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Journal of Neurology, Neurosurgery, and Psychiatry
|
June 20, 2001
No association between multiple sclerosis and the Notch3 gene responsible for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
S A Broadley, S J Sawcer, S J Chataway, et al.
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.
Brain : a Journal of Neurology
|
June 1, 1996
Spinal MRI in patients with suspected multiple sclerosis and negative brain MRI
J W Thorpe, D Kidd, I F Moseley, et al.
Clinical and Experimental Dermatology
|
September 1, 1988
Type III collagen mutations in Ehlers Danlos syndrome type IV and other related disorders
F M Pope, A C Nicholls, P Narcisi, et al.
Neurology
|
February 1, 1995
Correlations between changes in disability and T2-weighted brain MRI activity in multiple sclerosis: a follow-up study
M Filippi, D W Paty, L Kappos, et al.
British Journal of Neurosurgery
|
January 1, 1991
Type III collagen mutations cause fragile cerebral arteries
F M Pope, B E Kendall, G I Slapak, et al.
Neuroradiology
|
May 1, 2001
Detection of optic nerve atrophy following a single episode of unilateral optic neuritis by MRI using a fat-saturated short-echo fast FLAIR sequence
S J Hickman, P A Brex, C M Brierley, et al.
Neurology
|
January 27, 1998
Effects of intravenous methylprednisolone on outcome in MRI-based prognostic subgroups in acute optic neuritis
R Kapoor, D H Miller, S J Jones, et al.
Page
of 12
Search research articles
Search
Showing results (111-120 of 118) with videos related to
Sort By:
Page
of 12
You have reached the last page of results.
This site can display upto 118 results.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 20, 2001
No association between multiple sclerosis and the Notch3 gene responsible for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
S A Broadley, S J Sawcer, S J Chataway, et al.
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.
Brain : a Journal of Neurology
|
June 1, 1996
Spinal MRI in patients with suspected multiple sclerosis and negative brain MRI
J W Thorpe, D Kidd, I F Moseley, et al.
Clinical and Experimental Dermatology
|
September 1, 1988
Type III collagen mutations in Ehlers Danlos syndrome type IV and other related disorders
F M Pope, A C Nicholls, P Narcisi, et al.
Neurology
|
February 1, 1995
Correlations between changes in disability and T2-weighted brain MRI activity in multiple sclerosis: a follow-up study
M Filippi, D W Paty, L Kappos, et al.
British Journal of Neurosurgery
|
January 1, 1991
Type III collagen mutations cause fragile cerebral arteries
F M Pope, B E Kendall, G I Slapak, et al.
Neuroradiology
|
May 1, 2001
Detection of optic nerve atrophy following a single episode of unilateral optic neuritis by MRI using a fat-saturated short-echo fast FLAIR sequence
S J Hickman, P A Brex, C M Brierley, et al.
Neurology
|
January 27, 1998
Effects of intravenous methylprednisolone on outcome in MRI-based prognostic subgroups in acute optic neuritis
R Kapoor, D H Miller, S J Jones, et al.
Page
of 12