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Neurobiology of Disease
|
April 2, 2004
Evidence of widespread cerebral microglial activation in amyotrophic lateral sclerosis: an [11C](R)-PK11195 positron emission tomography study
M R Turner, A Cagnin, F E Turkheimer, et al.
Human Molecular Genetics
|
February 5, 1999
Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis
A Al-Chalabi, P M Andersen, P Nilsson, et al.
Clinical Genetics
|
May 23, 2009
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype
B N Smith, S Bevan, C Vance, et al.
Annals of Neurology
|
July 1, 1997
Copper and zinc levels in familial amyotrophic lateral sclerosis patients with CuZnSOD gene mutations
A Radunović, H T Delves, W Robberecht, et al.
Journal of Neurology
|
May 26, 2001
Hereditary pure lower motor neuron disease with adult onset and rapid progression
R M Van den Berg-Vos, L H Van den Berg, G H Jansen, et al.
Lancet (London, England)
|
January 20, 1996
Association of apolipoprotein E epsilon 4 allele with bulbar-onset motor neuron disease
A al-Chalabi, Z E Enayat, M C Bakker, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 19, 2005
Abnormal cortical excitability in sporadic but not homozygous D90A SOD1 ALS
M R Turner, A D Osei-Lah, A Hammers, et al.
Neurology
|
December 30, 2004
No association of the SOD1 locus and disease susceptibility or phenotype in sporadic ALS
W J Broom, M J Parton, C A Vance, et al.
Neuroepidemiology
|
September 28, 2007
Amyotrophic lateral sclerosis in South-East England: a population-based study. The South-East England register for amyotrophic lateral sclerosis (SEALS Registry)
K Abhinav, B Stanton, C Johnston, et al.
Neurology
|
March 25, 2009
Natural history and clinical features of the flail arm and flail leg ALS variants
L C Wijesekera, S Mathers, P Talman, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 76) with videos related to
Sort By:
Page
of 8
Neurobiology of Disease
|
April 2, 2004
Evidence of widespread cerebral microglial activation in amyotrophic lateral sclerosis: an [11C](R)-PK11195 positron emission tomography study
M R Turner, A Cagnin, F E Turkheimer, et al.
Human Molecular Genetics
|
February 5, 1999
Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis
A Al-Chalabi, P M Andersen, P Nilsson, et al.
Clinical Genetics
|
May 23, 2009
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype
B N Smith, S Bevan, C Vance, et al.
Annals of Neurology
|
July 1, 1997
Copper and zinc levels in familial amyotrophic lateral sclerosis patients with CuZnSOD gene mutations
A Radunović, H T Delves, W Robberecht, et al.
Journal of Neurology
|
May 26, 2001
Hereditary pure lower motor neuron disease with adult onset and rapid progression
R M Van den Berg-Vos, L H Van den Berg, G H Jansen, et al.
Lancet (London, England)
|
January 20, 1996
Association of apolipoprotein E epsilon 4 allele with bulbar-onset motor neuron disease
A al-Chalabi, Z E Enayat, M C Bakker, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 19, 2005
Abnormal cortical excitability in sporadic but not homozygous D90A SOD1 ALS
M R Turner, A D Osei-Lah, A Hammers, et al.
Neurology
|
December 30, 2004
No association of the SOD1 locus and disease susceptibility or phenotype in sporadic ALS
W J Broom, M J Parton, C A Vance, et al.
Neuroepidemiology
|
September 28, 2007
Amyotrophic lateral sclerosis in South-East England: a population-based study. The South-East England register for amyotrophic lateral sclerosis (SEALS Registry)
K Abhinav, B Stanton, C Johnston, et al.
Neurology
|
March 25, 2009
Natural history and clinical features of the flail arm and flail leg ALS variants
L C Wijesekera, S Mathers, P Talman, et al.
Page
of 8