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All Genetics
Citations 81-90 of 679 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Interrelationships among the MTHFR 677C>T polymorphism, migraine, and cardiovascular disease
- Markus Schürks, Robert Y.L. Zee, Julie E. Buring, and Tobias Kurth
Neurology 2008; 71: 505-513.
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- ARTICLES
SPG11 compound mutations in spastic paraparesis with thin corpus callosum
- L. Samaranch, M. Riverol, J. C. Masdeu, E. Lorenzo, J. M. Vidal-Taboada, J. Irigoyen, M. A. Pastor, P. de Castro, and P. Pastor
Neurology 2008; 71: 332-336.
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- SPECIAL ARTICLES: INVITED ARTICLES
Invited Article: The expanding impact of molecular biology on the diagnosis and treatment of gliomas
- Warren P. Mason and J. Gregory Cairncross
Neurology 2008; 71: 365-373.
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- NEUROIMAGES
Susceptibility-weighted imaging in familial cerebral cavernous malformations
- Alex D. Cooper, Norbert G. Campeau, and Irene Meissner
Neurology 2008; 71: 382.
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- ARTICLES
Progranulin genetic variability contributes to amyotrophic lateral sclerosis
- K. Sleegers, N. Brouwers, S. Maurer-Stroh, M. A. van Es, P. Van Damme, P.W.J. van Vught, J. van der Zee, S. Serneels, T. De Pooter, M. Van den Broeck, M. Cruts, J. Schymkowitz, P. De Jonghe, F. Rousseau, L. H. van den Berg, W. Robberecht, and C. Van Broeckhoven
Neurology 2008; 71: 253-259.
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- ARTICLES
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes
- B. A. Neubauer, S. Waldegger, J. Heinzinger, A. Hahn, G. Kurlemann, B. Fiedler, F. Eberhard, H. Muhle, U. Stephani, S. Garkisch, O. Eeg-Olofsson, U. Müller, and T. Sander
Neurology 2008; 71: 177-183.
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- EDITORIALS
Detecting Alzheimer disease before it happens: The key to prevention?
- Joseph Quinn and Marwan N. Sabbagh
Neurology 2008; 71: 78-79.
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- ARTICLES
Biochemical markers in persons with preclinical familial Alzheimer disease
- J. M. Ringman, S. G. Younkin, D. Pratico, W. Seltzer, G. M. Cole, D. H. Geschwind, Y. Rodriguez-Agudelo, B. Schaffer, J. Fein, S. Sokolow, E. R. Rosario, K. H. Gylys, A. Varpetian, L. D. Medina, and J. L. Cummings
Neurology 2008; 71: 85-92.
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- ARTICLES
Reduced brain choline in homocystinuria due to remethylation defects
- F. -G. Debray, Y. Boulanger, A. Khiat, J. -C. Decarie, J. Orquin, M. -S. Roy, A. Lortie, F. Ramos, N. M. Verhoeven, E. Struys, H. J. Blom, C. Jakobs, E. Levy, G. A. Mitchell, and M. Lambert
Neurology 2008; 71: 44-49.
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- ARTICLES
Sensitivity and specificity of decreased CSF asialotransferrin for eIF2B-related disorder
- A. Vanderver, Y. Hathout, J. Maletkovic, E. S. Gordon, M. Mintz, M. Timmons, E. P. Hoffman, L. Horzinski, F. Niel, A. Fogli, O. Boespflug-Tanguy, and R. Schiffmann
Neurology 2008; 70: 2226-2232.
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