In Focus
Editorials
- Family history in juvenile Huntington diseaseDo the signs point to “yes” or “very doubtful”?Rebecca K. Lehman, Martha Nance
In Memoriam
Articles
- Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson diseaseKaren 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
- The challenge of juvenile Huntington diseaseTo test or not to testGeorgios Koutsis, Georgia Karadima, Athina Kladi, Marios Panas
- Elevation of proinflammatory cytokines in patients with Aicardi-Goutières syndromeAsako 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
- Multiple molecular mechanisms for a single GABAA mutation in epilepsyChristopher A. Reid, Taehwan Kim, A. Marie Phillips, Jun Low, Samuel F. Berkovic, Bernhard Luscher, Steven Petrou
- CHADS2, CHA2DS2-VASc, and long-term stroke outcome in patients without atrial fibrillationGeorge Ntaios, Gregory Y.H. Lip, Konstantinos Makaritsis, Vasileios Papavasileiou, Anastasia Vemmou, Eleni Koroboki, Paraskevi Savvari, Efstathios Manios, Haralampos Milionis, Konstantinos Vemmos
- Disability in multiple sclerosisA reference for patients and cliniciansIlya Kister, Eric Chamot, Amber R. Salter, Gary R. Cutter, Tamar E. Bacon, Joseph Herbert
- Cognitive impairment in MSImpact of white matter integrity, gray matter volume, and lesionsHanneke 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
- CSF1R mutations link POLD and HDLS as a single disease entityAlexandra 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
- Modulation of neural activation following treatment of hepatic encephalopathyMark 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
- Prediction of dementia in MCI patients based on core diagnostic markers for Alzheimer diseaseAnnapaola 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
Contemporary Issues
Clinical/Scientific Notes
- A novel α-synuclein missense mutation in Parkinson diseaseChristos Proukakis, Christopher G. Dudzik, Timothy Brier, Donna S. MacKay, J. Mark Cooper, Glenn L. Millhauser, Henry Houlden, Anthony H. Schapira
Reflections: Neurology and the Humanities
Video NeuroImages
- Chvostek sign, frequently found in healthy subjects, is not a useful clinical signAurélie Méneret, Stéphanie Guey, Bertrand Degos
Resident and Fellow Section
- Clinical Reasoning: A 12-year-old boy with ascending weaknessKris F. French, Meghan S. Candee, Jessica L. Stahl, Lisa L. Giles, Tiffany S. Glasgow, Denise C. Morita
- Pearls and Oy-sters: Carotid dissection with normal arterial lumenJitphapa Pongmoragot, Aditya Bharatha, Gustavo Saposnik
- Teaching NeuroImages: Acute cerebellitis caused by Salmonella typhimuriumPhilippe Rizek, Florence Morriello, Manas Sharma, Teneille Gofton
- Teaching NeuroImages: A neurosyphilis case presenting with atypical neuroradiologic findingsNergiz Agayeva, Kader Karli-Oguz, Esen Saka
WriteClick: Editor's Choice
- Disease-modifying drugs for multiple sclerosis in pregnancy: A systematic reviewAuthor ResponseJames A. Charles, Helen Tremlett, Ellen Lu, Colleen Guimond, A. Dessa Sadovnick
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