In This Issue
Editorial Message
- Clinical Trials Recruiting SectionA new resource for a daunting problemSteven R. Schwid, John R. Marler
Editorials
- “Do try this at home”Self-treatment of BPPVJoseph M. Furman, Timothy C. Hain
Articles
- Left ventricular hypertrophy is associated with cerebral microbleeds in hypertensive patientsS. -H. Lee, J. -M. Park, S. -J. Kwon, H. Kim, Y. H. Kim, J. K. Roh, B. W. Yoon
- Does acute occlusion of the carotid T invariably have a poor outcome?D. Georgiadis, J. Oehler, S. Schwarz, V. Rousson, M. Hartmann, S. Schwab
- High lipoprotein (a), diabetes, and the extent of symptomatic intracranial atherosclerosisJ. F. Arenillas, C. A. Molina, P. Chacón, A. Rovira, J. Montaner, P. Coscojuela, E. Sánchez, M. Quintana, J. Álvarez-Sabín
- Copper deficiency myelopathy produces a clinical picture like subacute combined degenerationNeeraj Kumar, John B. Gross, J. Eric Ahlskog
- Paroxysmal eyelid movementsA confusing feature of generalized photosensitive epilepsyC. S. Camfield, P. R. Camfield, M. Sadler, S. Rahey, K. Farrell, S. Chayasirisobbon, I. Scheffer
- Absence of antibodies to glutamate receptor type 3 (GluR3) in Rasmussen encephalitisR. Watson, Y. Jiang, I. Bermudez, L. Houlihan, L. Clover, K. McKnight, J. H. Cross, I. K. Hart, A. Roubertie, J. Valmier, Y. Hart, J. Palace, D. Beeson, A. Vincent, B. Lang
- Germline and mosaic mutations of FLN1 in men with periventricular heterotopiaR. Guerrini, D. Mei, S. Sisodiya, F. Sicca, B. Harding, Y. Takahashi, T. Dorn, A. Yoshida, J. Campistol, G. Krämer, F. Moro, W. B. Dobyns, E. Parrini
- A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardationR. Borgatti, C. Zucca, A. Cavallini, M. Ferrario, C. Panzeri, P. Castaldo, M. V. Soldovieri, C. Baschirotto, N. Bresolin, B. Dalla Bernardina, M. Taglialatela, M. T. Bassi
- Onset and rate of striatal atrophy in preclinical Huntington diseaseE. H. Aylward, B. F. Sparks, K. M. Field, V. Yallapragada, B. D. Shpritz, A. Rosenblatt, J. Brandt, L. M. Gourley, K. Liang, H. Zhou, R. L. Margolis, C. A. Ross
- PET evidence for a role of the basal ganglia in patients with ring chromosome 20 epilepsyA. Biraben, F. Semah, M. -J. Ribeiro, G. Douaud, P. Remy, A. Depaulis
- Disorganized search on cancellation is not a consequence of neglectV. W. Mark, A. J. Woods, K. K. Ball, D. L. Roth, M. Mennemeier
- Alternative cerebrospinal fluid tests to diagnose neurosyphilis in HIV-infected individualsC. M. Marra, L. C. Tantalo, C. L. Maxwell, K. Dougherty, B. Wood
- Neocortical volume decrease in relapsing–remitting MS patients with mild cognitive impairmentM. P. Amato, M. L. Bartolozzi, V. Zipoli, E. Portaccio, M. Mortilla, L. Guidi, G. Siracusa, S. Sorbi, A. Federico, N. De Stefano
- Medial temporal lobe atrophy on MRI predicts dementia in patients with mild cognitive impairmentEsther S.C. Korf, Lars-Olof Wahlund, Pieter Jelle Visser, Philip Scheltens
- Postmenopausal hormone therapy and risk of cognitive decline in community-dwelling aging womenJae H. Kang, Jennifer Weuve, Francine Grodstein
- Predicting the rate of cognitive decline in aging and early Alzheimer diseaseS. Adak, K. Illouz, W. Gorman, R. Tandon, E. A. Zimmerman, R. Guariglia, M. M. Moore, J. A. Kaye
- Mild cognitive impairment, amnestic typeAn epidemiologic studyMary Ganguli, Hiroko H. Dodge, Changyu Shen, Steven T. DeKosky
- Preserved visual–vestibular interaction in patients with bilateral vestibular failureS. Bense, A. Deutschländer, Th. Stephan, P. Bartenstein, M. Schwaiger, Th. Brandt, M. Dieterich
- Pathology of early- vs late-onset TTR Met30 familial amyloid polyneuropathyH. Koike, K. Misu, M. Sugiura, M. Iijima, K. Mori, M. Yamamoto, N. Hattori, E. Mukai, Y. Ando, S. Ikeda, G. Sobue
Views & Reviews
- Ictal SPECT analysis in epilepsySubtraction and statistical parametric mapping techniquesRobert C. Knowlton, Nicholas D. Lawn, James M. Mountz, Ruben I. Kuzniecky
Medical Hypothesis
- White matter lesion progressionA surrogate endpoint for trials in cerebral small-vessel diseaseR. Schmidt, Ph. Scheltens, T. Erkinjuntti, L. Pantoni, H. S. Markus, A. Wallin, F. Barkhof, F. Fazekas
Clinical/Scientific Notes
- Thoracic syringomyelia and suspected multiple sclerosis: Cause and effect or coincidence?James A. Charles, Mark Berger, Stuart D. Cook
- CSF volume loss in spontaneous intracranial hypotensionNuno Canas, Elmira Medeiros, Ana Teresa Fonseca, Fernanda Palma-Mira
- Noninvasive imaging of carotid plaque inflammationR. A. Trivedi, J. M. U-King-Im, M. J. Graves, P. J. Kirkpatrick, J. H. Gillard
- Tremor and deep white matter changes in α-methylacyl-CoA racemase deficiencyC. E. Clarke, S. Alger, M. A. Preece, M. A. Burdon, S. Chavda, S. Denis, S. Ferdinandusse, R. J.A. Wanders
- Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2AS. Pereira, J. P. Vieira, F. Barroca, P. Roll, R. Carvalhas, P. Cau, S. Sequeira, P. Genton, P. Szepetowski
- Emotional prosody in primary progressive aphasiaJack W. Tsao, David H. Dickey, Kenneth M. Heilman
NeuroImages
- Midbrain vasculitic aneurysmsHyung-Min Kwon, Jae-Kyu Roh, Gregory Youngnam Chang
- Kluver-Bucy syndrome related to gliomaMichael A. Badruddoja, James Vredenburgh, Terry S. Peery, David A. Reardon
Patient Page
Correspondence
- Late onset Charcot-Marie-Tooth 2 syndrome caused by two novel mutations in the MPZ geneJohn Kamholz, Michael E. Shy
- A CAV3 microdeletion differentially affects skeletal muscle and myocardiumJosef Finsterer, Claudia Stoellberger
- Involvement of the human subthalamic nucleus in movement preparationGuglielmo Foffani, Alberto Priori
Resident and Fellow Page
- Update for the Neurology Residents and Fellows from the Neurology Residency Review Committee (NRRC)Noah Rosen, Jasper R. Daube, Larry Sulton
Departments
Brief Communications
- Detection of novel mutations in the SMN Tudor domain in type I SMA patientsI. Cuscó, M. Jesus Barceló, E. del Río, M. Baiget, E. F. Tizzano
- Self-treatment of benign paroxysmal positional vertigoSemont maneuver vs Epley procedureA. Radtke, M. von Brevern, K. Tiel-Wilck, A. Mainz-Perchalla, H. Neuhauser, T. Lempert
- l-Dopa-induced dyskinesia improvement after STN-DBS depends upon medication reductionH. Russmann, J. Ghika, P. Combrement, J. G. Villemure, J. Bogousslavsky, P. R. Burkhard, F. J.G. Vingerhoets
- Anti-basal ganglia antibodies in patients with atypical dystonia and ticsA prospective studyM. J. Edwards, E. Trikouli, D. Martino, M. Bozi, R. C. Dale, A. J. Church, A. Schrag, A. J. Lees, N. P. Quinn, G. Giovannoni, K. P. Bhatia
- On-line anosognosiaUnawareness for chorea in real time but not on videotape delayJ. I. Shenker, S. A. Wylie, K. Fuchs, C. A. Manning, K. M. Heilman
- Development and initial validation of a screening tool for Parkinson disease surgical candidatesM. S. Okun, H. H. Fernandez, O. Pedraza, M. Misra, K. E. Lyons, R. Pahwa, D. Tarsy, L. Scollins, K. Corapi, G. M. Friehs, J. Grace, J. Romrell, K. D. Foote
- Near-infrared spectrophotoscopy of finger venules in assessment of autonomic dysfunctionK. Obayashi, Y. Ando, M. Nakamura, T. Yamashita, M. Ueda, K. Haraoka, H. Terazaki, M. Uchino
- Clonal evolution as pathogenetic mechanism in relapse of primary CNS lymphomaH. Pels, M. Montesinos-Rongen, C. Schaller, D. Van Roost, U. Schlegel, O. D. Wiestler, M. Deckert
- Three-dimensional proton spectroscopy of deep gray matter nuclei in relapsing–remitting MSM. Inglese, S. Liu, J. S. Babb, L. J. Mannon, R. I. Grossman, O. Gonen
- Possible association of nicastrin polymorphisms and Alzheimer disease in the Finnish populationS. Helisalmi, B. Dermaut, M. Hiltunen, A. Mannermaa, M. Van den Broeck, M. Lehtovirta, A. M. Koivisto, S. Iivonen, M. Cruts, H. Soininen, C. Van Broeckhoven
- Ventilatory support in facioscapulohumeral muscular dystrophyM. Wohlgemuth, E. L. van der Kooi, R. G. van Kesteren, S. M. van der Maarel, G. W. Padberg
- Improvement of a CIDP associated with hepatitis C virus infection using antiviral therapyP. Corcia, D. Barbereau, A. M. Guennoc, B. de Toffol, Y. Bacq
- Cerebral lipiodol embolism during transcatheter arterial chemoembolizationK. M. Yoo, B. G. Yoo, K. S. Kim, S. U. Lee, B. H. Han
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