메뉴 건너뛰기




Volumn 25, Issue SUPPL. 4, 2004, Pages

Devic's neuromyelitis optica and mitochondrial DNA mutation: A case report

Author keywords

Devic's sneuromyelitis optica; Leber's optic atrophy; Mitochondrial DNA mutation; Multiple sclerosis

Indexed keywords

CORTICOSTEROID; MITOCHONDRIAL DNA;

EID: 10044258880     PISSN: 15901874     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10072-004-0347-8     Document Type: Article
Times cited : (15)

References (13)
  • 2
    • 10744233604 scopus 로고    scopus 로고
    • Clinical characteristics, course and prognosis of relapsing Devic's neuromyelitis optica
    • Ghezzi A, Bergamaschi R, Martinelli V et al (2004) Clinical characteristics, course and prognosis of relapsing Devic's neuromyelitis optica. J Neurol 251:47-52
    • (2004) J. Neurol. , vol.251 , pp. 47-52
    • Ghezzi, A.1    Bergamaschi, R.2    Martinelli, V.3
  • 3
    • 17644435064 scopus 로고    scopus 로고
    • Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations
    • Penisson-Besnier I, Moreau C, Roger JC, Dubas F, Reynier P (2001) Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations. Rev Neurol 157:537-541
    • (2001) Rev. Neurol. , vol.157 , pp. 537-541
    • Penisson-Besnier, I.1    Moreau, C.2    Roger, J.C.3    Dubas, F.4    Reynier, P.5
  • 4
    • 0035657392 scopus 로고    scopus 로고
    • Leber's hereditary optic neuropathy mutations in Korean patients with multiple sclerosis
    • Hwang JM, Chang BL, Park SS (2001) Leber's hereditary optic neuropathy mutations in Korean patients with multiple sclerosis. Ophtalmologica 215:398-400
    • (2001) Ophtalmologica , vol.215 , pp. 398-400
    • Hwang, J.M.1    Chang, B.L.2    Park, S.S.3
  • 5
    • 0034000267 scopus 로고    scopus 로고
    • Multiple secondary Leber's hereditary optic neuropathy mutations in Italian patients with multiple sclerosis
    • Franciotta D, Bergamaschi R, Piccolo G, Zardini E, Cosi V (2000) Multiple secondary Leber's hereditary optic neuropathy mutations in Italian patients with multiple sclerosis. J Neurol 247:304-305
    • (2000) J. Neurol. , vol.247 , pp. 304-305
    • Franciotta, D.1    Bergamaschi, R.2    Piccolo, G.3    Zardini, E.4    Cosi, V.5
  • 8
    • 0026782507 scopus 로고
    • Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mithocondrial DNA mutation
    • Harding AE, Sweeney MG, Miller DH et al (1992) Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mithocondrial DNA mutation. Brain 115:979-989
    • (1992) Brain , vol.115 , pp. 979-989
    • Harding, A.E.1    Sweeney, M.G.2    Miller, D.H.3
  • 9
    • 0033879510 scopus 로고    scopus 로고
    • Mithocondrial mutations of Leber's hereditary optic neuropathy: A risk factor for multiple sclerosis
    • Vanopdenbosh L, Dubois B, D'Hooge MB, Meire F, Carton H (2000) Mithocondrial mutations of Leber's hereditary optic neuropathy: A risk factor for multiple sclerosis. J Neurol 247:535-543
    • (2000) J. Neurol. , vol.247 , pp. 535-543
    • Vanopdenbosh, L.1    Dubois, B.2    D'Hooge, M.B.3    Meire, F.4    Carton, H.5
  • 10
    • 0035056945 scopus 로고    scopus 로고
    • Magnetic resonance imaging, magnetisation tranfer imaging, and diffusion weighted imaging correlates of optic nerve, brain, and cervical cord damage in Leber's hereditary optic neuropathy
    • Inglese M, Rovaris M, Bianchi S, LaMantia L, Mancardi GL, Ghezzi A, Montagna P, Salvi F, Filippi M (2001) Magnetic resonance imaging, magnetisation tranfer imaging, and diffusion weighted imaging correlates of optic nerve, brain, and cervical cord damage in Leber's hereditary optic neuropathy. J Neurol Neurosurg Psychiatry 70:444-449
    • (2001) J. Neurol. Neurosurg. Psychiatry , vol.70 , pp. 444-449
    • Inglese, M.1    Rovaris, M.2    Bianchi, S.3    LaMantia, L.4    Mancardi, G.L.5    Ghezzi, A.6    Montagna, P.7    Salvi, F.8    Filippi, M.9
  • 11
    • 0036785956 scopus 로고    scopus 로고
    • Visual recovery in a man with the rare combination of mtDNA 11778 LHON mutation and a MS-like disease after mitoxantrone theraphy
    • Buhmann C, Gbadamosi J, Heesen C (2002) Visual recovery in a man with the rare combination of mtDNA 11778 LHON mutation and a MS-like disease after mitoxantrone theraphy. Acta Neuro Scand 106:236-239
    • (2002) Acta Neuro. Scand. , vol.106 , pp. 236-239
    • Buhmann, C.1    Gbadamosi, J.2    Heesen, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.