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

By:

Waterston, John A.;
Barnes, Graham R.;
Grealy, Madeleine A.;
Collins, Sue

Publication type:

Article

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

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 818, doi. 10.1002/ana.410390622

By:

Holloway, Robert G.

Publication type:

Article

News and Comment.

Published in:: Annals of Neurology, 1996, v. 39, n. 6, p. A42, doi. 10.1002/ana.410390633
Publication type:: Article

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

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 693, doi. 10.1002/ana.410390604

By:

Griffin, John W.;
Griggs, Robert C.;
Barchi, Robert;
Schneck, Stuart A.;
Moses, Hamilton

Publication type:

Article

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 789, doi. 10.1002/ana.410390615

By:

Santorelli, F. M.;
Sciacco, M.;
Tanji, K.;
Shanske, S.;
Vu, T. H.;
Golzi, V.;
Griggs, R. C.;
Mendell, J. R.;
Hays, A. P.;
Bertorini, T. E.;
Pestronk, A.;
Bonilla, E.;
Dimauro, S.

Publication type:

Article

Letters.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 826, doi. 10.1002/ana.410390626

By:

Johnston, S. Claiborne;
Simon, Roger P.

Publication type:

Article

The syndrome of posterior choroidal artery territory ifarction.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 779, doi. 10.1002/ana.410390614

By:

Neau, Jean-Philippe;
Bogousslavsky, Julien

Publication type:

Article

Gender differences in autoimmune demyelination in the mouse: Implications for multiple sclerosis.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 724, doi. 10.1002/ana.410390608

By:

Voskuhl, Rhonda R.;
Pitchekian-Halabi, Hilda;
Mackenzie-Graham, Allan;
McFarland, Henry F.;
Raine, Cedric S.

Publication type:

Article

Molecular basis of phenotypic variability in sporadc creudeldt-jakob disease.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 767, doi. 10.1002/ana.410390613

By:

Parchi, Piero;
Castellani, Rudolph;
Capellari, Sabina;
Ghetti, Bernardino;
Young, Katherine;
Chen, Shu G.;
Farlow, Martin;
Dickson, Dennis W.;
Sima, Anders A. F.;
Trojanowski, John Q.;
Petersen, Robert B.;
Gambetti, Pierluigi

Publication type:

Article

Evidence for anticipation and association of deletion size with severity in facioscapulohumerd muscular dystrophy.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 744, doi. 10.1002/ana.410390610

By:

Tawil, Rabi;
Forrester, James;
Griggs, Robert C.;
Mendell, Jerry;
Kissel, John;
McDermott, Michael;
King, Wendy;
Weiffenbach, Barbara;
Figlewicz, Denise

Publication type:

Article

Reply.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 829, doi. 10.1002/ana.410390632

By:

Glass, Jonathan D.;
McArthur, Justin C.

Publication type:

Article

Polymerase chain reaction in situ hybridization-opening Pandora's box?

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 691, doi. 10.1002/ana.410390603

By:

Wiley, Clayton A.

Publication type:

Article

Familial cerebral cavernous angioma: A gene localized to a 15-cm interval on chromosome 7q.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 807, doi. 10.1002/ana.410390619

By:

Gil-Nagel, A.;
Dubovsky, J.;
Wilcox, K. J.;
Stewart, J. M.;
Anderson, V. E;
Leppik, I. E;
Orr, H. T;
Johnson, E. W;
Weber, J. L.;
Rich, S. S.

Publication type:

Article

Sudden death from hypoventilation during epileptic seizures.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 825, doi. 10.1002/ana.410390625

By:

Nelson, Dewey A;
Ray, Charles D

Publication type:

Article

Ultrastructural PMP22 expression in inherited demyelinating neuropathies.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 813, doi. 10.1002/ana.410390621

By:

Vallat, Jean-Michel;
Sindou, Philippe;
Preux, Pierre-Marie;
Tabaraud, Fransois;
Milor, André-Michel;
Couratier, Philippe;
Leguern, Eric;
Brice, Alexis

Publication type:

Article

A β-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 712, doi. 10.1002/ana.410390607

By:

Gomez, Christopher M.;
Maselli, Ricardo;
Gammack, Jason;
Lasalde, Jose;
Tamamizu, Shiori;
Cornblath, David R.;
Lehar, Mohamed;
McNamee, Mark;
Kuncl, Ralph W.

Publication type:

Article

Evaluation of Cisplatin Neuroprotection by NT-3.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 827, doi. 10.1002/ana.410390629

By:

Cavaletti, Guido;
Tredicit, Giovanni

Publication type:

Article

Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 810, doi. 10.1002/ana.410390620

By:

Orell, Richard W.;
Habgood, James;
Rudge, Petter;
Lane, Russell J. M.;
de Belleroche, Jackie S.

Publication type:

Article

Human Immunodeficiency Virus in Brain and Correlation with Dementia.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 828, doi. 10.1002/ana.410390631

By:

Brew, Bruce James

Publication type:

Article

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

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 689, doi. 10.1002/ana.410390602

By:

Mayeux, Richard

Publication type:

Article

DR2/DQwl Inheritance and haplotype sharing in affected siblings from multiple sclergis families.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 804, doi. 10.1002/ana.410390618

By:

Voskuhl, Rhonda R.;
Goldstein, Alisa M.;
Voskuhl, Toni;
Davey, Richard J.;
McFarland, Henry F.

Publication type:

Article

Reply.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 824, doi. 10.1002/ana.410390624

By:

Beal, M. Flint

Publication type:

Article

Localization of HIV-1 in human brain using polymerase chain reaction/in situ hybridization and immunocytochemistry.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 705, doi. 10.1002/ana.410390606

By:

Takahashi, Kiyomi;
Wesselingh, Steven L.;
Griffin, Diane E.;
McArthur, Justin C.;
Johnson, Richard T.;
Glass, Jonathan D.

Publication type:

Article

Lack of association of trinucleotide repeat polymorphisms in the very-low-density lipoprotein receptor gene with Alzhelner's disease.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 800, doi. 10.1002/ana.410390617

By:

Chung Ba, Haeyong;
Roberts, Carol T.;
Greenberg, Steven;
Rebeck, G. William;
Christie Bs, Richard;
Wallace, Robert;
Jacob, Howard J.;
Hyman, Bradley T.

Publication type:

Article

Reply.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 826, doi. 10.1002/ana.410390628

By:

Grafton, Scott T.;
Waters, Cheryl;
Lew, Mark;
Sutton, James

Publication type:

Article

Reply.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 827, doi. 10.1002/ana.410390630

By:

Gao, Wei-Qiang;
Winslow, John W.

Publication type:

Article

Masthead.

Published in:: Annals of Neurology, 1996, v. 39, n. 6, p. fmi, doi. 10.1002/ana.410390601
Publication type:: Article

MELAS- and kearns-sayre-type with myopathy and autoimmune polyendocrinopahy.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 761, doi. 10.1002/ana.410390612

By:

Ohno, Kinji;
Yamamoto, Masahiko;
Engel, Andrew G.;
Michel, C. Michel;
Roberts, Lewis R.;
Tan, Gerry H.;
Fatourechi, Vahab

Publication type:

Article

mtDNA contributes to neural loss in aging.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 824, doi. 10.1002/ana.410390623

By:

Byrne, Edward

Publication type:

Article

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

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 700, doi. 10.1002/ana.410390605

By:

Pericak-Vance, M. A.;
Johnson, C. C.;
Rimmler, J. B.;
Saunders, A. M.;
Robinson, L. C.;
D'Hondr, E. G.;
Jackson, C. E.;
Haines, J. L.

Publication type:

Article

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

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 796, doi. 10.1002/ana.410390616

By:

Jackson, Mandy;
Morrison, Karen E.;
Al-Chalabi, Ammar;
Baldier, Martijn;
Leigh, Peter N.

Publication type:

Article

Stereotaxic posteroventral pallidotomy in idiopathic Parkinson's disease.

Published in:

1996

By:

Quinn, N. P.

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

By:

Sima, A. A. F.;
Defendini, R.;
Keohane, C.;
D'Amato, C.;
Foster, N. L.;
Parchi, P.;
Gambetti, P.;
Lynch, T.;
Wilhelmsen, K. C.

Publication type:

Article