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All Genetics
Citations 11-20 of 676 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations
- J. L. Whitwell, C. R. Jack, Jr, B. F. Boeve, M. L. Senjem, M. Baker, R. J. Ivnik, D. S. Knopman, Z. K. Wszolek, R. C. Petersen, R. Rademakers, and K. A. Josephs
Neurology 2009; 73: 1058-1065.
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- SPECIAL ARTICLE
Practice Parameter: Evaluation of the child with microcephaly (an evidence-based review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
- Stephen Ashwal, David Michelson, Lauren Plawner, and William B. Dobyns
Neurology 2009; 73: 887-897.
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- CLINICAL/SCIENTIFIC NOTES
ATAXIA WITH OPHTHALMOPLEGIA OR SENSORY NEUROPATHY IS FREQUENTLY CAUSED BY POLG MUTATIONS
- Claudia Schulte, Matthis Synofzik, Thomas Gasser, and Ludger Schöls
Neurology 2009; 73: 898-900.
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- EDITORIALS
Another gene for ALS. Mutations in sporadic cases and the rare variant hypothesis
- Kevin Talbot
Neurology first published on September 9, 2009 as doi: WNL.0b013e3181bd1161.
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- ARTICLES
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
- N. Ticozzi, V. Silani, A. L. LeClerc, P. Keagle, C. Gellera, A. Ratti, F. Taroni, T. J. Kwiatkowski, Jr., D. M. McKenna-Yasek, P. C. Sapp, R. H. Brown, Jr., and J. E. Landers
Neurology first published on September 9, 2009 as doi: WNL.0b013e3181bbff05.
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- ARTICLES
Mutations in FUS cause FALS and SALS in French and French Canadian populations
- V. V. Belzil, P. N. Valdmanis, P. A. Dion, H. Daoud, E. Kabashi, A. Noreau, J. Gauthier, for the S2D team, P. Hince, A. Desjarlais, J.-P. Bouchard, L. Lacomblez, F. Salachas, P.-F. Pradat, W. Camu, V. Meininger, N. Dupré, and G. A. Rouleau
Neurology first published on September 9, 2009 as doi: WNL.0b013e3181bbfeef.
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- EDITORIALS
Multiple sclerosis: Evidence of maternal effects and an increasing incidence in women
- John W. Rose
Neurology 2009; 73: 578-579.
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- ARTICLES
Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotes
- S. C. Blumen, J. -P. Bouchard, B. Brais, R. L. Carasso, D. Paleacu, V. E. Drory, S. Chantal, N. Blumen, and I. Braverman
Neurology 2009; 73: 596-601.
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- ARTICLES
Parent-of-origin effect in multiple sclerosis: Observations from interracial matings
- S. V. Ramagopalan, I. M. Yee, D. A. Dyment, S. -M. Orton, R. A. Marrie, A. D. Sadovnick, G. C. Ebers For the Canadian Collaborative Study Group
Neurology 2009; 73: 602-605.
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- ARTICLES
Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His
- J. van der Zee, D. Pirici, T. Van Langenhove, S. Engelborghs, R. Vandenberghe, M. Hoffmann, G. Pusswald, M. Van den Broeck, K. Peeters, M. Mattheijssens, J. -J. Martin, P. P. De Deyn, M. Cruts, D. Haubenberger, S. Kumar-Singh, A. Zimprich, and C. Van Broeckhoven
Neurology 2009; 73: 626-632.
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