|
All Genetics
Citations 501-510 of 676 total displayed.
|
Past content
(since Jan 2001):
|
- BRIEF COMMUNICATIONS
Transthyretin Val122Ile, accumulated Aß, and inclusion-body myositis aspects in cultured muscle
- Valerie Askanas, W. King Engel, Janis McFerrin, and Gaetano Vattemi
Neurology 2003; 61: 257-260.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Polyalanine expansion of ARX associated with cryptogenic West syndrome
- M. Kato, S. Das, K. Petras, Y. Sawaishi, and W.B. Dobyns
Neurology 2003; 61: 267-276.
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Serum prolactin in symptomatic and asymptomatic dopa-responsive dystonia due to a GCH1 mutation
- Y. Furukawa, M. Guttman, H. Wong, S.A. Farrell, S. Furtado, and S.J. Kish
Neurology 2003; 61: 269-270.
[Full text]
[PDF]
- EDITORIALS
PD or not PD?: That is the question
- Caroline M. Tanner
Neurology 2003; 61: 5-6.
[Full text]
[PDF]
- ARTICLES
Validity of family history data on PD: Evidence for a family information bias
- A. Elbaz, S.K. McDonnell, D.M. Maraganore, K.J. Strain, D.J. Schaid, J.H. Bower, J.E. Ahlskog, and W.A. Rocca
Neurology 2003; 61: 11-17.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Accuracy of family history data on Parkinson’s disease
- K. Marder, G. Levy, E. D. Louis, H. Mejia–Santana, L. Cote, H. Andrews, J. Harris, C. Waters, B. Ford, S. Frucht, S. Fahn, and R. Ottman
Neurology 2003; 61: 18-23.
[Abstract]
[Full text]
[PDF]
- ARTICLES
A distinct phenotype of distal myopathy in a large Finnish family
- I. Mahjneh, H. Haravuori, A. Paetau, L.V.B. Anderson, A. Saarinen, B. Udd, and H. Somer
Neurology 2003; 61: 87-92.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Single section Western blot: Improving the molecular diagnosis of the muscular dystrophies
- Sandra T. Cooper, Harriet P. Lo, and Kathryn N. North
Neurology 2003; 61: 93-97.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP
- H.R. Morris, Y. Osaki, J. Holton, A.J. Lees, N.W. Wood, T. Revesz, and N. Quinn
Neurology 2003; 61: 102-104.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy
- R. Nabbout, E. Gennaro, B. Dalla Bernardina, O. Dulac, F. Madia, E. Bertini, G. Capovilla, C. Chiron, G. Cristofori, M. Elia, E. Fontana, R. Gaggero, T. Granata, R. Guerrini, M. Loi, L. La Selva, M. L. Lispi, A. Matricardi, A. Romeo, V. Tzolas, D. Valseriati, P. Veggiotti, F. Vigevano, L. Vallée, F. Dagna Bricarelli, A. Bianchi, and F. Zara
Neurology 2003; 60: 1961-1967.
[Abstract]
[Full text]
[PDF]
|
|
