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Trinucleotide repeat diseases
Citations 11-20 of 55 total displayed.
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Past content
(since Jan 2001):
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- NEUROIMAGES
Cerebellar T2 hyperintensities in a patient with tremor
- Menachem Sadeh and Alexander Lossos
Neurology 2008; 70: 578.
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- ARTICLES
Pathophysiologic insights into motor axonal function in Kennedy disease
- Steve Vucic and Matthew C. Kiernan
Neurology 2007; 69: 1828-1835.
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- ARTICLES
Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease
- P. T. Luoma, J. Eerola, S. Ahola, A. H. Hakonen, O. Hellström, K. T. Kivistö, P. J. Tienari, and A. Suomalainen
Neurology 2007; 69: 1152-1159.
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- ARTICLES
Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS)
- J. S. Adams, P. E. Adams, D. Nguyen, J. A. Brunberg, F. Tassone, W. Zhang, K. Koldewyn, S. M. Rivera, J. Grigsby, L. Zhang, C. DeCarli, P. J. Hagerman, and R. J. Hagerman
Neurology 2007; 69: 851-859.
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- EDITORIALS
The ARX story: A new twist
- Cecil D. Hahn
Neurology 2007; 69: 421-422.
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- CLINICAL/SCIENTIFIC NOTES
LIMBIC ENCEPHALITIS AS PRESENTATION OF A SAP DEFICIENCY
- H. Verhelst, R. Van Coster, N. Bockaert, G. Laureys, S. Latour, A. Fischer, and F. Haerynck
Neurology 2007; 69: 218-219.
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- ARTICLES
Neural transplantation in Huntington disease: Long-term grafts in two patients
- C. D. Keene, J. A. Sonnen, P. D. Swanson, O. Kopyov, J. B. Leverenz, T. D. Bird, and T. J. Montine
Neurology 2007; 68: 2093-2098.
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- CLINICAL/SCIENTIFIC NOTES
ATYPICAL CLINICAL COURSE OF FXTAS: RAPIDLY PROGRESSIVE DEMENTIA AS THE MAJOR SYMPTOM
- M.R.R. Gonçalves, L. P. Capelli, R. Nitrini, E. R. Barbosa, C. S. Porto, L. T. Lucato, and A. M. Vianna-Morgante
Neurology 2007; 68: 1864-1866.
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- ARTICLES
Molecular and imaging correlates of the fragile X–associated tremor/ataxia syndrome
- S. Cohen, K. Masyn, J. Adams, D. Hessl, S. Rivera, F. Tassone, J. Brunberg, C. DeCarli, L. Zhang, J. Cogswell, D. Loesch, M. Leehey, J. Grigsby, P. J. Hagerman, and R. Hagerman
Neurology 2006; 67: 1426-1431.
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- BRIEF COMMUNICATIONS
Clinicopathologic investigation of a family with expanded SCA8 CTA/CTG repeats
- H. Ito, H. Kawakami, R. Wate, S. Matsumoto, T. Imai, A. Hirano, and H. Kusaka
Neurology 2006; 67: 1479-1481.
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