Articles
- The Lewy body variant of Alzheimer's diseaseA clinical and pathologic entityL. Hansen, D. Salmon, D. Galasko, E. Masliah, R. Katzman, R. DeTeresa, L. Thal, M. M. Pay, R. Hofstetter, M. Klauber, V. Rice, N. Butters, M. Alford
- Measurement and prediction of functional capacity in Alzheimer's diseaseYaakov Stern, Dale Hesdorffer, Mary Sano, Richard Mayeux
- Focal Alzheimer's diseaseWilliam J. Jagust, Peter Davies, Janice K. Tiller-Borcich, Bruce R. Reed
- What excitotoxin kills striatal neurons in Huntington's disease? Clues from neurochemical studiesThomas L. Perry, Shirley Hansen
- Widespread tissue distribution of mitochondrial DNA deletions in Kearns‐Sayre syndromeS. Shanske, C. T. Moraes, A. Lombes, A. F. Miranda, E. Bonilla, P. Lewis, M. A. Whelan, C. A. Ellsworth, S. DiMauro
- Treatment of visual loss in pseudotumor cerebri associated with uremiaJ. Guy, P. K. Johnston, J. J. Corbett, A. L. Day, J. S. Glaser
- Age‐induced cognitive disturbances in Parkinson's diseaseB. Dubois, B. Pillon, N. Sternic, F. Lhermitte, Y. Agid
- The changing patterns of death rates in parkinsonismJohn F. Kurtzke, Frances M. Murphy
- Neologistic speech automatisms during complex partial seizuresWilliam L. Bell, Jennifer Homer, Patrick Logue, Rodney A. Radtke
- Common dopaminergic mechanism for epileptic photosensitivity in progressive myoclonus epilepsiesEsa Mervaala, Frederick Andermann, Luis Felipe Quesney, Michael Krelina
- The movement disorder of reflex sympathetic dystrophyRobert J. Schwartzman, James Kerrigan
- Post‐traumatic midbrain tremorsM. Reza Samie, John B. Selhorst, William C. Koller
- Dopa‐responsive dystoniaThe spectrum of clinical manifestations in a large North American familyTorbjoern G. Nygaard, Joel M. Trugman, Justo G. de Yebenes, Stanley Fahn
- Pharmacodynamic modeling of concentration‐effect relationships after controlled‐release carbidopa/levodopa (Sinemet CR4) in Parkinson's diseaseM. V. Nelson, R. C. Berchou, P. A. Le Witt, D. Kareti, M. P. Galloway
- Combined depth and subdural electrode investigation in uncontrolled epilepsySusan S. Spencer, Dennis D. Spencer, Peter D. Williamson, Richard Mattson
- Primary CNS lymphomaCombined treatment with chemotherapy and radiotherapyL. M. DeAngelis, J. Yahalom, M-H. Heinemann, C. Cirrincione, H. T. Thaler, G. Krol
- Focal functional anatomy of dorsolateral frontocentral seizuresW. W. Sutherling, M. W. Risinger, P. H. Crandall, D. P. Becker, C. Baumgartner, L. D. Cahan, C. Wilson, M. F. Levesque
- Cerebral blood flow variations in CNS lupusM. J. Kushner, M. Tobin, F. Fazekas, J. Chawluk, D. Jamieson, B. Freundlich, S. Grenell, L. Freemen, M. Reivich
- Recurrent respiratory insufficiency and depressed ventilatory drive complicating mitochondrial myopathiesRichard J. Barohn, Thomas Clanton, Zarife Sahenk, Jerry R. Mendell
- Acute changes in blood glucose affect resistance to ischemic nerve conduction failureGareth J. Parry, Hitoshi Kohzu
- Rapid detection of Creutzfeldt‐Jakob disease and scrapie prion proteinsDan Serban, Albert Taraboulos, Stephen J. DeArmond, Stanley B. Prusiner
- A syndrome of asymmetric limb weakness with motor conduction blockC. Krarup, J. D. Stewart, A. J. Sumner, A. Pestronk, S. A. Lipton
- Adult sphingomyelinase deficiencyReport of 2 patients who initially presented with psychiatric disordersG. Dubois, J.-M. Mussini, M. Auclair, J. Battesti, J.-M. Boutry, J.-L. Kemeny, J.-C. Mazière, J.-C. Turpin, J.-J. Hauw
- Segmental analysis of neuropeptide concentrations in normal human spinal cordEduardo E. Benarroch, Lisa D. Aimone, Tony L. Yaksh
- The juvenile and chronic forms of GM2 gangliosidosisClinical and enzymatic heterogeneityN. Specola, M. T. Vanier, F. Goutières, J. Mikol, J. Aicardi
Views & Reviews
- How frequently does classic amyotrophic lateral sclerosis develop in survivors of poliomyelitis?Carmel Armon, Jasper R. Daube, Anthony J. Windebank, Leonard T. Kurland
- Characteristics of American neurology chairs, 1988A demographic snapshotElliott L. Mancall, Sharon A. VanderWeide, Martin E. Grosse
- Dysphagia as the sole manifestation of adult type I Arnold‐Chiari malformationA. Achiron, A. Kuritzky
Correspondence
- Reply from the AuthorsJohn J. Halperin, Benjamin J. Luft, David J. Volkman, Raymond J. Dattwyler
- Amantadine for Friedreich's ataxiaClaudio Mariani, Margherita Canesi, Sergio Barbieri, Gianni Pezzoli
Brief Communications
- Herpes simplex labialis and trigeminal neuropathyStasha Gominak, Didier Cros, David Paydarfar
- Transient focal neurologic deficits complicating interleukin‐2 therapyJ. T. Bernard, S. Ameriso, R. A. Kempf, P. Rosen, M. S. Mitchell, M. Fisher
- Episodic symptoms mistaken for seizures in the neurologically impaired childJane F. Donat, Francis S. Wright
- The role of radiation therapy following resection of single brain metastasis from melanomaNeil A. Hagen, Constance Cirrincione, Howard T. Thaler, Lisa M. DeAngelis
- Transient inhibitory seizures mimicking crescendo TIAsHenry Lee, Alfred Lerner
- Neurologic involvement in toxemia of pregnancyReversible MRI lesionsHenry G. Raroque, William W. Orrison, Gary A. Rosenberg
- Occurrence of invasive thymoma after thymectomy for myasthenia gravisReport of a caseFarhat Husain, Nell J. Ryan, Gwendolyn R. Hogan, Enrique Gonzalez
Historical Neurology
- Henry F. Campbell and the secretory nervous systemKimford J. Meador, David W. Loring
Book Reviews
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Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis
Dr. Robert Pitceathly and Dr. William Macken
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