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Volumn 58, Issue 4, 2002, Pages 615-620

Axonal multifocal motor neuropathy without conduction block or other features of demyelination

Author keywords

[No Author keywords available]

Indexed keywords

GANGLIOSIDE ANTIBODY; GANGLIOSIDE GM1; IMMUNOGLOBULIN; PREDNISONE;

EID: 0037176810     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.58.4.615     Document Type: Article
Times cited : (107)

References (26)
  • 6
    • 0030679614 scopus 로고    scopus 로고
    • Multifocal motor neuropathy. Serum IgM anti-GM1 ganglioside antibodies in most patients detected using covalent linkage of GM1 to ELISA plates
    • (1997) Neurology , vol.49 , pp. 1289-1292
    • Pestronk, A.1    Choksi, R.2
  • 9
    • 0028142392 scopus 로고
    • El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis
    • Subcommittee on Motor Neuron Diseases Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial "Clinical limits of amyotrophic lateral sclerosis" workshop contributors
    • (1994) J Neurol Sci , vol.124 , pp. 96-107
    • Brooks, B.1
  • 19
    • 0030943761 scopus 로고    scopus 로고
    • Motor nerve terminal degeneration provides a potential mechanism for rapid recovery in acute motor axonal neuropathy after Campylobacter infection
    • (1997) Neurology , vol.48 , pp. 717-724
    • Ho, T.W.1    Hsieh, S.T.2    Nachamkin, I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.