Articles

• Ictal motor signs and interictal regional cerebral hypometabolism

  G. Schlaug, C. Antke, H. Holthausen, S. Arnold, A. Ebner, I. Tuxhorn, L. Jäncke, H. Lüders, O. W. Witte, R. J. Seitz

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• Treatment of multiple sclerosis with the monoclonal anti-CD4 antibody cM-T412: Results of a randomized, double-blind, placebo-controlled MR-monitored phase II trial

  B. W. van Oosten, M. Lai, S. Hodgkinson, F. Barkhof, D. H. Miller, I. F. Moseley, A. J. Thompson, P. Rudge, A. McDougall, J. G. McLeod, H. J. Adèr, C. H. Polman

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• Impact of interferon beta-1a on neurologic disability in relapsing multiple sclerosis

  R. A. Rudick, D. E. Goodkin, L. D. Jacobs, D. L. Cookfair, R. M. Herndon, J. R. Richert, A. M. Salazar, J. S. Fischer, C. V. Granger, J. H. Simon, J. J. Alam, N. A. Simonian, M. K. Campion, D. M. Bartoszak, D. N. Bourdette, J. Braiman, C. M. Brownscheidle, M. E. Coats, S. L. Cohan, D. S. Dougherty, R. P. Kinkel, M. K. Mass, F. E. Munschauer, R. L. Priore, P. M. Pullicino, B. J. Scherokman, B. Weistock-Guttman, R. H. Whitham, The Multiple Sclerosis Collaborative Research Group (MSCRG)

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• Multiple sclerosis lesion detection in the brain: A comparison of fast fluid-attenuated inversion recovery and conventional T2-weighted dual spin echo

  M. L. Gawne-Cain, J. I. O'Riordan, A. J. Thompson, I. F. Moseley, D. H. Miller

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• Interscanner variation in brain MRI lesion load measurements in MS: Implications for clinical trials

  M. Filippi, J. H. van Waesberghe, M. A. Horsfield, S. Bressi, C. Gasperini, T. A. Yousry, M. L. Gawne-Cain, S. P. Morrissey, M. A. Rocca, F. Barkhof, G. J. Lycklama à Nijeholt, S. Bastianello, D. H. Miller

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• Genetic variation in the tumor necrosis factor alpha gene and the outcome of multiple sclerosis

  B. G. Weinshenker, D. M. Wingerchuk, Q. Liu, A. S. Bissonet, D. J. Schaid, S. S. Sommer

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• Interferon-β interferes with the proliferation but not with the cytokine secretion of myelin basic protein-specific, T-helper type 1 lymphocytes

  M. Pette, D. F. Pette, P. A. Muraro, E. Farnon, R. Martin, H. F. McFarland

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• Ropinirole for the treatment of early Parkinson's disease

  C. H. Adler, K. D. Sethi, R. A. Hauser, T. L. Davis, J. P. Hammerstad, J. Bertoni, R. L. Taylor, J. Sanchez-Ramos, C. F. O'Brien, Ropinirole Study Group

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• Familial nature and continuing morbidity of the amyotrophic lateral sclerosis-parkinsonism dementia complex of Guam

  P. L. McGeer, C. Schwab, E. G. McGeer, R. L. Haddock, J. C. Steele

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• A volumetric MRI study of Gilles de la Tourette's syndrome

  J. Moriarty, A. R. Varma, J. Stevens, M. Fish, M. R. Trimble, M. M. Robertson

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• Functional MRI mapping of occipital and frontal cortical activity during voluntary and imagined saccades

  I. Bodis-Wollner, S. F. Bucher, K. C. Seelos, W. Paulus, M. Reiser, W. H. Oertel

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• Potential therapeutic use of the selective dopamine D₁ receptor agonist, A-86929: An acute study in parkinsonian levodopa-primed monkeys

  Richard Grondin, Paul J. Bédard, Donald R. Britton, Kazumi Shiosaki

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• High prevalence of Parkinson's disease in the Faroe Islands

  Lene Wermuth, Poul Joensen, Nick Bünger, Bernard Jeune

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• Spinal pseudoathetosis: A rare, forgotten syndrome, with a review of old and recent descriptions

  J. Ghika, J. Bogousslavsky

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• Changes in putamen N-acetylaspartate and choline ratios in untreated and levodopa-treated Parkinson's disease: A proton magnetic resonance spectroscopy study

  C. M. Ellis, G. Lemmens, S.C. R. Williams, A. Simmons, J. Dawson, P. N. Leigh, K. Ray Chaudhuri

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• Randomized, double-blind, placebo-controlled crossover trial of modafinil in the treatment of excessive daytime sleepiness in narcolepsy

  R. J. Broughton, J.A. E. Fleming, C.F. P. George, J. D. Hill, M. H. Kryger, H. Moldofsky, J. Y. Montplaisir, R. L. Morehouse, A. Moscovitch, W. F. Murphy

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• Spinal epidural metastasis as the initial manifestation of malignancy: Clinical features and diagnostic approach

  David Schiff, B. P. O'Neill, Vera J. Suman

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• Conceptual apraxia from lateralized lesions

  Kenneth M. Heilman, Lynn M. Maher, Margaret L. Greenwald, Leslie J. G. Rothi

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• Pure topographic disorientation due to right retrosplenial lesion

  N. Takahashi, M. Kawamura, J. Shiota, N. Kasahata, K. Hirayama

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• Audiogenic startle reflex in acute hemiplegia

  Ph. Voordecker, N. Mavroudakis, S. Blecic, J. Hildebrand, D. Zegers de Beyl

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• Selective deficit of praxis imagery in ideomotor apraxia

  Cynthia Ochipa, Steven Z. Rapcsak, Lynn M. Maher, Leslie J. Gonzalez Rothi, Dawn Bowers, Kenneth M. Heilman

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• Individual prediction of change in delayed recall of prose passages after left-sided anterior temporal lobectomy

  H. Jokeit, A. Ebner, H. Holthausen, H. J. Markowitsch, A. Moch, H. Pannek, R. Schulz, I. Tuxhorn

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• Lateralized effects of self-induced sadness and happiness on corticospinal excitability

  Jose Maria Tormos, Carlos Cañete, Francisco Tarazona, M. Dolores Catalá, Alvaro Pascual-Leone Pascual, Alvaro Pascual-Leone

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• Partial ocular tilt reaction due to unilateral cerebellar lesion

  Stuart Mossman, G. Michael Halmagyi

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• Anterior opercular syndrome, caused by herpes simplex encephalitis

  N. M. McGrath, N. E. Anderson, J.K.A. Hope, M. C. Croxson, K. F. Powell

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• Frequency and frequently overlooked: Treatment-induced endocrine dysfunction in adult long-term survivors of primary brain tumors

  W. Arlt, U. Hove, B. Müller, M. Reincke, U. Berweiler, F. Schwab, B. Allolio

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• Increased intra-abdominal pressure and cardiac filling pressures in obesity-associated pseudotumor cerebri

  H. J. Sugerman, E. J. DeMaria, W. L. Felton, M. Nakatsuka, A. Sismanis

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• Evidence for association of HLA-A2 allele with onset age of Alzheimer's disease

  H. Payami, G. D. Schellenberg, S. Zareparsi, J. Kaye, G. J. Sexton, M. A. Head, S. S. Matsuyama, L. F. Jarvik, B. Miller, D. Q. McManus, T. D. Bird, R. Katzman, L. Heston, D. Norman, G. W. Small

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• Expression of game-related and generic knowledge by dementia patients who retain skill at playing dominoes

  F. Greiner, S. English, K. Dean, K. A. Olson, P. Winn, W. W. Beatty

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• Probable diffuse Lewy body disease presenting as REM sleep behavior disorder

  R. S. Turner, R. D. Chervin, K. A. Frey, S. Minoshima, D. E. Kuhl

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• Relationship between mesial temporal seizure focus and elevated serum prolactin in temporal lobe epilepsy

  Y. Y. Lin, M. S. Su, C. H. Yiu, Y. H. Shih, D. J. Yen, S. Y. Kwan, Z. A. Wu, S.H.H. Chan

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• Risk factors for status epilepticus in children with symptomatic epilepsy

  Gerald Novak, Joseph Maytal, Anna Alshansky, Catherine Ascher

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• Decreased postexercise facilitation of motor evoked potentials in patients with cerebellar degeneration

  A. Samii, E. M. Wassermann, M. Hallett

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• Risk of serious cutaneous disorders after initiation of use of phenytoin, carbamazepine, or sodium valproate: A record linkage study

  Patricia Tennis, Robert S. Stern

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• An MRI study of autism: The cerebellum revisited

  Joseph Piven, Khalil Saliba, James Bailey, Stephan Arndt

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• The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred

  C. A. McLean, E. Storey, R.J.M. Gardner, A. E.G. Tannenberg, L. Cervenáková, P. Brown

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• The thigh may not be suitable as an injection site for patients self-injecting sumatriptan

  Anders Frid, Jan-Erik Hardebo

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• Acetylcholine receptor autoantibody secretion by thymocytes: Relationship to myasthenia gravis

  Hiroaki Yoshikawa, Vanda A. Lennon

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• Spinobulbar muscular atrophy can mimic ALS: The importance of genetic testing in male patients with atypical ALS

  J. S. Parboosingh, D. A. Figlewicz, A. Krizus, V. Meininger, N. A. Azad, D. S. Newman, G. A. Rouleau

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• Longitudinal study of fiber density and motor unit number estimate in patients with amyotrophic lateral sclerosis

  Eric C. Yuen, Richard K. Olney

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• Deficiency of syntrophin, dystroglycan, and merosin in a female infant with a congenital muscular dystrophy phenotype lacking cysteine-rich and C-terminal domains of dystrophin

  N. Tachi, K. Ohya, S. Chiba, M. Matsuo, S. Y. Patria, K. Matsumura

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• α-Tocopherol transfer protein gene: Exon skipping of all transcripts causes ataxia

  Y. Tamaru, M. Hirano, H. Kusaka, H. Ito, T. Imai, S. Ueno

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• A mitochondrial DNA tRNA^Val point mutation associated with adult-onset Leigh syndrome

  R. M. Chalmers, P. J. Lamont, I. Nelson, D. W. Ellison, N. H. Thomas, A. E. Harding, S. R. Hammans

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