Works matching IS 03645134 AND DT 1996 AND VI 39 AND IP 6
Results: 33
Abnormalities of smooth eye and head movement control in parhson's disease.
- Published in:
- Annals of Neurology, 1996, v. 39, n. 6, p. 749, doi. 10.1002/ana.410390611
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- Article
Cost-effectiveness analysis: What is it and how it influence neurology.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 818, doi. 10.1002/ana.410390622
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- Article
News and Comment.
- Published in:
- Annals of Neurology, 1996, v. 39, n. 6, p. A42, doi. 10.1002/ana.410390633
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- Article
Opportunities and challenges in academic neurology: Report of long range planning committee of the american neurological association.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 693, doi. 10.1002/ana.410390604
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- Article
Ultrastructural PMP22 expression in inherited demyelinating neuropathies.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 813, doi. 10.1002/ana.410390621
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Letters.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 826, doi. 10.1002/ana.410390626
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- Article
Gender differences in autoimmune demyelination in the mouse: Implications for multiple sclerosis.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 724, doi. 10.1002/ana.410390608
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- Article
Familial cerebral cavernous angioma: A gene localized to a 15-cm interval on chromosome 7q.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 807, doi. 10.1002/ana.410390619
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- Article
Evidence for anticipation and association of deletion size with severity in facioscapulohumerd muscular dystrophy.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 744, doi. 10.1002/ana.410390610
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- Article
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 789, doi. 10.1002/ana.410390615
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- Article
Reply.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 829, doi. 10.1002/ana.410390632
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Polymerase chain reaction in situ hybridization-opening Pandora's box?
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- Annals of Neurology, 1996, v. 39, n. 6, p. 691, doi. 10.1002/ana.410390603
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- Article
The syndrome of posterior choroidal artery territory ifarction.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 779, doi. 10.1002/ana.410390614
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- Article
Sudden death from hypoventilation during epileptic seizures.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 825, doi. 10.1002/ana.410390625
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- Publication type:
- Article
A β-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 712, doi. 10.1002/ana.410390607
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- Article
DR2/DQwl Inheritance and haplotype sharing in affected siblings from multiple sclergis families.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 804, doi. 10.1002/ana.410390618
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- Article
mtDNA contributes to neural loss in aging.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 824, doi. 10.1002/ana.410390623
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- Article
Evaluation of Cisplatin Neuroprotection by NT-3.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 827, doi. 10.1002/ana.410390629
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- Article
Human Immunodeficiency Virus in Brain and Correlation with Dementia.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 828, doi. 10.1002/ana.410390631
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Reply.
- Published in:
- Annals of Neurology, 1996, v. 39, n. 6, p. 827, doi. 10.1002/ana.410390630
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Understanding Alzheimer's disease: Expect more genes and other things.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 689, doi. 10.1002/ana.410390602
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Reply.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 824, doi. 10.1002/ana.410390624
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- Article
Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 810, doi. 10.1002/ana.410390620
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- Article
Localization of HIV-1 in human brain using polymerase chain reaction/in situ hybridization and immunocytochemistry.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 705, doi. 10.1002/ana.410390606
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Reply.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 826, doi. 10.1002/ana.410390628
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Molecular basis of phenotypic variability in sporadc creudeldt-jakob disease.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 767, doi. 10.1002/ana.410390613
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Masthead.
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- Annals of Neurology, 1996, v. 39, n. 6, p. fmi, doi. 10.1002/ana.410390601
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- Article
MELAS- and kearns-sayre-type with myopathy and autoimmune polyendocrinopahy.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 761, doi. 10.1002/ana.410390612
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Lack of association of trinucleotide repeat polymorphisms in the very-low-density lipoprotein receptor gene with Alzhelner's disease.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 800, doi. 10.1002/ana.410390617
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Alzheimer's disease and apolipoprotein e-4 allele in an amish population.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 700, doi. 10.1002/ana.410390605
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- Article
Analysis of chromosome 5q13 genes in amyotrophic lateral sclerosis: Homozygous naip deletion in a sporadic case.
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- Annals of Neurology, 1996, v. 39, n. 6, p. 796, doi. 10.1002/ana.410390616
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Stereotaxic posteroventral pallidotomy in idiopathic Parkinson's disease.
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- 1996
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- Publication type:
- Letter
The neuropathology of chromosome 17-linked dementia.
- Published in:
- Annals of Neurology, 1996, v. 39, n. 6, p. 734, doi. 10.1002/ana.410390609
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- Article