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Neurology
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All Genetics

Citations 121-130 of 679 total displayed.

Past content (since Jan 2001):

ARTICLES
{alpha}-Synuclein gene duplication is present in sporadic Parkinson disease
T. -B. Ahn, S. Y. Kim, J. Y. Kim, S. -S. Park, D. S. Lee, H. J.. Min, Y. K. Kim, S. E. Kim, J. -M. Kim, H. -J. Kim, J. Cho, and B. S. Jeon
Neurology 2008; 70: 43-49. [Abstract] [Full text] [PDF]  

ARTICLES
A structural basis for reading fluency: White matter defects in a genetic brain malformation
B. S. Chang, T. Katzir, T. Liu, K. Corriveau, M. Barzillai, K. A. Apse, A. Bodell, D. Hackney, D. Alsop, S. Wong, and C. A. Walsh
Neurology 2007; 69: 2146-2154. [Abstract] [Full text] [PDF]  

VIEWS & REVIEWS
Parkinson disease, 10 years after its genetic revolution: Multiple clues to a complex disorder
Christine Klein and Michael G. Schlossmacher
Neurology 2007; 69: 2093-2104. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

EDITORIALS
Lrrk2 in the limelight!
Matthew J. Farrer
Neurology 2007; 69: 1732-1733. [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

ARTICLES
{alpha}-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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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* Related collections:
 Genetics
 All Genetics
 Neurofibromatosis
 Other neurocutaneous disorders
 Genetic linkage
 Association studies in genetics
 Gene expression studies
 Gene therapy
 Mitochondrial disorders
 Ion channel gene defects
 Spinocerebellar ataxia
 Trinucleotide repeat diseases
 Chromosomes


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