Articles

• Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the β‐amyloid precursor protein gene

  H. Karlinsky, G. Vaula, J. L. Haines, J. Ridgley, C. Bergeron, M. Mortilla, R. G. Tupler, M. E. Percy, Y. Robitaille, N. E. Noldy, T. C. K. Yip, R. E. Tanzi, J. F. Gusella, R. Becker, J. M. Berg, D. R. Crapper McLachlan, P. H. St. George-Hyslop

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• Parkinson's disease in twins

  P. Vieregge, K. A. Schiffke, H. J. Friedrich, B. Müller, H. P. Ludin

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• Asymmetric cortical degenerative syndromesClinical and radiologic correlations

  R. J. Caselli, C. R. Jack, R. C. Petersen, H. W. Wahner, T. Yanagihara

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• A double‐blind, randomized, crossover trial of pemoline in fatigue associated with multiple sclerosis

  B. G. Weinshenker, M. Penman, B. Bass, G. C. Ebers, G. P. A. Rice

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• Epidemiology of human immunodeficiency virus encephalopathy in the United States

  Robert S. Janssen, Okey C. Nwanyanwu, Richard M. Selik, Jeanette K. Stehr-Green

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• Adult‐onset motor neuron disease and infantile Werdnig‐Hoffmann disease (spinal muscular atrophy type 1) in the same family

  P. J. Shaw, P. G. Ince, J. Goodship, J. Burn, J. Slade, D. Bates, D. Gardner Medwin

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• A case‐control study of Alzheimer's disease in China

  G. Li, Y. C. Shen, Y. T. Li, C. H. Chen, Y. W. Zhau, J. M. Silverman

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• Intrafamilial heterogeneity in hereditary motor neuron disease

  J. S. Appelbaum, R. P. ROOS, E. F. Salazar-Grueso, A. Buchman, S. Iannaccone, R. Glantz, T. Siddique, R. Maselli

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• Cognitive planning deficit in patients with cerebellar atrophy

  J. Grafman, I. Litvan, S. Massaquoi, M. Stewart, A. Sirigu, M. Hallett

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• Cerebrovascular complications of bacterial meningitis in adults

  Hans-Walter Pfister, Gian Domenico Borasio, Ulrich Dirnagl, Michael Bauer, Karl Max Einhäupl

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• Embolism from vertebral artery origin occlusive disease

  L. R. Caplan, P. Amarenco, A. Rosengart, E. F. Lafranchise, P. A. Teal, M. Belkin, L. D. DeWitt, M. S. Pessin

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• Characteristics of intractable seizures following meningitis and encephalitis

  David A. Marks, Jung Kim, Dennis D. Spencer, Susan S. Spencer

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• Headache in type I Chiari malformation

  Julio Pascual, Agustín Oterino, José Berciano

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• Antimigraine drug sumatriptan increases blood flow velocity in large cerebral arteries during migraine attacks

  J.F.V. Caekebeke, M. D. Ferrari, C. P. Zwetsloot, J. Jansen, P. R. Saxena

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• Pendular pseudonystagmus arising as a combination of head tremor and vestibular failure

  A. M. Bronstein, M. A. Gresty, S. S. Mossman

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• Elevated plasma glucagon in amyotrophic lateral sclerosis

  R. W. Hubbard, A. D. Will, G. W. Peterson, A. Sanchez, W. W. Gillan, S. A. Tan

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• Amyotrophic lateral sclerosisIncreased solubility of skin collagen

  Seiitsu Ono, Mitsuo Yamauchi

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• Positron emission tomography demonstrates frontal cortex and basal ganglia hypometabolism in dystonia

  H. Karbe, V. A. Holthoff, J. Rudolf, K. Herholz, W. D. Heiss

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• Linkage studies in progressive myoclonus epilepsyUnverricht‐Lundborg and Lafora's diseases

  A.-E. Lehesjoki, M. Koskiniemi, M. Pandolfo, A. Antonelli, M. Kyllerman, J. Wahlström, A. Nergårdh, M. Burmeister, P. Sistonen, R. Norio, A. de la Chapelle

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• Effect of BAEP monitoring on hearing preservation during acoustic neuroma resection

  C. M. Harper, S. G. Harner, D. H. Slavit, W. J. Litchy, J. R. Daube, C. W. Beatty, M. J. Ebersold

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• Isolated tremor and disruption of the nigrostriatal dopaminergic systemAn ¹⁸F‐dopa PET study

  D. J. Brooks, E. D. Playford, V. Ibanez, G. V. Sawle, P. D. Thompson, L. J. Findley, C. D. Marsden

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• Linkage analysis of candidate loci in autosomal dominant myotonia congenita

  J. A. Abdalla, W. L. Casley, A. J. Hudson, E. G. Murphy, H. K. Cousin, H. A. Armstrong, G. C. Ebers

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• Motor and nonmotor behavioral deficits in monkeys made hemiparkinsonian by intracarotid MPTP infusion

  J. S. Schneider, W. W. McLaughlin, D. P. Roeltgen

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• Striatal monoamine neurotransmitters and metabolites in dominantly inherited olivopontocerebellar atrophy

  S. J. Kish, Y. Robitaille, M. El-Awar, B. Clark, L. Schut, M. J. Ball, L. T. Young, R. Currier, K. Shannak

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• N‐acetyl‐L‐aspartate and other amino acid metabolites in Alzheimer's disease brainA preliminary proton nuclear magnetic resonance study

  W. E. Klunk, K. Panchalingam, J. MOOSSY, R. J. McClure, J. W. Pettegrew

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• In vivo ³¹P nuclear magnetic resonance spectroscopy of human temporal lobe epilepsy

  R. Kuzniecky, G. A. Elgavish, H. P. Hetherington, W. T. Evanochko, G. M. Pohost

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• Propriospinal myoclonusA neurophysiologic analysis

  S. Chokroverty, A. Walters, T. Zimmerman, M. Picone

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• Prospective serial analysis of interleukin‐2 and soluble interleukim‐2 receptor in relapsing‐remitting multiple sclerosis

  M. S. Freedman, K. L. Muth, J. L. Trotter, C. N. Yoshizawa, J. P. Antel

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• Aortic plaque in patients with brain ischemiaDiagnosis by transesophageal echocardiography

  Deborah R. Horowitz, Stanley Tuhrim, Jacqui Budd, Martin E. Goldman

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• Interaction of random electromyographic activity with averaged sensory evoked potentials

  Marlene M. Normand, Jasper R. Daube

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• Expression of monocyte activation antigen Mo3 on the surface of peripheral blood monocytes from patients with multiple sclerosis

  Paula Dore-Duffy, Carol Donovan, Robert F. Todd

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• Vimentin and desmin in maturing skeletal muscle and developmental myopathies

  Harvey B. Sarnat

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