Articles
- Coexistence of migraine and idiopathic intracranial hypertension without papilledemaNinan T. Mathew, K. Ravishankar, Luis C. Sanin
- Frontal lobe injuries, violence, and aggressionA report of the Vietnam Head Injury StudyJ. Grafman, K. Schwab, D. Warden, A. Pridgen, H. R. Brown, A. M. Salazar
- Neural basis of confabulationD. F. Benson, A. Djenderedjian, B. L. Miller, N. A. Pachana, L. Chang, L. Itti, I. Mena
- Pontine lesions in idiopathic narcolepsyG. Plazzi, P. Montagna, F. Provini, A. Bizzi, M. Cohen, E. Lugaresi
- Cataplexy and monoamine oxidase deficiency in Norrie diseaseD. G. Vossler, A. R. Wyler, R. J. Wilkus, G. Gardner-Walker, B. W. Vlcek
- Does monoamine oxidase type B play a role in dopaminergic nerve cell death in Parkinson's disease?Philippe Damier, Anne Kastner, Yves Agid, Etienne C. Hirsch
- Case‐control study of idiopathic Parkinson's disease and dietary vitamin E intakeD. M. Morens, A. Grandinetti, C. I. Waslien, C. B. Park, G. W. Ross, L. R. White
- Possible environmental, occupational, and other etiologic factors for Parkinson's diseaseA case‐control study in GermanyA. Seidler, W. Hellenbrand, B.-P. Robra, P. Vieregge, P. Nischan, J. Joerg, W. H. Oertel, G. Ulm, E. Schneider
- Limited usefulness of electroconvulsive therapy in progressive supranuclear palsyC. L. Barclay, J. Duff, P. Sandor, A. E. Lang
- Risk factors for Creutzfeldt‐Jakob diseaseA reanalysis of case‐control studiesD. P.W.M. Wientjens, Z. Davanipour, A. Hofman, K. Kondo, W. B. Matthews, R. G. Will, C. M. van Duijn
- Intracranial hemorrhage associated with cocaine abuseA prospective autopsy studyKurt B. Nolte, Lawrence M. Brass, Carol F. Fletterick
- Extensive brain calcifications, leukodystrophy, and formation of parenchymal cystsA new progressive disorder due to diffuse cerebral microangiopathyP. Labrune, C. Lacroix, F. Goutiéres, J. de Laveaucoupet, P. Chevalier, M. Zerah, B. Husson, P. Landrieu
- Stroke recurrence in patients with patent foramen ovaleThe Lausanne StudyJ. Bogousslavsky, S. Garazi, X. Jeanrenaud, N. Aebischer, G. Van Melle
- Botulinum toxin type A in the treatment of upper extremity spasticityA randomized, double‐blind, placebo‐controlled trialD. M. Simpson, D. N. Alexander, C. F. O'Brien, M. Tagliati, A. S. Aswad, J. M. Leon, J. Gibson, J. M. Mordaunt, E. P. Monaghan
- Linkage and mutation analysis of Charcot‐Marie‐Tooth neuropathy type 2 families with chromosomes 1p35‐p36 and Xq13V. Timmerman, P. De Jonghe, P. Spoelders, S. Simokovic, A. Löfgren, E. Nelis, J. Vance, J.-J. Martin, C. Van Broeckhoven
- Autosornal recessive hereditary motor and sensory neuropathy with focally folded myelin sheathsClinical, electrophysiologic, and genetic aspects of a large familyA. Quattrone, A. Gambardella, F. Bono, U. Aguglia, A. Bolino, A. C. Bruni, M. P. Montesi, R. L. Oliveri, M. Sabatelli, O. Tamburrini, P. Valentino, C. Van Broeckhoven, M. Zappia
- Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara JewsS. C. Blumen, M. Sadeh, A. D. Korczyn, A. Rouche, P. Nisipeanu, A. Asherov, F.M.S. Tomé
- Multiple mitochondria1 DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathyS. Bohlega, K. Tanji, F. M. Santorelli, M. Hirano, A. al-Jishi, S. DiMauro
- A MERRF/PEO overlap syndrome associated with the mitochondria1 DNA 3243 mutationAshok Verma, Carlos T. Moraes, Robert T. Shebert, Walter G. Bradley
- Late‐onset muscle weakness in partial phosphofructokinase deficiencyA unique myopathy with vacuoles, abnormal mitochondria, and absence of the common exon 5/intron 5 junction point mutationKumaraswamy Sivakumar, Olavo Vasconcelos, Lev Goldfarb, Marinos C. Dalakas
- Respiratory‐chain enzyme activities in isolated mitochondria of lymphocytes from untreated Parkinson's disease patientsM. A. Martín, J. A. Molina, F. J. Jiménez-Jiménez, J. Benito-León, M. Ortí-Pareja, Y. Campos, J. Arenas, The Grupo Centro de Trastornos del Movimiento
- A Japanese boy with myalgia and cramps has a novel in‐frame deletion of the dystrophin geneC. Ishigaki, S. Y. Patria, H. Nishio, M. Yabe, M. Matsuo
- Prenatal diagnosis of Duchenne muscular dystrophy using a single fetal nucleated erythrocyte in maternal bloodA. Sekizawa, T. Kimura, M. Sasaki, S. Nakamura, R. Kobayashi, T. Sato
- Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiencyC. Minetti, M. Bado, G. Morreale, M. Pedemont, G. Cordone
- Central motor loop oscillations in parkinsonian resting tremor revealed magnetoencephalographyJ. Volkmann, M. Joliot, A. Mogilner, A. A. Ioannides, F. Lado, E. Fazzini, U. Ribary, R. Llinás
- Abnormal cortical motor excitability in dystoniaK. Ikoma, A. Samii, B. Mercuri, E. M. Wassermann, M. Hallett
- Characterization of postexercise facilitation and depression of motor evoked potentials to transcranial magnetic stimulationA. Samii, E. M. Wassermann, K. Ikoma, B. Mercuri, M. Hallett
- Dose‐response curve of human extensor digitorum brevis muscle function to intramuscularly injected botulinum toxin type AR. R. Sloop, R. O. Escutin, J. A. Matus, B. A. Cole, G. W. Peterson
- Activity‐dependent conduction in single motor unitsJeremy M. Shefner, David C. Preston, Eric L. Logigian
- Calcium channel blockers and transmitter release at the normal human neurornuscular junctionDario A. Protti, Ricardo Reisin, Tomas Angelillo Mackinley, Osvaldo D. Uchitel
- Cortical projections to spinal motoneuronsChanges with aging and amyotrophic lateral sclerosisAndrew Eisen, Mohammed Entezari-Taher, Heather Stewart
- Intensity dependence of auditory evoked potentials is pronounced in migraineAn indication of cortical potentiation and low serotonergic neurotransmission?Wei Wang, Martine Timsit-Berthier, Jean Schoenen
- Frequency of MBP and MBP peptide‐reactive T cells in the HPRT mutant T‐cell population of MS patientsPatricia A. Lodge, Chad Johnson, Subramaniam Sriram
- Clinical and radiologic correlates of a novel T lymphocyte γ‐interferon‐activated Ca2+ influx in patients with relapsing remitting multiple sclerosisG. Martino, M. Filippi, V. Martinelli, E. Brambilla, G. Comi, L.M.E. Grimaldi
- Topography of interictal glucose hypometabolism in unilateral mesiotemporal epilepsyS. Arnold, G. Schlaug, H. Niemann, A. Ebner, H. Luders, O. W. Witte, R. J. Seitz
- Levodopa‐induced changes in synaptic dopamine in patients with Parkinson's disease as measured by [11C]raclopride displacement and PETJ. Tedroff, Marie Pedersen, S-M. Aquilonius, P. Hartvig, Gunilla Jacobsson, B. Långström
- Synthetic peptide derived from the Bordetella pertussis bacterium reduces infarct volume after transient middle cerebral artery occlusion in the ratR. L. Zhang, M. Chopp, W. X. Tang, Z. G. Zhang, S. D. Putney, R. M. Starzyk
Views & Reviews
- How familial is familial tremor?The genetic epidemiology of essential tremorElan D. Louis, Ruth Ottman
Clinical/Scientific Notes
- Apolipoprotein E allele in centenariansT. Asada, T. Kariya, Z. Yamagata, T. Kinoshita, A. Asaka
- A simple and efficient method for apolipoprotein E genotype determinationJoab Chapman, Juan Estupiñan, Alexander Asherou, Lev G. Goldfarb
- Misdiagnosis revealed by genetic linkage analysis in a family with Wilson diseaseDominique Vidaud, Brigitte Assouline, Patrick Lecoz, Jean-François Cadranel, Philippe Chappuis
- Anti‐Yo‐associated paraneoplastic cerebellar degeneration in a man with adenocarcinoma of unknown originJ. Krakauer, C. Balmaceda, J. Torres Gluck, J. B. Posner, M. R. Fetell, J. Dalmau
Correspondence
- The human primary motor cortexAnne L. Foundas, Kim Hong, Christiana M. Leonard, Kenneth M. Heilman
- The human primary motor cortexS. M. Rao, J. R. Binder, T. A. Hammeke, P. A. Bandettini, J. A. Bobholz, J. A. Frost, B. M. Myklebust, R. D. Jacobson, J. S. Hyde
- Lewy body disease in a patient with REM sleep disorderPaul Jácomo Negro, Raymond Faber
- Lewy body disease in a patient with REM sleep disorderMakoto Uchiyama, Kuniaki Tanaka, Kunihiro Isse, Masako Okawa
- Polyneuropathy in the mtDNA base pair 3243 point mutationM. D. King, G. O'Neill, J. Poulton, M. Moran, M. Burke, J. Redmond, M. A. Furrell
- Polyneuropathy in the mtDNA base pair 3243 point mutationK. Majamaa, U. Tolonen, H. Rusanen, A. M. Rernes, R. Myllylä, I. E. Hassinen
- Cough headache and the competency of jugular venous valvesVolker A. Knappertz
- Rhabdomyolysis and the acquired immunodeficiency syndromeDavid Beversdorf, H. Reid Mattison
- Rhabdomyolysis and the acquired immunodeficiency syndromePatrick Chariot, Romain K. Gherardi
Brief Communications
- Relationship of the Tufts Quantitative Neuromuscular Exam (TQNE) and the Sickness Impact Profile (SIP) in measuring progression of ALSD. McGuire, L. Garrison, C. Armon, R. Barohn, W. Bryan, R. Miller, G. Parry, J. Petajan, M. Ross, The SSNJV/CNTF ALS Study Group
- Elevated serum levels of manganese superoxide dismutase in polymyositis and dermatomyositisK. Mokuno, K. Kiyosawa, H. Honda, Y. Hirose, T. Murayama, S. Yoneyama, K. Kato
- Necrotizing myopathy with pipestem capillaries and minimal cellular infiltrationA case associated with cutaneous signs of dermatomyositisF. J. Authier, H. Kondo, R. T. Ghnassia, J. Revuz, R. K. Gherardi
- Cure of a solitary abscess with antibiotic therapyCase reportJ. R. Fulgham, Eelco F.M. Wijdicks, Alan J. Wright
- Inflammatory trigeminal sensory neuropathy mimicking trigeminal neurinomaMark B. Rorick, Krishan Chandar, Benedict J. Colombi
- Felbamate‐associated fatal acute hepatic necrosisM. G. O'Neil, C. S. Perdun, M. B. Wilson, S. T. McGown, S. Patel
- Human brain GABA levels rise after initiation of vigabatrin therapy but fail to rise further with increasing doseOgnen A.C. Petroff, Douglas L. Rothman, Kevin L. Behar, Richard H. Mattson
Historical Neurology
Special Articles
- Consensus statement on the definition of orthostatic hypotension, pure autonomic failure, and multiple system atrophyThe Consensus Committee of the American Autonomic Society and the American Academy of Neurology
- Report of the AAN Task Force on access to health careThe effect of no personal health insurance on health care for people with neurologic disordersMichael P. Earnest, Jill M. Norris, Mark S. Eberhardt, George H. Sands, The Task Force on Access to Health Care of the American Academy of Neurology
- Ethics education in neurology residency programsResults of a surveyAlison Wichman, Richard Foa