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Volumn 63, Issue 12, 2004, Pages 2451-2452

Leber hereditary optic neuropathy with chorea and dementia resembling Huntington disease

Author keywords

[No Author keywords available]

Indexed keywords

CYSTEINE ETHYL ESTER TC 99M; HALOPERIDOL;

EID: 11144275225     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000147321.38129.ED     Document Type: Article
Times cited : (21)

References (5)
  • 1
    • 0029166941 scopus 로고
    • Leber's "plus": Neurological abnormalities in patients with Leber's hereditary optic neuropathy
    • Nikoskelainen EK, Marttila RJ, Huoponen K, et al. Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy. J Neurol Neurosurg Psychiatry 1995;59:160-164.
    • (1995) J Neurol Neurosurg Psychiatry , vol.59 , pp. 160-164
    • Nikoskelainen, E.K.1    Marttila, R.J.2    Huoponen, K.3
  • 2
    • 0027180961 scopus 로고
    • Leber's hereditary optic neuropathy. New genetic considerations
    • Newman NJ. Leber's hereditary optic neuropathy. New genetic considerations. Arch Neurol 1993;50:540-548.
    • (1993) Arch Neurol , vol.50 , pp. 540-548
    • Newman, N.J.1
  • 3
    • 0032752681 scopus 로고    scopus 로고
    • Choreic movements and MRI abnormalities in the subthalamic nuclei reversible after administration of Coenzyme Q10 and multiple vitamins in a patient with bilateral optic neuropathy
    • Chariot P, Brugieres P, Eliezer-Vanerot M-C, Geny C, Binaghi M, Cesaro P. Choreic movements and MRI abnormalities in the subthalamic nuclei reversible after administration of Coenzyme Q10 and multiple vitamins in a patient with bilateral optic neuropathy. Mov Disord 1999;14:855-859.
    • (1999) Mov Disord , vol.14 , pp. 855-859
    • Chariot, P.1    Brugieres, P.2    Eliezer-Vanerot, M.-C.3    Geny, C.4    Binaghi, M.5    Cesaro, P.6
  • 4
    • 0942279746 scopus 로고    scopus 로고
    • Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation
    • Gropman A, Chen T-J, Perng C-L, et al. Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation. Am J Med Genet 2004;124A:377-382.
    • (2004) Am J Med Genet , vol.124 A , pp. 377-382
    • Gropman, A.1    Chen, T.-J.2    Perng, C.-L.3
  • 5
    • 0942290696 scopus 로고    scopus 로고
    • Clinical variability in maternally inherited Leber hereditary optic neuropathy with the G14459A mutation
    • Tarnopolsky MA, Baker SK, Myint T, Maxner CE, Robitaille J, Robinson BH. Clinical variability in maternally inherited Leber hereditary optic neuropathy with the G14459A mutation. Am J Med Genet 2004;124A:372-376.
    • (2004) Am J Med Genet , vol.124 A , pp. 372-376
    • Tarnopolsky, M.A.1    Baker, S.K.2    Myint, T.3    Maxner, C.E.4    Robitaille, J.5    Robinson, B.H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.