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Neurology
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All Clinical Neurology

Citations 131-140 of 226 total displayed.

Past content (since Mar 2001):

CLINICAL/SCIENTIFIC NOTES
THE FIRST CEREBROTENDINOUS XANTHOMATOSIS FAMILY FROM ARGENTINA: A NEW MUTATION IN CYP27A1 GENE
M. Szlago, G. N. Gallus, A. Schenone, M. E. Patiño, Z. Sfaelo, A. Rufa, P. Da Pozzo, E. Cardaioli, M. T. Dotti, and A. Federico
Neurology 2008; 70: 402-404. [Full text] [PDF]  

EDITORIALS
MS and cognition and APOE: The ongoing conundrum about biomarkers
A. Dessa Sadovnick and Daniel H. Jacobs
Neurology 2008; 70: 164-165. [Full text] [PDF]  

ARTICLES
APOE {varepsilon}4 allele is associated with cognitive impairment in patients with multiple sclerosis
J. Shi, C. B. Zhao, T. L. Vollmer, T. M. Tyry, and S. M. Kuniyoshi
Neurology 2008; 70: 185-190. [Abstract] [Full text] [PDF]  

ARTICLES
Cortical areas involved in Arabic number reading
F. -E. Roux, V. Lubrano, V. Lauwers-Cances, C. Giussani, and J. -F. Démonet
Neurology 2008; 70: 210-217. [Abstract] [Full text] [PDF]  

ARTICLES
Elevated plasma homocysteine levels in patients with amyotrophic lateral sclerosis
S. Zoccolella, I. L. Simone, P. Lamberti, V. Samarelli, R. Tortelli, L. Serlenga, and G. Logroscino
Neurology 2008; 70: 222-225. [Abstract] [Full text] [PDF]  

ARTICLES
Joint effect of stroke and APOE 4 on dementia risk: The Canadian Study of Health and Aging
Y. P. Jin, T. Østbye, J. W. Feightner, S. Di Legge, and V. Hachinski
Neurology 2008; 70: 9-16. [Abstract] [Full text] [PDF]  

ARTICLES
What causes paramyotonia in the United Kingdom?: Common and new SCN4A mutations revealed
E. Matthews, S. V. Tan, D. Fialho, M. G. Sweeney, R. Sud, A. Haworth, E. Stanley, G. Cea, M. B. Davis, and M. G. Hanna
Neurology 2008; 70: 50-53. [Abstract] [Full text] [PDF]  

ARTICLES
Altered functional and structural connectivities in patients with MS: A 3-T study
M. A. Rocca, E. Pagani, M. Absinta, P. Valsasina, A. Falini, G. Scotti, G. Comi, and M. Filippi
Neurology 2007; 69: 2136-2145. [Abstract] [Full text] [PDF]  

ARTICLES
Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine
B. de Vries, T. Freilinger, K.R.J. Vanmolkot, J. B. Koenderink, A. H. Stam, G. M. Terwindt, E. Babini, E. H. van den Boogerd, J. J.M.W. van den Heuvel, R. R. Frants, J. Haan, M. Pusch, A. M.J.M. van den Maagdenberg, M. D. Ferrari, and M. Dichgans
Neurology 2007; 69: 2170-2176. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
FERTILITY IN WOMEN WITH ACTIVE EPILEPSY
Katriina Viinikainen, Seppo Heinonen, Kai Eriksson, and Reetta Kälviäinen
Neurology 2007; 69: 2107-2108. [Full text] [PDF]  

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