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See Latest ArticlesFree sialic acid storage disease without sialuria
Annals of Neurology , 07/02/09
Mochel F et al. - The findings demonstrate that mutations in the SLC17A5 gene have to be considered in patients with hypomyelination, even in the absence of sialuria.
Today in Basic Science/Genetics...keeping you current
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Effect of IFN-beta therapy on the frequency and function of CD4+CD25+ regulatory T cells and Foxp3 gene expression in relapsing–remitting multiple sclerosis (RRMS): A preliminary study
Journal of Neuroimmunology, 11/25/09
Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders
Human Molecular Genetics, 11/25/09
Lack of association between five serotonin metabolism-related genes and medication overuse headache
The Journal of Headache and Pain, 11/25/09
Today in Demyelinating Disorders...keeping you current
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Effect of IFN-beta therapy on the frequency and function of CD4+CD25+ regulatory T cells and Foxp3 gene expression in relapsing–remitting multiple sclerosis (RRMS): A preliminary study
Journal of Neuroimmunology, 11/25/09
Magnetic resonance imaging characteristics of children and adults with paediatric-onset multiple sclerosis
Brain, 11/25/09
Post-transcriptional control of neurofilaments: New roles in development, regeneration and neurodegenerative disease
Trends in Neurosciences, 11/25/09
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