• Issue

    Annals of Neurology: Volume 39, Issue 6

    fmi, 689-829, A42-A43
    June 1996
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Masthead

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Masthead

  • Page: fmi
  • First Published: June 1996

Editorials

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Understanding Alzheimer's disease: Expect more genes and other things

Richard Mayeux MD, MSE, 
  • Pages: 689-690
  • First Published: June 1996
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Polymerase chain reaction in situ hybridization—opening Pandora's box?

Clayton A. Wiley MD, PhD, 
  • Pages: 691-692
  • First Published: June 1996

Speclal Reports

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Opportunities and challenges in academic neurology: Report of long range planning committee of the american neurological association

John W. Griffin MD,  Robert C. Griggs MD,  Robert Barchi MD, PhD,  Stuart A. Schneck MD,  Hamilton Moses III MD,  Long Range Planning Committee , 
  • Pages: 693-699
  • First Published: June 1996

Original Articles

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Alzheimer's disease and apolipoprotein e-4 allele in an amish population

M. A. Pericak-Vance PhD,  C. C. Johnson PhD,  J. B. Rimmler Ms,  A. M. Saunders PhD,  L. C. Robinson Bs,  E. G. D'Hondr BS,  C. E. Jackson MD,  J. L. Haines PhD, 
  • Pages: 700-704
  • First Published: June 1996
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Localization of HIV-1 in human brain using polymerase chain reaction/in situ hybridization and immunocytochemistry

Kiyomi Takahashi MD,  Steven L. Wesselingh MBBS, PhD,  Diane E. Griffin MBBS, PhD,  Justin C. McArthur MBBS, MPH,  Richard T. Johnson MD,  Dr Jonathan D. Glass MD, 
  • Pages: 705-711
  • First Published: June 1996
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A β-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome

Dr Christopher M. Gomez MD, PhD,  Ricardo Maselli MD,  Jason Gammack BS,  Jose Lasalde PhD,  Shiori Tamamizu PhD,  David R. Cornblath,  Mohamed Lehar MD,  Mark McNamee PhD,  Ralph W. Kuncl MD, PhD, 
  • Pages: 712-723
  • First Published: June 1996
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Gender differences in autoimmune demyelination in the mouse: Implications for multiple sclerosis

Dr Rhonda R. Voskuhl MD,  Hilda Pitchekian-Halabi MS,  Allan Mackenzie-Graham BS,  Henry F. McFarland MD,  Cedric S. Raine PhD, DSc, FRCPath, 
  • Pages: 724-733
  • First Published: June 1996
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The neuropathology of chromosome 17-linked dementia

Dr A. A. F. Sima MD, PhD,  R. Defendini MD,  C. Keohane FRCpath,  C. D'Amato BS,  N. L. Foster MD,  P. Parchi MD,  P. Gambetti MD,  T. Lynch MRCPI,  K. C. Wilhelmsen MD, PhD, 
  • Pages: 734-743
  • First Published: June 1996
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Evidence for anticipation and association of deletion size with severity in facioscapulohumerd muscular dystrophy

Dr Rabi Tawil MD,  James Forrester BS,  Robert C. Griggs MD,  Jerry Mendell MD,  John Kissel MD,  Michael McDermott PhD,  Wendy King PT,  Barbara Weiffenbach PhD,  Denise Figlewicz PhD,  The FSH-DY Group , 
  • Pages: 744-748
  • First Published: June 1996
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Abnormalities of smooth eye and head movement control in parhson's disease

Dr John A. Waterston MD,  Graham R. Barnes PhD,  Madeleine A. Grealy BSc,  Sue Collins BSc, 
  • Pages: 749-760
  • First Published: June 1996
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MELAS- and kearns-sayre-type with myopathy and autoimmune polyendocrinopahy

Kinji Ohno MD, PhD,  Masahiko Yamamoto MD,  Dr Andrew G. Engel MD,  C. Michel Michel MD,  Lewis R. Roberts MD,  Gerry H. Tan MD,  Vahab Fatourechi MD, 
  • Pages: 761-766
  • First Published: June 1996
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Molecular basis of phenotypic variability in sporadc creudeldt-jakob disease

Piero Parchi MD,  Rudolph Castellani MD,  Sabina Capellari MD,  Bernardino Ghetti MD,  Katherine Young PhD,  Shu G. Chen PhD,  Martin Farlow MD,  Dennis W. Dickson MD,  Anders A. F. Sima MD, PhD,  John Q. Trojanowski MD, PhD,  Robert B. Petersen PhD,  Dr Pierluigi Gambetti MD, 
  • Pages: 767-778
  • First Published: June 1996

Editorials

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The syndrome of posterior choroidal artery territory ifarction

Jean-Philippe Neau MD,  Dr Julien Bogousslavsky MD, 
  • Pages: 779-788
  • First Published: June 1996
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Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients

F. M. Santorelli MD,  M. Sciacco MD,  K. Tanji MD,  S. Shanske PhD,  T. H. Vu MD,  V. Golzi MD,  R. C. Griggs MD,  J. R. Mendell MD,  A. P. Hays MD,  T. E. Bertorini MD,  A. Pestronk MD,  E. Bonilla MD,  Dr S. Dimauro MD, 
  • Pages: 789-795
  • First Published: June 1996

Brief Communications

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Analysis of chromosome 5q13 genes in amyotrophic lateral sclerosis: Homozygous naip deletion in a sporadic case

Mandy Jackson BSc,  Dr Karen E. Morrison Dphil,  Ammar Al-Chalabi MRCP,  Martijn Baldier MMS,  Peter N. Leigh FRCP, 
  • Pages: 796-800
  • First Published: June 1996
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Lack of association of trinucleotide repeat polymorphisms in the very-low-density lipoprotein receptor gene with Alzhelner's disease

Haeyong Chung Ba,  Carol T. Roberts MS, NP,  Steven Greenberg MD, PhD,  G. William Rebeck PhD,  Richard Christie Bs,  Robert Wallace MD,  Howard J. Jacob PhD,  Dr Bradley T. Hyman MD, PhD, 
  • Pages: 800-803
  • First Published: June 1996
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DR2/DQwl Inheritance and haplotype sharing in affected siblings from multiple sclergis families

Rhonda R. Voskuhl MD,  Alisa M. Goldstein PhD,  Dr Toni Voskuhl CHS,  Richard J. Davey MD,  Henry F. McFarland MD, 
  • Pages: 804-807
  • First Published: June 1996
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Familial cerebral cavernous angioma: A gene localized to a 15-cm interval on chromosome 7q

A. Gil-Nagel MD,  J. Dubovsky PhD,  K. J. Wilcox PhD,  J. M. Stewart MD,  V. E Anderson PhD,  I. E Leppik MD,  H. T Orr PhD,  E. W Johnson PhD,  J. L. Weber PhD,  S. S. Rich PhD, 
  • Pages: 807-810
  • First Published: June 1996
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Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis

Richard W. Orell MRCP,  James Habgood BSc,  Petter Rudge FRCP,  Russell J. M. Lane FRCP,  Jackie S. de Belleroche PhD, 
  • Pages: 810-812
  • First Published: June 1996
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Ultrastructural PMP22 expression in inherited demyelinating neuropathies

Dr Jean-Michel Vallat MD,  Philippe Sindou PhD,  Pierre-Marie Preux MD,  Fransois Tabaraud MD,  André-Michel Milor MD,  Philippe Couratier MD,  Eric Leguern MD, PhD,  Alexis Brice MD, 
  • Pages: 813-817
  • First Published: June 1996

Point of Views

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Cost-effectiveness analysis: What is it and how it influence neurology

Dr Robert G. Holloway MD, 
  • Pages: 818-823
  • First Published: June 1996

Letters

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mtDNA contributes to neural loss in aging

Edward Byrne, 
  • Page: 824
  • First Published: June 1996
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Reply

M. Flint Beal MD, 
  • Pages: 824-825
  • First Published: June 1996
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Sudden death from hypoventilation during epileptic seizures

Dewey A Nelson MD,  Charles D Ray MD, 
  • Pages: 825-826
  • First Published: June 1996
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Letters

S. Claiborne Johnston MD,  Roger P. Simon MD, 
  • Page: 826
  • First Published: June 1996
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Stereotaxic posteroventral pallidotomy in idiopathic parkinson's disease

N. P. Quinn, 
  • Page: 826
  • First Published: June 1996
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Reply

Scott T. Grafton MD,  Cheryl Waters MD,  Mark Lew MD,  James Sutton MD, 
  • Pages: 826-827
  • First Published: June 1996
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Evaluation of Cisplatin Neuroprotection by NT-3

Guido Cavaletti,  Giovanni Tredicit, 
  • Page: 827
  • First Published: June 1996
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Reply

Wei-Qiang Gao,  John W. Winslow, 
  • Pages: 827-828
  • First Published: June 1996
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Human Immunodeficiency Virus in Brain and Correlation with Dementia

Bruce James Brew MBBS, MD, Fracp, 
  • Pages: 828-829
  • First Published: June 1996
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Reply

Jonathan D. Glass MD,  Justin C. McArthur MBBS, MPH, 
  • Page: 829
  • First Published: June 1996

News and comment

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News and Comment

  • Pages: A42-A43
  • First Published: June 1996