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All Genetics
Citations 101-110 of 676 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
- K. Haugarvoll, R. Rademakers, J. M. Kachergus, K. Nuytemans, O. A. Ross, J. M. Gibson, E-K Tan, C. Gaig, E. Tolosa, S. Goldwurm, M. Guidi, G. Riboldazzi, L. Brown, U. Walter, R. Benecke, D. Berg, T. Gasser, J. Theuns, P. Pals, P. Cras, P. Paul De Deyn, S. Engelborghs, B. Pickut, R. J. Uitti, T. Foroud, W. C. Nichols, J. Hagenah, C. Klein, A. Samii, C. P. Zabetian, V. Bonifati, C. Van Broeckhoven, M. J. Farrer, and Z. K. Wszolek
Neurology 2008; 70: 1456-1460.
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- EDITORIALS
TRAPS and MS: Two diseases or an MS mimic?
- Subramaniam Sriram
Neurology 2008; 70: 1077-1078.
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- ARTICLES
Integrating risk factors: HLA-DRB1*1501 and Epstein–Barr virus in multiple sclerosis
- P. L. De Jager, K. C. Simon, K. L. Munger, J. D. Rioux, D. A. Hafler, and A. Ascherio
Neurology 2008; 70: 1113-1118.
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- ARTICLES
Investigating genotype–phenotype relationships in Rett syndrome using an international data set
- A. Bebbington, A. Anderson, D. Ravine, S. Fyfe, M. Pineda, N. de Klerk, B. Ben-Zeev, N. Yatawara, A. Percy, W. E. Kaufmann, and H. Leonard
Neurology 2008; 70: 868-875.
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- CLINICAL/SCIENTIFIC NOTES
ASSOCIATION BETWEEN GENETIC VARIANTS IN SORL1 AND AUTOPSY-CONFIRMED ALZHEIMER DISEASE
- J. H. Lee, R. Cheng, L. S. Honig, J-P G. Vonsattel, L. Clark, and R. Mayeux
Neurology 2008; 70: 887-889.
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- ARTICLES
GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease
- M. Henneke, P. Combes, S. Diekmann, E. Bertini, K. Brockmann, A. P. Burlina, J. Kaiser, A. Ohlenbusch, B. Plecko, D. Rodriguez, O. Boespflug-Tanguy, and J. Gärtner
Neurology 2008; 70: 748-754.
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- ARTICLES
Motoneuron-specific NR3B gene: No association with ALS and evidence for a common null allele
- S. Niemann, J. E. Landers, M. J. Churchill, B. Hosler, P. Sapp, W. C. Speed, B. T. Lahn, K. K. Kidd, R. H. Brown, Jr, and Y. Hayashi
Neurology 2008; 70: 666-676.
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- ARTICLES
Neuropathology of primary adult-onset dystonia
- J. L. Holton, S. A. Schneider, T. Ganesharajah, S. Gandhi, C. Strand, P. Shashidharan, J. Barreto, N. W. Wood, A. J. Lees, K. P. Bhatia, and T. Revesz
Neurology 2008; 70: 695-699.
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- ARTICLES
Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations
- A. S. Chen-Plotkin, W. Yuan, C. Anderson, E. McCarty Wood, H. I. Hurtig, C. M. Clark, B. L. Miller, V. M.-Y. Lee, J. Q. Trojanowski, M. Grossman, and V. M. Van Deerlin
Neurology 2008; 70: 521-527.
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- ARTICLES
Prevalence of SOD1 mutations in the Italian ALS population
- A. Chiò, B. J. Traynor, F. Lombardo, M. Fimognari, A. Calvo, P. Ghiglione, R. Mutani, and G. Restagno
Neurology 2008; 70: 533-537.
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