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Annals of Neurology
|
September 11, 1999
Genetic association of alpha2-macroglobulin with Alzheimer's disease in a Finnish elderly population
L Myllykangas, T Polvikoski, R Sulkava, et al.
Current Alzheimer Research
|
October 26, 2013
Relationships between white matter hyperintensities, cerebral amyloid angiopathy and dementia in a population-based sample of the oldest old
M Tanskanen, R N Kalaria, I-L Notkola, et al.
Neuroscience Letters
|
May 4, 2000
No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease
M Baker, D Graff-Radford, F Wavrant DeVrièze, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 28, 2019
Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease
V Boczonadi, M S King, A C Smith, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 25, 2015
Mutational spectrum and phenotypic variability of VCP-related neurological disease in the UK
S Figueroa-Bonaparte, J Hudson, R Barresi, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
Annals of Neurology
|
September 11, 1999
Genetic association of alpha2-macroglobulin with Alzheimer's disease in a Finnish elderly population
L Myllykangas, T Polvikoski, R Sulkava, et al.
Current Alzheimer Research
|
October 26, 2013
Relationships between white matter hyperintensities, cerebral amyloid angiopathy and dementia in a population-based sample of the oldest old
M Tanskanen, R N Kalaria, I-L Notkola, et al.
Neuroscience Letters
|
May 4, 2000
No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease
M Baker, D Graff-Radford, F Wavrant DeVrièze, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 28, 2019
Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease
V Boczonadi, M S King, A C Smith, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 25, 2015
Mutational spectrum and phenotypic variability of VCP-related neurological disease in the UK
S Figueroa-Bonaparte, J Hudson, R Barresi, et al.
Page
of 3