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Volumn 48, Issue 6, 2008, Pages 419-421

A case of Charcot-Marie-Tooth disease type 1A with increased cerebrospinal fluid proteins and nerve root hypertrophy

Author keywords

CMT1A; High CSF proteins; Nerve root hypertrophy

Indexed keywords

PERIPHERAL MYELIN PROTEIN 22;

EID: 51149087257     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: 10.5692/clinicalneurol.48.419     Document Type: Article
Times cited : (13)

References (9)
  • 1
    • 85036855538 scopus 로고    scopus 로고
    • Japanese source
    • Japanese source
  • 2
    • 85036852228 scopus 로고    scopus 로고
    • Japanese source
    • Japanese source
  • 3
    • 27644516384 scopus 로고    scopus 로고
    • European Federation of Neurological Societies and the Peripheral Nerve Society
    • Joint Task Force of the EFNS and the PNS
    • Joint Task Force of the EFNS and the PNS: European Federation of Neurological Societies and the Peripheral Nerve Society. J Peripher Nerv Syst 2005; 10: 220-228
    • (2005) J Peripher Nerv Syst , vol.10 , pp. 220-228
  • 4
    • 0035102069 scopus 로고    scopus 로고
    • Terminal latency index and modified F ratio in distinction of chronic demyelinating neuropathies
    • Attarian S, Azulay JP, Boucraut J, et al: Terminal latency index and modified F ratio in distinction of chronic demyelinating neuropathies. Clinical Neurophysiology 2001; 112: 457-463
    • (2001) Clinical Neurophysiology , vol.112 , pp. 457-463
    • Attarian, S.1    Azulay, J.P.2    Boucraut, J.3
  • 5
    • 0032744517 scopus 로고    scopus 로고
    • MRI of the cauda equina in CIDP: Clinical correlations
    • Midroni G, de Tilly LN, Gray B, et al: MRI of the cauda equina in CIDP: clinical correlations. J Neurol Sci 1999; 170: 36-44
    • (1999) J Neurol Sci , vol.170 , pp. 36-44
    • Midroni, G.1    de Tilly, L.N.2    Gray, B.3
  • 6
    • 0024439779 scopus 로고
    • Compression syndromes due to hypertrophic nerve roots in hereditary motor sensory neuropathy type I
    • Rosen SA, Wang H, Cornblath DR, et al: Compression syndromes due to hypertrophic nerve roots in hereditary motor sensory neuropathy type I. Neurology 1989; 39: 1173-1177
    • (1989) Neurology , vol.39 , pp. 1173-1177
    • Rosen, S.A.1    Wang, H.2    Cornblath, D.R.3
  • 7
    • 0038813880 scopus 로고    scopus 로고
    • Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins?
    • Pareyson D, Testa D, Morbin M, et al: Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins? Neurology 2003; 60: 1721-1722
    • (2003) Neurology , vol.60 , pp. 1721-1722
    • Pareyson, D.1    Testa, D.2    Morbin, M.3
  • 8
    • 0023139580 scopus 로고
    • The leakage of serum proteins across the blood-nerve barrier in hereditary and inflammatory neuropathy
    • Neuen E, Seitz RJ, Langenbach M, et al: The leakage of serum proteins across the blood-nerve barrier in hereditary and inflammatory neuropathy. Acta Neuropathol (Berl) 1987; 73: 53-61
    • (1987) Acta Neuropathol (Berl) , vol.73 , pp. 53-61
    • Neuen, E.1    Seitz, R.J.2    Langenbach, M.3
  • 9
    • 0346097880 scopus 로고    scopus 로고
    • Coexistent hereditary and inflammatory neuropathy
    • Ginsberg L, Malik O, Kenton AR, et al: Coexistent hereditary and inflammatory neuropathy. Brain 2004; 127: 193-202
    • (2004) Brain , vol.127 , pp. 193-202
    • Ginsberg, L.1    Malik, O.2    Kenton, A.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.