Works matching IS 03645134 AND DT 2002 AND VI 52 AND IP 4

Results: 30

A PLP splicing abnormality is associated with an unusual presentation of PMD.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 477, doi. 10.1002/ana.10320

By:

Hobson, Grace M.;
Huang, Zhong;
Sperle, Karen;
Stabley, Deborah L.;
Marks, Harold G.;
Cambi, Franca

Publication type:

Article

Interleukin-12 p40 polymorphism and susceptibility to multiple sclerosis.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 524, doi. 10.1002/ana.10348

By:

Alloza, Iraide;
Heggarty, Shirley;
Goris, An;
Graham, Colin A.;
Dubois, Bénédicte;
McDonnell, Gavin;
Hawkins, Stanley A.;
Carton, Herwig;
Vandenbroeck, Koen

Publication type:

Article

Linkage of Parkinsonism and Alzheimer's disease with Lewy body pathology to chromosome 12.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 524, doi. 10.1002/ana.10330

By:

Scott, William K.;
Vance, Jeffery M.;
Haines, Jonathan L.;
Pericak-Vance, Margaret A.

Publication type:

Article

Reply.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 524, doi. 10.1002/ana.10331

By:

Funayama, Manabu;
Hasegawa, Kazuko;
Obata, Fumiya

Publication type:

Article

Treatment of multiple sclerosis with the pregnancy hormone estriol.

Published in:

2002

By:

Sicotte NL;
Liva SM;
Klutch R;
Pfeiffer P;
Bouvier S;
Odesa S;
Wu TCJ;
Voskuhl RR

Publication type:

Journal Article

Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 435, doi. 10.1002/ana.10304

By:

Abbruzzese, Claudia;
Costanzi Porrini, Sandro;
Mariani, Bruno;
Gould, Fiona K.;
Mcabney, John P.;
Monckton, Darren G.;
Ashizawa, Tetsuo;
Giacanelli, Manlio

Publication type:

Article

Febrile seizures.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 527, doi. 10.1002/ana.10335

By:

Gilbert, Donald L.

Publication type:

Article

Treatment of multiple sclerosis with the pregnancy hormone estriol.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 421, doi. 10.1002/ana.10301

By:

Sicotte, Nancy L.;
Liva, Stephanie M.;
Klutch, Rochelle;
Pfeiffer, Paul;
Bouvier, Seth;
Odesa, Sylvia;
Wu, T. C. Jackson;
Voskuhl, Rhonda R.

Publication type:

Article

A novel mutation in the GNE gene and a linkage disequilibrium in Japanese pedigrees.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 516, doi. 10.1002/ana.10341

By:

Arai, Aki;
Tanaka, Keiko;
Ikeuchi, Takeshi;
Igarashi, Shuichi;
Kobayashi, Hisashi;
Asaka, Tomoya;
Date, Hidetoshi;
Saito, Masaaki;
Tanaka, Hajime;
Kawasaki, Sari;
Uyama, Eiichiro;
Mizusawa, Hidehiro;
Fukuhara, Nobuyoshi;
Tsuji, Shoji

Publication type:

Article

Evidence that accumulation of ceramides and cholesterol esters mediates oxidative stress-induced death of motor neurons in amyotrophic lateral sclerosis.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 448, doi. 10.1002/ana.10312

By:

Cutler, Roy G.;
Pedersen, Ward A.;
Camandola, Simonetta;
Rothstein, Jeffrey D.;
Mattson, Mark P.

Publication type:

Article

Gliomatosis cerebri: Molecular pathology and clinical course.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 389, doi. 10.1002/ana.10363

By:

Burger, Peter C.

Publication type:

Article

Neurologic complications of critical illness, 2nd ed.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 527, doi. 10.1002/ana.10334

By:

Bhardwaj, Anish

Publication type:

Article

Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 429, doi. 10.1002/ana.10305

By:

Paulson, Henry L.;
Garbern, James Y.;
Hoban, Timothy F.;
Krajewski, Karen M.;
Lewis, Richard A.;
Fischbeck, Kenneth H.;
Grossman, Robert I.;
Lenkinski, Robert;
Kamholz, John A.;
Shy, Michael E.

Publication type:

Article

Concerns with the use of T2* signal intensity to differentiate hippocampal subregions.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 525, doi. 10.1002/ana.10345

By:

Darby, David G.;
Tress, Brain M.

Publication type:

Article

Preserved visual function in a case of occipitoparietal microgyria.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 492, doi. 10.1002/ana.10327

By:

Zesiger, Pascal;
Kiper, Daniel;
Maeder, Philippe;
Deonna, Thierry;
Innocenti, Giorgio M.

Publication type:

Article

Alzheimer's second patient: Johann F. and his family.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 520, doi. 10.1002/ana.10309

By:

Klünemann, Hans H.;
Fronhöfer, Wolfgang;
Wurster, Herbert;
Fischer, Wolfgang;
Ibach, Bernd;
Klein, Helmfried E.

Publication type:

Article

Gliomatosis cerebri: molecular pathology and clinical course.

Published in:

2002

By:

Herrlinger, Ulrich;
Felsberg, Jörg;
Küker, Wilhelm;
Bornemann, Antje;
Plasswilm, Ludwig;
Knobbe, Christiane B.;
Strik, Herwig;
Wick, Wolfgang;
Meyermann, Richard;
Dichgans, Johannes;
Bamberg, Michael;
Reifenberger, Guido;
Weller, Michael;
Felsberg, Jörg;
Küker, Wilhelm

Publication type:

journal article

Wld s mice are resistant to paclitaxel (taxol) neuropathy.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 442, doi. 10.1002/ana.10300

By:

Wang, Min Sheng;
Davis, Albert A.;
Culver, Deborah G.;
Glass, Jonathan D.

Publication type:

Article

An R5L τ mutation in a subject with a progressive supranuclear palsy phenotype.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 511, doi. 10.1002/ana.10340

By:

Poorkaj, Parvoneh;
Muma, Nancy A.;
Zhukareva, Victoria;
Cochran, Elizabeth J.;
Shannon, Kathleen M.;
Hurtig, Howard;
Koller, William C.;
Bird, Thomas D.;
Trojanowski, John Q.;
Lee, Virginia M.-Y.;
Schellenberg, Gerard D.

Publication type:

Article

Imaging the metabolic footprint of Glut1 deficiency on the brain.

Published in:

2002

By:

Pascual, Juan M.;
van Heertum, Ronald L.;
Wang, Dong;
Engelstad, Kristin;
De Vivo, Darryl C.

Publication type:

journal article

Assessment of different treatment failure criteria in a cohort of relapsing-remitting multiple sclerosis patients treated with interferon β: Implications for clinical trials.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 400, doi. 10.1002/ana.10290

By:

Río, Jordi;
Nos, Carlos;
Tintoré, Mar;
Borrás, Cecilia;
Galán, Ingrid;
Comabella, Manuel;
Montalban, Xavier

Publication type:

Article

Aggregation of actin and cofilin in identical twins with juvenile-onset dystonia.

Published in:

2002

By:

Gearing, Marla;
Juncos, Jorge L.;
Procaccio, Vincent;
Gutekunst, Claire-Anne;
Marino-Rodriguez, Elaine M.;
Gyure, Kymberly A.;
Ono, Shoichiro;
Santoianni, Robert;
Krawiecki, Nicolas S.;
Wallace, Douglas C.;
Wainer, Bruce H.

Publication type:

journal article

Myoclonus-dystonia syndrome: ε-sarcoglycan mutations and phenotype.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 489, doi. 10.1002/ana.10325

By:

Asmus, Friedrich;
Zimprich, Alexander;
Tezenas Du Montcel, Sophie;
Kabus, Christian;
Deuschl, Günther;
Kupsch, Andreas;
Ziemann, Ulf;
Castro, Mirna;
Kühn, Andrea A.;
Strom, Tim M.;
Vidailhet, Marie;
Bhatia, Kailash P.;
Dürr, Alexandra;
Wood, Nicholas W.;
Brice, Alexis;
Gasser, Thomas

Publication type:

Article

Interictal high-frequency oscillations (80-500Hz) in the human epileptic brain: Entorhinal cortex.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 407, doi. 10.1002/ana.10291

By:

Bragin, Anatol;
Wilson, Charles L.;
Staba, Richard J.;
Reddick, Mark;
Fried, Itzhak;
Engel, Jerome

Publication type:

Article

Quinacrine does not prolong survival in a murine Creutzfeldt-Jakob disease model.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 503, doi. 10.1002/ana.10336

By:

Collins, Steven J.;
Lewis, Victoria;
Brazier, Marcus;
Hill, Andrew F.;
Fletcher, Ashley;
Masters, Colin L.

Publication type:

Article

Reply.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 526, doi. 10.1002/ana.10346

By:

Small, Scott A.

Publication type:

Article

Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locus.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 506, doi. 10.1002/ana.10339

By:

Fogli, Anne;
Wong, Kondi;
Eymard-Pierre, Eleonore;
Wenger, Jack;
Bouffard, John-Paul;
Goldin, Ehud;
Black, Deborah N.;
Boespflug-Tanguy, Odile;
Schiffmann, Raphael

Publication type:

Article

News and comment.

Published in:: Annals of Neurology, 2002, v. 52, n. 4, p. A36, doi. 10.1002/ana.1320
Publication type:: Article

Valproic acid treatment results in increased accumulation of prion proteins.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 416, doi. 10.1002/ana.10298

By:

Shaked, Gideon M.;
Engelstein, Roni;
Avraham, Inbal;
Rosenmann, Hannah;
Gabizon, Ruth

Publication type:

Article

Involvement of lysosomes in the pathogenesis of CAG repeat diseases.

Published in:

Annals of Neurology, 2002, v. 52, n. 4, p. 498, doi. 10.1002/ana.10328

By:

Yamada, Mitsunori;
Tsuji, Shoji;
Takahashi, Hitoshi

Publication type:

Article

Works matching IS 03645134 AND DT 2002 AND VI 52 AND IP 4

A PLP splicing abnormality is associated with an unusual presentation of PMD.

Interleukin-12 p40 polymorphism and susceptibility to multiple sclerosis.

Linkage of Parkinsonism and Alzheimer's disease with Lewy body pathology to chromosome 12.

Reply.

Treatment of multiple sclerosis with the pregnancy hormone estriol.

Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1.

Febrile seizures.

Treatment of multiple sclerosis with the pregnancy hormone estriol.

A novel mutation in the GNE gene and a linkage disequilibrium in Japanese pedigrees.

Evidence that accumulation of ceramides and cholesterol esters mediates oxidative stress-induced death of motor neurons in amyotrophic lateral sclerosis.

Gliomatosis cerebri: Molecular pathology and clinical course.

Neurologic complications of critical illness, 2nd ed.

Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease.

Concerns with the use of T2* signal intensity to differentiate hippocampal subregions.

Preserved visual function in a case of occipitoparietal microgyria.

Alzheimer's second patient: Johann F. and his family.

Gliomatosis cerebri: molecular pathology and clinical course.

Wld<sup> s</sup> mice are resistant to paclitaxel (taxol) neuropathy.

An <sup>R</sup>5<sup>L</sup> τ mutation in a subject with a progressive supranuclear palsy phenotype.

Imaging the metabolic footprint of Glut1 deficiency on the brain.

Assessment of different treatment failure criteria in a cohort of relapsing-remitting multiple sclerosis patients treated with interferon β: Implications for clinical trials.

Aggregation of actin and cofilin in identical twins with juvenile-onset dystonia.

Myoclonus-dystonia syndrome: ε-sarcoglycan mutations and phenotype.

Interictal high-frequency oscillations (80-500Hz) in the human epileptic brain: Entorhinal cortex.

Quinacrine does not prolong survival in a murine Creutzfeldt-Jakob disease model.

Reply.

Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locus.

News and comment.

Valproic acid treatment results in increased accumulation of prion proteins.

Involvement of lysosomes in the pathogenesis of CAG repeat diseases.