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Brain : a Journal of Neurology
|
July 2, 1999
Spatial mapping of T2 and gadolinium-enhancing T1 lesion volumes in multiple sclerosis: evidence for distinct mechanisms of lesion genesis?
M A Lee, S Smith, J Palace, et al.
Neurology
|
September 25, 2003
Rapsyn mutations in hereditary myasthenia: distinct early- and late-onset phenotypes
G Burke, J Cossins, S Maxwell, et al.
Pilot and Feasibility Studies
|
February 7, 2018
A protocol for a randomised double-blind placebo-controlled feasibility study to determine whether the daily consumption of flavonoid-rich pure cocoa has the potential to reduce fatigue in people with relapsing and remitting multiple sclerosis (RRMS)
S Coe, J Collett, H Izadi, et al.
Neurology
|
February 4, 2012
Serologic diagnosis of NMO: a multicenter comparison of aquaporin-4-IgG assays
P J Waters, A McKeon, M I Leite, et al.
Neuromuscular Disorders : NMD
|
October 19, 2010
Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myasthenia
P Munot, D Lashley, H Jungbluth, et al.
BMJ Open
|
May 27, 2015
Protocol for a multicentre randomiSed controlled TRial of IntraVEnous immunoglobulin versus standard therapy for the treatment of transverse myelitis in adults and children (STRIVE)
M Absoud, J Gadian, J Hellier, et al.
Neurology
|
July 14, 2004
Absence of antibodies to glutamate receptor type 3 (GluR3) in Rasmussen encephalitis
R Watson, Y Jiang, I Bermudez, et al.
Journal of Neurology
|
November 16, 2007
MRI characteristics of atypical idiopathic inflammatory demyelinating lesions of the brain : A review of reported findings
A Seewann, C Enzinger, M Filippi, et al.
Journal of Neuroimmunology
|
August 19, 2008
Congenital myasthenic syndromes in childhood: diagnostic and management challenges
M Kinali, D Beeson, M C Pitt, et al.
Neurology
|
January 8, 2010
MRI criteria for MS in patients with clinically isolated syndromes
X Montalban, M Tintoré, J Swanton, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 104) with videos related to
Sort By:
Page
of 11
Brain : a Journal of Neurology
|
July 2, 1999
Spatial mapping of T2 and gadolinium-enhancing T1 lesion volumes in multiple sclerosis: evidence for distinct mechanisms of lesion genesis?
M A Lee, S Smith, J Palace, et al.
Neurology
|
September 25, 2003
Rapsyn mutations in hereditary myasthenia: distinct early- and late-onset phenotypes
G Burke, J Cossins, S Maxwell, et al.
Pilot and Feasibility Studies
|
February 7, 2018
A protocol for a randomised double-blind placebo-controlled feasibility study to determine whether the daily consumption of flavonoid-rich pure cocoa has the potential to reduce fatigue in people with relapsing and remitting multiple sclerosis (RRMS)
S Coe, J Collett, H Izadi, et al.
Neurology
|
February 4, 2012
Serologic diagnosis of NMO: a multicenter comparison of aquaporin-4-IgG assays
P J Waters, A McKeon, M I Leite, et al.
Neuromuscular Disorders : NMD
|
October 19, 2010
Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myasthenia
P Munot, D Lashley, H Jungbluth, et al.
BMJ Open
|
May 27, 2015
Protocol for a multicentre randomiSed controlled TRial of IntraVEnous immunoglobulin versus standard therapy for the treatment of transverse myelitis in adults and children (STRIVE)
M Absoud, J Gadian, J Hellier, et al.
Neurology
|
July 14, 2004
Absence of antibodies to glutamate receptor type 3 (GluR3) in Rasmussen encephalitis
R Watson, Y Jiang, I Bermudez, et al.
Journal of Neurology
|
November 16, 2007
MRI characteristics of atypical idiopathic inflammatory demyelinating lesions of the brain : A review of reported findings
A Seewann, C Enzinger, M Filippi, et al.
Journal of Neuroimmunology
|
August 19, 2008
Congenital myasthenic syndromes in childhood: diagnostic and management challenges
M Kinali, D Beeson, M C Pitt, et al.
Neurology
|
January 8, 2010
MRI criteria for MS in patients with clinically isolated syndromes
X Montalban, M Tintoré, J Swanton, et al.
Page
of 11