|
Cortical dysplasia
Citations 51-56 of 56 total displayed.
|
Past content
(since Jul 2001):
|
- 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.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Anterior commissure absence without callosal agenesis: A new brain malformation
- T. N. Mitchell, J. M. Stevens, S. L. Free, J. W. Sander, S. D. Shorvon, and S. M. Sisodiya
Neurology 2002; 58: 1297-1299.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- VIEWS & REVIEWS
Classification system for malformations of cortical development: Update 2001
- A. J. Barkovich, R. I. Kuzniecky, G. D. Jackson, R. Guerrini, and W. B. Dobyns
Neurology 2001; 57: 2168-2178.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Fluid-attenuated inversion recovery: Correlations of hippocampal cell densities with signal abnormalities
- B. Diehl, I. Najm, A. Mohamed, E. Wyllie, T. Babb, Z. Ying, A. Hilbig, W. Bingaman, H. O. Lüders, and P. Ruggieri
Neurology 2001; 57: 1029-1032.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene
- L. Demelas, G. Serra, M. Conti, A. Achene, C. Mastropaolo, N. Matsumoto, L.L. Dudlicek, P.L. Mills, W.B. Dobyns, D.H. Ledbetter, and S. Das
Neurology 2001; 57: 327-330.
[Abstract]
[Full text]
[PDF]
|
|
