|
All Epilepsy/Seizures
Citations 61-70 of 642 total displayed.
|
Past content
(since Jan 2000):
|
- ARTICLES
Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features
- Michael J. Rosanoff and Ruth Ottman
Neurology 2008; 71: 567-571.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Treating obstructive sleep apnea in adults with epilepsy: A randomized pilot trial
- B. A. Malow, N. Foldvary-Schaefer, B. V. Vaughn, L. M. Selwa, R. D. Chervin, K. J. Weatherwax, L. Wang, and Y. Song
Neurology 2008; 71: 572-577.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Drowning in people with epilepsy: How great is the risk?
- G. S. Bell, A. Gaitatzis, C. L. Bell, A. L. Johnson, and J. W. Sander
Neurology 2008; 71: 578-582.
[Abstract]
[Full text]
[PDF]
- RESIDENT AND FELLOW SECTION
Pearls & Oy-sters: Selective postictal aphasia: Cerebral language organization in bilingual patients
- Yasser Aladdin, Thomas J. Snyder, and S. Nizam Ahmed
Neurology 2008; 71: e14-17e.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Generic substitution in the treatment of epilepsy: Case evidence of breakthrough seizures
- M. J. Berg, R. A. Gross, K. J. Tomaszewski, W. M. Zingaro, and L. S. Haskins
Neurology 2008; 71: 525-530.
[Abstract]
[Full text]
[PDF]
- NEUROIMAGES
Interictal hypermetabolic subcortical band on brain FDG-PET in doublecortin mutation
- Joanna Fong, Guiyun Wu, Elaine Wyllie, and Ajay Gupta
Neurology 2008; 71: 535.
[Full text]
[PDF]
- NEUROIMAGES
Susceptibility-weighted imaging in familial cerebral cavernous malformations
- Alex D. Cooper, Norbert G. Campeau, and Irene Meissner
Neurology 2008; 71: 382.
[Full text]
[PDF]
- ARTICLES
Topiramate in pregnancy: Preliminary experience from the UK Epilepsy and Pregnancy Register
- S. Hunt, A. Russell, W. H. Smithson, L. Parsons, I. Robertson, R. Waddell, B. Irwin, P. J. Morrison, J. Morrow, and J. Craig
Neurology 2008; 71: 272-276.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Outcome and predictors of interstitial radiosurgery in the treatment of gelastic epilepsy
- A. Schulze-Bonhage, M. Trippel, K. Wagner, T. Bast, F. V. Deimling, A. Ebner, C. Elger, T. Mayer, R. Keimer, B. J. Steinhoff, J. Spreer, S. Fauser, and C. Ostertag
Neurology 2008; 71: 277-282.
[Abstract]
[Full text]
[PDF]
- ARTICLES
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes
- B. A. Neubauer, S. Waldegger, J. Heinzinger, A. Hahn, G. Kurlemann, B. Fiedler, F. Eberhard, H. Muhle, U. Stephani, S. Garkisch, O. Eeg-Olofsson, U. Müller, and T. Sander
Neurology 2008; 71: 177-183.
[Abstract]
[Full text]
[PDF]
|
|
