Articles

• Parental transmission of MS in a population-based Canadian cohort

  B. M. Herrera, S. V. Ramagopalan, S. Orton, M. J. Chao, I. M. Yee, A. D. Sadovnick, G. C. Ebers

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• Thalamic atrophy and cognition in multiple sclerosis

  M. K. Houtchens, R.H.B. Benedict, R. Killiany, J. Sharma, Z. Jaisani, B. Singh, B. Weinstock-Guttman, C. R.G. Guttmann, R. Bakshi

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• Incidence and prevalence of multiple sclerosis in Saskatoon, Saskatchewan

  Walter J. Hader, Irene M.L. Yee

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• A composite score to predict short-term disease activity in patients with relapsing-remitting MS

  Maria Pia Sormani, Marco Rovaris, Giancarlo Comi, Massimo Filippi

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• Limbic encephalitis as a precipitating event in adult-onset temporal lobe epilepsy

  C. G. Bien, H. Urbach, J. Schramm, B. M. Soeder, A. J. Becker, R. Voltz, A. Vincent, C. E. Elger

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• Clinical characterization of the HOXA1 syndrome BSAS variant

  T. M. Bosley, M. A. Salih, I. A. Alorainy, D. T. Oystreck, M. Nester, K. K. Abu-Amero, M. A. Tischfield, E. C. Engle

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• New POMT2 mutations causing congenital muscular dystrophyIdentification of a founder mutation

  A. Yanagisawa, C. Bouchet, P.Y.K. Van den Bergh, J. -M. Cuisset, L. Viollet, F. Leturcq, N. B. Romero, S. Quijano-Roy, M. Fardeau, N. Seta, P. Guicheney

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• Prominent brain axonal damage and functional reorganization in “pure” adrenomyeloneuropathy

  S. Marino, M. De Luca, M. T. Dotti, M. L. Stromillo, P. Formichi, P. Galluzzi, M. Mondelli, P. Bramanti, A. Federico, N. De Stefano

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• Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease

  L. N. Clark, B. M. Ross, Y. Wang, H. Mejia-Santana, J. Harris, E. D. Louis, L. J. Cote, H. Andrews, S. Fahn, C. Waters, B. Ford, S. Frucht, R. Ottman, K. Marder

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• San Francisco/Oakland Bay Bridge Welder StudyOlfactory function

  Marcelo B. Antunes, Rosemarie Bowler, Richard L. Doty

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