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All Genetics
Citations 101-110 of 679 total displayed.
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Past content
(since Jan 2001):
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- CLINICAL/SCIENTIFIC NOTES
EXTRACEPHALIC CLUSTER (CLUSTER SINE HEADACHE)
- Esma Dilli and David W. Dodick
Neurology 2008; 70: 1362-1363.
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- EDITORIALS
Complicated autosomal recessive hereditary spastic paraplegia: A complex picture is emerging
- Peter Hedera and Oliver Bandmann
Neurology 2008; 70: 1375-1376.
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- ARTICLES
FMR1 CGG repeat length predicts motor dysfunction in premutation carriers
- M. A. Leehey, E. Berry-Kravis, C. G. Goetz, L. Zhang, D. A. Hall, L. Li, C. D. Rice, R. Lara, J. Cogswell, A. Reynolds, L. Gane, S. Jacquemont, F. Tassone, J. Grigsby, R. J. Hagerman, and P. J. Hagerman
Neurology 2008; 70: 1397-1402.
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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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