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Neurology
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Trinucleotide repeat diseases

Citations 31-40 of 55 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Sudden cardiac death in myotonic dystrophy type 2
B. G.H. Schoser, K. Ricker, C. Schneider-Gold, C. Hengstenberg, J. Dürre, B. Bültmann, W. Kress, J. W. Day, and L. P.W. Ranum
Neurology 2004; 63: 2402-2404. [Abstract] [Full text] [PDF]  

ARTICLES
Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome
C. S. Kogan, A. Bertone, K. Cornish, I. Boutet, V. M. Der Kaloustian, E. Andermann, J. Faubert, and A. Chaudhuri
Neurology 2004; 63: 1634-1639. [Abstract] [Full text] [PDF]  

ARTICLES
Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3
U. Rüb, K. Bürk, L. Schöls, E. R. Brunt, R. A.I. de Vos, G. Orozco Diaz, K. Gierga, E. Ghebremedhin, C. Schultz, D. Del Turco, M. Mittelbronn, G. Auburger, T. Deller, and H. Braak
Neurology 2004; 63: 1258-1263. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort
E. K. Tan, Y. Zhao, K. Y. Puong, H. Y. Law, L. L. Chan, K. Yew, C. Tan, H. Shen, V. R. Chandran, M. L. Teoh, Y. Yih, R. Pavanni, M. C. Wong, and I. S. Ng
Neurology 2004; 63: 362-363. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Intergenerational instability and marked anticipation in SCA-17
F. Maltecca, A. Filla, I. Castaldo, G. Coppola, N.A. Fragassi, M. Carella, A. Bruni, S. Cocozza, G. Casari, A. Servadio, and G. De Michele
Neurology 2003; 61: 1441-1443. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
GAA expansion size and age at onset of Friedreich’s ataxia
I. Mateo, J. Llorca, V. Volpini, J. Corral, J. Berciano, and O. Combarros
Neurology 2003; 61: 274-275. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2
A. Vihola, G. Bassez, G. Meola, S. Zhang, H. Haapasalo, A. Paetau, E. Mancinelli, A. Rouche, J.Y. Hogrel, P. Laforêt, T. Maisonobe, J.F. Pellissier, R. Krahe, B. Eymard, and B. Udd
Neurology 2003; 60: 1854-1857. [Abstract] [Full text] [PDF]  

EDITORIALS
Idebenone for treatment of Friedreich’s ataxia?
Alessandro Filla and Arthur J. Moss
Neurology 2003; 60: 1569-1570. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Idebenone treatment in Friedreich patients: One-year-long randomized placebo-controlled trial
C. Mariotti, A. Solari, D. Torta, L. Marano, C. Fiorentini, and S. Di Donato
Neurology 2003; 60: 1676-1679. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Idebenone treatment in Friedreich’s ataxia: Neurological, cardiac, and biochemical monitoring
G. Buyse, L. Mertens, G. Di Salvo, I. Matthijs, F. Weidemann, B. Eyskens, W. Goossens, N. Goemans, G. R. Sutherland, and J. L.K. Van Hove
Neurology 2003; 60: 1679-1681. [Abstract] [Full text] [PDF]  

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* Related collections:
 Genetics
 All Genetics
 Neurofibromatosis
 Other neurocutaneous disorders
 Genetic linkage
 Association studies in genetics
 Gene expression studies
 Gene therapy
 Mitochondrial disorders
 Ion channel gene defects
 Spinocerebellar ataxia
 Trinucleotide repeat diseases
 Chromosomes


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