Articles

• Cerebrospinal fluid diversion procedures in pseudotumor cerebri

  M. L. Rosenberg, J. J. Corbett, C. Smith, J. Goodwin, R. Sergott, P. Savino, N. Schatz

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• Schizophrenia in epilepsySeizure and psychosis variables

  Mario F. Mendez, Rosario Grau, Robert C. Doss, Jody L. Taylor

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• Epileptic negative myoclonus

  R. Guerrini, C. Dravet, P. Genton, M. Bureau, J. Roger, G. Rubboli, C. A. Tassinari

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• Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsyAn MRI volumetric study

  F. Cendes, F. Andermann, F. Dubeau, P. Gloor, A. Evans, M. Jones-Gotman, A. Olivier, E. Andermann, Y. Robitaille, I. Lopes-Cendes, T. Peters, D. Melanson

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• Temporal lobe hypometabolism on PETPredictor of seizure control after temporal lobectomy

  R. A. Radtke, M. W. Hanson, J. M. Hoffman, B. J. Crain, T. S. Walczak, D. V. Lewis, C. Beam, R. E. Coleman, A. H. Friedman

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• Detection of Borrelia burgdorferi antigens in cerebrospinal fluid

  P. K. Coyle, Z. Deng, S. E. Schutzer, A. L. Belman, J. Benach, L. B. Krupp, B. Luft

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• Human immunodeficiency virus‐related headache

  Bruce J. Brew, John Miller

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• Plasmapheresis in acute episodes of fulminant CNS inflammatory demyelination

  Moses Rodriguez, William E. Karnes, J. D. Bartleson, Alvaro A. Pineda

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• Acetazolamide‐induced nephrolithiasisImplications for treatment of neuromuscular disorders

  Rabi Tawil, Richard T. Moxley, Robert C. Griggs

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• Transient neurologic and ocular manifestations in primary thrombocythemia

  Jan J. Michiels, Peter J. Koudstaal, Andries H. Mulder, Huub H.D.M. van Vliet

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• Complications of therapy for venous thromboembolic disease in patients with brain tumors

  J. M. Levin, D. Schiff, J. S. Loeffler, H. A. Fine, P. McL. Black, P. Y. Wen

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• Prevalence of diabetic neuropathy with somatic symptomsA door‐to‐door survey in two Sicilian municipalities

  G. Savettieri, W. A. Rocca, G. Salemi, F. Meneghini, F. Grigoletto, L. Morgante, A. Reggio, V. Costa, M. A. Coraci, R. Di Perri

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• Familial sensory autonomic neuropathy with arthropathy in Navajo children

  Stanley D. Johnsen, Peter C. Johnson, Stephen R. Stein

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• Conduction block as an early sign of reversible injury in ischemic monomelic neuropathy

  David A. Kaku, Richard I. Malamut, Daniel J. Frey, Gareth J. Parry

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• Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1Clinical and genetic analysis of 10 French families

  C. Khati, G. Stevanin, A. Durr, H. Chneiweiss, S. Belal, A. Seek, H. Cann, A. Brice, Y. Agid

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• Skin sympathetic nerve activity in acquired idiopathic generalized anhidrosis

  K. Murakami, G. Sobue, S. Iwase, T. Mitsuma, T. Mano

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• The Sorbinil Retinopathy TrialNeuropathy results

  Sorbinil Retinopathy Trial Research Group, Sorbinil Retinopathy Trial Research Group.

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• Environmental antecedents of young‐onset Parkinson's disease

  P. G. Butterfield, B. G. Valanis, P. S. Spencer, C. A. Lindeman, J. G. Nutt

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• Identical twins with similar onset of Parkinson's diseaseA case report

  Rajesh Pahwa, Karen Busenbark, Carolyn Gray, William C. Roller

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• Oral pulse levodopa therapy in mild Parkinson's disease

  Aldo Quattrone, Mario Zappia

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• Myasthenia gravisQuantitative immunocytochemical analysis of inflammatory cells and detection of complement membrane attack complex at the end‐plate in 30 patients

  Satoshi Nakano, Andrew G. Engel

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• Parkinson's diseaseA test of the multifactorial etiologic hypothesis

  Karen M. Semchuk, Edgar J. Love, Robert G. Lee

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• β‐Adrenoceptor expression on circulating mononuclear cells of idiopathic Parkinson's disease and autonomic failure patients before and after reduction of central sympathetic outflow by clonidine

  Y. Zoukos, T. Thomaides, D. V. Pavitt, M. L. Cuzner, C. J. Mathias

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• Sensitivity and specificity of transcranial Doppler ultrasonography in the detection of high‐grade carotid stenosis

  Roger E. Kelley, Richard A. Namon, Lily L. Mantelle, Jen Y. Chang

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• Antigen processing gene polymorphisms in HLA‐DR2 multiple sclerosis

  R. Liblau, P. M. van Endert, M. Sandberg-Wollheim, S. D. Patel, M. T. Lopez, S. Land, L. Fugger, H. O. McDevitt

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• Uniform tissue distribution of tRNA^Lys mutation in mitochondrial DNA in MERRF patients

  Y. Tanno, M. Yoneda, K. Tanaka, R. Kondo, I. Hozumi, K. Wakabayashi, M. Yamada, N. Fukuhara, F. Ikuta, S. Tsuji

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• Clinical features associated with the A → G transition at nucleotide 8344 of mtDNA (“MERRF mutation”)

  G. Silvestri, E. Ciafaloni, F. M. Santorelli, S. Shanske, S. Servidei, W. D. Graf, M. Sumi, S. DiMauro

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• HLA‐DQ polymorphisms do not explain HLA class II associations with multiple sclerosis in two Canadian patient groups

  D. G. Haegert, G. S. Francis

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• Asymmetric sweating in strokeA prospective quantitative study of patients with hemispheral brain infarction

  Juha T. Korpelainen, Kyosti A. Sotaniemi, Vilho V. Myllylä

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• Optic neuritis and multiple sclerosisAnti‐MBP and anti‐MBP peptide antibody‐secreting cells are accumulated in CSF

  Mats Söderström, Hans Link, Zhenyi Xu, Sten Fredriksson

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• A receptor for cathepsin Gα₁‐antichymotrypsin complexes on mouse spinal cord astrocytes

  Ming Chen, Kelly-Jo Conn, Barry W. Festoff

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• Effects of fish oil supplementation on acute ischemic brain injury in the rat

  M. L. Lai, C. Y. Hsu, T. H. Liu, Y. Y. He, J. Xu, M. Navidi, G. Sun, E. L. Hogan

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