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All Genetics
Citations 381-390 of 676 total displayed.
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Past content
(since Jan 2001):
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- EDITORIALS
Can "blue" genes affect mood and movement?
- Irene Hegeman Richard and William M. McDonald
Neurology 2004; 63: 610-611.
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- ARTICLES
Increased risk for recurrent major depression in DYT1 dystonia mutation carriers
- G. A. Heiman, R. Ottman, R. J. Saunders-Pullman, L. J. Ozelius, N. J. Risch, and S. B. Bressman
Neurology 2004; 63: 631-637.
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- ARTICLES
Parkin-positive autosomal recessive juvenile parkinsonism with  -synuclein-positive inclusions
- Shoichi Sasaki, Akiko Shirata, Kiyomi Yamane, and Makoto Iwata
Neurology 2004; 63: 678-682.
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- BRIEF COMMUNICATIONS
Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene
- P. F. Chinnery, S. M. Keers, M. J. Holden, V. Ramesh, and A. Dalton
Neurology 2004; 63: 710-712.
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- BRIEF COMMUNICATIONS
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS
- C. Münch, R. Sedlmeier, T. Meyer, V. Homberg, A. D. Sperfeld, A. Kurt, J. Prudlo, G. Peraus, C. O. Hanemann, G. Stumm, and A. C. Ludolph
Neurology 2004; 63: 724-726.
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- BRIEF COMMUNICATIONS
Hearing loss as the first feature of late-onset axonal CMT disease due to a novel P0 mutation
- P. Seeman, R. Mazanec, K. Huehne, P. Suslíková, O. Keller, and B. Rautenstrauss
Neurology 2004; 63: 733-735.
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- VIEWS & REVIEWS
Genetically modified adenoviruses against gliomas: From bench to bedside
- Candelaria Gomez-Manzano, W.K. Alfred Yung, Ramon Alemany, and Juan Fueyo
Neurology 2004; 63: 418-426.
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- BRIEF COMMUNICATIONS
A limited role for DJ1 in Parkinson disease susceptibility
- D. M. Maraganore, K. Wilkes, T. G. Lesnick, K. J. Strain, M. de Andrade, W. A. Rocca, J. H. Bower, J. E. Ahlskog, S. Lincoln, and M. J. Farrer
Neurology 2004; 63: 550-553.
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- BRIEF COMMUNICATIONS
SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies
- J. Johnson, S. M. Hague, M. Hanson, A. Gibson, K. E. Wilson, E. W. Evans, A. A. Singleton, A. McInerney-Leo, R. L. Nussbaum, D. G. Hernandez, M. Gallardo, I. G. McKeith, D. J. Burn, M. Ryu, O. Hellstrom, B. Ravina, J. Eerola, R. H. Perry, E. Jaros, P. Tienari, R. Weiser, K. Gwinn-Hardy, C. M. Morris, J. Hardy, and A. B. Singleton
Neurology 2004; 63: 554-556.
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- BRIEF COMMUNICATIONS
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL
- R. Mazzei, F. L. Conforti, P. L. Lanza, T. Sprovieri, M. R. Lupo, O. Gallo, A. Patitucci, A. Magariello, M. Caracciolo, A. L. Gabriele, F. Fera, P. Valentino, F. Bono, G. Cenacchi, G. Santoro, M. Muglia, and A. Quattrone
Neurology 2004; 63: 561-564.
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