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All Clinical Neurology
Citations 151-160 of 226 total displayed.
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Past content
(since Mar 2001):
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- EDITORIALS
Neutralizing antibodies to biological therapies: A "touch of gray" vs a "black and white" story
- Mark S. Freedman and Andrew R. Pachner
Neurology 2007; 69: 1386-1387.
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- ARTICLES
Minocycline treatment in acute stroke: An open-label, evaluator-blinded study
- Y. Lampl, M. Boaz, R. Gilad, M. Lorberboym, R. Dabby, A. Rapoport, M. Anca-Hershkowitz, and M. Sadeh
Neurology 2007; 69: 1404-1410.
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- ARTICLES
Serum uric acid and brain ischemia in normal elderly adults
- D. J. Schretlen, A. B. Inscore, T. D. Vannorsdall, M. Kraut, G. D. Pearlson, B. Gordon, and H. A. Jinnah
Neurology 2007; 69: 1418-1423.
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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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- ARTICLES
Electrographic seizures and periodic discharges after intracerebral hemorrhage
- J. Claassen, N. Jetté, F. Chum, R. Green, M. Schmidt, H. Choi, J. Jirsch, J. A. Frontera, E. Sander Connolly, R. G. Emerson, S. A. Mayer, and L. J. Hirsch
Neurology 2007; 69: 1356-1365.
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- REFLECTIONS: NEUROLOGY AND THE HUMANITIES
Black substance
- Dawn McGuire
Neurology 2007; 69: 1380.
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- ARTICLES
Prominent brain axonal damage and functional reorganization in "pure" adrenomyeloneuropathy
- S. Marino, M. De Luca, M. T. Dotti, M. L. Stromillo, P. Formichi, P. Galluzzi, M. Mondelli, P. Bramanti, A. Federico, and N. De Stefano
Neurology 2007; 69: 1261-1269.
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- ARTICLES
Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease
- L. N. Clark, B. M. Ross, Y. Wang, H. Mejia-Santana, J. Harris, E. D. Louis, L. J. Cote, H. Andrews, S. Fahn, C. Waters, B. Ford, S. Frucht, R. Ottman, and K. Marder
Neurology 2007; 69: 1270-1277.
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- VIEWS AND REVIEWS
Phenotypic clustering of lamin A/C mutations in neuromuscular patients
- S. Benedetti, I. Menditto, M. Degano, C. Rodolico, L. Merlini, A. D’Amico, L. Palmucci, A. Berardinelli, E. Pegoraro, C. P. Trevisan, L. Morandi, I. Moroni, G. Galluzzi, E. Bertini, A. Toscano, M. Olivè, G. Bonne, F. Mari, R. Caldara, R. Fazio, I. Mammì, P. Carrera, D. Toniolo, G. Comi, A. Quattrini, M. Ferrari, and S. C. Previtali
Neurology 2007; 69: 1285-1292.
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- ARTICLES
Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan
- M. Okada, G. Kawahara, S. Noguchi, K. Sugie, K. Murayama, I. Nonaka, Y. K. Hayashi, and I. Nishino
Neurology 2007; 69: 1035-1042.
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