±±¾©:ÖйúкÍÒ½¿Æ´óѧ³ö°æÉç,2003:24.
[6] Saida K.Treatment of neuro-immunologic diseases by immunosuppressants[J].Nihon Rinsho,1994,52(11):3046-3052.
[7] Debono Miguel,Ghobadi Cyrus,Rostami-Hodjegan Amin,et al.Modified-release hydrocortisone to provide circadian cortisol profiles[J].J Clin Endocrinol Metab,2009,94(5):1548-1554.
[8] Utsugisawa Kimiaki,Nagane Yuriko.Therapeutic strategies against myasthenia gravis[J].Nihon Rinsho,2013,71(5):881-886.
[9] Anlar Banu,Senbil Nesrin,Köse Gül ÿðþ ‰D en,et al.Serological follow-up in juvenile myasthenia: clinical and acetylcholine receptor antibody status of patients followed for at least 2 years[J].Neuromuscul Disord,2005,15(5):355-357.
[10] Hirano.T-The biology of interleukin-6[J].Chem fmmunol,1992,9(4):153.
[11] Matusevicuis D,Navikas V,Palasik W,et al.Tumornecrosis factor-alpha,lymphotoxin,interleukin[J].-6,IL-10,IL-12 and perforin mRNA expression in monouclearcells in responsetoacety lcholinereceptoris augmented in myasthenia gravis¡²J¡³.Neuroimmunol,1996,71(1):191-193.
[12] ãÆÏþ²¨,ÍõάÖÎ,º«Íþ.ÖØÖ¢¼¡ÎÞÁ¦cICAM-1¼°TNF-¦ÁˮƽµÄ¼ì²â[J].ÖйúÉñ¾ÃâÒßѧºÍÉñ¾²¡Ñ§ÔÓÖ¾,2002,9(2):79-81.
[13] Deren H,Ritva PS.Tumo r necr osis factor-¦Á polymorphism and secretion in myasthenia gravis[J].J Neuroimmunol,1999,94(8):165-171.
[14] ÀµÏéÇà,ÑîÃ÷ɽ,Ðì½ðÖ¦,µÈ.ÖØÖ¢¼¡ÎÞÁ¦»¼ÕßÃâÒß·¢²¡»úÖƵÄÑо¿[J].Öйú²¡ÀíÉúÀíÔÓÖ¾,2001,17(7):662-664.