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All Genetics
Citations 11-20 of 679 total displayed.
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Past content
(since Jan 2001):
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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 2009; 73: 1180-1185.
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- ARTICLES
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum
- C. Goizet, A. Boukhris, D. Maltete, L. Guyant-Maréchal, J. Truchetto, E. Mundwiller, S. Hanein, P. Jonveaux, F. Roelens, J. Loureiro, E. Godet, S. Forlani, J. Melki, M. Auer-Grumbach, J. C. Fernandez, P. Martin-Hardy, I. Sibon, G. Sole, I. Orignac, C. Mhiri, P. Coutinho, A. Durr, A. Brice, and G. Stevanin
Neurology 2009; 73: 1111-1119.
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- ARTICLES
Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy
- A. van der Walt, J. Stankovich, M. Bahlo, B. V. Taylor, I.A.F. van der Mei, S. J. Foote, T. J. Kilpatrick, J. P. Rubio, and H. Butzkueven
Neurology 2009; 73: 1018-1025.
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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.
[Abstract]
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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.
[Abstract]
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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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