-
1
-
-
0027731794
-
Association of the 11,778 mitochondrial DNA mutation and demyelinating disease
-
Flanigan KM, Johns DR. Association of the 11,778 mitochondrial DNA mutation and demyelinating disease. Neurology 1993; 43: 2720-2722.
-
(1993)
Neurology
, vol.43
, pp. 2720-2722
-
-
Flanigan, K.M.1
Johns, D.R.2
-
2
-
-
0026782507
-
Occurrence of multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation
-
Harding AE, Sweeney MG, Millerb H et al. Occurrence of 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
Millerb, H.3
-
3
-
-
0028957580
-
Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harboring the mitochondrial DNA 11.778 mutation
-
Olsen NK, Hansen AW, Norby S, Edal AL, Jorgensen JR, Rosenberg T. Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harboring the mitochondrial DNA 11.778 mutation. Acta Neurologica Scandinavica 1995; 91: 326-329.
-
(1995)
Acta Neurologica Scandinavica
, vol.91
, pp. 326-329
-
-
Olsen, N.K.1
Hansen, A.W.2
Norby, S.3
Edal, A.L.4
Jorgensen, J.R.5
Rosenberg, T.6
-
4
-
-
0028595987
-
Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis
-
Hanefeld FA, Ernst BP, Wilichowski E, Cristen HJ. Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis. Neuropediatrics 1994; 25: 331.
-
(1994)
Neuropediatrics
, vol.25
, pp. 331
-
-
Hanefeld, F.A.1
Ernst, B.P.2
Wilichowski, E.3
Cristen, H.J.4
-
6
-
-
0028147810
-
Biochemical alterations in multiple sclerosis lesions and normal-appearing white matter detected by in vivo 31P and 1H spectroscopic imaging
-
Husted CA, Goodin DS, Hugg JW et al. Biochemical alterations in multiple sclerosis lesions and normal-appearing white matter detected by in vivo 31P and 1H spectroscopic imaging. Annals of Neurology 1994; 36: 157-165.
-
(1994)
Annals of Neurology
, vol.36
, pp. 157-165
-
-
Husted, C.A.1
Goodin, D.S.2
Hugg, J.W.3
-
7
-
-
0029075525
-
A magnetization transfer imaging study of normal-appearing white matter in multiple sclerosis
-
Filippi M, Campi A, Dousset V et al. A magnetization transfer imaging study of normal-appearing white matter in multiple sclerosis. Neurology 1995; 45: 478-482.
-
(1995)
Neurology
, vol.45
, pp. 478-482
-
-
Filippi, M.1
Campi, A.2
Dousset, V.3
-
8
-
-
0018394631
-
A histological, histochemical and biochemical study of the macroscopically normal white matter in multiple sclerosis
-
Allen IV, McKeon SR. A histological, histochemical and biochemical study of the macroscopically normal white matter in multiple sclerosis. Journal of the Neurological Sciences 1979; 41: 81-91.
-
(1979)
Journal of the Neurological Sciences
, vol.41
, pp. 81-91
-
-
Allen, I.V.1
McKeon, S.R.2
-
10
-
-
11244291105
-
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
-
11
-
-
0034662806
-
Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis
-
Lu F, Selak M, O'Connor J et al. Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis. Journal of the Neurological Sciences 2000; 177: 95-103.
-
(2000)
Journal of the Neurological Sciences
, vol.177
, pp. 95-103
-
-
Lu, F.1
Selak, M.2
O'Connor, J.3
-
13
-
-
0030247011
-
Characterization of the mitochondrial DNA in patients with multiple sclerosis
-
Kalman B, Lublin FD, Alder H. Characterization of the mitochondrial DNA in patients with multiple sclerosis. Journal of the Neurological Sciences 1996; 140: 75-84.
-
(1996)
Journal of the Neurological Sciences
, vol.140
, pp. 75-84
-
-
Kalman, B.1
Lublin, F.D.2
Alder, H.3
-
14
-
-
0032897253
-
Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians
-
Kalman B, Li S, Chatterjee D et al. Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians. Acta Neurologica Scandinavica 1999; 99: 16-25.
-
(1999)
Acta Neurologica Scandinavica
, vol.99
, pp. 16-25
-
-
Kalman, B.1
Li, S.2
Chatterjee, D.3
-
15
-
-
0012394085
-
New diagnostic criteria for multiple sclerosis: Guidelines for research protocols
-
Poser CM, Paty DW, Scheinberg L. et al. New diagnostic criteria for multiple sclerosis: guidelines for research protocols. Annals of Neurology 1983; 33: 1444-1452.
-
(1983)
Annals of Neurology
, vol.33
, pp. 1444-1452
-
-
Poser, C.M.1
Paty, D.W.2
Scheinberg, L.3
-
16
-
-
0030468182
-
Classification of European mtDNAs from an analysis of three European populations
-
Torroni A, Huoponen K, Francalacci P et al. Classification of European mtDNAs from an analysis of three European populations. Genetics 1996; 144: 1835-1850.
-
(1996)
Genetics
, vol.144
, pp. 1835-1850
-
-
Torroni, A.1
Huoponen, K.2
Francalacci, P.3
-
18
-
-
17644435064
-
Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations
-
Penisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P. Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations. Revue Neurologique 2001; 157: 537-541.
-
(2001)
Revue Neurologique
, vol.157
, pp. 537-541
-
-
Penisson-Besnier, I.1
Moreau, C.2
Jacques, C.3
Roger, J.C.4
Dubas, F.5
Reynier, P.6
-
19
-
-
0028337837
-
Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis
-
Kellar-Wood H, Robertson N, Govan GG, Comoston DAS, Harding AE. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Annals of Neurology 1994; 36: 109-112.
-
(1994)
Annals of Neurology
, vol.36
, pp. 109-112
-
-
Kellar-Wood, H.1
Robertson, N.2
Govan, G.G.3
Comoston, D.A.S.4
Harding, A.E.5
-
20
-
-
0028872087
-
Leber's hereditary optic neuropathy (LHON)-related mitochondrial DNA sequence changes in Italian patients presenting with sporadic bilateral optic neuritis
-
Sartore M, Grasso M, Piccolo G et al. Leber's hereditary optic neuropathy (LHON)-related mitochondrial DNA sequence changes in Italian patients presenting with sporadic bilateral optic neuritis. Biochemical and Molecular Medicine 1995; 56: 45-51.
-
(1995)
Biochemical and Molecular Medicine
, vol.56
, pp. 45-51
-
-
Sartore, M.1
Grasso, M.2
Piccolo, G.3
-
21
-
-
0026587335
-
Mitochondrial genetics: A paradigm for aging and degenerative diseases?
-
Wallace DC. Mitochondrial genetics: a paradigm for aging and degenerative diseases? Science 1992; 256: 628-632.
-
(1992)
Science
, vol.256
, pp. 628-632
-
-
Wallace, D.C.1
-
22
-
-
16944363113
-
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484
-
Torroni A, Petrozzi M, D'Urbano L et al. Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. American Journal of human genetics 1997; 60: 1107-1121.
-
(1997)
American Journal of human genetics
, vol.60
, pp. 1107-1121
-
-
Torroni, A.1
Petrozzi, M.2
D'Urbano, L.3
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