-
1
-
-
0018394631
-
A histological, histochemical and biochemical study of the macroscopically normal white matter in multiple sclerosis
-
Allen, I.V. and McKeon, S.R. (1979) A histological, histochemical and biochemical study of the macroscopically normal white matter in multiple sclerosis. J. Neurol. Sci., 41: 81-91.
-
(1979)
J. Neurol. Sci.
, vol.41
, pp. 81-91
-
-
Allen, I.V.1
McKeon, S.R.2
-
2
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
Anderson, S., Bankier, A.T., Barell, B.G., deBruijn, M.H.L., Coulson, A.R., Drouin, J., Eperon, I.C., Nierlich, D.P., Roe, B.A., Sanger, F., Schreier, P.H., Smith, A.J.H., Staden, R. and Young, I.G. (1981) Sequence and organization of the human mitochondrial genome. Nature, 290: 457-464.
-
(1981)
Nature
, vol.290
, pp. 457-464
-
-
Anderson, S.1
Bankier, A.T.2
Barell, B.G.3
DeBruijn, M.H.L.4
Coulson, A.R.5
Drouin, J.6
Eperon, I.C.7
Nierlich, D.P.8
Roe, B.A.9
Sanger, F.10
Schreier, P.H.11
Smith, A.J.H.12
Staden, R.13
Young, I.G.14
-
3
-
-
0019983804
-
Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome
-
Anderson, S., DeBruijn, M.H.L., Coulson, A.R., Eperon, I.C., Sanger, F. and Young, I.G. (1982) Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome. J. Mol. Biol., 156: 683-717.
-
(1982)
J. Mol. Biol.
, vol.156
, pp. 683-717
-
-
Anderson, S.1
DeBruijn, M.H.L.2
Coulson, A.R.3
Eperon, I.C.4
Sanger, F.5
Young, I.G.6
-
4
-
-
0027235992
-
Susceptibility for multiple sclerosis is determined, in part, by inheritance of a 175-kb region of the TCR Vβ chain locus and HLA class II genes
-
Beall, S.S., Biddison, W.E., McFarlin, D.E., McFarland, H.F. and Hood, L.E. (1993) Susceptibility for multiple sclerosis is determined, in part, by inheritance of a 175-kb region of the TCR Vβ chain locus and HLA class II genes. J. Neuroimmunol., 45: 53-60.
-
(1993)
J. Neuroimmunol.
, vol.45
, pp. 53-60
-
-
Beall, S.S.1
Biddison, W.E.2
McFarlin, D.E.3
McFarland, H.F.4
Hood, L.E.5
-
5
-
-
0019837699
-
Sequence and gene organization of mouse mitochondrial DNA
-
Bibb, M.J., Van Etten, R.A., Wright, C.T., Walberg, M.W. and Clayton, D.A. (1981) Sequence and gene organization of mouse mitochondrial DNA. Cell, 26: 167-180.
-
(1981)
Cell
, vol.26
, pp. 167-180
-
-
Bibb, M.J.1
Van Etten, R.A.2
Wright, C.T.3
Walberg, M.W.4
Clayton, D.A.5
-
6
-
-
0025317768
-
DNA length polymorphism 5″ to the myelin basic protein gene is associated with multiple sclerosis
-
Boylan, K.B., Takahashi, N., Paty, D.W., Sadovnick, A.D., Diamond, M., Hood, L.E. and Prusiner, S.B. (1990) DNA length polymorphism 5″ to the myelin basic protein gene is associated with multiple sclerosis. Ann. Neurol., 27: 291-297.
-
(1990)
Ann. Neurol.
, vol.27
, pp. 291-297
-
-
Boylan, K.B.1
Takahashi, N.2
Paty, D.W.3
Sadovnick, A.D.4
Diamond, M.5
Hood, L.E.6
Prusiner, S.B.7
-
7
-
-
0024457283
-
Idiopathic dystonia among Ashkenazi Jews: Evidence for autosomal dominant inheritence
-
Bressman, S.B., de Leon, D., Brin, M.F., Risch, N., Burke, R.E., Greene, P.E., Shale, H. and Fahn, S. (1989) Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritence. Ann. Neurol., 26: 612-620.
-
(1989)
Ann. Neurol.
, vol.26
, pp. 612-620
-
-
Bressman, S.B.1
De Leon, D.2
Brin, M.F.3
Risch, N.4
Burke, R.E.5
Greene, P.E.6
Shale, H.7
Fahn, S.8
-
8
-
-
0026702249
-
Leber's hereditary optic neuropathy: A model for mitochondrial neurodegenerative diseases
-
Brown, M.D., Voljavec, A.S., Lott, M.T., MacDonald, I. and Wallace, D.C. (1992a) Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases. FASEB J., 6: 2791-2799.
-
(1992)
FASEB J.
, vol.6
, pp. 2791-2799
-
-
Brown, M.D.1
Voljavec, A.S.2
Lott, M.T.3
MacDonald, I.4
Wallace, D.C.5
-
9
-
-
0026531040
-
Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy
-
Brown, M.D., Voljavec, A.S., Lott, M.T., Torroni, A., Yang, C.C. and Wallace, D.C. (1992b) Mitochondrial DNA Complex I and III mutations associated with Leber's hereditary optic neuropathy. Genetics, 130: 163-173.
-
(1992)
Genetics
, vol.130
, pp. 163-173
-
-
Brown, M.D.1
Voljavec, A.S.2
Lott, M.T.3
Torroni, A.4
Yang, C.C.5
Wallace, D.C.6
-
10
-
-
0002699021
-
A sex-linked heredo-degenerative neurological disorder, associated with Leber's optic atrophy. Part I. Clinical studies
-
Bruyn, G.W. and Went, L.N. (1964) A sex-linked heredo-degenerative neurological disorder, associated with Leber's optic atrophy. Part I. Clinical studies. J. Neurol. Sci., 1: 59-80.
-
(1964)
J. Neurol. Sci.
, vol.1
, pp. 59-80
-
-
Bruyn, G.W.1
Went, L.N.2
-
11
-
-
0029014947
-
Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis
-
Chalmers, R.M., Robertson, N., Kellar-Wood, H., Compston, D.A.S. and Harding, A.E. (1995) Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis. J. Neurol., 242: 332-334.
-
(1995)
J. Neurol.
, vol.242
, pp. 332-334
-
-
Chalmers, R.M.1
Robertson, N.2
Kellar-Wood, H.3
Compston, D.A.S.4
Harding, A.E.5
-
12
-
-
0022271984
-
The mitochondrial DNA molecule of Drosophila yakuba: Nucleotide sequence, gene organization and genetic code
-
Clary, D.O. and Wolstenholme, D.R. (1985) The mitochondrial DNA molecule of Drosophila yakuba: nucleotide sequence, gene organization and genetic code. J. Mol. Evol., 22: 252-271.
-
(1985)
J. Mol. Evol.
, vol.22
, pp. 252-271
-
-
Clary, D.O.1
Wolstenholme, D.R.2
-
13
-
-
0026049670
-
HLA-DR and -DQ allelic sequences in multiple sclerosis patients are identical to those found in the general population
-
Cowan, E.P., Pierce, M.L., McFarland, H.F. and McFarlin, D.E. (1991) HLA-DR and -DQ allelic sequences in multiple sclerosis patients are identical to those found in the general population. Hum. Immunol., 32: 203-210.
-
(1991)
Hum. Immunol.
, vol.32
, pp. 203-210
-
-
Cowan, E.P.1
Pierce, M.L.2
McFarland, H.F.3
McFarlin, D.E.4
-
14
-
-
0001174007
-
Leber's optic atrophy and its relation to the heredo-familial ataxias
-
Ferguson, F.R. and Critchley, M. (1928) Leber's optic atrophy and its relation to the heredo-familial ataxias. J. Neurol. Psychol., 9: 120-132.
-
(1928)
J. Neurol. Psychol.
, vol.9
, pp. 120-132
-
-
Ferguson, F.R.1
Critchley, M.2
-
15
-
-
0029075525
-
A magnetization transfer imaging study of normal-appearing white matter in multiple sclerosis
-
Filippi, M., Campi, A., Dousset, V., Baratti, C., Martinelli, V., Canal, N., Scotti, G. and Comi, G. (1995) A magnetization transfer imaging study of normal-appearing white matter in multiple sclerosis. Neurology, 45: 478-482.
-
(1995)
Neurology
, vol.45
, pp. 478-482
-
-
Filippi, M.1
Campi, A.2
Dousset, V.3
Baratti, C.4
Martinelli, V.5
Canal, N.6
Scotti, G.7
Comi, G.8
-
16
-
-
0027731794
-
Association of the 11778 mitochondrial DNA mutation and demyelinating disease
-
Flanigan, K.M. and Johns, D.R. (1993) Association of the 11778 mitochondrial DNA mutation and demyelinating disease. Neurology, 43: 2720-2722.
-
(1993)
Neurology
, vol.43
, pp. 2720-2722
-
-
Flanigan, K.M.1
Johns, D.R.2
-
17
-
-
0028595987
-
Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis
-
Hanefeld, F.A., Ernst, B.P., Wilichowski, E. and Cristen, H.-J. (1994) Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis. Neuropediatrics, 25: 331.
-
(1994)
Neuropediatrics
, vol.25
, pp. 331
-
-
Hanefeld, F.A.1
Ernst, B.P.2
Wilichowski, E.3
Cristen, H.-J.4
-
18
-
-
0026782507
-
Occurrence of multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation
-
Harding, A.E., Sweeney, M.G., Miller, D.H., Mumford, C.J., Kellar-Wood, H., Menard, D., McDonald, W.I. and Compston, D.A.S. (1992) Occurrence of multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation. Brain, 115: 979-989.
-
(1992)
Brain
, vol.115
, pp. 979-989
-
-
Harding, A.E.1
Sweeney, M.G.2
Miller, D.H.3
Mumford, C.J.4
Kellar-Wood, H.5
Menard, D.6
McDonald, W.I.7
Compston, D.A.S.8
-
19
-
-
0001782589
-
HLA-Dw2 in multiple sclerosis: A world-wide association and a close segregation with disease in multiplex families
-
Hillert, J., Kall, T. and Ollerup, O. (1993) HLA-Dw2 in multiple sclerosis: a world-wide association and a close segregation with disease in multiplex families. Hum. Immunol., 36: 50.
-
(1993)
Hum. Immunol.
, vol.36
, pp. 50
-
-
Hillert, J.1
Kall, T.2
Ollerup, O.3
-
20
-
-
0025897119
-
Leber hereditary optic neuropathy: Involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation
-
Howell, N., Kubacka, I., Xu, M. and McCullough, D.A, (1991) Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation. Am. J. Hum. Genet., 48: 935-942.
-
(1991)
Am. J. Hum. Genet.
, vol.48
, pp. 935-942
-
-
Howell, N.1
Kubacka, I.2
Xu, M.3
McCullough, D.A.4
-
21
-
-
0026654907
-
The sequence of human mtDNA: The question of errors versus polymorphism
-
Howell, N., McCullough, D.A., Kubacka, I., Halvorson, S. and Macley, D. (1992) The sequence of human mtDNA: The question of errors versus polymorphism. Am. J. Hum. Genet., 50: 1333-1337.
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 1333-1337
-
-
Howell, N.1
McCullough, D.A.2
Kubacka, I.3
Halvorson, S.4
Macley, D.5
-
22
-
-
0028218473
-
Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy
-
Houshmand, M., Larsson, N.G., Holme, E., Oldfors, A., Tulinius, M.H. and Andersen, O. (1994) Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy. Biochim. Biophys. Acta. 1226: 49-55.
-
(1994)
Biochim. Biophys. Acta
, vol.1226
, pp. 49-55
-
-
Houshmand, M.1
Larsson, N.G.2
Holme, E.3
Oldfors, A.4
Tulinius, M.H.5
Andersen, O.6
-
23
-
-
0028147810
-
1H spectroscopic imaging
-
1H spectroscopic imaging. Ann. Neurol., 36: 157-165.
-
(1994)
Ann. Neurol.
, vol.36
, pp. 157-165
-
-
Husted, C.A.1
Goodin, D.S.2
Hugg, J.W.3
Maudsley, A.A.4
Tsuruda, J.S.5
De Bie, S.H.6
Fein, G.7
Matson, G.B.8
Weiner, M.W.9
-
24
-
-
0026757115
-
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy
-
Johns, D.R., Neufeld, M.J. and Park, R.D. (1992) An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy. Biochem. Biophys. Res. Commun., 187: 1551-1557.
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.187
, pp. 1551-1557
-
-
Johns, D.R.1
Neufeld, M.J.2
Park, R.D.3
-
25
-
-
0028342847
-
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene with maternally inherited Leber hereditary optic neuropathy and dystonia
-
Jun, A.S., Brown, M.D. and Wallace, D.C. (1994) A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene with maternally inherited Leber hereditary optic neuropathy and dystonia. Proc. Natl. Acad. Sci. USA, 91: 6206-6210.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 6206-6210
-
-
Jun, A.S.1
Brown, M.D.2
Wallace, D.C.3
-
26
-
-
0029279163
-
Mitochondrial DNA mutations in multiple sclerosis
-
Kalman, B., Lublin, F.D. and Alder, H. (1995) Mitochondrial DNA mutations in multiple sclerosis. Multiple Sclerosis, 1: 32-36.
-
(1995)
Multiple Sclerosis
, vol.1
, pp. 32-36
-
-
Kalman, B.1
Lublin, F.D.2
Alder, H.3
-
27
-
-
0028337837
-
Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis
-
Kellar-Wood, H., Robertson, N., Govan, G.G., Compston, D.A.S. and Harding, A.E. (1994) Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Ann. Neurol., 36: 109-112.
-
(1994)
Ann. Neurol.
, vol.36
, pp. 109-112
-
-
Kellar-Wood, H.1
Robertson, N.2
Govan, G.G.3
Compston, D.A.S.4
Harding, A.E.5
-
28
-
-
0000514888
-
Leber's disease with symptoms resembling disseminated sclerosis
-
Lees, F., MacDonald, A.-M. and Aldren Turner, J.W. (1964) Leber's disease with symptoms resembling disseminated sclerosis. J. Neurol. Neurosurg. Psychiatry, 27: 415-421.
-
(1964)
J. Neurol. Neurosurg. Psychiatry
, vol.27
, pp. 415-421
-
-
Lees, F.1
MacDonald, A.-M.2
Aldren Turner, J.W.3
-
29
-
-
0025312304
-
Maternally transmitted histocompatibility antigen of mice: A hydrophobic peptide of a mitochondrially encoded protein
-
Loveland, B., Wang, C.R., Yonekawa, H., Hermel, E. and Lindahl, K.F. (1990) Maternally transmitted histocompatibility antigen of mice: A hydrophobic peptide of a mitochondrially encoded protein. Cell, 60: 971-980.
-
(1990)
Cell
, vol.60
, pp. 971-980
-
-
Loveland, B.1
Wang, C.R.2
Yonekawa, H.3
Hermel, E.4
Lindahl, K.F.5
-
30
-
-
0002387271
-
Leber's disease. A genealogic, genetic and clinical study of 101 cases of retrobulbar optic neuritis in 20 Danish families
-
Lundsgaard, R. (1994) Leber's disease. A genealogic, genetic and clinical study of 101 cases of retrobulbar optic neuritis in 20 Danish families. Acta Ophthalmol. (Suppl.), 21: 300-306.
-
(1994)
Acta Ophthalmol.
, vol.21
, Issue.SUPPL.
, pp. 300-306
-
-
Lundsgaard, R.1
-
31
-
-
0026609572
-
Discordance of the T-cell receptor alpha-chain gene in familial multiple sclerosis
-
Lynch, S.G., Rose, J.W., Petajan, J.H. and Leppert, M. (1992) Discordance of the T-cell receptor alpha-chain gene in familial multiple sclerosis. Neurology, 42: 839-844.
-
(1992)
Neurology
, vol.42
, pp. 839-844
-
-
Lynch, S.G.1
Rose, J.W.2
Petajan, J.H.3
Leppert, M.4
-
32
-
-
0025986996
-
Discordance of T-cell receptor β-chain genes in familial multiple sclerosis
-
Lynch, S.G., Rose, J.W., Petajan, J.H., Stauffer, D., Kamerath, C. and Leppert, M. (1991) Discordance of T-cell receptor β-chain genes in familial multiple sclerosis. Ann. Neurol., 30: 402-410.
-
(1991)
Ann. Neurol.
, vol.30
, pp. 402-410
-
-
Lynch, S.G.1
Rose, J.W.2
Petajan, J.H.3
Stauffer, D.4
Kamerath, C.5
Leppert, M.6
-
33
-
-
0026746739
-
A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology
-
Mackey, D. and Howell, N. (1992) A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology. Am. J. Hum. Genet., 51: 1218-1228.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 1218-1228
-
-
Mackey, D.1
Howell, N.2
-
34
-
-
0026409821
-
Normal variants of human mitochondrial DNA and translation products: The building of a reference data base
-
Marzuki, S., Noer, A.S., Letrit, P., Thyagarajan, D., Kapsa, R., Utthanaphol, P. and Byrne, E. (1991) Normal variants of human mitochondrial DNA and translation products: the building of a reference data base. Hum. Genet., 88: 139-145.
-
(1991)
Hum. Genet.
, vol.88
, pp. 139-145
-
-
Marzuki, S.1
Noer, A.S.2
Letrit, P.3
Thyagarajan, D.4
Kapsa, R.5
Utthanaphol, P.6
Byrne, E.7
-
35
-
-
0001296348
-
Reply to Howell et al: The need for a joint effort in the construction of a reference data base for normal sequence variants of human mtDNA
-
Marzuki, S., Letrit, P., Noer, A.S., Kapsa, R., Sudoyo, R.M.I., Byrne, E. and Thyagarajan, D. (1992) Reply to Howell et al: the need for a joint effort in the construction of a reference data base for normal sequence variants of human mtDNA. Am. J. Hum. Genet. 50: 1337-1340.
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 1337-1340
-
-
Marzuki, S.1
Letrit, P.2
Noer, A.S.3
Kapsa, R.4
Sudoyo, R.M.I.5
Byrne, E.6
Thyagarajan, D.7
-
36
-
-
0027180961
-
Leber's hereditary optic neuropathy. New genetic considerations. Review article
-
Newman, N.J. (1993) Leber's hereditary optic neuropathy. New genetic considerations. Review article. Arch. Neurol., 50: 540-547.
-
(1993)
Arch. Neurol.
, vol.50
, pp. 540-547
-
-
Newman, N.J.1
-
37
-
-
0026468520
-
Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy
-
Obayashi, T., Hattori, K., Sugiyama, S., Tanaka, M., Tanaka, T., Itoyama, S., Deguchi, H., Kawamura, K., Koga, Y., Toshima, H., Takeda, N., Nagano, M., Ito, T. and Ozawa, T. (1992) Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy. Am. Heart J., 124: 1263-1269.
-
(1992)
Am. Heart J.
, vol.124
, pp. 1263-1269
-
-
Obayashi, T.1
Hattori, K.2
Sugiyama, S.3
Tanaka, M.4
Tanaka, T.5
Itoyama, S.6
Deguchi, H.7
Kawamura, K.8
Koga, Y.9
Toshima, H.10
Takeda, N.11
Nagano, M.12
Ito, T.13
Ozawa, T.14
-
38
-
-
0028957580
-
Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harboring the mitochondrial DNA 11778 mutation
-
Olsen, N.K., Hansen, A.W., Norby, S., Edal, A.L., Jorgensen, J.R. and Rosenberg, T. (1995) Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harboring the mitochondrial DNA 11778 mutation. Acta Neurol. Scand., 91: 326-329.
-
(1995)
Acta Neurol. Scand.
, 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
-
39
-
-
0019424530
-
Immunoglobulin G heavy chain (Gm) allotypes in multiple sclerosis
-
Pandey, J.P., Goust, J.M. and Salier, J.P. (1981) Immunoglobulin G heavy chain (Gm) allotypes in multiple sclerosis. J. Clin. Invest., 67: 1797-1800.
-
(1981)
J. Clin. Invest.
, vol.67
, pp. 1797-1800
-
-
Pandey, J.P.1
Goust, J.M.2
Salier, J.P.3
-
40
-
-
0020686503
-
New diagnostic criteria for multiple sclerosis: Guidelines for research protocols
-
Poser, C.M., Paty, D.W., Scheinberg, L., McDonald, W.I., Davis, F.A., Ebers, G.C., Johnson, K.P., Sibley, W.A., Silberberg, D.H. and Tourtelotte, W.W. (1983) New diagnostic criteria for multiple sclerosis: guidelines for research protocols. Ann. Neurol., 13: 227-231.
-
(1983)
Ann. Neurol.
, vol.13
, pp. 227-231
-
-
Poser, C.M.1
Paty, D.W.2
Scheinberg, L.3
McDonald, W.I.4
Davis, F.A.5
Ebers, G.C.6
Johnson, K.P.7
Sibley, W.A.8
Silberberg, D.H.9
Tourtelotte, W.W.10
-
41
-
-
0027226069
-
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromatic deafness
-
Prezant, T.R., Agapian, J.V., Bohlman, M.C., Bu, X., Oztas, S., Qiu, W.Q., Arnos, K.S., Coropassi, G.A., Jaber, L., Rotter, J.I., Shohat, M. and Fischel-Ghodsian, N. (1993) Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromatic deafness. Nature Genet., 4: 289-294.
-
(1993)
Nature Genet.
, vol.4
, pp. 289-294
-
-
Prezant, T.R.1
Agapian, J.V.2
Bohlman, M.C.3
Bu, X.4
Oztas, S.5
Qiu, W.Q.6
Arnos, K.S.7
Coropassi, G.A.8
Jaber, L.9
Rotter, J.I.10
Shohat, M.11
Fischel-Ghodsian, N.12
-
42
-
-
0028949749
-
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mulation
-
Riordan-Eva, P., Sanders, M.D., Govan, G.G., Sweeney, M.G., Da Costa, J. and Harding, A.E. (1995) The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mulation. Brain, 118: 319-337.
-
(1995)
Brain
, vol.118
, pp. 319-337
-
-
Riordan-Eva, P.1
Sanders, M.D.2
Govan, G.G.3
Sweeney, M.G.4
Da Costa, J.5
Harding, A.E.6
-
43
-
-
0026013435
-
Parent child concordance in multiple sclerosis
-
Sadovnick, A.D., Bulman, D. and Ebers, G.C. (1991) Parent child concordance in multiple sclerosis. Ann. Neurol., 29: 252-255.
-
(1991)
Ann. Neurol.
, vol.29
, pp. 252-255
-
-
Sadovnick, A.D.1
Bulman, D.2
Ebers, G.C.3
-
44
-
-
0025232653
-
A mitochondrial encephalomyopathy with specific deficiencies of two respiratory chain polypeptides and a circulating auto-antibody to a mitochondrial matrix protein
-
Schapira, A.H.V., Cooper, J.M., Manneschi, L., Vital, C., Morgan-Hughes, J.A. and Clark, J.B. (1990) A mitochondrial encephalomyopathy with specific deficiencies of two respiratory chain polypeptides and a circulating auto-antibody to a mitochondrial matrix protein. Brain, 113: 419-432
-
(1990)
Brain
, vol.113
, pp. 419-432
-
-
Schapira, A.H.V.1
Cooper, J.M.2
Manneschi, L.3
Vital, C.4
Morgan-Hughes, J.A.5
Clark, J.B.6
-
45
-
-
0024406282
-
A susceptibility locus for multiple sclerosis is linked to the T cell receptor β chain complex
-
Seboun, E., Robinson, M.A., Doolittle, T.H., Ciulla, T.A., Kindt, T.J. and Hauser, S.L. (1989) A susceptibility locus for multiple sclerosis is linked to the T cell receptor β chain complex. Cell, 57: 1095-1100.
-
(1989)
Cell
, vol.57
, pp. 1095-1100
-
-
Seboun, E.1
Robinson, M.A.2
Doolittle, T.H.3
Ciulla, T.A.4
Kindt, T.J.5
Hauser, S.L.6
-
46
-
-
0027200741
-
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients
-
Shoffner, J.M., Brown, M.D., Torroni, A., Lott, M.T., Cabell, M.F., Mirra, S.S., Beal, M.F., Yang, C.C., Gearing, M., Salvo, R., Watts, R.L., Juncos, J.L., Hansen, L.A., Crain, B.J., Fayad, M., Reckord, C.L. and Wallace, D.C. (1993) Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. Genomics, 17: 171-184.
-
(1993)
Genomics
, vol.17
, pp. 171-184
-
-
Shoffner, J.M.1
Brown, M.D.2
Torroni, A.3
Lott, M.T.4
Cabell, M.F.5
Mirra, S.S.6
Beal, M.F.7
Yang, C.C.8
Gearing, M.9
Salvo, R.10
Watts, R.L.11
Juncos, J.L.12
Hansen, L.A.13
Crain, B.J.14
Fayad, M.15
Reckord, C.L.16
Wallace, D.C.17
-
47
-
-
0029041731
-
Antibodies to human optic nerve in Leber's hereditary optic neuropathy
-
Smith, P.R., Cooper, J.M., Govan, G.G., Riordan-Eva, P., Harding, A.E. and Schapira, A.H.V. (1995) Antibodies to human optic nerve in Leber's hereditary optic neuropathy. J. Neurol. Sci., 130: 134-138.
-
(1995)
J. Neurol. Sci.
, vol.130
, pp. 134-138
-
-
Smith, P.R.1
Cooper, J.M.2
Govan, G.G.3
Riordan-Eva, P.4
Harding, A.E.5
Schapira, A.H.V.6
-
48
-
-
0025292979
-
Association between the lack of HLA DQw6 and the low incidence of multiple sclerosis in Hungarian Gypsies
-
Takacs, K., Kalman, B., Gyodi, E., Tauszik, T., Palffy, Gy., Kuntar, L., Guseo, A., Nagy, Cs. and Petranyi, Gy. (1990) Association between the lack of HLA DQw6 and the low incidence of multiple sclerosis in Hungarian Gypsies. Immunogenetics, 31: 383-385.
-
(1990)
Immunogenetics
, vol.31
, pp. 383-385
-
-
Takacs, K.1
Kalman, B.2
Gyodi, E.3
Tauszik, T.4
Palffy, Gy.5
Kuntar, L.6
Guseo, A.7
Nagy, Cs.8
Petranyi, Gy.9
-
49
-
-
0026670087
-
Genetic susceptibility to multiple sclerosis linked to myelin basic protein gene
-
Tienari, P.J., Wikstrom, J., Sajantila, A., Palo, J. and Peltonen, L. (1992) Genetic susceptibility to multiple sclerosis linked to myelin basic protein gene. Lancet, 340: 987-991.
-
(1992)
Lancet
, vol.340
, pp. 987-991
-
-
Tienari, P.J.1
Wikstrom, J.2
Sajantila, A.3
Palo, J.4
Peltonen, L.5
-
51
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
Wallace, D.C., Singh, G., Lou, M.T., Hodge, J.A., Schurr, T.G., Lezza, M.S., Elsas II, E.J. and Nikoskelainen, E.K. (1988) Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science, 242: 1427-1430.
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lou, M.T.3
Hodge, J.A.4
Schurr, T.G.5
Lezza, M.S.6
Elsas E.J. II7
Nikoskelainen, E.K.8
-
52
-
-
0001944794
-
Report of the committee on human mitochondrial DNA
-
Wallace, D.C., Lott, M.T., Torroni, A., Brown, M.D. and Shoffner, J.M. (1993) Report of the committee on human mitochondrial DNA. Human Gene Mapping, pp. 813-845.
-
(1993)
Human Gene Mapping
, pp. 813-845
-
-
Wallace, D.C.1
Lott, M.T.2
Torroni, A.3
Brown, M.D.4
Shoffner, J.M.5
-
53
-
-
0021132161
-
Is the myelin membrane abnormal in multiple sclerosis?
-
Wood, D.D. and Moscarello, M.A. (1984) Is the myelin membrane abnormal in multiple sclerosis? J. Membr. Biol., 79: 195-201.
-
(1984)
J. Membr. Biol.
, vol.79
, pp. 195-201
-
-
Wood, D.D.1
Moscarello, M.A.2
|