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All Epilepsy/Seizures
Citations 551-560 of 642 total displayed.
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Past content
(since Jan 2000):
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- ARTICLES
Predicting surgical outcome in temporal lobe epilepsy patients using MRI and MRSI
- S. B. Antel, L. M. Li, F. Cendes, D. L. Collins, R. E. Kearney, R. Shinghal, and D. L. Arnold
Neurology 2002; 58: 1505-1512.
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- BRIEF COMMUNICATIONS
Rapidly progressive hippocampal atrophy: Evidence for a seizure-induced mechanism
- G. A. Worrell, D. Sencakova, C. R. Jack, K. D. Flemming, J. R. Fulgham, and E. L. So
Neurology 2002; 58: 1553-1556.
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- BRIEF COMMUNICATIONS
Males with epilepsy, complete subcortical band heterotopia, and somatic mosaicism for DCX
- N. P. Poolos, S. Das, G. D. Clark, D. Lardizabal, J. L. Noebels, E. Wyllie, and W. B. Dobyns
Neurology 2002; 58: 1559-1562.
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- VIEWS & REVIEWS
Seizure-like phenomena and propofol: A systematic review
- Bernhard Walder, Martin R. Tramèr, and Margitta Seeck
Neurology 2002; 58: 1327-1332.
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- ARTICLES
Resection of the lesion in patients with hypothalamic hamartomas and catastrophic epilepsy
- A. Palmini, C. Chandler, F. Andermann, J. Costa da Costa, E. Paglioli–Neto, C. Polkey, B. Rosenblatt, J. Montes, J. V. Martínez, J. P. Farmer, B. Sinclair, K. Aronyk, E. Paglioli, L. Coutinho, S. Raupp, and M. Portuguez
Neurology 2002; 58: 1338-1347.
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- BRIEF COMMUNICATIONS
Generalized epilepsy with febrile seizures plus: Mutation of the sodium channel subunit SCN1B
- R. H. Wallace, I. E. Scheffer, G. Parasivam, S. Barnett, G. B. Wallace, G. R. Sutherland, S. F. Berkovic, and J. C. Mulley
Neurology 2002; 58: 1426-1429.
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- BRIEF COMMUNICATIONS
Familial temporal lobe epilepsy with febrile seizures
- C. Depondt, W. Van Paesschen, G. Matthijs, E. Legius, K. Martens, P. Demaerel, and G. Wilms
Neurology 2002; 58: 1429-1433.
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- ARTICLES
Epilepsy, cysticercosis, and toxocariasis: A population-based case-control study in rural Bolivia
- A. Nicoletti, A. Bartoloni, A. Reggio, F. Bartalesi, M. Roselli, V. Sofia, J. Rosado Chavez, H. Gamboa Barahona, F. Paradisi, G. Cancrini, V. C.W. Tsang, and A. J. Hall
Neurology 2002; 58: 1256-1261.
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- BRIEF COMMUNICATIONS
Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy
- T. Sugawara, E. Mazaki–Miyazaki, K. Fukushima, J. Shimomura, T. Fujiwara, S. Hamano, Y. Inoue, and K. Yamakawa
Neurology 2002; 58: 1122-1124.
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- ARTICLES
Familial periventricular heterotopia: Missense and distal truncating mutations of the FLN1 gene
- F. Moro, R. Carrozzo, P. Veggiotti, G. Tortorella, D. Toniolo, A. Volzone, and R. Guerrini
Neurology 2002; 58: 916-921.
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