Trinucleotide repeat diseases

Citations 51-55 of 55 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Pathogenic effect of an intermediate-size SCA-6 allele (CAG)₁₉ in a homozygous patient

C. Mariotti, C. Gellera, M. Grisoli, R. Mineri, A. Castucci, and S. Di Donato
Neurology 2001; 57: 1502-1504. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
SCA8 repeat expansions in ataxia: A controversial association

M.-J. Sobrido, J. A. Cholfin, S. Perlman, S. M. Pulst, and D. H. Geschwind
Neurology 2001; 57: 1310-1312. [Abstract] [Full text] [PDF]  

ARTICLES
Striatal volume loss in HD as measured by MRI and the influence of CAG repeat

H. D. Rosas, J. Goodman, Y. I. Chen, B. G. Jenkins, D. N. Kennedy, N. Makris, M. Patti, L. J. Seidman, M. F. Beal, and W. J. Koroshetz
Neurology 2001; 57: 1025-1028. [Abstract] [Full text] [PDF]  

ARTICLES
Frequency and stability of the myotonic dystrophy type 1 premutation

L. Martorell, D.G. Monckton, A. Sanchez, A. Lopez de Munain, and M. Baiget
Neurology 2001; 56: 328-335. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Severe infantile dentatorubral pallidoluysian atrophy with extreme expansion of CAG repeats

Y. Shimojo, Y. Osawa, M. Fukumizu, S. Hanaoka, H. Tanaka, F. Ogata, M. Sasaki, and K. Sugai
Neurology 2001; 56: 277-278. [Full text] [PDF]  

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