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Trinucleotide repeat diseases
Citations 21-30 of 55 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Periventricular heterotopia in fragile X syndrome
- F. Moro, T. Pisano, B. Dalla Bernardina, R. Polli, A. Murgia, L. Zoccante, F. Darra, A. Battaglia, T. Pramparo, O. Zuffardi, and R. Guerrini
Neurology 2006; 67: 713-715.
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- NEUROIMAGES
Extravasation of hyperalimentation into the spinal epidural space from a central venous line
- M. Scott Perry and Lisa Billars
Neurology 2006; 67: 715.
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- BRIEF COMMUNICATIONS
Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions
- M. -E. Arsenault, C. Prévost, A. Lescault, C. Laberge, J. Puymirat, and J. Mathieu
Neurology 2006; 66: 1248-1250.
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- ARTICLES
The association of CAG repeat length with clinical progression in Huntington disease
- A. Rosenblatt, K. -Y. Liang, H. Zhou, M. H. Abbott, L. M. Gourley, R. L. Margolis, J. Brandt, and C. A. Ross
Neurology 2006; 66: 1016-1020.
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- BRIEF COMMUNICATIONS
Electrophysiologic characterization in spinocerebellar ataxia 17
- F. Manganelli, A. Perretti, M. Nolano, B. Lanzillo, A. C. Bruni, G. De Michele, A. Filla, and L. Santoro
Neurology 2006; 66: 932-934.
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- BRIEF COMMUNICATIONS
Dopamine transporter imaging study in parkinsonism occurring in fragile X premutation carriers
- R. Ceravolo, A. Antonini, D. Volterrani, C. Rossi, S. Goldwurm, E. Di Maria, L. Kiferle, U. Bonuccelli, and L. Murri
Neurology 2005; 65: 1971-1973.
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- BRIEF COMMUNICATIONS
Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS)
- D. A. Hall, E. Berry-Kravis, S. Jacquemont, C. D. Rice, J. Cogswell, L. Zhang, R. J. Hagerman, P. J. Hagerman, and M. A. Leehey
Neurology 2005; 65: 299-301.
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- BRIEF COMMUNICATIONS
Laryngospasm: An underdiagnosed symptom of X-linked spinobulbar muscular atrophy
- Anne-Dorte Sperfeld, C. Oliver Hanemann, Albert C. Ludolph, and Jan Kassubek
Neurology 2005; 64: 753-754.
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- BRIEF COMMUNICATIONS
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia
- A. Brussino, C. Gellera, A. Saluto, C. Mariotti, C. Arduino, B. Castellotti, M. Camerlingo, V. de Angelis, L. Orsi, P. Tosca, N. Migone, F. Taroni, and A. Brusco
Neurology 2005; 64: 145-147.
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- ARTICLES
Truncated ClC-1 mRNA in myotonic dystrophy exerts a dominant-negative effect on the Cl current
- Jim Berg, Hong Jiang, Charles A. Thornton, and Stephen C. Cannon
Neurology 2004; 63: 2371-2375.
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