Articles

• Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2

  H. Houlden, M. Laura, F. Wavrant–De Vrièze, J. Blake, N. Wood, M. M. Reilly

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• A novel dominant mutation of the Na_v1.4 α-subunit domain I leading to sodium channel myotonia

  S. Petitprez, L. Tiab, L. Chen, L. Kappeler, K. M. Rösler, D. Schorderet, H. Abriel, J-M Burgunder

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• Diffusion tensor imaging of the pyramidal tracts in infants with motor dysfunction

  N. A. Ludeman, J. I. Berman, Y. W. Wu, R. J. Jeremy, J. Kornak, A. I. Bartha, A. J. Barkovich, D. M. Ferriero, R. G. Henry, O. A. Glenn

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• GM1/GalNAc-GD1a complexA target for pure motor Guillain-Barré syndrome

  K. Kaida, M. Sonoo, G. Ogawa, K. Kamakura, M. Ueda-Sada, M. Arita, K. Motoyoshi, S. Kusunoki

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• Neurologic improvement after peripheral blood stem cell transplantation in POEMS syndrome

  S. Kuwabara, S. Misawa, K. Kanai, Y. Suzuki, Y. Kikkawa, S. Sawai, T. Hattori, M. Nishimura, C. Nakaseko

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  CME Course
• Atrial fibrillation detected by mobile cardiac outpatient telemetry in cryptogenic TIA or stroke

  A. H. Tayal, M. Tian, K. M. Kelly, S. C. Jones, D. G. Wright, D. Singh, J. Jarouse, J. Brillman, S. Murali, R. Gupta

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• Growth hormone secretagogue MK-677No clinical effect on AD progression in a randomized trial

  J. J. Sevigny, J. M. Ryan, C. H. van Dyck, Y. Peng, C. R. Lines, M. L. Nessly

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• Early-onset dementia with prolonged occipital seizuresAn atypical case of Kufs disease

  A. Zini, G. Cenacchi, P. Nichelli, E. Zunarelli, A. Todeschini, S. Meletti

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• Transient loss of consciousness through the eyes of a witness

  R. D. Thijs, W. A. Wagenaar, H.A.M. Middelkoop, W. Wieling, J. G. van Dijk

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• SEEG-guided thermocoagulationsA palliative treatment of nonoperable partial epilepsies

  H. Catenoix, F. Mauguière, M. Guénot, P. Ryvlin, A. Bissery, M. Sindou, J. Isnard

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• Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore

  C. H. Lin, E. K. Tan, M. L. Chen, L. C. Tan, H. Q. Lim, G. S. Chen, R. M. Wu

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