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1987
2025

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

Year Number of Results
1987 3
1989 2
1990 1
1992 1
1993 1
1994 3
1995 2
1996 3
1997 3
1998 3
1999 3
2000 5
2001 6
2002 10
2003 4
2004 8
2005 5
2006 10
2007 6
2008 12
2009 9
2010 14
2011 18
2012 15
2013 18
2014 15
2015 20
2016 25
2017 21
2018 22
2019 38
2020 51
2021 54
2022 44
2023 58
2024 70
2025 5

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477 results

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Page 1
Epilepsy and cannabidiol: a guide to treatment.
Arzimanoglou A, Brandl U, Cross JH, Gil-Nagel A, Lagae L, Landmark CJ, Specchio N, Nabbout R, Thiele EA, Gubbay O, The Cannabinoids International Experts Panel; Collaborators. Arzimanoglou A, et al. Epileptic Disord. 2020 Feb 1;22(1):1-14. doi: 10.1684/epd.2020.1141. Epileptic Disord. 2020. PMID: 32096470 Free article. Review.
The growing interest in cannabidiol (CBD), specifically a pure form of CBD, as a treatment for epilepsy, among other conditions, is reflected in recent changes in legislation in some countries. ...However, just as we are beginning to understand the significance of CBD as a …
The growing interest in cannabidiol (CBD), specifically a pure form of CBD, as a treatment for epilepsy, among other conditions, is r …
Developmental and epileptic encephalopathies: recognition and approaches to care.
Raga S, Specchio N, Rheims S, Wilmshurst JM. Raga S, et al. Epileptic Disord. 2021 Feb 1;23(1):40-52. doi: 10.1684/epd.2021.1244. Epileptic Disord. 2021. PMID: 33632673 Review.
The term "developmental and epileptic encephalopathy" (DEE) refers to when cognitive functions are influenced by both seizure and interictal epileptiform activity and the neurobiological process behind the epilepsy. ...In this setting, neurocognition, …
The term "developmental and epileptic encephalopathy" (DEE) refers to when cognitive functions are influenced by both s …
Cerebral palsy.
Graham HK, Rosenbaum P, Paneth N, Dan B, Lin JP, Damiano DL, Becher JG, Gaebler-Spira D, Colver A, Reddihough DS, Crompton KE, Lieber RL. Graham HK, et al. Nat Rev Dis Primers. 2016 Jan 7;2:15082. doi: 10.1038/nrdp.2015.82. Nat Rev Dis Primers. 2016. PMID: 27188686 Free PMC article. Review.
Cerebral palsy is the most common cause of childhood-onset, lifelong physical disability in most countries, affecting about 1 in 500 neonates with an estimated prevalence of 17 million people worldwide. Cerebral palsy is not a disease entity in the traditional sense but a …
Cerebral palsy is the most common cause of childhood-onset, lifelong physical disability in most countries, affecting about 1 in 500 …
West syndrome: a comprehensive review.
Pavone P, Polizzi A, Marino SD, Corsello G, Falsaperla R, Marino S, Ruggieri M. Pavone P, et al. Neurol Sci. 2020 Dec;41(12):3547-3562. doi: 10.1007/s10072-020-04600-5. Epub 2020 Aug 22. Neurol Sci. 2020. PMID: 32827285 Free PMC article. Review.
Since its first clinical description (on his son) by William James West (1793-1848) in 1841, and the definition of the classical triad of (1) infantile spasms; (2) hypsarrhythmia, and (3) developmental arrest or regression as "West syndrome", new and relevant advanc …
Since its first clinical description (on his son) by William James West (1793-1848) in 1841, and the definition of the classical triad of ( …
Cerebral plasticity: Windows of opportunity in the developing brain.
Ismail FY, Fatemi A, Johnston MV. Ismail FY, et al. Eur J Paediatr Neurol. 2017 Jan;21(1):23-48. doi: 10.1016/j.ejpn.2016.07.007. Epub 2016 Aug 9. Eur J Paediatr Neurol. 2017. PMID: 27567276 Review.
Neuroplasticity in the healthy developing brain exhibits a heterochronus cortex-specific developmental profile and is heightened during "critical and sensitive periods" of pre and postnatal brain development that enable the construction and consolidation of e …
Neuroplasticity in the healthy developing brain exhibits a heterochronus cortex-specific developmental profile and is heighten …
Developmental and epileptic encephalopathies.
Scheffer IE, Zuberi S, Mefford HC, Guerrini R, McTague A. Scheffer IE, et al. Nat Rev Dis Primers. 2024 Sep 5;10(1):61. doi: 10.1038/s41572-024-00546-6. Nat Rev Dis Primers. 2024. PMID: 39237642 Review.
Developmental and epileptic encephalopathies, the most severe group of epilepsies, are characterized by seizures and frequent epileptiform activity associated with developmental slowing or regression. ...More than 900 genes have been identified as mono
Developmental and epileptic encephalopathies, the most severe group of epilepsies, are characterized by seizures and fr
The complete European guidelines on phenylketonuria: diagnosis and treatment.
van Wegberg AMJ, MacDonald A, Ahring K, Bélanger-Quintana A, Blau N, Bosch AM, Burlina A, Campistol J, Feillet F, Giżewska M, Huijbregts SC, Kearney S, Leuzzi V, Maillot F, Muntau AC, van Rijn M, Trefz F, Walter JH, van Spronsen FJ. van Wegberg AMJ, et al. Orphanet J Rare Dis. 2017 Oct 12;12(1):162. doi: 10.1186/s13023-017-0685-2. Orphanet J Rare Dis. 2017. PMID: 29025426 Free PMC article. Review.
If left untreated, PKU results in increased phenylalanine concentrations in blood and brain, which cause severe intellectual disability, epilepsy and behavioural problems. ...
If left untreated, PKU results in increased phenylalanine concentrations in blood and brain, which cause severe intellectual disabili …
Lennox-Gastaut Syndrome: Current Treatments, Novel Therapeutics, and Future Directions.
Nelson JA, Knupp KG. Nelson JA, et al. Neurotherapeutics. 2023 Sep;20(5):1255-1262. doi: 10.1007/s13311-023-01397-x. Epub 2023 Jun 23. Neurotherapeutics. 2023. PMID: 37353676 Free PMC article. Review.
Lennox-Gastaut syndrome is a severe drug-resistant developmental and epileptic encephalopathy with slow spike and wave on EEG (DEE-SSW) composing about 1-2% of epilepsy patients. ...The updated definition by the International League Against E
Lennox-Gastaut syndrome is a severe drug-resistant developmental and epileptic encephalopathy with slow spike and wave …
From Genetic Testing to Precision Medicine in Epilepsy.
Striano P, Minassian BA. Striano P, et al. Neurotherapeutics. 2020 Apr;17(2):609-615. doi: 10.1007/s13311-020-00835-4. Neurotherapeutics. 2020. PMID: 31981099 Free PMC article. Review.
In the last two decades, a genetic etiology has been revealed in more than half of all epilepsies and single gene defects in ion channels or neurotransmitter receptors have been associated with most inherited forms of epilepsy, including some focal and lesional forms as we …
In the last two decades, a genetic etiology has been revealed in more than half of all epilepsies and single gene defects in ion channels or …
SCN8A Epilepsy, Developmental Encephalopathy, and Related Disorders.
Talwar D, Hammer MF. Talwar D, et al. Pediatr Neurol. 2021 Sep;122:76-83. doi: 10.1016/j.pediatrneurol.2021.06.011. Epub 2021 Aug 3. Pediatr Neurol. 2021. PMID: 34353676 Review.
In this review we describe the identification of a new epileptic encephalopathy caused by a de novo mutation in the SCN8A gene, which encodes for Na(V)1.6, a vital sodium channel in the central nervous system. ...Following the original discovery in 2012 of a …
In this review we describe the identification of a new epileptic encephalopathy caused by a de novo mutation in the SCN8A gene …
477 results