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Neurology
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July 27, 2001
Patterns of disease in concordant parent-child pairs with multiple sclerosis
R Hupperts, S Broadley, A Mander, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
April 25, 2000
Multiple sclerosis and tonsillectomy: no evidence for an influence on the development of disease or clinical phenotype
S A Broadley, J Deans, S J Chataway, et al.
Journal of Neurology
|
May 1, 1995
Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis
R M Chalmers, N Robertson, H Kellar-Wood, et al.
Immunology
|
May 1, 1992
Oligodendrocytes lack glycolipid anchored proteins which protect them against complement lysis. Restoration of resistance to lysis by incorporation of CD59
M G Wing, J Zajicek, D J Seilly, et al.
Annals of Neurology
|
July 1, 1994
Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis
H Kellar-Wood, N Robertson, G G Govan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 1, 1992
EDMUS, a European database for multiple sclerosis
C Confavreux, D A Compston, O R Hommes, et al.
Immunology
|
August 1, 1989
Reversible injury of cultured rat oligodendrocytes by complement
N J Scolding, W A Houston, B P Morgan, et al.
Lancet (London, England)
|
December 5, 1981
Optic neuritis and multiple sclerosis: do factor B alleles influence progression of disease?
A H Fielder, J R Batchelor, B N Vakarelis, et al.
Brain : a Journal of Neurology
|
August 1, 1989
The role of complement in the pathogenesis of experimental allergic encephalomyelitis
C Linington, B P Morgan, N J Scolding, et al.
Journal of Neuroimmunology
|
May 1, 1989
Myelin-oligodendrocyte glycoprotein (MOG) is a surface marker of oligodendrocyte maturation
N J Scolding, S Frith, C Linington, et al.
Page
of 12
Search research articles
Search
Showing results (71-80 of 118) with videos related to
Sort By:
Page
of 12
Neurology
|
July 27, 2001
Patterns of disease in concordant parent-child pairs with multiple sclerosis
R Hupperts, S Broadley, A Mander, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
April 25, 2000
Multiple sclerosis and tonsillectomy: no evidence for an influence on the development of disease or clinical phenotype
S A Broadley, J Deans, S J Chataway, et al.
Journal of Neurology
|
May 1, 1995
Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis
R M Chalmers, N Robertson, H Kellar-Wood, et al.
Immunology
|
May 1, 1992
Oligodendrocytes lack glycolipid anchored proteins which protect them against complement lysis. Restoration of resistance to lysis by incorporation of CD59
M G Wing, J Zajicek, D J Seilly, et al.
Annals of Neurology
|
July 1, 1994
Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis
H Kellar-Wood, N Robertson, G G Govan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 1, 1992
EDMUS, a European database for multiple sclerosis
C Confavreux, D A Compston, O R Hommes, et al.
Immunology
|
August 1, 1989
Reversible injury of cultured rat oligodendrocytes by complement
N J Scolding, W A Houston, B P Morgan, et al.
Lancet (London, England)
|
December 5, 1981
Optic neuritis and multiple sclerosis: do factor B alleles influence progression of disease?
A H Fielder, J R Batchelor, B N Vakarelis, et al.
Brain : a Journal of Neurology
|
August 1, 1989
The role of complement in the pathogenesis of experimental allergic encephalomyelitis
C Linington, B P Morgan, N J Scolding, et al.
Journal of Neuroimmunology
|
May 1, 1989
Myelin-oligodendrocyte glycoprotein (MOG) is a surface marker of oligodendrocyte maturation
N J Scolding, S Frith, C Linington, et al.
Page
of 12