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Page 1
Dental health in persons with disability.
Devinsky O, Boyce D, Robbins M, Pressler M. Devinsky O, et al. Epilepsy Behav. 2020 Sep;110:107174. doi: 10.1016/j.yebeh.2020.107174. Epub 2020 Jun 9. Epilepsy Behav. 2020. PMID: 32531727 Review.
Expert opinion: Proposed diagnostic and treatment algorithms for Lennox-Gastaut syndrome in adult patients.
Montouris G, Aboumatar S, Burdette D, Kothare S, Kuzniecky R, Rosenfeld W, Chung S. Montouris G, et al. Epilepsy Behav. 2020 Sep;110:107146. doi: 10.1016/j.yebeh.2020.107146. Epub 2020 Jun 18. Epilepsy Behav. 2020. PMID: 32563898 Free article. Review.
Lennox-Gastaut syndrome (LGS) is a severe developmental epileptic encephalopathy diagnosed in childhood that persists through adolescence and into adulthood. ...
Lennox-Gastaut syndrome (LGS) is a severe developmental epileptic encephalopathy diagnosed in childhood that persists t …
Genetics and SUDEP: Challenges and Future Directions.
Whitney R, Sharma S, Jones KC, RamachandranNair R. Whitney R, et al. Seizure. 2023 Aug;110:188-193. doi: 10.1016/j.seizure.2023.07.002. Epub 2023 Jul 2. Seizure. 2023. PMID: 37413779 Review.
Sudden unexpected death in epilepsy (SUDEP) is the leading cause of epilepsy-related deaths in children and adults with epilepsy. ...Pleiotropy may occur in which a single gene when altered may cause multiple phenotypes (i.e., epilepsy and cardiac arrh …
Sudden unexpected death in epilepsy (SUDEP) is the leading cause of epilepsy-related deaths in children and adults with epi
Dyke-Davidoff-Masson Syndrome: Main clinical and radiological findings- systematic literature review.
Rondão MBA, Hsu BRRHS, Centeno RS, de Aguiar PHP. Rondão MBA, et al. Seizure. 2023 Aug;110:58-68. doi: 10.1016/j.seizure.2023.04.020. Epub 2023 Jun 3. Seizure. 2023. PMID: 37327751 Review.
RESULTS: The mean age of the patients was 19.44 (0-83 years), and the majority were male (55.32%). The most common types of epileptic seizures were generalised tonic-clonic seizures (31 cases), focal impaired awareness seizures (20 cases), focal motor seizures (13 cases), …
RESULTS: The mean age of the patients was 19.44 (0-83 years), and the majority were male (55.32%). The most common types of epileptic
MicroRNA-induced silencing in epilepsy: Opportunities and challenges for clinical application.
Tiwari D, Peariso K, Gross C. Tiwari D, et al. Dev Dyn. 2018 Jan;247(1):94-110. doi: 10.1002/dvdy.24582. Epub 2017 Oct 4. Dev Dyn. 2018. PMID: 28850760 Free PMC article. Review.
Indeed, several years of research in rodent models have provided strong evidence that acute or recurrent seizures change microRNA expression and function. Moreover, altered microRNA expression has been observed in brain and blood from patients with various epilepsy
Indeed, several years of research in rodent models have provided strong evidence that acute or recurrent seizures change microRNA expression …
The mTOR signalling cascade: paving new roads to cure neurological disease.
Crino PB. Crino PB. Nat Rev Neurol. 2016 Jul;12(7):379-92. doi: 10.1038/nrneurol.2016.81. Epub 2016 Jun 24. Nat Rev Neurol. 2016. PMID: 27340022 Review.
Alterations in the dual contributions of mTOR - regulation of cell growth and proliferation, as well as autophagy and cell death - have been found in developmental brain malformations, epilepsy, autism and intellectual disability, hypoxic-ischaemic and trauma …
Alterations in the dual contributions of mTOR - regulation of cell growth and proliferation, as well as autophagy and cell death - have been …
alpha-[11C]-methyl-L-tryptophan PET for tracer localization of epileptogenic brain regions: clinical studies.
Kumar A, Asano E, Chugani HT. Kumar A, et al. Biomark Med. 2011 Oct;5(5):577-84. doi: 10.2217/bmm.11.68. Biomark Med. 2011. PMID: 22003906 Free PMC article. Review.
AMT PET appears to be particularly useful in patients with tuberous sclerosis complex and in patients with cortical developmental malformations. Although the sensitivity of AMT PET in finding the epileptic focus is about 70%, its specificity is almost 100%, indicati …
AMT PET appears to be particularly useful in patients with tuberous sclerosis complex and in patients with cortical developmental mal …