Articles

• MFN2 mutations cause severe phenotypes in most patients with CMT2A

  S.M.E. Feely, M. Laura, C.E. Siskind, S. Sottile, M. Davis, V.S. Gibbons, M.M. Reilly, M.E. Shy

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• Clinical outcomes of natalizumab-associated progressive multifocal leukoencephalopathy

  P. Vermersch, L. Kappos, R. Gold, J.F. Foley, T. Olsson, D. Cadavid, C. Bozic, S. Richman

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• A case of multiple sclerosis presenting with inflammatory cortical demyelination

  B.F.Gh. Popescu, R.F. Bunyan, J.E. Parisi, R.M. Ransohoff, C.F. Lucchinetti

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• Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias

  P. Vitali, E. Maccagnano, E. Caverzasi, R.G. Henry, A. Haman, C. Torres-Chae, D.Y. Johnson, B.L. Miller, M.D. Geschwind

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• Clinical features and APOE genotype of pathologically proven early-onset Alzheimer disease

  M. Balasa, E. Gelpi, A. Antonell, M.J. Rey, R. Sánchez-Valle, J.L. Molinuevo, A. Lladó, For the Neurological Tissue Bank/University of Barcelona/Hospital Clínic NTB/UB/HC Collaborative Group

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  CME Course
• Are networks for residual language function and recovery consistent across aphasic patients?

  Peter E. Turkeltaub, Samuel Messing, Catherine Norise, Roy H. Hamilton

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• Outcomes and prognostic factors of intracranial unruptured vertebrobasilar artery dissection

  B.M. Kim, S.H. Kim, D.I. Kim, Y.S. Shin, S.H. Suh, D.J. Kim, S.I. Park, K.Y. Park, S.S. Ahn

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• Silent brain infarcts, leukoaraiosis, and long-term prognosis in young ischemic stroke patients

  J. Putaala, E. Haapaniemi, M. Kurkinen, O. Salonen, M. Kaste, T. Tatlisumak

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