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March 12, 2002; 58 (5)

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In This Issue

  • March 12 Highlights
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Editorials

  • We need something better, and we need it nowFetal striatal transplantation in Huntington’s disease?
    J. Timothy Greenamyre, Ira Shoulson
    • Full Text
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  • B cells and epilepsyThe odd couple
    James O. McNamara
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Articles

  • Bilateral human fetal striatal transplantation in Huntington’s disease
    R. A. Hauser, S. Furtado, C. R. Cimino, H. Delgado, S. Eichler, S. Schwartz, D. Scott, G. M. Nauert, E. Soety, V. Sossi, D. A. Holt, P. R. Sanberg, A. J. Stoessl, T. B. Freeman
    • Abstract
    • Full Text
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  • Regional and progressive thinning of the cortical ribbon in Huntington’s disease
    H. D. Rosas, A. K. Liu, S. Hersch, M. Glessner, R. J. Ferrante, D. H. Salat, A. van der Kouwe, B. G. Jenkins, A. M. Dale, B. Fischl
    • Abstract
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  • Spinocerebellar ataxias in the NetherlandsPrevalence and age at onset variance analysis
    B.P.C. van de Warrenburg, R.J. Sinke, C.C. Verschuuren–Bemelmans, H. Scheffer, E.R. Brunt, P.F. Ippel, J.A. Maat–Kievit, D. Dooijes, N.C. Notermans, D. Lindhout, N.V.A.M. Knoers, H.P.H. Kremer
    • Abstract
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  • Analysis of antibody gene rearrangement, usage, and specificity in chronic focal encephalitis
    S.E. Baranzini, K. Laxer, R. Saketkhoo, M.K. Elkins, J.M. Parent, R. Mantegazza, J.R. Oksenberg
    • Abstract
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  • Low incidence of abnormal 18FDG-PET in children with new-onset partial epilepsyA prospective study
    W.D. Gaillard, L. Kopylev, S. Weinstein, J. Conry, P.L. Pearl, M.V. Spanaki, S. Fazilat, S. Fazilat, L.G. Venzina, E. Dubovsky, W.H. Theodore
    • Abstract
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  • Clinical, EEG, and quantitative MRI differences in pediatric frontal and temporal lobe epilepsy
    J.A. Lawson, M.J. Cook, S. Vogrin, L. Litewka, D. Strong, A.F. Bleasel, A.M.E. Bye
    • Abstract
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  • Abnormal cobalamin-dependent transmethylation in AIDS-associated myelopathy
    A. Di Rocco, T. Bottiglieri, P. Werner, A. Geraci, D. Simpson, J. Godbold, S. Morgello
    • Abstract
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  • Does dichotic listening probe temporal lobe functions?
    L. Jäncke, N.J. Shah
    • Abstract
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  • The effect of APOE ε4 allele on cerebral glucose metabolism in AD is a function of age at onset
    N. Hirono, M. Hashimoto, M. Yasuda, K. Ishii, S. Sakamoto, H. Kazui, E. Mori
    • Abstract
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  • Antemortem MRI findings correlate with hippocampal neuropathology in typical aging and dementia
    C. R. Jack, D. W. Dickson, J. E. Parisi, Y. C. Xu, R. H. Cha, P. C. O’Brien, S. D. Edland, G. E. Smith, B. F. Boeve, E. G. Tangalos, E. Kokmen, R. C. Petersen
    • Abstract
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  • Functional deficits in patients with mild cognitive impairmentPrediction of AD
    M. H. Tabert, S. M. Albert, L. Borukhova-Milov, Y. Camacho, G. Pelton, X. Liu, Y. Stern, D. P. Devanand
    • Abstract
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  • ALS and PDC of GuamForty-year follow-up
    C.C. Plato, D. Galasko, R.M. Garruto, M. Plato, A. Gamst, U.-K. Craig, J. M. Torres, W. Wiederholt
    • Abstract
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  • Early detection and longitudinal changes in amyotrophic lateral sclerosis by 1H MRSI
    J. Suhy, R.G. Miller, R. Rule, N. Schuff, J. Licht, V. Dronsky, D. Gelinas, A.A. Maudsley, M.W. Weiner
    • Abstract
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  • Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age
    H. Tajsharghi, L.-E. Thornell, N. Darin, T. Martinsson, M. Kyllerman, J. Wahlström, A. Oldfors
    • Abstract
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  • Effect of time since onset of risk factors on the occurrence of ischemic stroke
    J. P. Whisnant, D. O. Wiebers, W. M. O’Fallon, J. D. Sicks, R. L. Frye
    • Abstract
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  • Adaptation in the motor cortex following cervical spinal cord injury
    D. J. Mikulis, M. T. Jurkiewicz, W. E. McIlroy, W. R. Staines, L. Rickards, S. Kalsi–Ryan, A. P. Crawley, M. G. Fehlings, M. C. Verrier
    • Abstract
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Views & Reviews

  • Clinical trial end pointsOn the road to nowhere?
    Robert G. Holloway, Andrew W. Dick
    • Abstract
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Clinical/Scientific Notes

  • Effects of l-arginine on the acute phase of strokes in three patients with MELAS
    Y. Koga, M. Ishibashi, I. Ueki, S. Yatsuga, R. Fukiyama, Y. Akita, T. Matsuishi
    • Full Text
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  • Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson’s disease
    D. Messina, G. Annesi, P. Serra, G. Nicoletti, A. Pasqua, F. Annesi, C. Tomaino, I.C. Cirò–Candiano, S. Carrideo, M. Caracciolo, P. Spadafora, M. Zappia, G. Savettieri, A. Quattrone
    • Full Text
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  • Alopecia induced by dopamine agonists
    Rowena E. Tabamo, Alessandro Di Rocco
    • Full Text
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  • Cabergoline can increase penile erections and libido
    Matthias Wittstock, Reiner Benecke, Dirk Dressler
    • Full Text
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  • Lack of effect of topiramate for central pain
    S. Canavero, V. Bonicalzi, R. Paolotti
    • Full Text
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Correspondence

  • The parkin gene is not involved in late-onset Parkinson’s disease
    M. Kann, K. Hedrich, P. Vieregge, H. Jacobs, B. Müller, N. Kock, E. Schwinger, C. Klein, K. Marder, J. Harris, H. Meija-Santana, S. Bressman, L.J. Ozelius, A.E. Lang, P.P. Pramstaller
    • Full Text
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  • A 1-year, randomized, placebo-controlled study of donepezil in patients with mild to moderate AD
    Dirk Deleu
    • Full Text
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  • Prognostic value of decremental responses to repetitive nerve stimulation in ALS patients
    Paula A. Kaires
    • Full Text
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  • Language and spatial attention can lateralize to the same hemisphere in healthy humans
    Leonidas Stefanis
    • Full Text
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  • Association study of dopamine D2, D3 receptor gene polymorphisms with motor fluctuations in PD
    Mario Zappia, Grazia Annesi, Aldo Quattrone
    • Full Text
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  • Differing patterns of temporal atrophy in Alzheimer’s disease and semantic dementia
    Dennis Chan, Nick Fox, Martin Rossor
    • Full Text
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  • Frequency of bowel movements and future risk of Parkinson’s disease
    Gershon T. Lesser
    • Full Text
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Corrections

  • Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy
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Departments

  • Calendar
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  • Book Reviews
    Lauren E. Abrey, Nancy J. Newman
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Filler

  • Access www.neurology.org now for full-text articles
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Brief Communications

  • Trochleitis and migraine headache
    Julio Yangüela, Juan A. Pareja, Nicolas Lopez, Margarita Sánchez del Río
    • Abstract
    • Full Text
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  • Accuracy of muscle localization without EMG: Implications for treatment of limb dystonia
    F. M. Molloy, H. A. Shill, A. Kaelin–Lang, B. I. Karp
    • Abstract
    • Full Text
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  • Parkin mutations in a patient with hemiparkinsonism–hemiatrophy: A clinical–genetic and PET study
    P. P. Pramstaller, G. Künig, K. Leenders, M. Kann, K. Hedrich, P. Vieregge, C. G. Goetz, C. Klein
    • Abstract
    • Full Text
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  • Early-onset, rapidly progressive familial tauopathy with R406W mutation
    Y. Saito, A. Geyer, R. Sasaki, S. Kuzuhara, E. Nanba, T. Miyasaka, K. Suzuki, S. Murayama
    • Abstract
    • Full Text
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  • Spontaneous CSF leaks: Underlying disorder of connective tissue
    Bahram Mokri, Cormac O. Maher, Drahomira Sencakova
    • Abstract
    • Full Text
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  • Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
    Sohei Yanagawa, Nobuo Ito, Kunimasa Arima, Shu-ichi Ikeda
    • Abstract
    • Full Text
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  • 1H MRSI predicts surgical outcome in MRI-negative temporal lobe epilepsy
    J. Suhy, K.D. Laxer, A.A. Capizzano, P. Vermathen, G.B. Matson, N.M. Barbaro, M.W. Weiner
    • Abstract
    • Full Text
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  • Intrathecal IgM synthesis in neurologic diseases: Relationship with disability in MS
    L. M. Villar, J. Masjuan, P. González–Porqué, J. Plaza, M. C. Sádaba, E. Roldán, A. Bootello, J. C. Alvarez–Cermeño
    • Abstract
    • Full Text
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NISUS: Neurology and the Humanities

  • Fiction: The last referral
    David Goldblatt
    • Full Text
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