|
Trinucleotide repeat diseases
Citations 41-50 of 55 total displayed.
|
Past content
(since Jan 2001):
|
- ARTICLES
Myotonic dystrophy type 2: Molecular, diagnostic and clinical spectrum
- J. W. Day, K. Ricker, J. F. Jacobsen, L. J. Rasmussen, K. A. Dick, W. Kress, C. Schneider, M. C. Koch, G. J. Beilman, A. R. Harrison, J. C. Dalton, and L. P.W. Ranum
Neurology 2003; 60: 657-664.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
REM sleep behavior disorder and SCA-3 (Machado-Joseph disease)
- Badar H. Syed, David B. Rye, and Gurwant Singh
Neurology 2003; 60: 148.
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Relationship between CAG repeat length and late-stage outcomes in Huntington’s disease
- K. Marder, S. Sandler, A. Lechich, J. Klager, and S.M. Albert
Neurology 2002; 59: 1622-1624.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Weight loss in early stage of Huntington’s disease
- L. Djoussé, B. Knowlton, L. A. Cupples, K. Marder, I. Shoulson, and R. H. Myers
Neurology 2002; 59: 1325-1330.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Presymptomatic testing in Huntington’s disease and autosomal dominant cerebellar ataxias
- C. Goizet, G. Lesca, and A. Dürr
Neurology 2002; 59: 1330-1336.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Clinical and genetic study of a large Italian family linked to SPG12 locus
- A. Orlacchio, T. Kawarai, E. Rogaeva, Y.Q. Song, A.D. Paterson, G. Bernardi, and P.H. St. George-Hyslop
Neurology 2002; 59: 1395-1401.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Jaw drop in Kennedy’s disease
- Charlotte J. Sumner and Kenneth H. Fischbeck
Neurology 2002; 59: 1471-1472.
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Expression of X-linked bulbospinal muscular atrophy (Kennedy disease) in two homozygous women
- Brian J. Schmidt, Cheryl R. Greenberg, Diane J. Allingham–Hawkins, and Elizabeth L. Spriggs
Neurology 2002; 59: 770-772.
[Abstract]
[Full text]
[PDF]
- ARTICLES
X-linked myoclonic epilepsy with spasticity and intellectual disability: Mutation in the homeobox gene ARX
- I. E. Scheffer, R. H. Wallace, F. L. Phillips, P. Hewson, K. Reardon, G. Parasivam, P. Stromme, S. F. Berkovic, J. Gecz, and J. C. Mulley
Neurology 2002; 59: 348-356.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Autosomal dominant chorea–acanthocytosis with polyglutamine-containing neuronal inclusions
- R. H. Walker, S. Morgello, B. Davidoff–Feldman, A. Melnick, M. J. Walsh, P. Shashidharan, and M. F. Brin
Neurology 2002; 58: 1031-1037.
[Abstract]
[Full text]
[PDF]
|
|
