Brief Communications

• Severity of sports-related concussion and neuropsychological test performance

  Anton D. Hinton-Bayre, Gina Geffen

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• Multiple sclerosis–associated retrovirus and MS prognosisAn observational study

  S. Sotgiu, C. Serra, G. Mameli, M. Pugliatti, G. Rosati, G. Arru, A. Dolei

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• Treatment of steroid-unresponsive tumefactive demyelinating disease with plasma exchange

  Yang Mao-Draayer, Steven Braff, William Pendlebury, Hillel Panitch

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• The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

  Catherine Lomen-Hoerth, Thomas Anderson, Bruce Miller

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• Familial dementia with Lewy bodiesClinicopathologic analysis of two kindreds

  J.E. Galvin, S.L. Lee, A. Perry, N. Havlioglu, D.W. McKeel, J.C. Morris

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• Main trunk tibial neuropathies

  Cornelia Drees, Asa J. Wilbourn, Glen H.J. Stevens

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• Postexercise facilitation of reflexes is not common in Lambert–Eaton myasthenic syndrome

  Z. Odabasi, M. Demirci, D.S. Kim, D.K. Lee, H.F. Ryan, G.C. Claussen, A. Tseng, S.J. Oh

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• Tick paralysis in childrenElectrophysiology and possibility of misdiagnosis

  V. Venkataraman Vedanarayanan, Owen B. Evans, S.H. Subramony

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• A novel murine myotonia congenita without molecular defects in the ClC-1 and the SCN4A

  T. Shirakawa, K. Sakai, Y. Kitagawa, A. Hori, G. Hirose

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• Cutaneous innervation in chronic inflammatory demyelinating polyneuropathy

  M.-C. Chiang, Y.-H. Lin, C.-L. Pan, T.-J. Tseng, W.-M. Lin, S.-T. Hsieh

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• Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13

  S.E. Noble-Topham, D.A. Dyment, M.Z. Cader, R. Ganapathy, J.D. Brown, G.P.A. Rice, G.C. Ebers

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• Neuroleptic malignant syndrome with prolonged catatonia in a dopa-responsive dystonia patient

  M. Ihara, N. Kohara, F. Urano, H. Ichinose, S. Takao, T. Nishida, H. Saiki, Y. Kawamoto, A. Ikeda, S. Takagi, H. Shibasaki

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• Heterogeneity of presenile dementia with bone cysts (Nasu–Hakola disease)Three genetic forms

  T. Kondo, K. Takahashi, N. Kohara, Y. Takahashi, S. Hayashi, H. Takahashi, H. Matsuo, M. Yamazaki, K. Inoue, K. Miyamoto, T. Yamamura

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• Presenilin-1 mutation (E280G), spastic paraparesis, and cranial MRI white-matter abnormalities

  S. O’Riordan, P. McMonagle, J. C. Janssen, N. C. Fox, M. Farrell, J. Collinge, M. N. Rossor, M. Hutchinson

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