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Neurology
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March 12, 2013; 80 (11)

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In Focus

  • Spotlight on the March 12 Issue
    Robert A. Gross
    • Full Text
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Editorials

  • The importance of rare DNA variation in neurologic diseaseCautionary tale
    Jonathan L. Haines
    • Full Text
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  • Family history in juvenile Huntington diseaseDo the signs point to “yes” or “very doubtful”?
    Rebecca K. Lehman, Martha Nance
    • Full Text
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  • Alzheimer disease biomarkers and insights into mild cognitive impairment
    David S. Knopman
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In Memoriam

  • Sheldon Kapen, MD (1935–2012)
    Robert P. Lisak, Joshua E. Adler
    • Full Text
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Articles

  • Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease
    Karen Nuytemans, Guney Bademci, Vanessa Inchausti, Amy Dressen, Daniel D. Kinnamon, Arpit Mehta, Liyong Wang, Stephan Züchner, Gary W. Beecham, Eden R. Martin, William K. Scott, Jeffery M. Vance
    • Abstract
    • Full Text
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  • The challenge of juvenile Huntington diseaseTo test or not to test
    Georgios Koutsis, Georgia Karadima, Athina Kladi, Marios Panas
    • Abstract
    • Full Text
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    CME Course
  • Elevation of proinflammatory cytokines in patients with Aicardi-Goutières syndrome
    Asako Takanohashi, Morgan Prust, Jichuan Wang, Heather Gordish-Dressman, Miriam Bloom, Gillian I. Rice, Johanna L. Schmidt, Yanick J. Crow, Pierre Lebon, Taco W. Kuijpers, Kanneboyina Nagaraju, Adeline Vanderver
    • Abstract
    • Full Text
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  • Multiple molecular mechanisms for a single GABAA mutation in epilepsy
    Christopher A. Reid, Taehwan Kim, A. Marie Phillips, Jun Low, Samuel F. Berkovic, Bernhard Luscher, Steven Petrou
    • Abstract
    • Full Text
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  • CHADS2, CHA2DS2-VASc, and long-term stroke outcome in patients without atrial fibrillation
    George Ntaios, Gregory Y.H. Lip, Konstantinos Makaritsis, Vasileios Papavasileiou, Anastasia Vemmou, Eleni Koroboki, Paraskevi Savvari, Efstathios Manios, Haralampos Milionis, Konstantinos Vemmos
    • Abstract
    • Full Text
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  • Disability in multiple sclerosisA reference for patients and clinicians
    Ilya Kister, Eric Chamot, Amber R. Salter, Gary R. Cutter, Tamar E. Bacon, Joseph Herbert
    • Abstract
    • Full Text
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  • Cognitive impairment in MSImpact of white matter integrity, gray matter volume, and lesions
    Hanneke E. Hulst, Martijn D. Steenwijk, Adriaan Versteeg, Petra J.W. Pouwels, Hugo Vrenken, Bernard M.J. Uitdehaag, Chris H. Polman, Jeroen J.G. Geurts, Frederik Barkhof
    • Abstract
    • Full Text
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  • CSF1R mutations link POLD and HDLS as a single disease entity
    Alexandra M. Nicholson, Matt C. Baker, NiCole A. Finch, Nicola J. Rutherford, Christian Wider, Neill R. Graff-Radford, Peter T. Nelson, H. Brent Clark, Zbigniew K. Wszolek, Dennis W. Dickson, David S. Knopman, Rosa Rademakers
    • Abstract
    • Full Text
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  • Modulation of neural activation following treatment of hepatic encephalopathy
    Mark J.W. McPhail, Robert Leech, Vijay P.B. Grover, Julie A. Fitzpatrick, Novraj S. Dhanjal, Mary M.E. Crossey, Henning Pflugrad, Brian K. Saxby, Keith Wesnes, M. Alex Dresner, Adam D. Waldman, Howard C. Thomas, Simon D. Taylor-Robinson
    • Abstract
    • Full Text
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  • Prediction of dementia in MCI patients based on core diagnostic markers for Alzheimer disease
    Annapaola Prestia, Anna Caroli, Wiesje M. van der Flier, Rik Ossenkoppele, Bart Van Berckel, Frederik Barkhof, Charlotte E. Teunissen, Anders E. Wall, Stephen F. Carter, Michael Schöll, Il Han Choo, Agneta Nordberg, Philip Scheltens, Giovanni B. Frisoni
    • Abstract
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    CME Course

Contemporary Issues

  • Ethical and quality pitfalls in electronic health records
    James L. Bernat
    • Abstract
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Clinical/Scientific Notes

  • A novel α-synuclein missense mutation in Parkinson disease
    Christos Proukakis, Christopher G. Dudzik, Timothy Brier, Donna S. MacKay, J. Mark Cooper, Glenn L. Millhauser, Henry Houlden, Anthony H. Schapira
    • Full Text
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Reflections: Neurology and the Humanities

  • The last exam
    Ludwig Gutmann
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Video NeuroImages

  • Chvostek sign, frequently found in healthy subjects, is not a useful clinical sign
    Aurélie Méneret, Stéphanie Guey, Bertrand Degos
    • Full Text
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Resident and Fellow Section

  • Clinical Reasoning: A 12-year-old boy with ascending weakness
    Kris F. French, Meghan S. Candee, Jessica L. Stahl, Lisa L. Giles, Tiffany S. Glasgow, Denise C. Morita
    • Full Text
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  • Pearls and Oy-sters: Carotid dissection with normal arterial lumen
    Jitphapa Pongmoragot, Aditya Bharatha, Gustavo Saposnik
    • Full Text
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  • Teaching NeuroImages: Acute cerebellitis caused by Salmonella typhimurium
    Philippe Rizek, Florence Morriello, Manas Sharma, Teneille Gofton
    • Full Text
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  • Teaching NeuroImages: A neurosyphilis case presenting with atypical neuroradiologic findings
    Nergiz Agayeva, Kader Karli-Oguz, Esen Saka
    • Full Text
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WriteClick: Editor's Choice

  • Tadpole pupilAuthor Response
    Robert A. Egan, Aki Kawasaki
    • Full Text
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  • Disease-modifying drugs for multiple sclerosis in pregnancy: A systematic reviewAuthor Response
    James A. Charles, Helen Tremlett, Ellen Lu, Colleen Guimond, A. Dessa Sadovnick
    • Full Text
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Corrections

  • Intrathecal EBV antibodies are part of the polyspecific immune response in multiple sclerosis
    • Full Text
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  • Provocation of migraine with aura using natural trigger factors
    • Full Text
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Departments

  • Book Review

    • Handbook of Atypical Parkinsonism
      Rodolfo Savica
      • Full Text
      • Full Text (PDF)
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Neurology: 80 (11)
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