-
2
-
-
0026013435
-
Parent-child concordance in multiple sclerosis
-
Sadovnick AD, Bulman D, Ebers GC. Parent-child concordance in multiple sclerosis. Ann Neurol 1991;29:252-255
-
(1991)
Ann Neurol
, vol.29
, pp. 252-255
-
-
Sadovnick, A.D.1
Bulman, D.2
Ebers, G.C.3
-
3
-
-
0026782507
-
Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondria! DNA mutation
-
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 mitochondria! 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
-
4
-
-
0028949749
-
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
-
Riordan-Eva P, Sanders MD, Govan GG, et al. The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation. Brain 1995:118:319-337
-
(1995)
Brain
, vol.118
, pp. 319-337
-
-
Riordan-Eva, P.1
Sanders, M.D.2
Govan, G.G.3
-
5
-
-
0026036025
-
Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy
-
Johns DR, Berman J. Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy. Bicohem Biophys Res Commun 1991:174:13241330
-
(1991)
Bicohem Biophys Res Commun
, vol.174
, pp. 13241330
-
-
Johns, D.R.1
Berman, J.2
-
6
-
-
0026337654
-
Cytochrome b mutations in Leber hereditary optic neuropathy
-
Johns DR, Neufeld MJ. Cytochrome b mutations in Leber hereditary optic neuropathy. Biochem Biophys Res Commun 1991:181:1358-1364
-
(1991)
Biochem Biophys Res Commun
, vol.181
, pp. 1358-1364
-
-
Johns, D.R.1
Neufeld, M.J.2
-
7
-
-
0028337837
-
Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis
-
Kellar-Wood H, Robertson N, Govan GG, et al. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Ann Neurol 1994:36:109-112
-
(1994)
Ann Neurol
, vol.36
, pp. 109-112
-
-
Kellar-Wood, H.1
Robertson, N.2
Govan, G.G.3
-
8
-
-
0025312304
-
Maternally transmitted histocompatibility antigen of mice: A hydrophobic peptide of a mitochondrially encoded protein
-
Loveland BE, Wang CR, Yonekawa H, et al. Maternally transmitted histocompatibility antigen of mice: a hydrophobic peptide of a mitochondrially encoded protein. Cell 1990;60:971 980
-
(1990)
Cell
, vol.60
, pp. 971980
-
-
Loveland, B.E.1
Wang, C.R.2
Yonekawa, H.3
-
9
-
-
0003377162
-
Antigen presentation by neoclassical MHC class I gene products in murine rodents
-
Wang CR, Livingstone A, Butcher GW, et al. Antigen presentation by neoclassical MHC class I gene products in murine rodents. In: Klein J, Klein D, eds. Nato ASI series, Vol H59: molecular evolution of the major histocompatibility complex. Berlin: Springer, 1991:441-462
-
(1991)
In: Klein J, Klein D, Eds. Nato ASI Series, Vol H59: Molecular Evolution of the Major Histocompatibility Complex. Berlin: Springer
, pp. 441-462
-
-
Wang, C.R.1
Livingstone, A.2
Butcher, G.W.3
-
11
-
-
0029014947
-
Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis
-
Chalmers RM, Robertson N, Kellar-Wood H, et al. Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis. J Neurol 1995:242:332-334
-
(1995)
J Neurol
, vol.242
, pp. 332-334
-
-
Chalmers, R.M.1
Robertson, N.2
Kellar-Wood, H.3
-
13
-
-
0028128084
-
The British Isles survey of multiple sclerosis in twins
-
Mumford CJ, Wood NW, Kellar-Wood H, et al. The British Isles survey of multiple sclerosis in twins. Neurology 1994;44: 11-15
-
(1994)
Neurology
, vol.44
, pp. 11-15
-
-
Mumford, C.J.1
Wood, N.W.2
Kellar-Wood, H.3
-
14
-
-
0019423856
-
Sequence and organisation of the human mitochondrial genome
-
Anderson S, Bankier AT, Barrell BG, et al. Sequence and organisation of the human mitochondrial genome. Nature 1981; 290:457-465
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
-
15
-
-
0002600547
-
Report of the committee on human mitochondrial DNA
-
Wallace DC, Lott MT, Brown MD, et al. Report of the committee on human mitochondrial DNA. In: Cuticchia AJ, ed. Human gene mapping 1995: a compendium. Baltimore; Johns Hopkins University Press, 1995:910-954
-
(1995)
In: Cuticchia AJ, Ed. Human Gene Mapping
, vol.1995
, pp. 910-954
-
-
Wallace, D.C.1
Lott, M.T.2
Brown, M.D.3
-
16
-
-
0028595987
-
Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis
-
Hanefeld FA, Ernst BP, Wilichowski E, Christen 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
Christen, H.J.4
-
18
-
-
0028221662
-
Leber's hereditary optic neuropathy: Correlations between mitochondrial genotype and visual outcome
-
Oostra RJ, Bolhuis PA, Wijburg FA, et al. Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome. J Med Genet 1994;31:280-286
-
(1994)
J Med Genet
, vol.31
, pp. 280-286
-
-
Oostra, R.J.1
Bolhuis, P.A.2
Wijburg, F.A.3
-
19
-
-
0028349620
-
Platelet mitochondrial function in Leber's hereditary optic neuropathy
-
Smith PR, Cooper JM, Govan GG, et al. Platelet mitochondrial function in Leber's hereditary optic neuropathy. J Neurol Sei 1994:122:80-83
-
(1994)
J Neurol Sei
, vol.122
, pp. 80-83
-
-
Smith, P.R.1
Cooper, J.M.2
Govan, G.G.3
-
20
-
-
0029041731
-
Antibodies to human optic nerve in patients with Leber's hereditary optic neuropathy
-
Smith PR, Cooper JM, Govan GG, et al. Antibodies to human optic nerve in patients with Leber's hereditary optic neuropathy. J Neurol Sei 1995:130:134-138
-
(1995)
J Neurol Sei
, vol.130
, pp. 134-138
-
-
Smith, P.R.1
Cooper, J.M.2
Govan, G.G.3
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