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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.
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Transient Ischemic Attack after Tissue Plasminogen Activator: Aborted Stroke or Unnecessary Stroke Therapy
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Magnetic Resonance Imaging Predictors of Conversion to Multiple Sclerosis in the BENEFIT Study
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