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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 11, 2007
Somatostatin receptor scintigraphy in the follow-up of myasthenia gravis
Z R Gao, C Kornblum, S Flacke, et al.
Journal of Neurology
|
April 1, 1997
Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus
K Bürk, G Stevanin, O Didierjean, et al.
American Journal of Human Genetics
|
January 1, 1995
Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity
S Gispert, N Santos, R Damen, et al.
Journal of Neurochemistry
|
February 12, 1998
Cooperative interception of neuronal apoptosis by BCL-2 and BAG-1 expression: prevention of caspase activation and reduced production of reactive oxygen species
J B Schulz, D Bremen, J C Reed, et al.
Journal of the Neurological Sciences
|
December 16, 1998
Risk factors for idiopathic cerebellar ataxia of late onset
T Klockgether, K Bürk, U Wüllner, et al.
Clinical Neuropathology
|
December 5, 2006
Neuronal intranuclear inclusions, dysregulation of cytokine expression and cell death in spinocerebellar ataxia type 3
B O Evert, J Schelhaas, H Fleischer, et al.
Acta Neuropathologica
|
May 18, 2001
Molecular genetic alterations in glioblastomas with oligodendroglial component
J A Kraus, K Lamszus, N Glesmann, et al.
Neuroscience Letters
|
October 27, 2009
The variant methylenetetrahydrofolate reductase c.1298A>C (p.E429A) is associated with multiple sclerosis in a German case-control study
L Klotz, M Farkas, N Bain, et al.
AJNR. American Journal of Neuroradiology
|
September 15, 2006
Does high-field MR imaging have an influence on the classification of patients with clinically isolated syndromes according to current diagnostic mr imaging criteria for multiple sclerosis?
M P Wattjes, M Harzheim, C K Kuhl, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 10, 1999
Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD)
T Klockgether, L Schöls, M Abele, et al.
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of 24
Search research articles
Search
Showing results (181-190 of 236) with videos related to
Sort By:
Page
of 24
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 11, 2007
Somatostatin receptor scintigraphy in the follow-up of myasthenia gravis
Z R Gao, C Kornblum, S Flacke, et al.
Journal of Neurology
|
April 1, 1997
Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus
K Bürk, G Stevanin, O Didierjean, et al.
American Journal of Human Genetics
|
January 1, 1995
Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity
S Gispert, N Santos, R Damen, et al.
Journal of Neurochemistry
|
February 12, 1998
Cooperative interception of neuronal apoptosis by BCL-2 and BAG-1 expression: prevention of caspase activation and reduced production of reactive oxygen species
J B Schulz, D Bremen, J C Reed, et al.
Journal of the Neurological Sciences
|
December 16, 1998
Risk factors for idiopathic cerebellar ataxia of late onset
T Klockgether, K Bürk, U Wüllner, et al.
Clinical Neuropathology
|
December 5, 2006
Neuronal intranuclear inclusions, dysregulation of cytokine expression and cell death in spinocerebellar ataxia type 3
B O Evert, J Schelhaas, H Fleischer, et al.
Acta Neuropathologica
|
May 18, 2001
Molecular genetic alterations in glioblastomas with oligodendroglial component
J A Kraus, K Lamszus, N Glesmann, et al.
Neuroscience Letters
|
October 27, 2009
The variant methylenetetrahydrofolate reductase c.1298A>C (p.E429A) is associated with multiple sclerosis in a German case-control study
L Klotz, M Farkas, N Bain, et al.
AJNR. American Journal of Neuroradiology
|
September 15, 2006
Does high-field MR imaging have an influence on the classification of patients with clinically isolated syndromes according to current diagnostic mr imaging criteria for multiple sclerosis?
M P Wattjes, M Harzheim, C K Kuhl, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 10, 1999
Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD)
T Klockgether, L Schöls, M Abele, et al.
Page
of 24