In This Issue
Editorials
In Memoriam
- Richard Lambert Masland, MD (1910–2003)Timothy A. Pedley, Lewis P. Rowland
Articles
- Enzyme replacement therapy improves function of C-, Aδ-, and Aβ-nerve fibers in Fabry neuropathyM. J. Hilz, M. Brys, H. Marthol, B. Stemper, M. Dütsch
- Triflusal vs aspirin for prevention of cerebral infarctionA randomized stroke studyA. Culebras, R. Rotta–Escalante, J. Vila, R. Domínguez, G. Abiusi, A. Famulari, R. Rey, L. Bauso–Tosselli, H. Gori, J. Ferrari, E. Reich, the TAPIRSS investigators
- Leukocyte CTG repeat length correlates with severity of myotonia in myotonic dystrophy type 1E. L. Logigian, R. T. Moxley, C. L. Blood, C. A. Barbieri, W. B. Martens, A. W. Wiegner, C. A. Thornton, R. T. Moxley
- Mutation in the AChR ion channel gate underlies a fast channel congenital myasthenic syndromeR. Webster, M. Brydson, R. Croxen, J. Newsom–Davis, A. Vincent, D. Beeson
- Large-scale disruption of microtubule pathways in morphologically normal human spastin muscleA. Molon, S. Di Giovanni, Y. W. Chen, P. M. Clarkson, C. Angelini, E. Pegoraro, E. P. Hoffman
- The effect of cannabis on tremor in patients with multiple sclerosisP. Fox, P. G. Bain, S. Glickman, C. Carroll, J. Zajicek
- Stimulation of STN impairs aspects of cognitive control in PDT. Hershey, F. J. Revilla, A. Wernle, P. Schneider Gibson, J. L. Dowling, J. S. Perlmutter
- LGI1 mutations in temporal lobe epilepsiesS. F. Berkovic, P. Izzillo, J. M. McMahon, L. A. Harkin, A. M. McIntosh, H. A. Phillips, R. S. Briellmann, R. H. Wallace, A. Mazarib, M. Y. Neufeld, A. D. Korczyn, I. E. Scheffer, J. C. Mulley
- LGI1 mutations in autosomal dominant partial epilepsy with auditory featuresR. Ottman, M. R. Winawer, S. Kalachikov, C. Barker-Cummings, T. C. Gilliam, T. A. Pedley, W. A. Hauser
- Epilepsy in twinsInsights from unique historical data of William LennoxL. Vadlamudi, E. Andermann, C. T. Lombroso, S. C. Schachter, R. L. Milne, J. L. Hopper, F. Andermann, S. F. Berkovic
- Primary trochlear headacheA new cephalgia generated and modulated on the trochlear regionJ. Yangüela, M. Sánchez-del-Rio, A. Bueno, A. Espinosa, P. Gili, N. Lopez-Ferrando, F. Barriga, J. C. Nieto, J. A. Pareja
- Alzheimer disease without neocortical neurofibrillary tangles“A second look”P. Tiraboschi, M. N. Sabbagh, L. A. Hansen, D. P. Salmon, A. Merdes, A. Gamst, E. Masliah, M. Alford, L. J. Thal, J. Corey-Bloom
- Cerebral infarctions and the likelihood of dementia from Alzheimer disease pathologyJ. A. Schneider, R. S. Wilson, J. L. Bienias, D. A. Evans, D. A. Bennett
- Dementia: The leading predictor of death in a defined elderly populationThe Cache County StudyJ. T. Tschanz, C. Corcoran, I. Skoog, A. S. Khachaturian, J. Herrick, K. M. Hayden, K. A. Welsh-Bohmer, T. Calvert, M. C. Norton, P. Zandi, J. C.S. Breitner, the Cache County Study Group
- Dissociation of numbers and objects in corticobasal degeneration and semantic dementiaC. H. Halpern, G. Glosser, R. Clark, J. Gee, P. Moore, K. Dennis, C. McMillan, A. Colcher, M. Grossman
- Polymorphisms in the CYP19 gene confer increased risk for Alzheimer diseaseS. Iivonen, E. Corder, M. Lehtovirta, S. Helisalmi, A. Mannermaa, S. Vepsäläinen, T. Hänninen, H. Soininen, M. Hiltunen
- Potentially reversible autoimmune limbic encephalitis with neuronal potassium channel antibodyM. J. Thieben, V. A. Lennon, B. F. Boeve, A. J. Aksamit, M. Keegan, S. Vernino
Views & Reviews
- Aromatic l-amino acid decarboxylase deficiencyClinical features, treatment, and prognosisR. Pons, B. Ford, C. A. Chiriboga, P. T. Clayton, V. Hinton, K. Hyland, R. Sharma, D. C. De Vivo
Clinical/Scientific Notes
- 4-Aminopyridine improves downbeat nystagmus, smooth pursuit, and VOR gainR. Kalla, S. Glasauer, F. Schautzer, N. Lehnen, U. Büttner, M. Strupp, T. Brandt
- Myoclonus–dystonia: Detection of novel, recurrent, and de novo SGCE mutationsK. Hedrich, E. -M. Meyer, B. Schüle, N. Kock, P. de Carvalho Aguiar, K. Wiegers, J. H. Koelman, J. Garrels, R. Dürr, L. Liu, E. Schwinger, L. J. Ozelius, B. Landwehrmeyer, A. J. Stoessl, M. A.J. Tijssen, C. Klein
- Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson diseaseR. Hering, S. Petrovic, E. -M. Mietz, C. Holzmann, D. Berg, P. Bauer, D. Woitalla, T. Müller, K. Berger, R. Krüger, O. Riess
- Transient insomnia induced by high-frequency deep brain stimulation in Parkinson diseaseC. Monaca, C. Ozsancak, L. Defebvre, S. Blond, A. Destée, J. D. Guieu, P. Derambure
- Botulinum toxin A improves involuntary limb movements in Rasmussen syndromeDora A. Lozsadi, Ian K. Hart, A. Peter Moore
- Neuralgic amyotrophy precipitated by Epstein–Barr virusBryan E. Tsao, Robin Avery, Robert W. Shields
- False-positive pulvinar sign on MRI in sporadic Creutzfeldt–Jakob diseaseG. C. Petzold, I. Westner, G. Bohner, K. M. Einhäupl, H. A. Kretzschmar, J. M. Valdueza
NeuroImages
- FDG-PET of poststroke oculomotor repairD. S. Liebeskind, B. M. Ances, A. B. Newberg, D. A. Jacobs, A. Alavi
- Focal polymicrogyria: Planar-surface MRIH. Urbach, A. Perez-Bouza, J. von Oertzen
Correspondence
- Prevalence of antigliadin antibodies in ataxia patientsKhalaf Bushara, Mark Hallett
- Language function and dysfunction in corticobasal degenerationAndrew J. Larner, Mark Doran
- Evidence of cardiac ischemia during seizures in drug refractory epilepsy patientsClaudia Stollberger, Joseph Finsterer
- Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaquesGianfranco Puoti, Lucia Limido, Roberto Cotrufo, Giuseppe Di Fede, Fabrizio Tagliavini
Resident and Fellow Page
Departments
Special Articles
- Practice Parameter: Recurrent stroke with patent foramen ovale and atrial septal aneurysm: [RETIRED]Report of the Quality Standards Subcommittee of the American Academy of Neurology*S. R. Messé, I. E. Silverman, J. R. Kizer, S. Homma, C. Zahn, G. Gronseth, S. E. Kasner
- The state of patient-oriented research in neurologyRalph L. Sacco, Beth A. Malow, Linda S. Williams
Brief Communications
- Pronunciation of irregular words is preserved in dementia, validating premorbid IQ estimationB. McGurn, J.M. Starr, J.A. Topfer, A. Pattie, M.C. Whiteman, H.A. Lemmon, L.J. Whalley, I.J. Deary
- Antiplatelet drug discontinuation is a risk factor for ischemic strokeIgor Sibon, Jean-Marc Orgogozo
- Alpha-1-antitrypsin deficiency alleles are not associated with cervical artery dissectionsC. Grond-Ginsbach, S. Engelter, I. Werner, I. Hausser, U. S. Müller, T. Brandt, P. Lyrer
- Feasibility and safety of norepinephrine-induced arterial hypertension in acute ischemic strokeA. S. Marzan, H. -J. Hungerbühler, A. Studer, R. W. Baumgartner, D. Georgiadis
- The impact of APOE on myocardial infarction, stroke, and dementiaThe Rotterdam StudyA.J. C. Slooter, M. Cruts, A. Hofman, P. J. Koudstaal, D. van der Kuip, M.A. J. de Ridder, J.C. M. Witteman, M.M. B. Breteler, C. Van Broeckhoven, C. M. van Duijn
- Behavioral symptoms in mild cognitive impairmentH. Feldman, P. Scheltens, E. Scarpini, N. Hermann, P. Mesenbrink, L. Mancione, S. Tekin, R. Lane, S. Ferris
- Retinal vascular abnormalities in CADASILC. Haritoglou, G. Rudolph, J. P. Hoops, C. Opherk, A. Kampik, M. Dichgans
- Leukoencephalopathy, cerebral calcifications, and cystsNew observationsL. M. Nagae-Poetscher, G. Bibat, M. Philippart, S. Rosemberg, A. Fatemi, M. T.C. Lacerda, M. O.R. Costa, F. Kok, C. Costa Leite, A. Horská, P. B. Barker, S. Naidu
- Temozolomide for treatment-resistant recurrent meningiomaMarc C. Chamberlain, Denice D. Tsao-Wei, Susan Groshen
- CCM1 mutation screen of sporadic cases with cerebral cavernous malformationsD. J. Verlaan, S. B. Laurent, U. Sure, H. Bertalanffy, E. Andermann, F. Andermann, G. A. Rouleau, A. M. Siegel
- Cognitive functioning in humans with mutations of the PAX6 geneP. J. Thompson, T. N. Mitchell, S. L. Free, K. A. Williamson, I. M. Hanson, V. van Heyningen, A. T. Moore, S. M. Sisodiya
- Developmental prosopagnosia and the Benton Facial Recognition TestBradley C. Duchaine, Ken Nakayama
- Laser scanning tomography of the optic nerve vs CSF opening pressure in idiopathic intracranial hypertensionJ.G. Heckmann, M. Weber, A.G. Jünemann, B. Neundörfer, C.Y. Mardin
- Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson diseaseN. L. Khan, R. Katzenschlager, H. Watt, K. P. Bhatia, N. W. Wood, N. Quinn, A. J. Lees
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