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All Genetics
Citations 121-130 of 676 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Sensorimotor integration is abnormal in asymptomatic Parkin mutation carriers: A TMS study
- T. Bäumer, P. P. Pramstaller, H. R. Siebner, S. Schippling, J. Hagenah, M. Peller, C. Gerloff, C. Klein, and A. Münchau
Neurology 2007; 69: 1976-1981.
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- ARTICLES
Dietary patterns and risk of dementia: The Three-City cohort study
- P. Barberger-Gateau, C. Raffaitin, L. Letenneur, C. Berr, C. Tzourio, J. F. Dartigues, and A. Alpérovitch
Neurology 2007; 69: 1921-1930.
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- EDITORIALS
Lrrk2 in the limelight!
- Matthew J. Farrer
Neurology 2007; 69: 1732-1733.
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- ARTICLES
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8
- W. C. Nichols, V. E. Elsaesser, N. Pankratz, M. W. Pauciulo, D. K. Marek, C. A. Halter, A. Rudolph, C. W. Shults, T. Foroud For the Parkinson Study Group– PROGENI Investigators
Neurology 2007; 69: 1737-1744.
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- ARTICLES
 -Synuclein and Parkinson disease susceptibility
- S. Winkler, J. Hagenah, S. Lincoln, M. Heckman, K. Haugarvoll, K. Lohmann-Hedrich, V. Kostic, M. Farrer, and C. Klein
Neurology 2007; 69: 1745-1750.
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- ARTICLES
The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: Is there a gender effect?
- A. Orr-Urtreger, C. Shifrin, U. Rozovski, S. Rosner, D. Bercovich, T. Gurevich, H. Yagev-More, A. Bar-Shira, and N. Giladi
Neurology 2007; 69: 1595-1602.
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- ARTICLES
Hormone therapy in menopausal women with cognitive complaints: A randomized, double-blind trial
- P. M. Maki, M. J. Gast, A. J. Vieweg, S. W. Burriss, and K. Yaffe
Neurology 2007; 69: 1322-1330.
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- EDITORIALS
Parental transmission of multiple sclerosis: Maternal, paternal, or neither?
- Maria Giovanna Marrosu
Neurology 2007; 69: 1202-1203.
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- ARTICLES
Parental transmission of MS in a population-based Canadian cohort
- B. M. Herrera, S. V. Ramagopalan, S. Orton, M. J. Chao, I. M. Yee, A. D. Sadovnick, and G. C. Ebers
Neurology 2007; 69: 1208-1212.
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- ARTICLES
Clinical characterization of the HOXA1 syndrome BSAS variant
- T. M. Bosley, M. A. Salih, I. A. Alorainy, D. T. Oystreck, M. Nester, K. K. Abu-Amero, M. A. Tischfield, and E. C. Engle
Neurology 2007; 69: 1245-1253.
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