Articles

• Postural imbalance and falls in PSP correlate with functional pathology of the thalamus

  A. Zwergal, C. la Fougère, S. Lorenzl, A. Rominger, G. Xiong, L. Deutschenbaur, J. Linn, S. Krafczyk, M. Dieterich, T. Brandt, M. Strupp, P. Bartenstein, K. Jahn

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• Preferential D2 or preferential D3 dopamine agonists in restless legs syndrome

  M. Manconi, R. Ferri, M. Zucconi, S. Clemens, L. Giarolli, V. Bottasini, L. Ferini-Strambi

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  CME Course
• Quantitative EEG as a predictive biomarker for Parkinson disease dementia

  B.T. Klassen, J.G. Hentz, H.A. Shill, E. Driver-Dunckley, V.G.H. Evidente, M.N. Sabbagh, C.H. Adler, J.N. Caviness

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• Plasma Aβ and PET PiB binding are inversely related in mild cognitive impairment

  D.P. Devanand, N. Schupf, Y. Stern, R. Parsey, G.H. Pelton, P. Mehta, R. Mayeux

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• Causes of death among people with convulsive epilepsy in rural West ChinaA prospective study

  J. Mu, L. Liu, Q. Zhang, Y. Si, J. Hu, J. Fang, Y. Gao, J. He, S. Li, W. Wang, J. Wu, J.W. Sander, D. Zhou

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  CME Course
• Prevalence, sensitivity, and specificity of chronic cerebrospinal venous insufficiency in MS

  R. Zivadinov, K. Marr, G. Cutter, M. Ramanathan, R.H.B. Benedict, C. Kennedy, M. Elfadil, A.E. Yeh, J. Reuther, C. Brooks, K. Hunt, M. Andrews, E. Carl, M.G. Dwyer, D. Hojnacki, B. Weinstock-Guttman

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• Breastfeeding is not related to postpartum relapses in multiple sclerosis

  E. Portaccio, A. Ghezzi, B. Hakiki, V. Martinelli, L. Moiola, F. Patti, L. La Mantia, G.L. Mancardi, C. Solaro, M.R. Tola, C. Pozzilli, L. De Giglio, R. Totaro, A. Lugaresi, G. De Luca, D. Paolicelli, M.G. Marrosu, G. Comi, M. Trojano, M.P. Amato, For the MS Study Group of the Italian Neurological Society

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• Low bone mass in newly diagnosed multiple sclerosis and clinically isolated syndrome

  S.M. Moen, E.G. Celius, L. Sandvik, L. Nordsletten, E.F. Eriksen, T. Holmøy

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• Genetic associations with brain microbleedsSystematic review and meta-analyses

  S.S. Maxwell, C.A. Jackson, L. Paternoster, C. Cordonnier, V. Thijs, R. Al-Shahi Salman, C.L.M. Sudlow

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• Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations

  J.M. Polke, M. Laurá, D. Pareyson, F. Taroni, M. Milani, G. Bergamin, V.S. Gibbons, H. Houlden, S.C. Chamley, J. Blake, C. DeVile, R. Sandford, M.G. Sweeney, M.B. Davis, M.M. Reilly

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• Comment: The increasing complexity of phenotype–genotype correlations in CMT

  Jonathan D. Glass

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