Articles

• Distinct genetic forms of frontotemporal dementia

  H. Seelaar, W. Kamphorst, S. M. Rosso, A. Azmani, R. Masdjedi, I. de Koning, J. A. Maat-Kievit, B. Anar, L. Donker Kaat, G. J. Breedveld, D. Dooijes, J. M. Rozemuller, I. F. Bronner, P. Rizzu, J. C. van Swieten

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  CME Course
• The logopenic/phonological variant of primary progressive aphasia

  M. L. Gorno-Tempini, S. M. Brambati, V. Ginex, J. Ogar, N. F. Dronkers, A. Marcone, D. Perani, V. Garibotto, S. F. Cappa, B. L. Miller

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• Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration

  R. Ghidoni, L. Benussi, M. Glionna, M. Franzoni, G. Binetti

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• Pronouncing brain deathContemporary practice and safety of the apnea test

  Eelco F.M. Wijdicks, Alejandro A. Rabinstein, Edward M. Manno, John D. Atkinson

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  CME Course
• Autosomal recessive myosclerosis myopathy is a collagen VI disorder

  L. Merlini, E. Martoni, P. Grumati, P. Sabatelli, S. Squarzoni, A. Urciuolo, A. Ferlini, F. Gualandi, P. Bonaldo

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• Motor axon loss is associated with hand dysfunction in Charcot-Marie-Tooth disease 1a

  A. J. Videler, J. P. van Dijk, A. Beelen, M. de Visser, F. Nollet, I. N. van Schaik

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• FTY720 therapy exerts differential effects on T cell subsets in multiple sclerosis

  M. Mehling, V. Brinkmann, J. Antel, A. Bar-Or, N. Goebels, C. Vedrine, C. Kristofic, J. Kuhle, R.L.P. Lindberg, L. Kappos

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• Herpetic encephalitis is a risk factor for acute retinal necrosis

  T. Vandercam, R. Q. Hintzen, J. H. de Boer, A. Van der Lelij

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