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All Genetics
Citations 441-450 of 676 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Leukocyte CTG repeat length correlates with severity of myotonia in myotonic dystrophy type 1
- E. L. Logigian, R. T. Moxley, IV, C. L. Blood, C. A. Barbieri, W. B. Martens, A. W. Wiegner, C. A. Thornton, and R. T. Moxley, III
Neurology 2004; 62: 1081-1089.
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- ARTICLES
Large-scale disruption of microtubule pathways in morphologically normal human spastin muscle
- A. Molon, S. Di Giovanni, Y. W. Chen, P. M. Clarkson, C. Angelini, E. Pegoraro, and E. P. Hoffman
Neurology 2004; 62: 1097-1104.
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- ARTICLES
LGI1 mutations in temporal lobe epilepsies
- S. F. Berkovic, P. Izzillo, J. M. McMahon, L. A. Harkin, A. M. McIntosh, H. A. Phillips, R. S. Briellmann, R. H. Wallace, A. Mazarib, M. Y. Neufeld, A. D. Korczyn, I. E. Scheffer, and J. C. Mulley
Neurology 2004; 62: 1115-1119.
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- ARTICLES
LGI1 mutations in autosomal dominant partial epilepsy with auditory features
- R. Ottman, M. R. Winawer, S. Kalachikov, C. Barker-Cummings, T. C. Gilliam, T. A. Pedley, and W. A. Hauser
Neurology 2004; 62: 1120-1126.
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- ARTICLES
Epilepsy in twins: Insights from unique historical data of William Lennox
- L. Vadlamudi, E. Andermann, C. T. Lombroso, S. C. Schachter, R. L. Milne, J. L. Hopper, F. Andermann, and S. F. Berkovic
Neurology 2004; 62: 1127-1133.
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- BRIEF COMMUNICATIONS
Alpha-1-antitrypsin deficiency alleles are not associated with cervical artery dissections
- C. Grond-Ginsbach, S. Engelter, I. Werner, I. Hausser, U. S. Müller, T. Brandt, and P. Lyrer
Neurology 2004; 62: 1190-1192.
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- BRIEF COMMUNICATIONS
CCM1 mutation screen of sporadic cases with cerebral cavernous malformations
- D. J. Verlaan, S. B. Laurent, U. Sure, H. Bertalanffy, E. Andermann, F. Andermann, G. A. Rouleau, and A. M. Siegel
Neurology 2004; 62: 1213-1215.
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- BRIEF COMMUNICATIONS
Cognitive functioning in humans with mutations of the PAX6 gene
- P. J. Thompson, T. N. Mitchell, S. L. Free, K. A. Williamson, I. M. Hanson, V. van Heyningen, A. T. Moore, and S. M. Sisodiya
Neurology 2004; 62: 1216-1218.
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- BRIEF COMMUNICATIONS
Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease
- N. L. Khan, R. Katzenschlager, H. Watt, K. P. Bhatia, N. W. Wood, N. Quinn, and A. J. Lees
Neurology 2004; 62: 1224-1226.
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- CLINICAL/SCIENTIFIC NOTES
Myoclonus–dystonia: Detection of novel, recurrent, and de novo SGCE mutations
- K. Hedrich, E. -M. Meyer, B. Schüle, N. Kock, P. de Carvalho Aguiar, K. Wiegers, J. H. Koelman, J. Garrels, R. Dürr, L. Liu, E. Schwinger, L. J. Ozelius, B. Landwehrmeyer, A. J. Stoessl, M. A.J. Tijssen, and C. Klein
Neurology 2004; 62: 1229-1231.
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