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All Genetics
Citations 481-490 of 676 total displayed.
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Past content
(since Jan 2001):
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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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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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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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Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 alleles
- M. Wohlgemuth, R. J. Lemmers, E. L. van der Kooi, M. J. van der Wielen, P. G. van Overveld, H. Dauwerse, E. Bakker, R. R. Frants, G. W. Padberg, and S. M. van der Maarel
Neurology 2003; 61: 909-913.
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- ARTICLES
Risk of action tremor in relatives of tremor-dominant and postural instability gait disorder PD
- E. D. Louis, G. Levy, H. Mejia-Santana, L. Cote, H. Andrews, J. Harris, C. Waters, B. Ford, S. Frucht, S. Fahn, R. Ottman, and K. Marder
Neurology 2003; 61: 931-936.
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- BRIEF COMMUNICATIONS
Charcot–Marie–Tooth disease with giant axons: A clinicopathological and genetic entity
- G. Lus, E. Nelis, A. Jordanova, A. Löfgren, T. Cavallaro, A. Ammendola, M. A.B. Melone, N. Rizzuto, V. Timmerman, R. Cotrufo, and P. De Jonghe
Neurology 2003; 61: 988-990.
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