Search research articles
Contact Us
Filters
Showing results (211-220 of 241) with videos related to
Page
of 25
Sort By:
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1985
A study of the relationship between neurological function and serum vitamin E concentrations in patients with cystic fibrosis
H J Willison, D P Muller, S Matthews, et al.
Annals of Neurology
|
April 1, 1995
A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European families
T T Warner, L D Williams, R W Walker, et al.
The Quarterly Journal of Medicine
|
January 1, 1988
Psychiatric and neurological manifestations in systemic lupus erythematosus
L Lim, M A Ron, I E Ormerod, et al.
QJM : Monthly Journal of the Association of Physicians
|
March 1, 1995
Management of mitochondrial disease on an intensive care unit
R S Howard, S Russell, N Losseff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 1, 1993
Linkage analysis with chromosome 9 markers in hereditary essential tremor
D Conway, P G Bain, T T Warner, et al.
Brain : a Journal of Neurology
|
June 1, 1993
Linkage analysis in British and French families with idiopathic torsion dystonia
T T Warner, N A Fletcher, M B Davis, 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.
Experimental Neurology
|
May 1, 1991
Insertions in the prion protein gene in atypical dementias
F Owen, M Poulter, J Collinge, et al.
Annals of Neurology
|
August 1, 1991
Presynaptic and postsynaptic striatal dopaminergic function in neuroacanthocytosis: a positron emission tomographic study
D J Brooks, V Ibanez, E D Playford, et al.
Brain : a Journal of Neurology
|
December 1, 1995
Persistent functional deficit in multiple sclerosis and autosomal dominant cerebellar ataxia is associated with axon loss
C A Davie, G J Barker, S Webb, et al.
Page
of 25
Search research articles
Search
Showing results (211-220 of 241) with videos related to
Sort By:
Page
of 25
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1985
A study of the relationship between neurological function and serum vitamin E concentrations in patients with cystic fibrosis
H J Willison, D P Muller, S Matthews, et al.
Annals of Neurology
|
April 1, 1995
A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European families
T T Warner, L D Williams, R W Walker, et al.
The Quarterly Journal of Medicine
|
January 1, 1988
Psychiatric and neurological manifestations in systemic lupus erythematosus
L Lim, M A Ron, I E Ormerod, et al.
QJM : Monthly Journal of the Association of Physicians
|
March 1, 1995
Management of mitochondrial disease on an intensive care unit
R S Howard, S Russell, N Losseff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 1, 1993
Linkage analysis with chromosome 9 markers in hereditary essential tremor
D Conway, P G Bain, T T Warner, et al.
Brain : a Journal of Neurology
|
June 1, 1993
Linkage analysis in British and French families with idiopathic torsion dystonia
T T Warner, N A Fletcher, M B Davis, 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.
Experimental Neurology
|
May 1, 1991
Insertions in the prion protein gene in atypical dementias
F Owen, M Poulter, J Collinge, et al.
Annals of Neurology
|
August 1, 1991
Presynaptic and postsynaptic striatal dopaminergic function in neuroacanthocytosis: a positron emission tomographic study
D J Brooks, V Ibanez, E D Playford, et al.
Brain : a Journal of Neurology
|
December 1, 1995
Persistent functional deficit in multiple sclerosis and autosomal dominant cerebellar ataxia is associated with axon loss
C A Davie, G J Barker, S Webb, et al.
Page
of 25