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Quoted phrase not found in phrase index: "Epilepsy, familial adult myoclonic, 5"
Page 1
Juvenile myoclonic epilepsy: Long-term prognosis and risk factors.
Pietrafusa N, La Neve A, de Palma L, Boero G, Luisi C, Vigevano F, Specchio N. Pietrafusa N, et al. Brain Dev. 2021 Jun;43(6):688-697. doi: 10.1016/j.braindev.2021.02.005. Epub 2021 Mar 27. Brain Dev. 2021. PMID: 33781581 Review.
OBJECTIVE: Our goal was to investigate the long-term clinical course of juvenile myoclonic epilepsy (JME) in a cohort of patients and to identify prognostic factors for refractoriness and seizure relapse after anti-seizure medications (ASMs) withdrawal …
OBJECTIVE: Our goal was to investigate the long-term clinical course of juvenile myoclonic epilepsy (JME) in a cohort o …
Familial adult myoclonic epilepsy: A new expansion repeats disorder.
Lagorio I, Zara F, Striano S, Striano P. Lagorio I, et al. Seizure. 2019 Apr;67:73-77. doi: 10.1016/j.seizure.2019.03.009. Epub 2019 Mar 19. Seizure. 2019. PMID: 30928698 Free article. Review.
Familial adult myoclonic epilepsy (FAME), also described with different acronyms (ADCME, BAFME, FEME, FCTE and others), is a high-penetrant autosomal dominant condition featuring cortical hand tremors, myoclonic jerks, and occasional/rare convul
Familial adult myoclonic epilepsy (FAME), also described with different acronyms (ADCME, BAFME, FEME, FCTE and o
Epilepsy in children.
Arnold ST, Dodson WE. Arnold ST, et al. Baillieres Clin Neurol. 1996 Dec;5(4):783-802. Baillieres Clin Neurol. 1996. PMID: 9068881 Review.
The idiopathic generalized absence epilepsies are usually easy to control with medication. They range from childhood absence epilepsy which tends to remit in adolescence to juvenile myoclonic epilepsy which is a lifelong condition. In contrast, the seizures o …
The idiopathic generalized absence epilepsies are usually easy to control with medication. They range from childhood absence epilepsy
Sex-specific disease modifiers in juvenile myoclonic epilepsy.
Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, Ng CC, Orsini A, Rees MI, Rubboli G, Selmer KK, Striano P, Syvertsen M, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK. Shakeshaft A, et al. Sci Rep. 2022 Feb 21;12(1):2785. doi: 10.1038/s41598-022-06324-2. Sci Rep. 2022. PMID: 35190554 Free PMC article.
Juvenile myoclonic epilepsy (JME) is a common idiopathic generalised epilepsy with variable seizure prognosis and sex differences in disease presentation. Here, we investigate the combined epidemiology of sex, seizure types and precipitants, and their …
Juvenile myoclonic epilepsy (JME) is a common idiopathic generalised epilepsy with variable seizure prognosis an …
Inherited epilepsies.
Walsh LE, McCandless D. Walsh LE, et al. Semin Pediatr Neurol. 2001 Sep;8(3):165-76. doi: 10.1053/spen.2001.26450. Semin Pediatr Neurol. 2001. PMID: 11575846 Review.
Epilepsy may be acquired or inherited. At least one half of epilepsy is genetic in origin; this figure is likely higher in children regardless of whether seizures are generalized or partial. ...To date, genetic mutations in the idiopathic inherited epilepsies affect
Epilepsy may be acquired or inherited. At least one half of epilepsy is genetic in origin; this figure is likely higher in chi
Prognosis of Juvenile myoclonic epilepsy with eye-closure sensitivity.
Uchida CGP, de Carvalho KC, Guaranha MSB, Guilhoto LMFF, de Araújo Filho GM, Yacubian EMT. Uchida CGP, et al. Seizure. 2018 Nov;62:17-25. doi: 10.1016/j.seizure.2018.09.006. Epub 2018 Sep 17. Seizure. 2018. PMID: 30248569 Free article.
PURPOSE: Eye closure sensitivity (ECS) has been described as a reflex trait in juvenile myoclonic epilepsy (JME). However, there is no consensus regarding its significance on prognosis. ...Except for photosensitivity (PS), any other reflex traits occurrence, …
PURPOSE: Eye closure sensitivity (ECS) has been described as a reflex trait in juvenile myoclonic epilepsy (JME). However, the …
Development and Validation of MRI-Based Radiomics Models for Diagnosing Juvenile Myoclonic Epilepsy.
Kim KM, Hwang H, Sohn B, Park K, Han K, Ahn SS, Lee W, Chu MK, Heo K, Lee SK. Kim KM, et al. Korean J Radiol. 2022 Dec;23(12):1281-1289. doi: 10.3348/kjr.2022.0539. Korean J Radiol. 2022. PMID: 36447416 Free PMC article.
OBJECTIVE: Radiomic modeling using multiple regions of interest in MRI of the brain to diagnose juvenile myoclonic epilepsy (JME) has not yet been investigated. This study aimed to develop and validate radiomics prediction models to distinguish patients with …
OBJECTIVE: Radiomic modeling using multiple regions of interest in MRI of the brain to diagnose juvenile myoclonic epilepsy (J …
Seizures and electrophysiological features in familial cortical myoclonic tremor with epilepsy 1.
Ding Y, Cen Z, Zheng Y, Qiu X, Ye Y, Chen X, Hu L, Wang B, Wang Z, Yin H, Shen C, Ming W, Ge Y, Xie F, Yang D, Ouyang Z, Wang H, Wu S, Ding M, Wang S, Luo W. Ding Y, et al. Ann Clin Transl Neurol. 2024 Feb;11(2):414-423. doi: 10.1002/acn3.51961. Epub 2023 Dec 7. Ann Clin Transl Neurol. 2024. PMID: 38059543 Free PMC article.
OBJECTIVES: To investigate and characterize epileptic seizures and electrophysiological features of familial cortical myoclonic tremor with epilepsy (FCMTE) type 1 patients in a large Chinese cohort. ...Overnight EEG of FCMTE patients displayed paradox …
OBJECTIVES: To investigate and characterize epileptic seizures and electrophysiological features of familial cortical myocl
Clonazepam. A review of a new anticonvulsant drug.
Browne TR. Browne TR. Arch Neurol. 1976 May;33(5):326-32. doi: 10.1001/archneur.1976.00500050012003. Arch Neurol. 1976. PMID: 817697 Review.
Clonazepam is a new benzodiazepine anticonvulsant recently approved by the Food and Drug Administration for the treatment of typical absence, infantile myoclonic, atypical absence, myoclonic, and akinetic seizures. It is rapidly absorbed by the oral route and appear …
Clonazepam is a new benzodiazepine anticonvulsant recently approved by the Food and Drug Administration for the treatment of typical absence …
Probability of Remission of the Main Epileptic Syndromes in Childhood.
Ramos-Lizana J, Martínez-Espinosa G, Aguilera-López P, Aguirre-Rodriguez J. Ramos-Lizana J, et al. J Child Neurol. 2022 Jan;37(1):89-97. doi: 10.1177/08830738211056780. Epub 2021 Nov 24. J Child Neurol. 2022. PMID: 34816766
AIM: To determine the long-term probability of remission without antiepileptic treatment of common epileptic syndromes and of children without a specific syndromic diagnosis. ...CONCLUSIONS: The study results highlight the long-term outcomes of the main epileptic
AIM: To determine the long-term probability of remission without antiepileptic treatment of common epileptic syndromes and of …
149 results