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March 26, 2002; 58 (6)

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In This Issue

  • March 26 Highlights
    • Full Text
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Editorials

  • An important first stepA standard curriculum for the neurology clerkship
    Robert C. Griggs, David C. Anderson
    • Full Text
    • Full Text (PDF)
  • ALADIN, but where’s the Genie?
    Richard W. Orrell, Adrian J.L. Clark
    • Full Text
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Articles

  • Neuropsychological and psychiatric sequelae of pallidotomy for PDClinical trial findings
    J. Green, W. M. McDonald, J. L. Vitek, M. Haber, H. Barnhart, R. A.E. Bakay, M. Evatt, A. Freeman, N. Wahlay, S. Triche, B. Sirockman, M. R. DeLong
    • Abstract
    • Full Text
    • Full Text (PDF)
  • Evidence for widespread movement-associated functional MRI changes in patients with PPMS
    M. A. Rocca, P. M. Matthews, D. Caputo, A. Ghezzi, A. Falini, G. Scotti, G. Comi, M. Filippi
    • Abstract
    • Full Text
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  • Ciguatera fish poisoningA double-blind randomized trial of mannitol therapy
    Hans Schnorf, M. Taurarii, T. Cundy
    • Abstract
    • Full Text
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  • Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene with Parkinson’s disease
    P.-Y. Xu, R. Liang, J. Jankovic, C. Hunter, Y.-X. Zeng, T. Ashizawa, D. Lai, W.-D. Le
    • Abstract
    • Full Text
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  • Migraine in the United StatesEpidemiology and patterns of health care use
    R. B. Lipton, A. I. Scher, K. Kolodner, J. Liberman, T. J. Steiner, W. F. Stewart
    • Abstract
    • Full Text
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  • Expression of JC virus T-antigen in a patient with MS and glioblastoma multiforme
    L. Del Valle, S. Delbue, J. Gordon, S. Enam, S. Croul, P. Ferrante, K. Khalili
    • Abstract
    • Full Text
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  • Proton MR spectroscopic imaging predicts lesion progression on MRI in X-linked adrenoleukodystrophy
    F. S. Eichler, P. B. Barker, C. Cox, D. Edwin, A. M. Ulug, H. W. Moser, G. V. Raymond
    • Abstract
    • Full Text
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  • Increased familial risk of the psychotic phenotype of Alzheimer disease
    R. A. Sweet, V. L. Nimgaonkar, B. Devlin, O. L. Lopez, S. T. DeKosky
    • Abstract
    • Full Text
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  • Prevalence and clinical importance of sleep apnea in the first night after cerebral infarction
    A. Iranzo, J. Santamaría, J. Berenguer, M. Sánchez, A. Chamorro
    • Abstract
    • Full Text
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  • Familial periventricular heterotopiaMissense and distal truncating mutations of the FLN1 gene
    F. Moro, R. Carrozzo, P. Veggiotti, G. Tortorella, D. Toniolo, A. Volzone, R. Guerrini
    • Abstract
    • Full Text
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  • Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy
    A. Filla, G. De Michele, S. Cocozza, A. Patrignani, G. Volpe, I. Castaldo, G. Ruggiero, V. Bonavita, C. Masters, G. Casari, A. Bruni
    • Abstract
    • Full Text
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  • Selective reduction of N-acetylaspartate in medial temporal and parietal lobes in AD
    N. Schuff, A. A. Capizzano, A. T. Du, D. L. Amend, J. O’Neill, D. Norman, J. Kramer, W. Jagust, B. Miller, O. M. Wolkowitz, K. Yaffe, M. W. Weiner
    • Abstract
    • Full Text
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  • The value of sleep deprivation as a diagnostic tool in adult sleepwalkers
    Steve Joncas, Antonio Zadra, Jean Paquet, Jacques Montplaisir
    • Abstract
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  • Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME)
    P. Labauge, L. O. Amer, M. Simonetta-Moreau, F. Attané, C. Tannier, M. Clanet, G. Castelnovo, I. An-Gourfinkel, Y. Agid, A. Brice, A. Ducros, E. LeGuern
    • Abstract
    • Full Text
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  • Normobaric hyperoxia reduces MRI diffusion abnormalities and infarct size in experimental stroke
    Aneesh B. Singhal, Rick M. Dijkhuizen, Bruce R. Rosen, Eng H. Lo
    • Abstract
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Special Article

  • The neurology clerkship core curriculum
    D.J. Gelb, C.H. Gunderson, K.A. Henry, H.S. Kirshner, R.F. Józefowicz
    • Abstract
    • Full Text
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Views & Reviews

  • Cerebral cavernous malformationsMutations in Krit1
    D. J. Verlaan, W. J. Davenport, H. Stefan, U. Sure, A. M. Siegel, G. A. Rouleau
    • Abstract
    • Full Text
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Medical Hypothesis

  • Cycad neurotoxins, consumption of flying foxes, and ALS-PDC disease in Guam
    Paul Alan Cox, Oliver W. Sacks
    • Abstract
    • Full Text
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Clinical/Scientific Notes

  • Spinocerebellar ataxia type 10 is rare in populations other than Mexicans
    T. Matsuura, L. P.W. Ranum, V. Volpini, M. Pandolfo, H. Sasaki, K. Tashiro, K. Watase, H. Y. Zoghbi, T. Ashizawa
    • Full Text
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  • Multifocal myoclonus due to verapamil overdose
    Lata Vadlamudi, Eelco F.M. Wijdicks
    • Full Text
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  • Isolated weakness of index finger due to small cortical infarction
    Jong S. Kim, Jong P. Chung, Sang W. Ha
    • Full Text
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NeuroImages

  • Intraluminal carotid thrombus
    Markus Busch, Randolf Klingebiel, Georg Bohner, Florian Masuhr
    • Full Text
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Correspondence

  • Ring chromosome 20 epilepsy syndrome in children: Electroclinical features
    Pedro Jesús Serrano-Castro
    • Full Text
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  • Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X
    David G. Munoz
    • Full Text
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  • CSF filtration is an effective treatment of Guillain–Barré syndrome: A randomized clinical trial
    Paolo L. Manfredi
    • Full Text
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  • Accuracy of clinical criteria for AD in the Honolulu–Asia Aging Study, a population-based study
    Kurt A. Jellinger
    • Full Text
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  • How many patients with psychogenic nonepileptic seizures also have epilepsy?
    W. Curt LaFrance
    • Full Text
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  • Limb immobilization for the treatment of focal occupational dystonia
    Daniel J. Lanska
    • Full Text
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Corrections

  • Treatment of drug-induced psychosis and clozapine with quetiapine and clozapine in Parkinson’s disease
    • Full Text
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Calendar

  • Calendar
    • Full Text
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Changes, People, Comments

  • Changes • People • Comments
    Robert J. Joynt
    • Full Text
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Filler

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Historical Neurology

  • The mystery of the Doctor’s son, or the riddle of West syndrome
    Paul Eling, Willy O. Renier, Joern Pomper, Tallie Z. Baram
    • Abstract
    • Full Text
    • Full Text (PDF)

Brief Communications

  • “Economy Class” stroke syndrome?
    Y. Isayev, R. K.T. Chan, P. M. Pullicino
    • Abstract
    • Full Text
    • Full Text (PDF)
  • Progressive bulbospinal amyotrophy in Triple A syndrome with AAAS gene mutation
    C. Goizet, B. Catargi, F. Tison, A. Tullio-Pelet, S. Hadj-Rabia, F. Pujol, A. Lagueny, S. Lyonnet, D. Lacombe
    • Abstract
    • Full Text
    • Full Text (PDF)
  • CAG/CTG repeat expansions at the Huntington’s disease–like 2 locus are rare in Huntington’s disease patients
    G. Stevanin, A. Camuzat, S. E. Holmes, C. Julien, R. Sahloul, C. Dodé, V. Hahn-Barma, C. A. Ross, R. L. Margolis, A. Durr, A. Brice
    • Abstract
    • Full Text
    • Full Text (PDF)
  • The cerebellum may be directly involved in cognitive functions
    M. Vokaer, J. C. Bier, S. Elincx, T. Claes, P. Paquier, S. Goldman, E. J. Bartholomé, M. Pandolfo
    • Abstract
    • Full Text
    • Full Text (PDF)
  • Midbrain deafness with normal brainstem auditory evoked potentials
    E. Vitte, F. Tankéré, I. Bernat, A. Zouaoui, G. Lamas, J. Soudant
    • Abstract
    • Full Text
    • Full Text (PDF)
  • HLA-A2 homozygosity but not heterozygosity is associated with Alzheimer disease
    S. Zareparsi, D. M. James, J. A. Kaye, T. D. Bird, G. D. Schellenberg, H. Payami
    • Abstract
    • Full Text
    • Full Text (PDF)
  • fMRI/EEG in paroxysmal activity elicited by elimination of central vision and fixation
    G. D. Iannetti, C. Di Bonaventura, P. Pantano, A. T. Giallonardo, P. L. Romanelli, L. Bozzao, M. Manfredi, G. B. Ricci
    • Abstract
    • Full Text
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  • Chronic inflammatory demyelinating polyneuropathy presenting with features of GBS
    K. Mori, N. Hattori, M. Sugiura, H. Koike, K. Misu, M. Ichimura, M. Hirayama, G. Sobue
    • Abstract
    • Full Text
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Departments

  • Book Reviews
    Rodger Elble
    • Full Text
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