Continuous spikes and waves during slow sleep in a child with karyotype 47, XYY

2014 ◽  
Vol 16 (2) ◽  
pp. 223-226
Author(s):  
Vittoria Cianci ◽  
Edoardo Ferlazzo ◽  
Giuseppe De Martino ◽  
Angela Vinci ◽  
Sara Gasparini ◽  
...  
Brain ◽  
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Vol 134 (5) ◽  
pp. e177-e177 ◽  
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S. Goldman ◽  
P. Van Bogaert

2013 ◽  
Vol 105 (1-2) ◽  
pp. 164-173 ◽  
Author(s):  
Roberto Horacio Caraballo ◽  
Pierangelo Veggiotti ◽  
María C. Kaltenmeier ◽  
Elena Piazza ◽  
Beatriz Gamboni ◽  
...  

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J.J. Ortega-Albás ◽  
J.L. Tripiana ◽  
M. Gil-Marqués ◽  
R. Salas-Pascual ◽  
...  

Epilepsia ◽  
2009 ◽  
Vol 50 (5) ◽  
pp. 1127-1131 ◽  
Author(s):  
Marina Nikanorova ◽  
Maria J. Miranda ◽  
Mary Atkins ◽  
Lene Sahlholdt

1996 ◽  
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A.-K. Wetterquist ◽  
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2008 ◽  
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pp. 489-491
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Meriem K. Bensalem-Owen ◽  
Toufic A. Fakhoury

Author(s):  
Michael Drees ◽  
Neil Kulkarni ◽  
Jorge Vidaurre

AbstractElectrical status epilepticus during sleep (ESES) is an age-related, self-limited epileptic encephalopathy characterized by heterogeneous clinical manifestations and a specific electroencephalographic pattern of continuous spikes and waves during slow sleep. The etiology of ESES is not completely clear, although structural brain lesions, abnormal immunological markers, and genetic mutations have been associated with the syndrome. ESES was first described in 1971 and since then, the diagnostic criteria have changed multiple times. Additionally, inconsistency between authors in how to record and evaluate the electroencephalogram also leads to variability between studies. These inconsistencies hamper objectivity, comparison, and generalization. Because of this, one of the first priorities of physicians treating this condition should be defining the parameters of this disease so that cooperative building can occur.


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