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Volumn 71, Issue 24, 2008, Pages 2010-2012

Fetal acetylcholine receptor inactivation syndrome and maternal myasthenia gravis

Author keywords

[No Author keywords available]

Indexed keywords

CHOLINERGIC RECEPTOR; CHOLINERGIC RECEPTOR ANTIBODY; IMMUNOGLOBULIN; PREDNISONE; PYRIDOSTIGMINE; AUTOANTIBODY; PROTEIN SUBUNIT;

EID: 58149389167     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/01.wnl.0000336929.38733.7a     Document Type: Article
Times cited : (42)

References (7)
  • 1
    • 0032924923 scopus 로고    scopus 로고
    • Plasma from human mothers of fetuses with severe arthrogryposismultiplex congenita causes deformities in mice
    • Jacobson L, Polizzi A, Morriss-Kay G, Vincent A. Plasma from human mothers of fetuses with severe arthrogryposismultiplex congenita causes deformities in mice. J Clin Invest 1999;103:1031-1038.
    • (1999) J Clin Invest , vol.103 , pp. 1031-1038
    • Jacobson, L.1    Polizzi, A.2    Morriss-Kay, G.3    Vincent, A.4
  • 4
    • 0026741980 scopus 로고
    • Follow-up study of muscle function in children of mothers with myasthenia gravis during pregnancy
    • Ahlsten G, Lefvert AK, Osterman PO, Stalberg E, Safwenberg J. Follow-up study of muscle function in children of mothers with myasthenia gravis during pregnancy. J Child Neurol 1992;7:264-269.
    • (1992) J Child Neurol , vol.7 , pp. 264-269
    • Ahlsten, G.1    Lefvert, A.K.2    Osterman, P.O.3    Stalberg, E.4    Safwenberg, J.5
  • 5
    • 38149000982 scopus 로고    scopus 로고
    • Isolated facial and bulbar paresis: A persistent manifestation of neonatal myasthenia gravis
    • Jeannet PY, Marcoz JP, Kuntzer T, Roulet-Perez E. Isolated facial and bulbar paresis: a persistent manifestation of neonatal myasthenia gravis. Neurology 2008;70: 237-238.
    • (2008) Neurology , vol.70 , pp. 237-238
    • Jeannet, P.Y.1    Marcoz, J.P.2    Kuntzer, T.3    Roulet-Perez, E.4
  • 6
    • 0034194862 scopus 로고    scopus 로고
    • Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotype
    • Brueton LA, Huson SM, Cox PM, et al. Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotype. Am J Med Genet 2000;92:1-6.
    • (2000) Am J Med Genet , vol.92 , pp. 1-6
    • Brueton, L.A.1    Huson, S.M.2    Cox, P.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.