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All Genetics
Citations 481-490 of 679 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Late onset Charcot–Marie–Tooth 2 syndrome caused by two novel mutations in the MPZ gene
- M. Auer–Grumbach, S. Strasser–Fuchs, T. Robl, C. Windpassinger, and K. Wagner
Neurology 2003; 61: 1435-1437.
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- BRIEF COMMUNICATIONS
Intergenerational instability and marked anticipation in SCA-17
- F. Maltecca, A. Filla, I. Castaldo, G. Coppola, N.A. Fragassi, M. Carella, A. Bruni, S. Cocozza, G. Casari, A. Servadio, and G. De Michele
Neurology 2003; 61: 1441-1443.
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- ARTICLES
 B-Crystallin genotype has impact on the multiple sclerosis phenotype
- T. van Veen, L. van Winsen, J. B.A. Crusius, N. F. Kalkers, F. Barkhof, A. S. Peña, C. H. Polman, and B. M.J. Uitdehaag
Neurology 2003; 61: 1245-1249.
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- BRIEF COMMUNICATIONS
Clinically disparate stiff-person syndrome with GAD65 autoantibody in a father and daughter
- T. M. Burns, H. R. Jones, L. H. Phillips, II, T. L. Bugawan, H. A. Erlich, and V. A. Lennon
Neurology 2003; 61: 1291-1293.
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- ARTICLES
Mosaic mutations of the LIS1 gene cause subcortical band heterotopia
- F. Sicca, A. Kelemen, P. Genton, S. Das, D. Mei, F. Moro, W.B. Dobyns, and R. Guerrini
Neurology 2003; 61: 1042-1046.
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- ARTICLES
Candidate gene studies in focal dystonia
- D. Sibbing, F. Asmus, I. R. König, S. Tezenas du Montcel, M. Vidailhet, S. Sangla, W. H. Oertel, A. Brice, A. Ziegler, T. Gasser, and O. Bandmann
Neurology 2003; 61: 1097-1101.
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- BRIEF COMMUNICATIONS
Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu)
- F. Portet, Y. Dauvilliers, D. Campion, G. Raux, J.J. Hauw, O. Lyon-Caen, W. Camu, and J. Touchon
Neurology 2003; 61: 1136-1137.
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- BRIEF COMMUNICATIONS
Brain metabolic differences between sporadic and familial Alzheimer’s disease
- L. Mosconi, S. Sorbi, B. Nacmias, M.T.R. De Cristofaro, M. Fayyaz, E. Cellini, S. Bagnoli, L. Bracco, K. Herholz, and A. Pupi
Neurology 2003; 61: 1138-1140.
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- BRIEF COMMUNICATIONS
Classical mitochondrial phenotypes without mtDNA mutations: The possible role of nuclear genes
- Teeratorn Pulkes, Danae Liolitsa, Isabelle P. Nelson, and Michael G. Hanna
Neurology 2003; 61: 1144-1147.
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- ARTICLES
Remarkable infidelity of polymerase  A associated with mutations in POLG1 exonuclease domain
- R. Del Bo, A. Bordoni, M. Sciacco, A. Di Fonzo, S. Galbiati, M. Crimi, N. Bresolin, and G. P. Comi
Neurology 2003; 61: 903-908.
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