SCOPUS 정보 검색 플랫폼

Journal of Neurology

Volumn 253, Issue 4, 2006, Pages 525-526

Spastic paraparesis as a manifestation of Leber's disease [2]

(8) Clarencon F a Touze E a Leroy Willig, A b Turmel, H a Naggara, O a Pavy, S c Brezin A d Mas, J L a

a CENTRE HOSPITALIER SAINTE ANNE (France)

b PITIÉ SALPÊTRIÈRE HOSPITAL (France)

c Hôpital Cochin (India)

d Hôpital Cochin Ophtalmology (India)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; CASE REPORT; CONTRAST ENHANCEMENT; GENE MUTATION; GENETIC DISORDER; HUMAN; LEBER CONGENITAL AMAUROSIS; LETTER; MALE; OPTIC NERVE ATROPHY; PEDIGREE; PRIORITY JOURNAL; SPASTIC PARESIS;

ADULT; BRAIN; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; NEUROLOGIC EXAMINATION; OPTIC ATROPHY, HEREDITARY, LEBER; PARAPARESIS, SPASTIC; PEDIGREE;

EID: 33745662162 PISSN: 03405354 EISSN: 14321459 Source Type: Journal
DOI: 10.1007/s00415-005-0994-6 Document Type: Letter

Times cited : (6)

References (5)

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2
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- Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy
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3
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- 31P NMR spectroscopy of calf muscles coupled with MRI and ergometry
- Paris
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4
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- Leber's "plus": Neurological abnormalities in patients with Leber's hereditary optic neuropathy
- Nikoskelainen EK, Marttila RJ, Huoponen K, Juvonen V, Lamminen T, Sonninen P, Savontaus ML (1995) Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy. J Neurol Neurosurg Psychiatry 59:160-164
- (1995) J Neurol Neurosurg Psychiatry , vol.59 , pp. 160-164
- Nikoskelainen, E.K.¹ Marttila, R.J.² Huoponen, K.³ Juvonen, V.⁴ Lamminen, T.⁵ Sonninen, P.⁶ Savontaus, M.L.⁷

5
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- Mitochondrial mutations of Leber's hereditary optic neuropathy: A risk factor for multiple sclerosis
- Vanopdenbosch L, Dubois B, D'Hooghe MB, Meire F, Carton H (2000) Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis. J Neurol 247:535-543
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.