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October 24, 2000; 55 (8)

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In This Issue

  • October 24 Highlights
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Editorials

  • Pelizaeus–Merzbacher diseaseSplice sites are nice sites for disease expression
    Alan K. Percy
    • Full Text
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  • Diversity in epilepsy and a newly recognized benign childhood syndrome
    A.T. Berg, C.P. Panayiotopoulos
    • Full Text
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Articles

  • Mutations in noncoding regions of the proteolipid protein gene in Pelizaeus–Merzbacher disease
    G.M. Hobson, A.P. Davis, N.C. Stowell, E.H. Kolodny, E.A. Sistermans, I.F. M. de Coo, V.L. Funanage, H.G. Marks
    • Abstract
    • Full Text
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  • Panayiotopoulos-type benign childhood occipital epilepsyA prospective study
    Roberto Caraballo, Ricardo Cersosimo, Carlos Medina, Natalio Fejerman
    • Abstract
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  • Idiopathic generalized epilepsyLack of significant microdysgenesis
    K. Opeskin, R.M. Kalnins, G. Halliday, H. Cartwright, S.F. Berkovic
    • Abstract
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  • Do carbamazepine and phenytoin aggravate juvenile myoclonic epilepsy?
    P. Genton, P. Gelisse, P. Thomas, C. Dravet
    • Abstract
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  • Seizure outcome after surgery for epilepsy due to malformation of cortical development
    J.C. Edwards, E. Wyllie, P.M. Ruggeri, W. Bingaman, H. Lüders, P. Kotagal, D.S. Dinner, H.H. Morris, R.A. Prayson, Y.G. Comair
    • Abstract
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  • Subclinical sensory neuropathy in late-onset restless legs syndrome
    M. Polydefkis, R.P. Allen, P. Hauer, C.J. Earley, J.W. Griffin, J.C. McArthur
    • Abstract
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  • Juvenile and adult-onset acid maltase deficiency in FranceGenotype–phenotype correlation
    P. Laforêt, M. Nicolino, B. Eymard, J.P. Puech, C. Caillaud, L. Poenaru, M. Fardeau
    • Abstract
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  • A novel laminin α2 isoform in severe laminin α2 deficient congenital muscular dystrophy
    E. Pegoraro, M. Fanin, C.P. Trevisan, C. Angelini, E.P. Hoffman
    • Abstract
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  • IV immunoglobulin does not reverse established weakness in MSA double-blind, placebo-controlled trial
    J.H. Noseworthy, P.C. O’Brien, B.G. Weinshenker, J.A. Weis, T.M. Petterson, B.J. Erickson, A.J. Windebank, J.P. Whisnant, K.A. Stolp–Smith, C.M. Harper, P.A. Low, L.J. Romme, M. Johnson, K.-N. An, M. Rodriguez
    • Abstract
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  • Past adult lead exposure is associated with longitudinal decline in cognitive function
    B.S. Schwartz, W.F. Stewart, K.I. Bolla, D. Simon, K. Bandeen-Roche, B. Gordon, J.M. Links, A.C. Todd
    • Abstract
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  • Activation of language cortex with automatic speech tasks
    S.Y. Bookheimer, T.A. Zeffiro, T.A. Blaxton, W. Gaillard, W.H. Theodore
    • Abstract
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  • Documented head injury in early adulthood and risk of Alzheimer’s disease and other dementias
    B.L. Plassman, R.J. Havlik, D.C. Steffens, M.J. Helms, T.N. Newman, D. Drosdick, C. Phillips, B.A. Gau, K.A. Welsh–Bohmer, J.R. Burke, J.M. Guralnik, J.C. S. Breitner
    • Abstract
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  • Left vagus nerve stimulation suppresses experimentally induced pain
    A. Kirchner, F. Birklein, H. Stefan, H.O. Handwerker
    • Abstract
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  • Interatrial septal abnormalities and strokeA meta-analysis of case-control studies
    J.R. Overell, I. Bone, K.R. Lees
    • Abstract
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  • Predictors of resource use after acute hospitalizationThe Northern Manhattan Stroke Study
    T. Rundek, H. Mast, A. Hartmann, B. Boden–Albala, L. Lennihan, I.-F. Lin, M.C. Paik, R.L. Sacco
    • Abstract
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  • Two affected boys in a Rett syndrome familyClinical and molecular findings
    L. Villard, A. Kpebe, C. Cardoso, J. Chelly, M. Tardieu, M. Fontes
    • Abstract
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  • AIDS-related focal brain lesions in the era of highly active antiretroviral therapy
    A. Ammassari, A. Cingolani, P. Pezzotti, A. De Luca, R. Murri, M.L. Giancola, L.M. Larocca, A. Antinori
    • Abstract
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Views & Reviews

  • Iatrogenic Creutzfeldt–Jakob disease at the millennium
    P. Brown, M. Preece, J.-P. Brandel, T. Sato, L. McShane, I. Zerr, A. Fletcher, R.G. Will, M. Pocchiari, N.R. Cashman, J.H. d’Aignaux, L. Cervenáková, J. Fradkin, L.B. Schonberger, S.J. Collins
    • Abstract
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Clinical/Scientific Notes

  • Cerebellar toxicity of cytosine arabinoside: Clinical and neuropsychological signs
    T. Zawacki, J.H. Friedman, J. Grace, N. Shetty
    • Full Text
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  • Sporadic inclusion body myositis not linked to prion protein codon 129 methionine homozygosity
    Michael Orth, Sarah J. Tabrizi, Anthony H. V. Schapira
    • Full Text
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  • Successful treatment of lamotrigine-induced erythroblastopenic crisis with folinic acid
    Marc Pulik, François Lionnet, Philippe Genet
    • Full Text
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  • Dystonia secondary to Sjögren–Larsson syndrome
    Esther Cubo, Christopher G. Goetz
    • Full Text
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  • Severe acute disseminated encephalomyelitis with normal MRI at presentation
    B.J. Murray, D. Apetauerova, T.E. Scammell
    • Full Text
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Correspondence

  • Oral zolmitriptan is effective in the acute treatment of cluster headache
    William Bernstein
    • Full Text
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  • Differentiation of atypical parkinsonian syndromes with routine MRI
    F. Yekhlef, G. Ballan, F. Macia, O. Delmer, C. Sourgen, C. Vital, F. Tison
    • Full Text
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  • Incidence of and risk factors for hallucinations and delusions in patients with probable AD
    Luca Rozzini, Alessandro Padovani, Barbara Borroni, Marco Trabucchi
    • Full Text
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  • Benign childhood epilepsy with centrotemporal spikes: Is it always benign?
    A. de Saint-Martin, R. Massa, M.N. Metz-Lutz, E. Hirsch, C. Marescaux
    • Full Text
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  • Progressive cerebral atrophy in MS: A serial study using registered, volumetric MRI
    Hans-Peter Adams, James A. Koziol
    • Full Text
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  • Periodic limb movements in sleep: State-dependent excitability of the spinal flexor reflex
    Martín Nogués, Ana Pardal, Fabio Barroso, Juan Vilés Gonzalez
    • Full Text
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  • Functional MRI cerebral activation and deactivation during finger movement
    H. Reddy, P.M. Matthews, M. Lassonde
    • Full Text
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Departments

  • Calendar
    • Full Text
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Expedited Publication

  • Glutamate transporter EAAT2 splice variants occur not only in ALS, but also in AD and controls
    L.S. Honig, D.D. Chambliss, E.H. Bigio, S.L. Carroll, J.L. Elliott
    • Abstract
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Filler

  • Access www.neurology.org now for full-text articles
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Historical Neurology

  • Romberg’s signDevelopment, adoption, and adaptation in the 19th century
    Douglas J. Lanska, Christopher G. Goetz
    • Abstract
    • Full Text
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Brief Communications

  • Natural history of cardiac involvement in myotonic dystrophy: Correlation with CTG repeats
    G. Antonini, F. Giubilei, A. Mammarella, P. Amicucci, M. Fiorelli, F. Gragnani, S. Morino, V. Ceschin, P.V. Fragola, M. Gennarelli
    • Abstract
    • Full Text
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  • A novel mutation in the mitochondrial tRNATyr gene associated with exercise intolerance
    T. Pulkes, A. Siddiqui, J.A. Morgan–Hughes, M.G. Hanna
    • Abstract
    • Full Text
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  • Increased skin lactate in complex regional pain syndrome: Evidence for tissue hypoxia?
    F. Birklein, M. Weber, B. Neundörfer
    • Abstract
    • Full Text
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  • Paroxetine in Parkinson’s disease: Effects on motor and depressive symptoms
    R. Ceravolo, A. Nuti, A. Piccinni, G. Dell’ Agnello, G. Bellini, G. Gambaccini, L. Dell’ Osso, L. Murri, U. Bonuccelli
    • Abstract
    • Full Text
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  • Long-term efficacy of posteroventral pallidotomy in the treatment of Parkinson’s disease
    E.C. Lai, J. Jankovic, J.K. Krauss, W.G. Ondo, R.G. Grossman
    • Abstract
    • Full Text
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  • The experience of Wernicke’s aphasia
    Ronald M. Lazar, Randolph S. Marshall, George D. Prell, John Pile-Spellman
    • Abstract
    • Full Text
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  • A Japanese patient with frontotemporal dementia and parkinsonism by a tau P301S mutation
    M. Yasuda, K. Yokoyama, T. Nakayasu, Y. Nishimura, M. Matsui, T. Yokoyama, K. Miyoshi, C. Tanaka
    • Abstract
    • Full Text
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  • Cortical reafferentation following left subcortical hemorrhage: A serial functional MR study
    M. Hund-Georgiadis, U. Lex, D.G. Norris, D.Y. von Cramon
    • Abstract
    • Full Text
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  • Acute effects of interferon beta-1a on plasma cytokine levels in patients with MS
    T. Kümpfel, F. Then Bergh, T. Pollmächer, F. Holsboer, C. Trenkwalder
    • Abstract
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