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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 2
1993 3
1995 1
1996 1
1997 1
1998 1
1999 1
2000 1
2001 4
2002 3
2003 4
2004 1
2005 3
2006 2
2007 3
2008 1
2009 1
2010 1
2011 3
2012 4
2013 2
2016 3
2017 1
2018 2
2019 2
2022 1
2024 0

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8 results

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Filters applied: Meta-Analysis, Review, Systematic Review, in the last 10 years. Clear all
Page 1
The glucose transporter type 1 (Glut1) syndromes.
Koch H, Weber YG. Koch H, et al. Epilepsy Behav. 2019 Feb;91:90-93. doi: 10.1016/j.yebeh.2018.06.010. Epub 2018 Jul 31. Epilepsy Behav. 2019. PMID: 30076047 Review.
A special form of transient movement disorders, the paroxysmal exertion-induced dyskinesia (PED), absence epilepsies particularly with an early onset absence epilepsy (EOAE) and childhood absence epilepsy (CAE), myoclonic astatic epilepsy (MAE), episodic chor …
A special form of transient movement disorders, the paroxysmal exertion-induced dyskinesia (PED), absence epilepsies particularly with an ea …
SCN1A Seizure Disorders.
Miller IO, Sotero de Menezes MA. Miller IO, et al. 2007 Nov 29 [updated 2022 Feb 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2007 Nov 29 [updated 2022 Feb 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301494 Free Books & Documents. Review.
Phenotypes with intractable seizures including Dravet syndrome are often associated with cognitive decline. Less commonly observed phenotypes include myoclonic astatic epilepsy (MAE), Lennox-Gastaut syndrome, infantile spasms, epilepsy with focal seizures, an …
Phenotypes with intractable seizures including Dravet syndrome are often associated with cognitive decline. Less commonly observed phenotype …
SYNGAP1-Related Intellectual Disability.
Holder JL Jr, Hamdan FF, Michaud JL. Holder JL Jr, et al. 2019 Feb 21. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2019 Feb 21. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 30789692 Free Books & Documents. Review.
The epilepsy is generalized; a subset of individuals with epilepsy have myoclonic astatic epilepsy (Doose syndrome) or epilepsy with myoclonic absences. ...
The epilepsy is generalized; a subset of individuals with epilepsy have myoclonic astatic epilepsy (Doose syndrome) or …
Ketogenic Diets in the Treatment of Epilepsy.
Elia M, Klepper J, Leiendecker B, Hartmann H. Elia M, et al. Curr Pharm Des. 2017;23(37):5691-5701. doi: 10.2174/1381612823666170809101517. Curr Pharm Des. 2017. PMID: 28799513 Review.
Preliminary findings indicate that KDs may be specifically effective in some epileptic syndromes, such as West syndrome, severe myoclonic epilepsy of infancy, myoclonic-astatic epilepsy, febrile infection related epileptic syndrome, and drug-resistant idiopat …
Preliminary findings indicate that KDs may be specifically effective in some epileptic syndromes, such as West syndrome, severe myoclonic ep …
Glucose Transporter Type 1 Deficiency Syndrome.
Wang D, Pascual JM, De Vivo D. Wang D, et al. 2002 Jul 30 [updated 2018 Mar 1]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2002 Jul 30 [updated 2018 Mar 1]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301603 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: The phenotypic spectrum of glucose transporter type 1 deficiency syndrome (Glut1 DS) is now known to be a continuum that includes the classic phenotype as well as paroxysmal exercise-induced dyskinesia and epilepsy (previously known as dystonia 18 [DYT18 …
CLINICAL CHARACTERISTICS: The phenotypic spectrum of glucose transporter type 1 deficiency syndrome (Glut1 DS) is now known to be a continuu …
The changing face of dietary therapy for epilepsy.
Pasca L, De Giorgis V, Macasaet JA, Trentani C, Tagliabue A, Veggiotti P. Pasca L, et al. Eur J Pediatr. 2016 Oct;175(10):1267-76. doi: 10.1007/s00431-016-2765-z. Epub 2016 Sep 1. Eur J Pediatr. 2016. PMID: 27586246 Review.
Ketogenic diet represents the treatment of choice for GLUT-1 deficiency syndrome and pyruvate dehydrogenase complex deficiency. Infantile spasms, Dravet syndrome and myoclonic-astatic epilepsy are epilepsy syndromes for which ketogenic diet should be consider …
Ketogenic diet represents the treatment of choice for GLUT-1 deficiency syndrome and pyruvate dehydrogenase complex deficiency. Infantile sp …
Non-pharmacological medical treatment in pediatric epilepsies.
Auvin S. Auvin S. Rev Neurol (Paris). 2016 Mar;172(3):182-5. doi: 10.1016/j.neurol.2015.12.009. Epub 2016 Mar 15. Rev Neurol (Paris). 2016. PMID: 26993568 Review.
It can be used during the investigation for epilepsy surgery even in case of structural abnormalities. In some epilepsy syndromes such as infantile spasms, myoclonic-astatic epilepsy and refractory status epilepticus, an early use seems helpful. ...
It can be used during the investigation for epilepsy surgery even in case of structural abnormalities. In some epilepsy syndromes such as in …
Late-onset periodic bradycardia during vagus nerve stimulation in a pediatric patient. A new case and review of the literature.
Cantarín-Extremera V, Ruíz-Falcó-Rojas ML, Tamaríz-Martel-Moreno A, García-Fernández M, Duat-Rodriguez A, Rivero-Martín B. Cantarín-Extremera V, et al. Eur J Paediatr Neurol. 2016 Jul;20(4):678-83. doi: 10.1016/j.ejpn.2016.02.014. Epub 2016 Mar 16. Eur J Paediatr Neurol. 2016. PMID: 27056279 Review.
We report a new child where vagally induced bradyarrhythmia, perfectly correlated with the stimulation periods. CLINICAL REPORT: 13-year-old girl with refractory myoclonic-astatic epilepsy since the age of two. When she was five years old, a VNS was implanted …
We report a new child where vagally induced bradyarrhythmia, perfectly correlated with the stimulation periods. CLINICAL REPORT: 13-year-old …