Works matching IS 03645134 AND DT 1992 AND VI 31 AND IP 3

Results: 24

Uncommon phenotype for a codon 178 mutation of the human PrP gene.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 345, doi. 10.1002/ana.410310321

By:

Laplanche, J. L.;
Chatelain, J.;
Thomas, S.;
Launay, J. M.;
Gaultier, C.;
Derouesne, C.

Publication type:

Article

Mild senile dementia of the Alzheimer type. 4. Evaluation of intervention.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 242, doi. 10.1002/ana.410310303

By:

Berg, Leonard;
Miller, J. Philip;
Baty, Jack;
Rubin, Eugene H.;
Morris, John C.;
Figiel, Gary

Publication type:

Article

T cells from normal and myasthenic individuals recognize the human acetylcholine receptor: Heterogeneity of antigenic sites on the α-subunit.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 311, doi. 10.1002/ana.410310314

By:

Melms, A.;
Malcherek, G.;
Gern, U.;
Wiethölter, H.;
Müller, C. A.;
Schoepfer, R.;
Lindstrom, J.

Publication type:

Article

The spectrum of neurological disease in patients with systemic cancer.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 268, doi. 10.1002/ana.410310307

By:

Clouston, Paul D.;
DeAngelis, Lisa M.;
Posner, Jerome B.

Publication type:

Article

Congenital hypomyelination neuropathy with arthrogryposis multiplex congenita.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 337, doi. 10.1002/ana.410310318

By:

Boylan, Kevin B.;
Ferriero, Donna M.;
Greco, Claudia M.;
Sheldon, R. Ann;
Dew, Michael

Publication type:

Article

Electroconvulsive therapy treatment of depression in a patient with adult GM2 gangliosidosis.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 342, doi. 10.1002/ana.410310320

By:

Renshaw, Perry F.;
Stern, Theodore A.;
Welch, Charles;
Schouten, Ronald;
Kolodny, Edwin H.

Publication type:

Article

Proton magnetic resonance spectroscopic imaging for metabolic characterization of demyelinating plaques.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 235, doi. 10.1002/ana.410310302

By:

Arnold, Douglas L.;
Matthews, Paul M.;
Francis, Gordon S.;
O'Connor, John;
Antel, Jack P.

Publication type:

Article

Collagen cross-linking of skin in patients with amyotrophic lateral sclerosis.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 305, doi. 10.1002/ana.410310313

By:

Ono, Seiitsu;
Yamauchi, Mitsuo

Publication type:

Article

News and Comment.

Published in:: Annals of Neurology, 1992, v. 31, n. 3, p. A47, doi. 10.1002/ana.410310324
Publication type:: Article

Multifocal inflammatory leukoencephalopathy with 5-fluorouracil and levamisole.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 262, doi. 10.1002/ana.410310306

By:

Hook, C. Christopher;
Kimmel, David W.;
Kvols, Larry K.;
Scheithauer, Bernd W.;
Forsyth, Peter A.;
Rubin, Joseph;
Moertel, Charles G.;
Rodriguez, Moses

Publication type:

Article

Revised estimate of the prevalence of multiple sclerosis in the united states.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 333, doi. 10.1002/ana.410310317

By:

Anderson, D. W.;
Ellenberg, J. H.;
Leventhal, C. M.;
Reingold, S. C.;
Rodriguez, M.;
Silberberg, D. H.

Publication type:

Article

Masthead.

Published in:: Annals of Neurology, 1992, v. 31, n. 3, p. fmi, doi. 10.1002/ana.410310301
Publication type:: Article

Cortically evoked motor responses in patients with Xp22.3-linked Kallmann's syndrome and in female gene carriers.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 299, doi. 10.1002/ana.410310312

By:

Danek, Adrian;
Heye, Babett;
Schroedter, Robert

Publication type:

Article

Reply.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 346, doi. 10.1002/ana.410310323

By:

Whitaker, John N.

Publication type:

Article

Late-onset metachromatic leukodystrophy: Molecular pathology in two siblings.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 256, doi. 10.1002/ana.410310305

By:

Kappler, Joachim;
von Figura, Kurt;
Gieselmann, Volkmar

Publication type:

Article

GM1 gangliosidosis in adults: Clinical and molecular analysis of 16 Japanese patients.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 328, doi. 10.1002/ana.410310316

By:

Yoshida, Kunihiro;
Oshima, Akihiro;
Sakuraba, Hitoshi;
Nakano, Takeshi;
Yanagisawa, Nobuo;
Inui, Koji;
Okada, Shintaro;
Uyama, Ei-ichiro;
Namba, Reiko;
Kondo, Kiyohiko;
Iwasaki, Shin-ichi;
Takamiya, Kiyoshi;
Suzuki, Yoshiyuki

Publication type:

Article

Phenotypic characteristics of familial Creutzfeldt-Jakob disease assoicated with the codon 178Asn PRNP mutation.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 282, doi. 10.1002/ana.410310309

By:

Brown, Paul;
Goldfarb, Lev G.;
Kovanen, Jussi;
Haltia, Mattie;
Cathala, Françoise;
Sulima, Michael;
Gibbs, C. J.;
Gajdusek, D. Carleton

Publication type:

Article

A follow-up study of isolated cases of suspected Huntington's disease.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 293, doi. 10.1002/ana.410310311

By:

Bateman, D.;
Boughey, A. M.;
Scaravilli, F.;
Marsden, C. D.;
Harding, A. E.

Publication type:

Article

Myelin basic protein peptides in urine.

Published in:

1992

By:

Barry, Richard;
Bolton, Christopher;
Glynn, Paul;
Groome, Nigel;
Barry, R;
Bolton, C;
Glynn, P;
Groome, N

Publication type:

Letter

Localization of extratemporal epileptic foci during ictal single photon emission computed tomography.

Published in:

1992

By:

Marks, David A.;
Katz, Amiram;
Hoffer, Paul;
Spencer, Susan S.;
Marks, D A;
Katz, A;
Hoffer, P;
Spencer, S S

Publication type:

journal article

In vivo imaging of glucose consumption and lactate concentration in human gliomas.

Published in:

1992

By:

Herholz, K.;
Heindel, W.;
Luyten, P. R.;
denHollander, J. A.;
Pietrzyk, U.;
Voges, J.;
Kugel, H.;
Friedmann, G.;
Heiss, W.-D.

Publication type:

journal article

Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 274, doi. 10.1002/ana.410310308

By:

Goldfarb, Lev G.;
Brown, Paul;
Haltia, Matti;
Cathala, Françoise;
McCombie, W. Richard;
Kovanen, Jussi;
Červen̆áková, Larisa;
Goldin, Lynn;
Nieto, Ana;
Godec, Mark S.;
Asher, David M.;
Gajdusek, D. Carleton

Publication type:

Article

Familial amyloidotic polyneuropathy: Report of patients heterozygous for the transthyretin Gly42 gene.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 340, doi. 10.1002/ana.410310319

By:

Murakami, Tatsufumi;
Yi, Shigehiro;
Yamamoto, Kenji;
Maruyama, Shoichi;
Araki, Shukuro

Publication type:

Article

Selective accumulation of aluminum and iron in the neurofibrillary tangles of Alzheimer's disease: A laser microprobe (LAMMA) study.

Published in:

Annals of Neurology, 1992, v. 31, n. 3, p. 286, doi. 10.1002/ana.410310310

By:

Good, Paul F.;
Perl, Daniel P.;
Bierer, Linda M.;
Schmeidler, James

Publication type:

Article

Works matching IS 03645134 AND DT 1992 AND VI 31 AND IP 3

Uncommon phenotype for a codon 178 mutation of the human PrP gene.

Mild senile dementia of the Alzheimer type. 4. Evaluation of intervention.

T cells from normal and myasthenic individuals recognize the human acetylcholine receptor: Heterogeneity of antigenic sites on the α-subunit.

The spectrum of neurological disease in patients with systemic cancer.

Congenital hypomyelination neuropathy with arthrogryposis multiplex congenita.

Electroconvulsive therapy treatment of depression in a patient with adult GM2 gangliosidosis.

Proton magnetic resonance spectroscopic imaging for metabolic characterization of demyelinating plaques.

Collagen cross-linking of skin in patients with amyotrophic lateral sclerosis.

News and Comment.

Multifocal inflammatory leukoencephalopathy with 5-fluorouracil and levamisole.

Revised estimate of the prevalence of multiple sclerosis in the united states.

Masthead.

Cortically evoked motor responses in patients with Xp22.3-linked Kallmann's syndrome and in female gene carriers.

Reply.

Late-onset metachromatic leukodystrophy: Molecular pathology in two siblings.

GM1 gangliosidosis in adults: Clinical and molecular analysis of 16 Japanese patients.

Phenotypic characteristics of familial Creutzfeldt-Jakob disease assoicated with the codon 178<sup>Asn</sup> PRNP mutation.

A follow-up study of isolated cases of suspected Huntington's disease.

Myelin basic protein peptides in urine.

Localization of extratemporal epileptic foci during ictal single photon emission computed tomography.

In vivo imaging of glucose consumption and lactate concentration in human gliomas.

Creutzfeldt-Jakob disease cosegregates with the codon 178<sup>Asn</sup> PRNP mutation in families of European origin.

Familial amyloidotic polyneuropathy: Report of patients heterozygous for the transthyretin Gly<sup>42</sup> gene.

Selective accumulation of aluminum and iron in the neurofibrillary tangles of Alzheimer's disease: A laser microprobe (LAMMA) study.