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Volumn 31, Issue 4, 2005, Pages 528-530

CMTX mimicking childhood chronic inflammatory demyelinating neuropathy with tremor

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOGLOBULIN;

EID: 15344343451     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/mus.20292     Document Type: Letter
Times cited : (28)

References (13)
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    • Bedlack, R.S.1    Vu, T.2    Hammans, S.3    Sparr, S.A.4    Myers, B.5    Morgenlander, J.6
  • 3
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    • Tremor as a feature of chronic relapsing and dysgammaglobulinemic polyneuropathies. Incidence and management
    • Dalakas MC, Teravainen H, Engel WK. Tremor as a feature of chronic relapsing and dysgammaglobulinemic polyneuropathies. Incidence and management. Arch Neurol 1984;41:711-714.
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    • Dalakas, M.C.1    Teravainen, H.2    Engel, W.K.3
  • 5
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    • Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): A clinicopathological study of 205 Japanese patients
    • Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, et al. Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients. Brain 2003;126:134-151.
    • (2003) Brain , vol.126 , pp. 134-151
    • Hattori, N.1    Yamamoto, M.2    Yoshihara, T.3    Koike, H.4    Nakagawa, M.5    Yoshikawa, H.6
  • 6
    • 15344347932 scopus 로고    scopus 로고
    • Pes cavus as the presenting sign of childhood neuropathies; EMG evaluation in 23 otherwise asymptomatic children
    • Jones HR, Hsu P. Pes cavus as the presenting sign of childhood neuropathies; EMG evaluation in 23 otherwise asymptomatic children [abstract]. Muscle Nerve 1997;20:1070.
    • (1997) Muscle Nerve , vol.20 , pp. 1070
    • Jones, H.R.1    Hsu, P.2
  • 7
    • 0033809078 scopus 로고    scopus 로고
    • Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis
    • Lewis RA, Sumner AJ, Shy ME. Electrophysiological features of inherited demyelinating neuropathies: a reappraisal in the era of molecular diagnosis. Muscle Nerve 2000;23:1472-1487.
    • (2000) Muscle Nerve , vol.23 , pp. 1472-1487
    • Lewis, R.A.1    Sumner, A.J.2    Shy, M.E.3
  • 8
    • 0026160813 scopus 로고
    • Report from an ad hoc Subcommittee of the American Academy of Neurology AIDS Task Force. Research criteria for diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP)
    • Report from an ad hoc Subcommittee of the American Academy of Neurology AIDS Task Force. Research criteria for diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP). Neurology 1991;41:617-618.
    • (1991) Neurology , vol.41 , pp. 617-618
  • 9
    • 0034255909 scopus 로고    scopus 로고
    • Childhood chronic inflammatory demyelinating polyneuropathy: Clinical course and long-term outcome
    • Ryan MM, Grattan-Smith PJ, Procopis PG, Morgan G, Ouvrier RA. Childhood chronic inflammatory demyelinating polyneuropathy: clinical course and long-term outcome. Neuromuscul Disord 2000;10:398-406.
    • (2000) Neuromuscul Disord , vol.10 , pp. 398-406
    • Ryan, M.M.1    Grattan-Smith, P.J.2    Procopis, P.G.3    Morgan, G.4    Ouvrier, R.A.5
  • 10
    • 0020585474 scopus 로고
    • Pathogenesis of pes cavus in Charcot-Marie-Tooth disease
    • Sabir M, Lyttle D. Pathogenesis of pes cavus in Charcot-Marie-Tooth disease. Clin Orthop 1983;175:173-178.
    • (1983) Clin Orthop , vol.175 , pp. 173-178
    • Sabir, M.1    Lyttle, D.2
  • 11
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    • Charcot-Marie-Tooth disease associated with "essential tremor": Report of 7 cases and a review of the literature
    • Salisachs P. Charcot-Marie-Tooth disease associated with "essential tremor": report of 7 cases and a review of the literature. J Neurol Sci 1976;28:17-40.
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    • Salisachs, P.1
  • 12
    • 0032812156 scopus 로고    scopus 로고
    • X-linked dominant Charcot-Marie-Tooth neuropathy: Clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations
    • Senderek J, Hermanns B, Bergmann C, Boroojerdi B, Bajbouj M, Hungs M, et al. X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations. J Neurol Sci 1999;167:90-101.
    • (1999) J Neurol Sci , vol.167 , pp. 90-101
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    • Demyelinating X-linked Charcot-Marie-Tooth disease: Unusual electrophysiological findings
    • Tabaraud F, Lagrange E, Sindou P, Vandenberghe A, Levy N, Vallat JM. Demyelinating X-linked Charcot-Marie-Tooth disease: unusual electrophysiological findings. Muscle Nerve 1999;22:1442-1447.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.