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All Clinical Neurology
Citations 131-140 of 227 total displayed.
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Past content
(since Mar 2001):
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- ARTICLES
Mesopontine cholinergic neuron involvement in Lewy body dementia and multiple system atrophy
- A. M. Schmeichel, L. C. Buchhalter, P. A. Low, J. E. Parisi, B. W. Boeve, P. Sandroni, and E. E. Benarroch
Neurology 2008; 70: 368-373.
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- 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.
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- EDITORIALS
MS and cognition and APOE: The ongoing conundrum about biomarkers
- A. Dessa Sadovnick and Daniel H. Jacobs
Neurology 2008; 70: 164-165.
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- ARTICLES
APOE  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.
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- 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.
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- 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.
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- 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.
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- 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.
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- 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.
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- 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.
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