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Volumn 16, Issue 6, 2006, Pages 394-395

Demyelinating polyneuropathy in Leber hereditary optic neuropathy

Author keywords

Demyelinating neuropathy; Leber hereditary optic neuropathy

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; DEMYELINATING DISEASE; DISEASE COURSE; ELECTROMYOGRAPHY; FAMILY HISTORY; HUMAN; LABORATORY TEST; LEBER HEREDITARY OPTIC NEUROPATHY; MALE; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; POLYNEUROPATHY; PRIORITY JOURNAL;

EID: 33744974249     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2006.03.006     Document Type: Article
Times cited : (15)

References (7)
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    • (1995) Brain , vol.118 , pp. 319-337
    • Riordan-Eva, P.1    Sanders, M.D.2    Govan, G.G.3    Sweeney, M.G.4    Da Costa, J.5    Harding, A.E.6
  • 2
    • 0029166941 scopus 로고
    • Leber's 'plus': neurological abnormalities in patients with Leber's hereditary optic neuropathy
    • Nikoskelainen E.K., Marttila R.J., Huoponen K., et al. Leber's 'plus': neurological abnormalities in patients with Leber's hereditary optic neuropathy. J Neurol Neurosurg Psychiatry 59 (1995) 160-164
    • (1995) J Neurol Neurosurg Psychiatry , vol.59 , pp. 160-164
    • Nikoskelainen, E.K.1    Marttila, R.J.2    Huoponen, K.3
  • 3
    • 11244291105 scopus 로고    scopus 로고
    • Neuropathology of white matter disease in Leber's hereditary optic neuropathy
    • Kovacs G.G., Hoftberger R., Majtenyi K., et al. Neuropathology of white matter disease in Leber's hereditary optic neuropathy. Brain 128 (2005) 35-41
    • (2005) Brain , vol.128 , pp. 35-41
    • Kovacs, G.G.1    Hoftberger, R.2    Majtenyi, K.3
  • 4
    • 0030048236 scopus 로고    scopus 로고
    • Leber's hereditary optic neuropathy with the 11778 mtDNA mutation and white matter disease resembling multiple sclerosis: clinical, MRI and MRS findings
    • Jansen P.H.P., van der Knaap M.S., and de Coo I.F.M. Leber's hereditary optic neuropathy with the 11778 mtDNA mutation and white matter disease resembling multiple sclerosis: clinical, MRI and MRS findings. J Neurol Sci 135 (1996) 176-180
    • (1996) J Neurol Sci , vol.135 , pp. 176-180
    • Jansen, P.H.P.1    van der Knaap, M.S.2    de Coo, I.F.M.3
  • 6
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    • The neuropathology of hereditary optic atrophy (Leber's disease); the first complete anatomic study
    • Kwittken J., and Barest H.D. The neuropathology of hereditary optic atrophy (Leber's disease); the first complete anatomic study. Am J Pathol 34 (1958) 185-207
    • (1958) Am J Pathol , vol.34 , pp. 185-207
    • Kwittken, J.1    Barest, H.D.2
  • 7
    • 0842281697 scopus 로고    scopus 로고
    • Mitochondrial dysfunction as a cause of optic neuropathies
    • Carelli V., Ross-Cisneros F.N., and Sadun A.A. Mitochondrial dysfunction as a cause of optic neuropathies. Prog Retin Eye Res 23 (2004) 53-89
    • (2004) Prog Retin Eye Res , vol.23 , pp. 53-89
    • Carelli, V.1    Ross-Cisneros, F.N.2    Sadun, A.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.