Leber's 'plus' disease: Optic neuropathy, parkinsonism and supranuclear ophtalmoplegia;Maladie de Leber 'plus': Neuropathie optique, syndrome parkinsonien et ophtalmoplegie supranucleaire

Revue Neurologique

Volumn 153, Issue 10, 1997, Pages 595-598

  Thobois, S ^a,c   Vighetto, A ^a   Grochowicki, M ^a   Godinot, C ^b   Broussolle, E ^a   Aimard, G ^a  

^a HÔPITAL NEUROLOGIQUE   (France)

^b CENTRE DE GÉNÉTIQUE MOLÉCULAIRE ET CELLULAIRE   (France)

^c Hop Neurologique Pierre Wertheimer   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; ARTICLE; BRAIN SCINTISCANNING; CASE REPORT; CLINICAL FEATURE; DYSTONIA; GENE MUTATION; HUMAN; LEBER CONGENITAL AMAUROSIS; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; OPHTHALMOPLEGIA; PARKINSONISM; RIGHT HANDEDNESS; GENETICS; HEREDITARY OPTIC ATROPHY; MUTATION; PARKINSON DISEASE;

ADULT; DNA, MITOCHONDRIAL; HUMANS; MALE; MUTATION; OPHTHALMOPLEGIA; OPTIC ATROPHIES, HEREDITARY; PARKINSON DISEASE, SECONDARY;

EID: 0030669154     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. BROWM M.D., WALLACE D.C. (1994). Spectrum of mitochondrial DNA mutations in Leber's hereditary optic neuropathy. Clin Neurosci, 2 : 1-8.
2. BRUYN G.W., BOTS G.T.A.M., WENT L.N., KLINKHAMER P.J.J.M. (1992). Hereditary spastic dystonia with Leber's hereditary optic neuropathy: neuropathological findings. J Neurol Sci, 113 : 55-61.
3. HANEMAN C.O., HEFTER H., SCHLANG G., SEITZ R.J., FREUND H.J., BENECKE R. (1996). Characterization of basal ganglia dysfonction in Leber plus disease. J Neurol, 243 : 297-300.
4. HARDING A.E., SWEENEY M.G., MILLER D.H., MUMFORD C.J., KELLAR-WOOD H., MENARD D. (1992). Ocurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial mutation. Brain, 115 : 979-989.
5. JOHNS D.R., SMITH K.H., MILLER M.R. (1992). Leber's hereditary optic neuropathy. Clinical manifestations of the 3,460 mutation. Arch Ophtamol, 110 : 1577-81.
6. JOHNS D.R., HEHER K.L., MILLER N.R. (1993). Leber's hereditary optic neuropathy. Clinical manifestations of the 14,484 mutation. Arch Ophtamol, 110 : 195-8.
7. JUN A.S., BROWN M.D., WALLACE D.C. (1994). A mitochondrial DNA mutation at nucleotide pair 14 459 of the NADH dehydrogenase