Articles

• GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease

  M. Henneke, P. Combes, S. Diekmann, E. Bertini, K. Brockmann, A. P. Burlina, J. Kaiser, A. Ohlenbusch, B. Plecko, D. Rodriguez, O. Boespflug-Tanguy, J. Gärtner

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• Cold-induced defects of sodium channel gating in atypical periodic paralysis plus myotonia

  Jadon Webb, Stephen C. Cannon

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• Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus

  C. La Morgia, A. Achilli, L. Iommarini, P. Barboni, M. Pala, A. Olivieri, C. Zanna, S. Vidoni, C. Tonon, R. Lodi, R. Vetrugno, B. Mostacci, R. Liguori, R. Carroccia, P. Montagna, M. Rugolo, A. Torroni, V. Carelli

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• The Toronto traumatic brain injury studyInjury severity and quantified MRI

  B. Levine, N. Kovacevic, E. I. Nica, G. Cheung, F. Gao, M. L. Schwartz, S. E. Black

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• Bevacizumab for recurrent malignant gliomasEfficacy, toxicity, and patterns of recurrence

  A. D. Norden, G. S. Young, K. Setayesh, A. Muzikansky, R. Klufas, G. L. Ross, A. S. Ciampa, L. G. Ebbeling, B. Levy, J. Drappatz, S. Kesari, P. Y. Wen

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• Psychological distress, major depressive disorder, and risk of stroke

  P. G. Surtees, N.W.J. Wainwright, R. N. Luben, N. J. Wareham, S. A. Bingham, K.-T Khaw

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• Polysomnography in Kleine-Levin syndrome

  Yu-Shu Huang, Yu-Hsuan Lin, Christian Guilleminault

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• Why do patients with PSP fall?Evidence for abnormal otolith responses

  K. Liao, J. Wagner, A. Joshi, I. Estrovich, M. F. Walker, M. Strupp, R. J. Leigh

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