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Neurology
Volumn 69, Issue 2, 2007, Pages 214-216
Primary spinal cord neurodegeneration in Leber hereditary optic neuropathy
Author keywords

[No Author keywords available]
Indexed keywords

ADULT; ARTICLE; CASE REPORT; FEMALE; GENE SEQUENCE; HUMAN; IMMUNOHISTOCHEMISTRY; LEBER HEREDITARY OPTIC NEUROPATHY; MEGALOCYTOSIS; NEUROPATHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SPINAL CORD ATROPHY;
EID: 34447341197     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000265598.76172.59     Document Type: Article
Times cited : (23)
References (7)
  • 1
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    • Harding AE, Sweeney MG, Miller DH, et al. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation. Brain 1992;115:979-989.
    • (1992) Brain , vol.115 , pp. 979-989
    • Harding, A.E.1    Sweeney, M.G.2    Miller, D.H.3
  • 2
    • 0000899960 scopus 로고
    • The neuropathology of hereditary optic atrophy (Leber's disease); the first complete anatomic study
    • Kwittken J, Barest HD. The neuropathology of hereditary optic atrophy (Leber's disease); the first complete anatomic study. Am J Pathol 1958;34:185-207.
    • (1958) Am J Pathol , vol.34 , pp. 185-207
    • Kwittken, J.1    Barest, H.D.2
  • 3
    • 11244291105 scopus 로고    scopus 로고
    • Neuropathology of white matter disease in Leber's hereditary optic neuropathy
    • Kovacs GG, Hoftberger R, Majtenyi K, et al. Neuropathology of white matter disease in Leber's hereditary optic neuropathy. Brain 2005;128:35-41.
    • (2005) Brain , vol.128 , pp. 35-41
    • Kovacs, G.G.1    Hoftberger, R.2    Majtenyi, K.3
  • 4
    • 0026566806 scopus 로고
    • Central nervous system changes in mitochondrial encephalomyopathy: Light and electron microscopic study
    • Mizukami K, Sasaki M, Suzuki T, et al. Central nervous system changes in mitochondrial encephalomyopathy: light and electron microscopic study. Acta Neuropathol (Berl) 1992;83:449-452.
    • (1992) Acta Neuropathol (Berl) , vol.83 , pp. 449-452
    • Mizukami, K.1    Sasaki, M.2    Suzuki, T.3
  • 5
    • 0028810370 scopus 로고
    • Alpers' syndrome presenting with seizures and multiple stroke-like episodes in a 17-year-old male
    • Montine TJ, Powers JM, Vogel FS, Radtke RA. Alpers' syndrome presenting with seizures and multiple stroke-like episodes in a 17-year-old male. Clin Neuropathol 1995;14:322-326.
    • (1995) Clin Neuropathol , vol.14 , pp. 322-326
    • Montine, T.J.1    Powers, J.M.2    Vogel, F.S.3    Radtke, R.A.4
  • 6
    • 0041320865 scopus 로고    scopus 로고
    • Howell N, Herrnstadt C, Shults C, Mackey DA. Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background. Am J Med Genet A 2003;119:147-151.
    • Howell N, Herrnstadt C, Shults C, Mackey DA. Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background. Am J Med Genet A 2003;119:147-151.
  • 7
    • 33748740746 scopus 로고    scopus 로고
    • Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis
    • Barcellos LF, Sawcer S, Ramsay PP, et al. Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis. Hum Mol Genet 2006;15:2813-2824.
    • (2006) Hum Mol Genet , vol.15 , pp. 2813-2824
    • Barcellos, L.F.1    Sawcer, S.2    Ramsay, P.P.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.