In Memoriam
Correspondence
- Multifocal motor neuropathy with conduction block after campylobacter jejuni enteritisM. Abbruzzese, L. Reni, A. Schenone, G. L. Mancardi, A. Primavera
- Reply from the AuthorsMultifocal motor neuropathy with conduction block after campylobacter jejuni enteritisJames R. White, George M. Sachs, James M. Gilchrist
- Brain edema after carotid endarterectomyB. van Harten, W. A. van Gool, H.M.E. Bienfait, J. Stam
- Reply from the AuthorsBrain edema after carotid endarterectomyJoan Breen, Michael Pessin, Louis Caplan
- Early frontal impairment as a predictor of dementia in Parkinson's diseaseMassimo Piccirilli, Patrizia D'Alessandro, Giancarlo Finali, Gianluigi Piccinin
- Reply from the AuthorsEarly frontal impairment as a predictor of dementia in Parkinson's diseaseD. M. Jacobs, K. Marder, L. J. Cote, M. Sano, Y. Stern, R. Mayeux
- Reply from the AuthorsPostoperative hyponatremiaJ. Carlos Ayus, Allen I. Arieff
- Reply from the AuthorsPreclinical ADDiane M. Jacobs, Mary Sano, George Dooneief, Karen Marder, Karen L. Bell, Yaakov Stern
- Occipital arteriovenous malformationsBruce E. Pollock, L. Dade Lunsford, Douglas Kondziolka
- Reply from the AuthorOccipital arteriovenous malformationsMark J. Kupersmith
- Dropped head syndromeAndrew J. Waclawik, Barend P. Lotz, Brad R. Beinlich, Benjamin Rix Brooks
- Dropped head syndromeJ. Howard Jaster, Tulio E. Bertorini, Melanie P. Swims, F. Curtis Dohan, Paul G. Menke, Tibor Becske, Klaus E. Monkemuller
- Reply from the AuthorsDropped head syndromeJ. S. Katz, G. I. Wolfe, D. K. Burns, W. W. Bryan, J. L. Fleckenstein, R. J. Barohn
- Reply from the AuthorsHereditary Alexander's diseaseJ. D. Schwankhaus, J. E. Parisi, W. R. Gulledge, R. D. Currier
- Reply from the AuthorsAssociated blepharospasm in lower pontine lesionsM. Aramideh, J. D. Speelman, B. W. Ongerboer de Visser
Corrections
View and Review
- The neurologist as neuroimagerJon Brillman, Richard Kasdan, Lawrence R. Wechsler
Article
- A multicenter, randomized, double-blind, placebo-controlled trial of influenza immunization in multiple sclerosisA. E. Miller, L. A. Morgante, L. Y. Buchwald, S. M. Nutile, P. K. Coyle, L. B. Krupp, C. A. Doscher, F. D. Lublin, R. L. Knobler, F. Trantas, L. Kelley, C. R. Smith, N. La Rocca, S. Lopez
- HTLV-associated myelopathy in a cohort of HTLV-I and HTLV-II-infected blood donorsE. L. Murphy, J. Fridey, J. W. Smith, J. Engstrom, R. A. Sacher, K. Miller, J. Gibble, J. Stevens, R. Thomson, D. Hansma, J. Kaplan, R. Khabbaz, G. Nemo
- Chronic inflammatory demyelinating polyneuropathyClinical features and response to treatment in 67 consecutive patients with and without a monoclonal gammopathyKenneth C. Gorson, Gregory Allam, Allan H. Ropper
- Pain in Guillain-Barre syndromeD. E. Moulin, N. Hagen, T. E. Feasby, R. Amireh, A. Hahn
- Development and preliminary validation of a pain measure specific to neuropathic painThe Neuropathic Pain ScaleBradley S. Galer, Mark P. Jensen
- Inflammatory myopathy in thyrotoxicosisO. Hardiman, F. Molloy, F. Brett, M. Farrell
- Crack cocaine use and stroke in young patientsA. I. Qureshi, M. S. Akbar, E. Czander, K. Safdar, R. S. Janssen, M. R. Frankel
- Validation of the ACAS TIA/stroke algorithmP. N. Karanjia, J. J. Nelson, D. S. Lefkowitz, A. R. Dick, J. F. Toole, L. E. Chambless, R. Hayes, V. J. Howard
- Cerebrospinal fluid creatine kinase BB isoenzyme activity and neurologic prognosis after cardiac arrestD. L. Tirschwell, W. T. Longstreth, M. E. Rauch-Matthews, W. L. Chandler, T. Rothstein, L. Wray, L. J. Eng, J. Fine, M. K. Copass
- Long-term effects of tetrabenazine in hyperkinetic movement disordersJoseph Jankovic, Jennifer Beach
- Cabergoline in the treatment of early parkinson's diseaseResults of the first year of treatment in a double-blind comparison of cabergoline and levodopaU. K. Rinne, F. Bracco, C. Chouza, E. Dupont, O. Gershanik, J. F. Marti Masso, J. L. Montastruc, C. D. Marsden, A. Dubini, N. Orlando, R. Grimaldi
- Apomorphine responses in parkinson's disease and the pathogenesis of motor complicationsL. Verhagen Metman, E. R. Locatelli, D. Bravi, M. M. Mouradian, T. N. Chase
- Laryngeal deglutition movement in parkinson's diseaseNorman A. Leopold, Marion C. Kagel
- Comparison of extrapyramidal features in 31 pathologically confirmed cases of diffuse lewy body disease and 34 pathologically confirmed cases of parkinson's diseaseElan D. Louis, Lisa A. Klatka, Yan Liu, Stanley Fahn
- Disappearance of motor tics after Wernicke's encephalopathy in a patient with Tourette's syndromeLeonardo Pantoni, Loredana Poggesi, Anna Repice, Domenico Inzitari
- Survival of patients with pathologically proven multiple system atrophyA meta-analysisY. Ben-Shlomo, G. K. Wenning, F. Tison, N. P. Quinn
- Longitudinal change in basal ganglia volume in patients with Huntington's diseaseE. H. Aylward, Q. Li, O. C. Stine, N. Ranen, M. Sherr, P. E. Barta, F. W. Bylsma, G. D. Pearlson, C. A. Ross
- Neuroanatomy in Rett syndromeCerebral cortex and posterior fossaBaskaran Subramaniam, Sakkubai Naidu, Allan L. Reiss
- The neurologic complications of B-cell chronic lymphocytic leukemiaJames H. Bower, Julie E. Hammack, Shannon K. McDonnell, Ayalew Tefferi
- CraniectomyAn aggressive treatment approach in severe encephalitisS. Schwab, E. Junger, M. Spranger, A. Dorfler, F. Albert, H. H. Steiner, W. Hacke
- Chronic encephalitis and epilepsy in adults and adolescentsA variant of Rasmussen's syndrome?Y. M. Hart, F. Andermann, D. R. Fish, F. Dubeau, Y. Robitaille, T. Rasmussen, S. Berkovic, R. Marino, E. M. Yakoubian, K. Spillane, F. Scaravilli
- Adult-onset temporal lobe epilepsy associated with smoldering herpes simplex 2 infectionMarcia E. Cornford, Georges F. McCormick
- The course of benign partial epilepsy of childhood with centrotemporal spikesA meta-analysisPaul A.D. Bouma, Anouk C. Bovenkerk, Rudi G.J. Westendorp, Oebele F. Brouwer
- Surgical treatment of patients with single and dual pathologyRelevance of lesion and of hippocampal atrophy to seizure outcomeL. M. Li, F. Cendes, C. Watson, F. Andermann, D. R. Fish, F. Dubeau, S. Free, A. Olivier, W. Harkness, D.G.T. Thomas, J. S. Duncan, J. W.A.S. Sander, S. D. Shorvon, M. J. Cook, D. L. Arnold
- Underexpression of messenger RNA for peripheral myelin protein 22 in hereditary neuropathy with liability to pressure palsiesA. Schenone, L. Nobbio, P. Mandich, E. Bellone, M. Abbruzzese, F. Aymar, G. L. Mancardi, A. J. Windebank
- A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsiesP. Young, H. Wiebusch, F. Stogbauer, B. Ringelstein, G. Assmann, H. Funke
- Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12S rRNA geneEvidence of heteroplasmyM. El-Schahawi, A. Lopez de Munain, A. M. Sarrazin, A. L. Shanske, M. Basirico, S. Shanske, S. DiMauro
- Dose-dependent, central effects of botulinum neurotoxin type AA pilot study in the alert behaving catB. Moreno-Lopez, A. M. Pastor, R. R. de la Cruz, J. M. Delgado-Garcia
- Indictment of the microglia as the villain in multiple sclerosisS. Sriram, M. Rodriguez
- Machado-Joseph disease in four Chinese pedigreesMolecular analysis of 15 patients including two juvenile cases and clinical correlationsY. X. Zhou, Y. Takiyama, S. Igarashi, Y. F. Li, B. Y. Zhou, D. C. Gui, K. Endo, H. Tanaka, Z. H. Chen, L. S. Zhou, M. Z. Fan, B. X. Yang, J. Weissenbach, G. X. Wang, S. Tsuji
- Dystrophin expression in a Duchenne muscular dystrophy Patient with a frame shift deletionT. W. Prior, C. Bartolo, A. C. Papp, P. J. Snyder, M. S. Sedra, A.H.M. Burghes, J. T. Kissel, M. H. Luquette, C.-Y. Tsao, J. R. Mendell
- A novel point mutation in the peripheral myelin protein 22 (PMP22) gene associated with Charcot-Marie-Tooth disease type 1AM. G. Marrosu, S. Vaccargiu, G. Marrosu, A. Vannelli, C. Cianchetti, F. Muntoni
- Autoantibodies to glutamate receptor subunit GluR2 in nonfamilial olivopontocerebellar degenerationLorise C. Gahring, Scott W. Rogers, Roy E. Twyman
- Intradermal recombinant human nerve growth factor induces pressure allodynia and lowered heat-pain threshold in humansP. J. Dyck, S. Peroutka, C. Rask, E. Burton, M. K. Baker, K. A. Lehman, D. A. Gillen, J. L. Hokanson, P. C. O'Brien
- Torsional eye movements in patients with skew deviation and spasmodic torticollisResponses to static and dynamic head rollL. Averbuch-Heller, K. G. Rottach, A. Z. Zivotofsky, J. I. Suarez, A. D. Pettee, B. F. Remler, R. J. Leigh
- Apolipoprotein E-epsilon 2 and Alzheimer's diseaseGenotype influences pathologic phenotypeC. F. Lippa, T. W. Smith, A. M. Saunders, C. Hulette, D. Pulaski-Salo, A. D. Roses
Brief Communication
- Subarachnoid hemorrhage in a patient with lyme diseaseM. Chehrenama, M. T. Zagardo, C. L. Koski
- Vascular lesions in Chinese patients with transient ischemic attacksY. N. Huang, S. Gao, S. W. Li, Y. Huang, J. F. Li, K. S. Wong, R. Kay
- Long-term follow-up of patients with subacute sclerosing panencephalitis treated with intraventricular alpha-interferonBanu Anlar, Kalbiye Yalaz, Ferhunde Oktem, Gulsen Kose
- Brainstem CMV encephalitis in AIDSClinical case and MRI featuresF. Pierelli, G. Tilia, A. Damiani, P. Coiro, M. C. Massara, F. Bianco, I. Mezzaroma
- Sydenham ChoreaMagnetic resonance imaging reveals permanent basal ganglia injuryE. Stanley Emery, Pedro T. Vieco
- Magnetization transfer imaging in progressive multifocal leukoencephalopathyScott E. Kasner, Steven L. Galetta, Joseph C. McGowan, Robert I. Grossman
Clinical Scientific Note
- How high is high in steroid treatment of Vogt-Koyanagi-Harada syndromeK. Ikeda, S. Suzuki, M. Ichijo, Y. Matsuoka, S. Irimajiri
- Spontaneous calcific cerebral embolusVijay Shanmugam, Ramesh Chhablani, Phillip B. Gorelick
- Isolated bilateral masseter atrophy in X-linked recessive bulbospinal neuronopathyT. Suzuki, K. Endo, S. Igarashi, M. Fukuda, M. Tanaka
- Use of fluid attenuating inversion recovery, MR angiogram, and diffusion-weighted MRI techniques for assessment of pontine infarction in a patient treated with radiation therapy for pituitary neoplasmLorin M. Graef, Helmi L. Lutsep, Alexander Norbash, Gregory W. Albers
Clinical Scientific Notes
- Inheritance of three distinct muscle chloride channel gene (CLCN1) mutations in a single recessive myotonia congenita familyKaren Sloan-Brown, Alfred L. George
Book Review
- Textbook of Hyperbaric Medicine, second revised editionR. N. Sawyer, P. M. Kortebein
- The Massachusetts General Hospital Handbook of Pain ManagementJennifer S. Kriegler