|
All Genetics
Citations 491-500 of 676 total displayed.
|
Past content
(since Jan 2001):
|
- BRIEF COMMUNICATIONS
Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD
- J. Eerola, D. Hernandez, J. Launes, O. Hellström, S. Hague, C. Gulick, J. Johnson, T. Peuralinna, J. Hardy, P. J. Tienari, and A. B. Singleton
Neurology 2003; 61: 1000-1002.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
PS1 Alzheimer’s disease family with spastic paraplegia: The search for a gene modifier
- E. Rogaeva, C. Bergeron, C. Sato, I. Moliaka, T. Kawarai, A. Toulina, Y-Q. Song, T. Kolesnikova, A. Orlacchio, G. Bernardi, and P. H. St. George-Hyslop
Neurology 2003; 61: 1005-1007.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Rapsyn mutations in hereditary myasthenia: Distinct early- and late-onset phenotypes
- G. Burke, J. Cossins, S. Maxwell, G. Owens, A. Vincent, S. Robb, M. Nicolle, D. Hilton–Jones, J. Newsom–Davis, J. Palace, and D. Beeson
Neurology 2003; 61: 826-828.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Genetic variation of the APOE promoter and outcome after head injury
- C. L. Lendon, J. M. Harris, A. L. Pritchard, J. A.R. Nicoll, G. M. Teasdale, and G. Murray
Neurology 2003; 61: 683-685.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Genetic heterogeneity of megalencephalic leukoencephalopathy and subcortical cysts
- C. Patrono, G. Di Giacinto, E. Eymard–Pierre, F. M. Santorelli, D. Rodriguez, N. De Stefano, A. Federico, R. Gatti, V. Benigno, A. Megarbané, B. Tabarki, O. Boespflug–Tanguy, and E. Bertini
Neurology 2003; 61: 534-537.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
A cluster headache family with possible autosomal recessive inheritance
- Roberto De Simone, Chiara Fiorillo, Salvatore Bonuso, and Giuseppe Castaldo
Neurology 2003; 61: 578-579.
[Full text]
[PDF]
- EDITORIALS
Mental retardation: X marks the spot
- Marc C. Patterson and Huda Y. Zoghbi
Neurology 2003; 61: 156-157.
[Full text]
[PDF]
- ARTICLES
D4F104S1 deletion in facioscapulohumeral muscular dystrophy: Phenotype, size, and detection
- R. J.L.F. Lemmers, M. Osborn, T. Haaf, M. Rogers, R. R. Frants, G. W. Padberg, D. N. Cooper, S. M. van der Maarel, and M. Upadhyaya
Neurology 2003; 61: 178-183.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia
- P.A. Wilkinson, A.H. Crosby, C. Turner, H. Patel, N.W. Wood, A.H. Schapira, and T.T. Warner
Neurology 2003; 61: 235-238.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Mutations in the  -sarcoglycan gene found to be uncommon in seven myoclonus–dystonia families
- F. Han, A. E. Lang, L. Racacho, D. E. Bulman, and D. A. Grimes
Neurology 2003; 61: 244-246.
[Abstract]
[Full text]
[PDF]
|
|
