Results 261 to 270 of about 356,587 (360)

Comparison of children and adults undergoing subdural grid electrode implantation or stereoelectroencephalography in a refractory epilepsy cohort from four European centers

Epilepsia, EarlyView.
Abstract Objective Children with refractory focal epilepsy differ from adults, although many centers will offer invasive electroencephalography (iEEG) to both. Outcomes in terms of likelihood of resection and subsequent seizure outcome after either subdural grid electrode implantation (SDE) or stereoelectroencephalography (SEEG) have, however, not been
Matea Rados, Shanice Beerepoot, Martin M. Tisdall, Ronit M. Pressler, J. Helen Cross, Rachel C. Thornton, Beate Diehl, Andrew W. McEvoy, Anna Miserocchi, Josemir W. Sander, John S. Duncan, Jane de Tisi, Francesco Cardinale, Laura Tassi, Giorgio Lo Russo, Stefano Francione, Herm J. Lamberink, Frans S. S. Leijten, Willem M. Otte, Sandra M. A. van der Salm, Kees P. J. Braun, Pieter van Eijsden   +21 more
wiley   +1 more source

IFIH1 variants are associated with generalised epilepsy preceded by febrile seizures. [PDF]

J Med Genet
Song W, Bian WJ, Li H, Guo QH, Wang J, Tang B, Zhang JY, Wei W, Liu XR, Liao WP, Li B, He N.   +11 more
europepmc   +1 more source

Serial MRI after experimental febrile seizures: Altered T2 signal without neuronal death [PDF]

, 2004
Céline Dubé, Hon J. Yu, Orhan Nalcioğlu, Tallie Z. Baram   +3 more
openalex   +1 more source

Familial SYNGAP1 variants define the boundaries of a complex neurodevelopmental disorder with epilepsy

Epilepsia, EarlyView.
Abstract Objective SYNGAP1‐related disorders are common neurodevelopmental conditions characterized by autism spectrum disorder, developmental delay, intellectual disability, and a range of generalized seizure types. Disease‐causing variants in SYNGAP1 typically occur de novo. This study aims to characterize inherited cases of SYNGAP1‐related disorders.
Alicia G. Harrison, Jan H. Magielski, Ian McSalley, Shiva Ganesan, Anna J. Prentice, Kristin G. Cunningham, Samuel R. Pierce, Michael J. Boland, Benjamin L. Prosser, Ingo Helbig, Jillian L. McKee   +10 more
wiley   +1 more source

Differential diagnostic value of electroencephalogram combined with NSE in pediatric febrile seizures and its predictive value for brain function prognosis. [PDF]

Am J Transl Res
Cao J, Xiao X, Li S.
europepmc   +1 more source

Iron Status: A Possible Risk Factor for the First Febrile Seizure

, 2002
Azhar S. Daoud, Anwar Batieha, Faisel Abu‐Ekteish, Nayef S. Gharaibeh, Saleh Ajlouni, Saad Hijazi   +5 more
openalex   +1 more source

An overview of epilepsy with a focus on the effects and implications of the condition for children and their families [PDF]

, 2009
Featherstone, VA
core   +1 more source

SCN9A should not be considered an epilepsy gene; Refuting a gene–disease association

Epilepsia, EarlyView.
Abstract Objective The SCN9A gene is primarily expressed in nociceptive pathways within the peripheral nervous system, and pathogenic variants are associated with human pain disorders. In recent years, several studies have proposed SCN9A as a monogenic cause of epilepsy.
Ismael Ghanty, Eduardo Perez‐Palma, Camilo Villaman, Daniel Stobo, Joseph Symonds, Sameer Zuberi, Dennis Lal, Andreas Brunklaus   +7 more
wiley   +1 more source

Clinical Significance of Lumbar Puncture in Children with First Febrile Seizures. [PDF]

Iran J Child Neurol
Kim YZ, Jung HW, Lee EH.
europepmc   +1 more source

Is routine EEG helpful in the management of complex febrile seizures? [PDF]

, 2004
Eduardo Cuestas
openalex   +1 more source