-
3
-
-
0031439343
-
Nitric oxide donors reversibly block axonal conduction: Demyelinated axons are especially susceptible
-
Redford EJ, Kapoor R, Smith KJ. Nitric oxide donors reversibly block axonal conduction: demyelinated axons are especially susceptible. Brain 1997;120:2149-57.
-
(1997)
Brain
, vol.120
, pp. 2149-2157
-
-
Redford, E.J.1
Kapoor, R.2
Smith, K.J.3
-
4
-
-
0035067635
-
Electrically active axons degenerate when exposed to nitric oxide
-
Smith KJ, Kapoor R, Hall SM, Davies M. Electrically active axons degenerate when exposed to nitric oxide. Ann Neurol 2001;49:470-6.
-
(2001)
Ann Neurol
, vol.49
, pp. 470-476
-
-
Smith, K.J.1
Kapoor, R.2
Hall, S.M.3
Davies, M.4
-
5
-
-
0036158610
-
Oligodendrocyte precursor cells in the demyelinated multiple sclerosis spinal cord
-
Wolswijk G. Oligodendrocyte precursor cells in the demyelinated multiple sclerosis spinal cord. Brain 2002;125:338-49.
-
(2002)
Brain
, vol.125
, pp. 338-349
-
-
Wolswijk, G.1
-
6
-
-
85039487102
-
The window of therapeutic opportunity in multiple sclerosis: Evidence from monoclonal antibody therapy in relapsing-remitting and secondary progressive disease
-
in press
-
Coles AJ, Le Page E, Cox AL, Goodin DS et al. The window of therapeutic opportunity in multiple sclerosis: evidence from monoclonal antibody therapy in relapsing-remitting and secondary progressive disease. Ann Neurol (in press).
-
Ann Neurol
-
-
Coles, A.J.1
Le Page, E.2
Cox, A.L.3
Goodin, D.S.4
-
7
-
-
0038452761
-
Oligodendrocytes promote neuronal survival and axonal length by distinct intracellular mechanisms: A novel role for oligodendrocyte-derived glial cell line-derived neurotrophic factor
-
Wilkins A, Majed H, Layfield R, Compston A et al. Oligodendrocytes promote neuronal survival and axonal length by distinct intracellular mechanisms: a novel role for oligodendrocyte-derived glial cell line-derived neurotrophic factor. J Neurosci 2003;23:4967-74.
-
(2003)
J Neurosci
, vol.23
, pp. 4967-4974
-
-
Wilkins, A.1
Majed, H.2
Layfield, R.3
Compston, A.4
-
8
-
-
0342906187
-
Heterogeneity of multiple sclerosis lesions: Implications for the pathogenesis of demyelination
-
Lucchinetti C, Brück W, Parisi J, Scheithauer B et al. Heterogeneity of multiple sclerosis lesions: Implications for the pathogenesis of demyelination. Ann Neurol 2000;47:707-17.
-
(2000)
Ann Neurol
, vol.47
, pp. 707-717
-
-
Lucchinetti, C.1
Brück, W.2
Parisi, J.3
Scheithauer, B.4
-
9
-
-
0000134011
-
Observations on the prevalence of multiple sclerosis in northern Scotland
-
Sutherland JM. Observations on the prevalence of multiple sclerosis in northern Scotland. Brain 1956;79:635-54.
-
(1956)
Brain
, vol.79
, pp. 635-654
-
-
Sutherland, J.M.1
-
10
-
-
0028020987
-
The dissemination of multiple sclerosis: A Viking Saga? A historical essay
-
Poser CM. The dissemination of multiple sclerosis: A Viking Saga? A historical essay. Ann Neurol 1994;36:S231-S234.
-
(1994)
Ann Neurol
, vol.36
-
-
Poser, C.M.1
-
11
-
-
0022726496
-
Who are the Orcadians?
-
Roberts DF. Who are the Orcadians? Anthrop Anzeiger 1986;44:93-104.
-
(1986)
Anthrop Anzeiger
, vol.44
, pp. 93-104
-
-
Roberts, D.F.1
-
12
-
-
0012444905
-
Myelite subaigue compliquee de nevrite optique
-
Devic E. Myelite subaigue compliquee de nevrite optique. Bull Med (Lyon) 1894;35:18-30.
-
(1894)
Bull Med (Lyon)
, vol.35
, pp. 18-30
-
-
Devic, E.1
-
14
-
-
0036310181
-
A role for humoral mechanisms in the pathogenesis of Devic's neuromyelitis optica
-
Lucchinetti CF, Mandler RN, McGavern D, Bruck W et al. A role for humoral mechanisms in the pathogenesis of Devic's neuromyelitis optica. Brain 2002;125:1450-61.
-
(2002)
Brain
, vol.125
, pp. 1450-1461
-
-
Lucchinetti, C.F.1
Mandler, R.N.2
McGavern, D.3
Bruck, W.4
-
15
-
-
0002374718
-
Neurological disorders in Nigeria
-
JD Spillane (ed). London: Oxford University Press
-
Osuntokun BO. Neurological disorders in Nigeria. In: JD Spillane (ed), Tropical neurology. London: Oxford University Press, 1973:161-90.
-
(1973)
Tropical Neurology
, pp. 161-190
-
-
Osuntokun, B.O.1
-
17
-
-
0035059815
-
Demyelinating disorder of the central nervous system occurring in black South Africans
-
Modi G, Mochan A, Modi M, Saffer D. Demyelinating disorder of the central nervous system occurring in black South Africans. J Neurol Neurosurg Psychiatry 2001;70:500-5.
-
(2001)
J Neurol Neurosurg Psychiatry
, vol.70
, pp. 500-505
-
-
Modi, G.1
Mochan, A.2
Modi, M.3
Saffer, D.4
-
18
-
-
0022408164
-
Multiple sclerosis: Indian experience in the last thirty years
-
Jain S, Maheshwari MC. Multiple sclerosis: Indian experience in the last thirty years. Neuroepidemiol 1985;4:96-107.
-
(1985)
Neuroepidemiol
, vol.4
, pp. 96-107
-
-
Jain, S.1
Maheshwari, M.C.2
-
19
-
-
0023895390
-
Multiple sclerosis in Malaysia
-
Tan CT. Multiple sclerosis in Malaysia. Arch Neurol 1988;45;624-7.
-
(1988)
Arch Neurol
, vol.45
, pp. 624-627
-
-
Tan, C.T.1
-
20
-
-
0014281338
-
Multiple sclerosis in Korea. Clinical features and prevalence
-
Kurzke JF, Park CS, Oh SJ. Multiple sclerosis in Korea. Clinical features and prevalence. J Neurol Sci 1968;6:463-81.
-
(1968)
J Neurol Sci
, vol.6
, pp. 463-481
-
-
Kurzke, J.F.1
Park, C.S.2
Oh, S.J.3
-
21
-
-
0024789540
-
Multiple sclerosis amongst Chinese in Hong Kong
-
Yu YL, Woo E, Hawkins BR, Ho HC, Huang CY. Multiple sclerosis amongst Chinese in Hong Kong. Brain 1989;112:1445-567.
-
(1989)
Brain
, vol.112
, pp. 1445-1567
-
-
Yu, Y.L.1
Woo, E.2
Hawkins, B.R.3
Ho, H.C.4
Huang, C.Y.5
-
22
-
-
0000094236
-
Multiple sclerosis and allied diseases in Japan. Clinical characteristics
-
Okinaka S, Tsubaki T, Kuroiwa Y, Toyokura Y et al. Multiple sclerosis and allied diseases in Japan. Clinical characteristics. Neurology 1958;8:756-63.
-
(1958)
Neurology
, vol.8
, pp. 756-763
-
-
Okinaka, S.1
Tsubaki, T.2
Kuroiwa, Y.3
Toyokura, Y.4
-
23
-
-
0019364238
-
Racial modification of clinical picture of multiple sclerosis; comparison between British and Japanese patients
-
Shibasaki H, McDonald WI, Kuroiwa Y. Racial modification of clinical picture of multiple sclerosis; comparison between British and Japanese patients. J Neurol Sci 1981;49:253-71.
-
(1981)
J Neurol Sci
, vol.49
, pp. 253-271
-
-
Shibasaki, H.1
McDonald, W.I.2
Kuroiwa, Y.3
-
24
-
-
0035852870
-
Aboriginals with multiple sclerosis: HLA types and predominance of neuromyelitis optica
-
Mirsattari SM, Johnston JB, McKenna R, Del Bigio MR et al. Aboriginals with multiple sclerosis: HLA types and predominance of neuromyelitis optica. Neurology 2001;56:317-23.
-
(2001)
Neurology
, vol.56
, pp. 317-323
-
-
Mirsattari, S.M.1
Johnston, J.B.2
McKenna, R.3
Del Bigio, M.R.4
-
26
-
-
0035957117
-
MS and neuromyelitis optica in Martinique (French West Indies)
-
Cabre P, Heinzlef O, Merle H, Buisson GG et al. MS and neuromyelitis optica in Martinique (French West Indies). Neurology 2001;56:507-14.
-
(2001)
Neurology
, vol.56
, pp. 507-514
-
-
Cabre, P.1
Heinzlef, O.2
Merle, H.3
Buisson, G.G.4
-
28
-
-
0033613643
-
The molecular genetics of European ancestry
-
Sykes B. The molecular genetics of European ancestry. Phil Trans R Soc Lon 1999;354:131-9.
-
(1999)
Phil Trans R Soc Lon
, vol.354
, pp. 131-139
-
-
Sykes, B.1
-
29
-
-
4243200965
-
Genetics and language in contemporary archaelogy
-
Cunliffe B, Davies W, Renfrew C (eds). Oxford: The British Academy/Oxford University Press
-
Renfrew C. Genetics and language in contemporary archaelogy, In: Cunliffe B, Davies W, Renfrew C (eds) Archaeology. The widening debate. Oxford: The British Academy/Oxford University Press, 2002: 43-76.
-
(2002)
Archaeology. The Widening Debate
, pp. 43-76
-
-
Renfrew, C.1
-
30
-
-
0029895378
-
Paleolithic and neolithic lineages in the European mitochondrial gene pool
-
Richards M, Corte-Real H, Forster P, Macaulay V et al. Paleolithic and neolithic lineages in the European mitochondrial gene pool. Am J Hum Genet 1996;59:185-203.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 185-203
-
-
Richards, M.1
Corte-Real, H.2
Forster, P.3
Macaulay, V.4
-
31
-
-
18344366125
-
Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major Afrian, Asian, and European haplogroups
-
Herrnstadt C, Elson JL, Fahy E, Preston G et al. Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major Afrian, Asian, and European haplogroups. Am J Hum Genet 2002;70:1152-71.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1152-1171
-
-
Herrnstadt, C.1
Elson, J.L.2
Fahy, E.3
Preston, G.4
-
32
-
-
0029759665
-
Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement
-
Mayr-Wohlfart U, Paulus C, Hennenberg A, Rodel G. Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement. Acta Neurol Scand 1996;94:167-71.
-
(1996)
Acta Neurol Scand
, vol.94
, pp. 167-171
-
-
Mayr-Wohlfart, U.1
Paulus, C.2
Hennenberg, A.3
Rodel, G.4
-
33
-
-
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, O'Connor J et al. Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians. Acta Neurol Scand 1999;99:16-25.
-
(1999)
Acta Neurol Scand
, vol.99
, pp. 16-25
-
-
Kalman, B.1
Li, S.2
Chatterjee, D.3
O'Connor, J.4
-
36
-
-
0026782507
-
Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation
-
Harding AE, Sweeney MG, Miller DH, Mumford CJ et al. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation. Brain 1992;115: 979-89.
-
(1992)
Brain
, vol.115
, pp. 979-989
-
-
Harding, A.E.1
Sweeney, M.G.2
Miller, D.H.3
Mumford, C.J.4
-
37
-
-
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, Sweeney MG et al. The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation. Brain 1995;118:319-37.
-
(1995)
Brain
, vol.118
, pp. 319-337
-
-
Riordan-Eva, P.1
Sanders, M.D.2
Govan, G.G.3
Sweeney, M.G.4
-
38
-
-
0028337837
-
Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis
-
Kellar-Wood H, Robertson N, Govan GG, Harding AE, Compston DAS. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Ann Neurol 1994b;36:109-12.
-
(1994)
Ann Neurol
, vol.36
, pp. 109-112
-
-
Kellar-Wood, H.1
Robertson, N.2
Govan, G.G.3
Harding, A.E.4
Compston, D.A.S.5
-
39
-
-
0030640474
-
Screening for Leber's hereditary optic neuropathy associated mitochondrial DNA mutations in patients with prominent optic neuritis
-
Kalman B, Rodriguez-Valdez JL, Bosch U, Lublin FD. Screening for Leber's hereditary optic neuropathy associated mitochondrial DNA mutations in patients with prominent optic neuritis. Multiple Sclerosis 1997;2:279-82.
-
(1997)
Multiple Sclerosis
, vol.2
, pp. 279-282
-
-
Kalman, B.1
Rodriguez-Valdez, J.L.2
Bosch, U.3
Lublin, F.D.4
-
40
-
-
0031027322
-
Neuromyelitis optica (Devic's syndrome): No association with the primary mitochondrial DNA mutations found in Leber hereditary optic neuropathy
-
Cock H, Mandler R, Ahmed W, Schapira AH. Neuromyelitis optica (Devic's syndrome): no association with the primary mitochondrial DNA mutations found in Leber hereditary optic neuropathy. J Neurol Neurosurg Psychiatry 1997;62:85-7.
-
(1997)
J Neurol Neurosurg Psychiatry
, vol.62
, pp. 85-87
-
-
Cock, H.1
Mandler, R.2
Ahmed, W.3
Schapira, A.H.4
-
41
-
-
0036231442
-
Studies of mitochondrial DNA in Devic's disease revealed no pathogenic mutations, but polymorphisms also found in association with multiple sclerosis
-
Kalman B, Mandler RN. Studies of mitochondrial DNA in Devic's disease revealed no pathogenic mutations, but polymorphisms also found in association with multiple sclerosis. Ann Neurol 2002;51:661-2.
-
(2002)
Ann Neurol
, vol.51
, pp. 661-662
-
-
Kalman, B.1
Mandler, R.N.2
-
42
-
-
0029153643
-
No association of the 11778 mitochondrial DNA mutation and multiple sclerosis in Japan
-
Nishimura M, Obayashi H, Ohta M, Uchiyama T et al. No association of the 11778 mitochondrial DNA mutation and multiple sclerosis in Japan. Neurology 1995;45:1333-4.
-
(1995)
Neurology
, vol.45
, pp. 1333-1334
-
-
Nishimura, M.1
Obayashi, H.2
Ohta, M.3
Uchiyama, T.4
-
43
-
-
0035657392
-
Leber's hereditary optic neuropathy mutations in Korean patients with multiple sclerosis
-
Hwang IM, Chang BL, Park SS. Leber's hereditary optic neuropathy mutations in Korean patients with multiple sclerosis. Ophthalmologica 2001;215:398-400.
-
(2001)
Ophthalmologica
, vol.215
, pp. 398-400
-
-
Hwang, I.M.1
Chang, B.L.2
Park, S.S.3
-
44
-
-
0029002151
-
Mitochondrial and nuclear genetic contribution of female founders to a contemporary population in Northeast Quebec
-
Heyer E. Mitochondrial and nuclear genetic contribution of female founders to a contemporary population in Northeast Quebec. Am J Hum Genet 1995;56:1450-5.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1450-1455
-
-
Heyer, E.1
-
46
-
-
0018575957
-
Genetic control of survival in epidemics
-
de Vries RR, Khan M, Bernini LF, van Loghem E, van Rood JJ. Genetic control of survival in epidemics. J Immunogenet 1979;6:271-87.
-
(1979)
J Immunogenet
, vol.6
, pp. 271-287
-
-
De Vries, R.R.1
Khan, M.2
Bernini, L.F.3
Van Loghem, E.4
Van Rood, J.J.5
-
47
-
-
0034661806
-
Evolutionary adaptation of inflammatory immune responses in human beings
-
Le Soeuf PN, Goldblatt J, Lynch NR. Evolutionary adaptation of inflammatory immune responses in human beings. Lancet 2000;356: 242-4.
-
(2000)
Lancet
, vol.356
, pp. 242-244
-
-
Le Soeuf, P.N.1
Goldblatt, J.2
Lynch, N.R.3
-
48
-
-
0344721480
-
Complete sequence and gene map of a human major histompatibility complex
-
The MHC Sequencing Consortium. Complete sequence and gene map of a human major histompatibility complex. Nature 1999;401:921-3.
-
(1999)
Nature
, vol.401
, pp. 921-923
-
-
-
50
-
-
0142186253
-
A meta-analysis of whole genome linkage screens in multiple sclerosis
-
GAMES and the Transatlantic Multiple Sclerosis genetics cooperative. A meta-analysis of whole genome linkage screens in multiple sclerosis. J Neuroimmunol 2003;143:39-46.
-
(2003)
J Neuroimmunol
, vol.143
, pp. 39-46
-
-
-
51
-
-
0031025579
-
HLA-DR polymorphism modulates the cytokine profile of Mycobacterium leprae HSP-reactive CD4+ T cells
-
Mitra DK, Rajalingam R, Taneja V, Bhattacharyya BC, Mehra NK. HLA-DR polymorphism modulates the cytokine profile of Mycobacterium leprae HSP-reactive CD4+ T cells. Clin Immunol Immunopathol 1997;82:60-7.
-
(1997)
Clin Immunol Immunopathol
, vol.82
, pp. 60-67
-
-
Mitra, D.K.1
Rajalingam, R.2
Taneja, V.3
Bhattacharyya, B.C.4
Mehra, N.K.5
-
52
-
-
0032126751
-
Notch receptor activation inhibits oligdenrocyte differentiation
-
Wang S, Sdrulla AD, Disibio G, Bush G et al. Notch receptor activation inhibits oligdenrocyte differentiation. Neuron 1998;21:63-75.
-
(1998)
Neuron
, vol.21
, pp. 63-75
-
-
Wang, S.1
Sdrulla, A.D.2
Disibio, G.3
Bush, G.4
-
53
-
-
0036799650
-
Multiple sclerosis: Re-expression of a developmental pathway that restricts oligodendrocyte maturation
-
John GR, Shankar SL, Shafit-Zagardo B, Massimi A et al. Multiple sclerosis: re-expression of a developmental pathway that restricts oligodendrocyte maturation. Nat Med 2002;8:1075-6.
-
(2002)
Nat Med
, vol.8
, pp. 1075-1076
-
-
John, G.R.1
Shankar, S.L.2
Shafit-Zagardo, B.3
Massimi, A.4
-
54
-
-
0036793245
-
A functional and structural basis for TCR cross-reactivity in multiple sclerosis
-
Lang HLE, Jacobsen H, Ikemizu S, Andersson C et al. A functional and structural basis for TCR cross-reactivity in multiple sclerosis. Nature Immunol 2002;3:940-43.
-
(2002)
Nature Immunol
, vol.3
, pp. 940-943
-
-
Lang, H.L.E.1
Jacobsen, H.2
Ikemizu, S.3
Andersson, C.4
-
55
-
-
0035967435
-
Molecular evolution of the alpha-herpesvirinae
-
McGeogh DJ. Molecular evolution of the alpha-herpesvirinae. Phil Trans R Soc Lond 2001;356:421-35.
-
(2001)
Phil Trans R Soc Lond
, vol.356
, pp. 421-435
-
-
McGeogh, D.J.1
-
56
-
-
0022577031
-
Viral infection in patients with multiple sclerosis and HLA-DR matched controls
-
Compston DAS, Vakarelis BN, Paul E, McDonald WI et al. Viral infection in patients with multiple sclerosis and HLA-DR matched controls. Brain 1986;109:325-44.
-
(1986)
Brain
, vol.109
, pp. 325-344
-
-
Compston, D.A.S.1
Vakarelis, B.N.2
Paul, E.3
McDonald, W.I.4
-
58
-
-
0042512328
-
Multiple sclerosis in the Japanese population
-
Kira J-I. Multiple sclerosis in the Japanese population. Lancet Neurology 2003;2:117-27.
-
(2003)
Lancet Neurology
, vol.2
, pp. 117-127
-
-
Kira, J.-I.1
-
59
-
-
0019480498
-
Multiple sclerosis and neuromyelitis optica in tropical and subtropical countries
-
Cosnett JE. Multiple sclerosis and neuromyelitis optica in tropical and subtropical countries. Med Hypoth 1981b;7:61-3.
-
(1981)
Med Hypoth
, vol.7
, pp. 61-63
-
-
Cosnett, J.E.1
|