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Genetic linkage
Citations 31-40 of 81 total displayed.
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Past content
(since Jan 2001):
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- EDITORIALS
Lrrk2 in the limelight!
- Matthew J. Farrer
Neurology 2007; 69: 1732-1733.
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- ARTICLES
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8
- W. C. Nichols, V. E. Elsaesser, N. Pankratz, M. W. Pauciulo, D. K. Marek, C. A. Halter, A. Rudolph, C. W. Shults, T. Foroud For the Parkinson Study Group– PROGENI Investigators
Neurology 2007; 69: 1737-1744.
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- ARTICLES
Clinical characterization of the HOXA1 syndrome BSAS variant
- T. M. Bosley, M. A. Salih, I. A. Alorainy, D. T. Oystreck, M. Nester, K. K. Abu-Amero, M. A. Tischfield, and E. C. Engle
Neurology 2007; 69: 1245-1253.
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- EDITORIALS
The ARX story: A new twist
- Cecil D. Hahn
Neurology 2007; 69: 421-422.
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- EDITORIALS
Dissecting the complexity of frontotemporal dementia: Genotypes, phenotypes, and phenocopies
- Christine Klein and Vincenzo Bonifati
Neurology 2007; 69: 129-130.
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- ARTICLES
Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3
- P. Hedera, M. A. Blair, E. Andermann, F. Andermann, D. D'Agostino, K. A. Taylor, L. Chahine, M. Pandolfo, Y. Bradford, J. L. Haines, and B. Abou-Khalil
Neurology 2007; 68: 2107-2112.
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- EDITORIALS
New evidence for a genetic link between epilepsy and migraine
- Melodie Winawer
Neurology 2007; 68: 1969-1970.
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- ARTICLES
Familial occipitotemporal lobe epilepsy and migraine with visual aura: Linkage to chromosome 9q
- L. Deprez, K. Peeters, W. Van Paesschen, K. G. Claeys, L.R.F. Claes, A. Suls, D. Audenaert, T. Van Dyck, D. Goossens, J. Del-Favero, and P. De Jonghe
Neurology 2007; 68: 1995-2002.
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- ARTICLES
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
- A. Di Fonzo, H. F. Chien, M. Socal, S. Giraudo, C. Tassorelli, G. Iliceto, G. Fabbrini, R. Marconi, E. Fincati, G. Abbruzzese, P. Marini, F. Squitieri, M. W. Horstink, P. Montagna, A. Dalla Libera, F. Stocchi, S. Goldwurm, J. J. Ferreira, G. Meco, E. Martignoni, L. Lopiano, L. B. Jardim, B. A. Oostra, E. R. Barbosa, The Italian Parkinson Genetics Network, and V. Bonifati
Neurology 2007; 68: 1557-1562.
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- BRIEF COMMUNICATIONS
A founder haplotype for autosomal dominant sensory ataxia in Eastern Canada
- P. N. Valdmanis, D. Brunet, J. St-Onge, L. Weston, G. A. Rouleau, and N. Dupré
Neurology 2006; 67: 2239-2242.
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