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Brain : a Journal of Neurology
|
August 1, 1992
Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation
A E Harding, M G Sweeney, D H Miller, et al.
Cell Death and Differentiation
|
January 29, 2011
Derivation of neural precursor cells from human ES cells at 3% O(2) is efficient, enhances survival and presents no barrier to regional specification and functional differentiation
S R L Stacpoole, B Bilican, D J Webber, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
July 1, 1996
CAMPATH-IH in multiple sclerosis
T Moreau, A Coles, M Wing, et al.
Journal of the Neurological Sciences
|
September 1, 1995
Affinity of antigen-specific IgG distinguishes multiple sclerosis from encephalitis
R W Luxton, A Zeman, H Holzel, et al.
Lancet (London, England)
|
November 24, 1999
Pulsed monoclonal antibody treatment and autoimmune thyroid disease in multiple sclerosis
A J Coles, M Wing, S Smith, et al.
Nature Protocols
|
July 30, 2011
Efficient derivation of NPCs, spinal motor neurons and midbrain dopaminergic neurons from hESCs at 3% oxygen
S R L Stacpoole, B Bilican, D J Webber, et al.
Journal of Neuroimmunology
|
October 25, 2003
A genome-wide screen for linkage disequilibrium in Australian HLA-DRB1*1501 positive multiple sclerosis patients
M Ban, S J Sawcer, R N S Heard, et al.
Genes and Immunity
|
July 31, 2001
A genome screen for multiple sclerosis in Italian families
S Broadley, S Sawcer, S D'Alfonso, et al.
Brain : a Journal of Neurology
|
November 3, 1998
The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen
J Chataway, R Feakes, F Coraddu, et al.
Neurogenetics
|
May 18, 1999
HLA typing in the United Kingdom multiple sclerosis genome screen
F Coraddu, S Sawcer, R Feakes, et al.
Page
of 25
Search research articles
Search
Showing results (211-220 of 243) with videos related to
Sort By:
Page
of 25
Brain : a Journal of Neurology
|
August 1, 1992
Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation
A E Harding, M G Sweeney, D H Miller, et al.
Cell Death and Differentiation
|
January 29, 2011
Derivation of neural precursor cells from human ES cells at 3% O(2) is efficient, enhances survival and presents no barrier to regional specification and functional differentiation
S R L Stacpoole, B Bilican, D J Webber, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
July 1, 1996
CAMPATH-IH in multiple sclerosis
T Moreau, A Coles, M Wing, et al.
Journal of the Neurological Sciences
|
September 1, 1995
Affinity of antigen-specific IgG distinguishes multiple sclerosis from encephalitis
R W Luxton, A Zeman, H Holzel, et al.
Lancet (London, England)
|
November 24, 1999
Pulsed monoclonal antibody treatment and autoimmune thyroid disease in multiple sclerosis
A J Coles, M Wing, S Smith, et al.
Nature Protocols
|
July 30, 2011
Efficient derivation of NPCs, spinal motor neurons and midbrain dopaminergic neurons from hESCs at 3% oxygen
S R L Stacpoole, B Bilican, D J Webber, et al.
Journal of Neuroimmunology
|
October 25, 2003
A genome-wide screen for linkage disequilibrium in Australian HLA-DRB1*1501 positive multiple sclerosis patients
M Ban, S J Sawcer, R N S Heard, et al.
Genes and Immunity
|
July 31, 2001
A genome screen for multiple sclerosis in Italian families
S Broadley, S Sawcer, S D'Alfonso, et al.
Brain : a Journal of Neurology
|
November 3, 1998
The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen
J Chataway, R Feakes, F Coraddu, et al.
Neurogenetics
|
May 18, 1999
HLA typing in the United Kingdom multiple sclerosis genome screen
F Coraddu, S Sawcer, R Feakes, et al.
Page
of 25