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

Results: 24

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
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
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
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
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
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

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

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

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

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.

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.

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.

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.

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