Articles

• Interferon beta-1b in secondary progressive MSA combined analysis of the two trials

  L. Kappos, B. Weinshenker, C. Pozzilli, A. J. Thompson, F. Dahlke, K. Beckmann, C. Polman, H. McFarland

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• Interferon beta-1b in secondary progressive MSResults from a 3-year controlled study

  The North American Study Group on Interferon beta-1b in Secondary Progressive MS

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• Prevalence of multiple sclerosis in a residential area bordering an oil refinery

  J. S. Neuberger, S. G. Lynch, M. L. Sutton, S. B. Hall, C. Feng, W. R. Schmidt

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• Linkage and association of febrile seizures to the IMPA2 gene on human chromosome 18

  J. Nakayama, N. Yamamoto, K. Hamano, N. Iwasaki, M. Ohta, S. Nakahara, A. Matsui, E. Noguchi, T. Arinami

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• Epileptic seizures in systemic lupus erythematosus

  Simone Appenzeller, Fernando Cendes, Lilian T.L. Costallat

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• Epileptic activity influences the lateralization of mesiotemporal fMRI activity

  J. Janszky, I. Ollech, H. Jokeit, K. Kontopoulou, M. Mertens, B. Pohlmann-Eden, A. Ebner, F. G. Woermann

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• Cortical reorganization in malformations of cortical developmentA magnetoencephalographic study

  Jorge G. Burneo, Ruben I. Kuzniecky, Martina Bebin, Robert C. Knowlton

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• Reorganization of language-specific cortex in patients with lesions or mesial temporal epilepsy

  E. Pataraia, P. G. Simos, E. M. Castillo, R. L. Billingsley-Marshall, A. L. McGregor, J. I. Breier, S. Sarkari, A. C. Papanicolaou

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• Atypical language cortex in the left temporal lobeRelationship to bilateral language

  R. A. Jabbour, P. E. Penovich, G. L. Risse, D. E. Kispert, M. B. Dunn, J. R. Gates

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• An fMRI study of cortical representation of mechanical allodynia in patients with neuropathic pain

  R. Peyron, F. Schneider, I. Faillenot, P. Convers, F.-G. Barral, L. Garcia-Larrea, B. Laurent

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• Natural history of nonketotic hyperglycinemia in 65 patients

  J. E. Hoover-Fong, S. Shah, J. L.K. Van Hove, D. Applegarth, J. Toone, A. Hamosh

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• Clinically mild encephalitis/encephalopathy with a reversible splenial lesion

  H. Tada, J. Takanashi, A. J. Barkovich, H. Oba, M. Maeda, H. Tsukahara, M. Suzuki, T. Yamamoto, T. Shimono, T. Ichiyama, T. Taoka, O. Sohma, H. Yoshikawa, Y. Kohno

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• Temporal bone histopathology in dominantly inherited audiovestibular syndrome

  A. Ishiyama, G. Ishiyama, I. Lopez, J. Jen, G. Kim, R. W. Baloh

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• The effect of tactile feedback on pantomime of tool use in apraxia

  G. Goldenberg, S. Hentze, J. Hermsdörfer

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• Association of cholesterol with stroke risk varies in stroke subtypes and patient subgroups

  D. L. Tirschwell, N. L. Smith, S. R. Heckbert, R. N. Lemaitre, W. T. Longstreth, B. M. Psaty

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• A 24-year follow-up of body mass index and cerebral atrophy

  D. Gustafson, L. Lissner, C. Bengtsson, C. Björkelund, I. Skoog

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• Vascular risk factors, incidence of MCI, and rates of progression to dementia

  V. Solfrizzi, F. Panza, A. M. Colacicco, A. D’Introno, C. Capurso, F. Torres, F. Grigoletto, S. Maggi, A. Del Parigi, E. M. Reiman, R. J. Caselli, E. Scafato, G. Farchi, A. Capurso

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• Hippocampal atrophy, whole brain volume, and white matter lesions in older hypertensive subjects

  R. M. Wiseman, B. K. Saxby, E. J. Burton, R. Barber, G. A. Ford, J. T. O’Brien

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• Impact of APOE in mild cognitive impairment

  M. R. Farlow, Y. He, S. Tekin, J. Xu, R. Lane, H. C. Charles

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• Diabetes mellitus in midlife and the risk of dementia three decades later

  M. Schnaider Beeri, U. Goldbourt, J. M. Silverman, S. Noy, J. Schmeidler, R. Ravona-Springer, A. Sverdlick, M. Davidson

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• Is fatigue an independent and persistent symptom in patients with Parkinson disease?

  G. Alves, T. Wentzel-Larsen, J. P. Larsen

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• Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease

  H. Hochstrasser, P. Bauer, U. Walter, S. Behnke, J. Spiegel, I. Csoti, B. Zeiler, A. Bornemann, J. Pahnke, G. Becker, O. Riess, D. Berg

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• Neuro-ophthalmology of late-onset Tay–Sachs disease (LOTS)

  J. C. Rucker, B. E. Shapiro, Y. H. Han, A. N. Kumar, S. Garbutt, E. L. Keller, R. J. Leigh

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• A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation

  Joseph J. Higgins, Joanna Pucilowska, Roni Q. Lombardi, John P. Rooney

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