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Year Number of Results
1948 1
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1966 2
1967 4
1968 1
1969 8
1970 3
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1972 3
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1974 4
1975 17
1976 16
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1978 16
1979 25
1980 28
1981 23
1982 26
1983 30
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1988 31
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1992 79
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1998 120
1999 174
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2001 220
2002 232
2003 202
2004 206
2005 241
2006 284
2007 296
2008 299
2009 357
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2011 422
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2021 846
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2024 286

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11,357 results

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Quoted phrase not found in phrase index: "Epileptic encephalopathy, infantile or early childhood, 3"
Page 1
ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions.
Zuberi SM, Wirrell E, Yozawitz E, Wilmshurst JM, Specchio N, Riney K, Pressler R, Auvin S, Samia P, Hirsch E, Galicchio S, Triki C, Snead OC, Wiebe S, Cross JH, Tinuper P, Scheffer IE, Perucca E, Moshé SL, Nabbout R. Zuberi SM, et al. Epilepsia. 2022 Jun;63(6):1349-1397. doi: 10.1111/epi.17239. Epub 2022 May 3. Epilepsia. 2022. PMID: 35503712 Free article.
The incidence of epilepsy is high in this age group and epilepsy is frequently associated with significant comorbidities and mortality. ...Syndromes are separated into self-limited syndromes, where there is likely to be spontaneous remission and developmental and …
The incidence of epilepsy is high in this age group and epilepsy is frequently associated with significant comorbidities and m …
Genetic Epilepsy Syndromes.
Myers KA. Myers KA. Continuum (Minneap Minn). 2022 Apr 1;28(2):339-362. doi: 10.1212/CON.0000000000001077. Continuum (Minneap Minn). 2022. PMID: 35393962 Review.
PURPOSE OF REVIEW: This article reviews the clinical features, typical EEG findings, treatment, prognosis, and underlying molecular etiologies of the more common genetic epilepsy syndromes. Genetic generalized epilepsy, self-limited focal epilepsy of child
PURPOSE OF REVIEW: This article reviews the clinical features, typical EEG findings, treatment, prognosis, and underlying molecular etiologi …
Epilepsy: Epileptic Syndromes and Treatment.
Katyayan A, Diaz-Medina G. Katyayan A, et al. Neurol Clin. 2021 Aug;39(3):779-795. doi: 10.1016/j.ncl.2021.04.002. Neurol Clin. 2021. PMID: 34215386 Review.
Epilepsy syndromes are the third and final level of epilepsy diagnosis, after classification of seizure and epilepsy types. Some epilepsy syndromes are self-limiting and pharmacoresponsive and others are pharmacoresistant and associated with poor devel
Epilepsy syndromes are the third and final level of epilepsy diagnosis, after classification of seizure and epilepsy ty
CDKL5 deficiency disorder: clinical features, diagnosis, and management.
Leonard H, Downs J, Benke TA, Swanson L, Olson H, Demarest S. Leonard H, et al. Lancet Neurol. 2022 Jun;21(6):563-576. doi: 10.1016/S1474-4422(22)00035-7. Epub 2022 Apr 25. Lancet Neurol. 2022. PMID: 35483386 Free PMC article. Review.
Although initially considered a variant of Rett syndrome, CDD is now recognised as an independent disorder and classified as a developmental epileptic encephalopathy. It is characterised by early-onset (generally within the first 2 months of life) seizures th …
Although initially considered a variant of Rett syndrome, CDD is now recognised as an independent disorder and classified as a developmental …
Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision Therapy.
Bayat A, Bayat M, Rubboli G, Møller RS. Bayat A, et al. Genes (Basel). 2021 Jul 8;12(7):1051. doi: 10.3390/genes12071051. Genes (Basel). 2021. PMID: 34356067 Free PMC article. Review.
These have been instrumental in providing insights into the pathophysiology of both early-onset benign and self-limited syndromes and devastating developmental and epileptic encephalopathies (DEEs). ...The aim of this study was to review the clinical and gene …
These have been instrumental in providing insights into the pathophysiology of both early-onset benign and self-limited syndromes and …
DEPDC5-related epilepsy: A comprehensive review.
Samanta D. Samanta D. Epilepsy Behav. 2022 May;130:108678. doi: 10.1016/j.yebeh.2022.108678. Epub 2022 Apr 14. Epilepsy Behav. 2022. PMID: 35429726 Review.
DEPDC5-related epilepsy includes several familial epilepsy syndromes, including familial focal epilepsy with variable foci (FFEVF) and rare sporadic nonlesional focal epilepsy. DEPDC5 has been identified as one of the more common epilepsy genes …
DEPDC5-related epilepsy includes several familial epilepsy syndromes, including familial focal epilepsy with variable f …
The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications.
Brunklaus A, Brünger T, Feng T, Fons C, Lehikoinen A, Panagiotakaki E, Vintan MA, Symonds J, Andrew J, Arzimanoglou A, Delima S, Gallois J, Hanrahan D, Lesca G, MacLeod S, Marjanovic D, McTague A, Nuñez-Enamorado N, Perez-Palma E, Scott Perry M, Pysden K, Russ-Hall SJ, Scheffer IE, Sully K, Syrbe S, Vaher U, Velayutham M, Vogt J, Weiss S, Wirrell E, Zuberi SM, Lal D, Møller RS, Mantegazza M, Cestèle S. Brunklaus A, et al. Brain. 2022 Nov 21;145(11):3816-3831. doi: 10.1093/brain/awac210. Brain. 2022. PMID: 35696452 Free PMC article.
Twenty-one patients presented later, between 2 weeks and 3 months of age, with a severe early infantile developmental and epileptic encephalopathy and a movement disorder. One patient presented after 3 months with developmental and epi
Twenty-one patients presented later, between 2 weeks and 3 months of age, with a severe early infantile developmental a …
Cannabis for the Treatment of Epilepsy: an Update.
Gaston TE, Szaflarski JP. Gaston TE, et al. Curr Neurol Neurosci Rep. 2018 Sep 8;18(11):73. doi: 10.1007/s11910-018-0882-y. Curr Neurol Neurosci Rep. 2018. PMID: 30194563 Review.
PURPOSE OF REVIEW: For millennia, there has been interest in the use of cannabis for the treatment of epilepsy. However, it is only recently that appropriately powered controlled studies have been completed. ...Future controlled studies of various ratios of CBD and THC are …
PURPOSE OF REVIEW: For millennia, there has been interest in the use of cannabis for the treatment of epilepsy. However, it is only r …
Epidemiology of Developmental and Epileptic Encephalopathy and of Intellectual Disability and Epilepsy in Children.
Poke G, Stanley J, Scheffer IE, Sadleir LG. Poke G, et al. Neurology. 2023 Mar 28;100(13):e1363-e1375. doi: 10.1212/WNL.0000000000206758. Epub 2022 Dec 29. Neurology. 2023. PMID: 36581463 Free PMC article.
BACKGROUND AND OBJECTIVES: We aimed to determine the population-based cumulative incidence and prevalence of developmental and epileptic encephalopathies (DEEs) and intellectual disability and epilepsy (ID+E) in children. ...Cumulative incidence for DEE was 1 …
BACKGROUND AND OBJECTIVES: We aimed to determine the population-based cumulative incidence and prevalence of developmental and epileptic
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