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Neurology
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Cortical dysplasia

Citations 1-10 of 50 total displayed.

Most recent content (18 Nov 2008):

ARTICLES
SEEG-guided thermocoagulations: A palliative treatment of nonoperable partial epilepsies
H. Catenoix, F. Mauguière, M. Guénot, P. Ryvlin, A. Bissery, M. Sindou, and J. Isnard
Neurology 2008; 71: 1719-1726. [Abstract] [Full text] [PDF]  

Past content (since Jul 2001):

ARTICLES
FDG-PET/MRI coregistration improves detection of cortical dysplasia in patients with epilepsy
N. Salamon, J. Kung, S. J. Shaw, J. Koo, S. Koh, J. Y. Wu, J. T. Lerner, R. Sankar, W. D. Shields, J. Engel, Jr, I. Fried, H. Miyata, W. H. Yong, H. V. Vinters, and G. W. Mathern
Neurology 2008; 71: 1594-1601. [Abstract] [Full text] [PDF]  

ARTICLES
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debré type
L. Van Maldergem, M. Yuksel-Apak, H. Kayserili, E. Seemanova, S. Giurgea, L. Basel-Vanagaite, E. Leao-Teles, J. Vigneron, M. Foulon, M. Greally, J. Jaeken, S. Mundlos, and W. B. Dobyns
Neurology 2008; 71: 1602-1608. [Abstract] [Full text] [PDF]  

ARTICLES
Subdural electrode analysis in focal cortical dysplasia: Predictors of surgical outcome
P. Widdess-Walsh, L. Jeha, D. Nair, P. Kotagal, W. Bingaman, and I. Najm
Neurology 2007; 69: 660-667. [Abstract] [Full text] [PDF]  

EDITORIALS
Smooth mosaics: Genotype and phenotype in lissencephaly
Hans H. Jung
Neurology 2007; 69: 425-426. [Full text] [PDF]  

ARTICLES
Location and type of mutation in the LIS1 gene do not predict phenotypic severity
G. Uyanik, D. J. Morris-Rosendahl, J. Stiegler, J. Klapecki, C. Gross, Y. Berman, P. Martin, L. Dey, S. Spranger, G. C. Korenke, I. Schreyer, C. Hertzberg, T. E. Neumann, P. Burkart, C. Spaich, M. Meng, H. Holthausen, L. Adès, J. Seidel, E. Mangold, G. Buyse, P. Meinecke, U. Schara, C. Zeschnigk, D. Muller, G. Helland, B. Schulze, M. L. Wright, S. Kortge-Jung, A. Hehr, U. Bogdahn, G. Schuierer, J. Kohlhase, L. Aigner, G. Wolff, U. Hehr, and J. Winkler
Neurology 2007; 69: 442-447. [Abstract] [Full text] [PDF]  

ARTICLES
Multiplex ligation-dependent probe amplification detects DCX gene deletions in band heterotopia
D. Mei, E. Parrini, M. Pasqualetti, G. Tortorella, E. Franzoni, U. Giussani, C. Marini, S. Migliarini, and R. Guerrini
Neurology 2007; 68: 446-450. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Pathologic and physiologic function in the subcortical band of double cortex
R. S. Briellmann, T. Little, A. S. Harvey, D. F. Abbott, R. Jacobs, A. B. Waites, and G. D. Jackson
Neurology 2006; 67: 1090-1093. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Periventricular heterotopia in fragile X syndrome
F. Moro, T. Pisano, B. Dalla Bernardina, R. Polli, A. Murgia, L. Zoccante, F. Darra, A. Battaglia, T. Pramparo, O. Zuffardi, and R. Guerrini
Neurology 2006; 67: 713-715. [Abstract] [Full text] [PDF]  

NEUROIMAGES
Extravasation of hyperalimentation into the spinal epidural space from a central venous line
M. Scott Perry and Lisa Billars
Neurology 2006; 67: 715. [Full text] [PDF]  

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* Related collections:
 Epilepsy/Seizures
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 Antiepileptic drugs
 EEG
 Epilepsy monitoring
 Epilepsy semiology
 Intracranial electrodes
 Epilepsy surgery
 WADA test
 Hippocampal sclerosis
 Video/ EEG use in epilepsy
 Epileptogenic zone
 Cortical localization
 Functional neuroimaging
 PET in epilepsy
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 Volumetric MRI use in epilepsy
 Generalized seizures
 Partial seizures
 Vagus nerve stimulation
 Neonatal seizures
 Status epilepticus
 Infantile spasms
 Absence seizures
 Complex partial seizures
 Nonepileptic seizures
 Cortical dysplasia


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