Absence seizures

Citations 1-5 of 5 total displayed.

Most recent content (27 May 2008):

ARTICLES
Novel mutations in Myoclonin1/EFHC1 in sporadic and familial juvenile myoclonic epilepsy

M. T. Medina, T. Suzuki, M. E. Alonso, R. M. Durón, I. E. Martínez-Juárez, J. N. Bailey, D. Bai, Y. Inoue, I. Yoshimura, S. Kaneko, M. C. Montoya, A. Ochoa, A. Jara Prado, M. Tanaka, J. Machado-Salas, S. Fujimoto, M. Ito, S. Hamano, K. Sugita, Y. Ueda, M. Osawa, H. Oguni, F. Rubio-Donnadieu, K. Yamakawa, and A. V. Delgado-Escueta
Neurology 2008; 70: 2137-2144. [Abstract] [Full text] [PDF]  

Past content (since Sep 2003):

ARTICLES
Electroclinical features of absence seizures in childhood absence epilepsy

L. G. Sadleir, K. Farrell, S. Smith, M. B. Connolly, and I. E. Scheffer
Neurology 2006; 67: 413-418. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Idiopathic generalized epilepsy and choice of antiepileptic drugs

Selim R. Benbadis, William O. Tatum, IV, and Maria Gieron
Neurology 2003; 61: 1793-1795. [Abstract] [Full text] [PDF]  

ARTICLES
Genetic influences on myoclonic and absence seizures

M. R. Winawer, D. Rabinowitz, T. A. Pedley, W. A. Hauser, and R. Ottman
Neurology 2003; 61: 1576-1581. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy

D. Audenaert, L. Claes, B. Ceulemans, A. Löfgren, C. Van Broeckhoven, and P. De Jonghe
Neurology 2003; 61: 854-856. [Abstract] [Full text] [PDF]