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Myoclonus.
Shibasaki H. Shibasaki H. Curr Opin Neurol. 1995 Aug;8(4):331-4. doi: 10.1097/00019052-199508000-00015. Curr Opin Neurol. 1995. PMID: 7582053 Review.
Genetic studies have suggested homogeneity between the Baltic-type and Mediterranean-type progressive myoclonic epilepsy. Magnetoencephalography was applied to elucidate the mechanism underlying the giant evoked responses in cortical reflex myoc …
Genetic studies have suggested homogeneity between the Baltic-type and Mediterranean-type progressive myoclonic
A systematic review of the efficacy of perampanel as treatment for myoclonic seizures and symptomatic myoclonus.
Mir A, Alghamdi A, Alotaibi W, Samreen D, Alotaibi M, Albaradie R, Bashir S. Mir A, et al. Epileptic Disord. 2022 Aug 1;24(4):633-646. doi: 10.1684/epd.2022.1439. Epileptic Disord. 2022. PMID: 35770766 Review. English.
Epileptic myoclonus or myoclonic seizures can occur in idiopathic generalized epilepsy (IGE) and progressive myoclonus epilepsy (PME). ...We also analysed the number of patients who were already on levetiracetam (LEV) or valproic acid (VPA) at the time …
Epileptic myoclonus or myoclonic seizures can occur in idiopathic generalized epilepsy (IGE) and progressive myoclonus …
[Unverricht-Lundborg disease (PME1)].
Genton P. Genton P. Rev Neurol (Paris). 2006 Sep;162(8-9):819-26. doi: 10.1016/s0035-3787(06)75084-6. Rev Neurol (Paris). 2006. PMID: 17028542 Review. French.
Unverricht-Lundborg disease (ULD) is the purest and least severe type of progressive myoclonus epilepsy (PME), and is not associated with progressive cognitive deficit. ...The disorder follows an autosomal recessive transmission pattern, with onset bet …
Unverricht-Lundborg disease (ULD) is the purest and least severe type of progressive myoclonus epilepsy (PME), and is n …
Progressive Myoclonus Epilepsy in Congenital Generalized Lipodystrophy type 2: Report of 3 cases and literature review.
Opri R, Fabrizi GM, Cantalupo G, Ferrarini M, Simonati A, Dalla Bernardina B, Darra F. Opri R, et al. Seizure. 2016 Nov;42:1-6. doi: 10.1016/j.seizure.2016.08.008. Epub 2016 Sep 5. Seizure. 2016. PMID: 27632409 Free article. Review.
Herein we describe clinical and EEG features of three patients presenting with Progressive Myoclonus Epilepsy (PME) and Congenital Generalized Lipodystrophy type 2 (CGL2) related to novel Seipin mutations. ...RESULTS: The CGL2-PME syndrome co-segregated with …
Herein we describe clinical and EEG features of three patients presenting with Progressive Myoclonus Epilepsy (PME) and Congen …
Exploring the Evidence for Broad-Spectrum Effectiveness of Perampanel: A Systematic Review of Clinical Data in Generalised Seizures.
Trinka E, Lattanzi S, Carpenter K, Corradetti T, Nucera B, Rinaldi F, Shankar R, Brigo F. Trinka E, et al. CNS Drugs. 2021 Aug;35(8):821-837. doi: 10.1007/s40263-021-00831-y. Epub 2021 Jul 7. CNS Drugs. 2021. PMID: 34232492 Free PMC article.
The most commonly reported epilepsy type was IGE (N = 378) and the most common syndromes were juvenile myoclonic epilepsy (N = 92), progressive myoclonic epilepsies (N = 59) and absence epilepsies (N = 43). ...Data from othe …
The most commonly reported epilepsy type was IGE (N = 378) and the most common syndromes were juvenile myoclonic epi
Progressive myoclonus epilepsies: clinical and neurophysiological diagnosis.
Berkovic SF, So NK, Andermann F. Berkovic SF, et al. J Clin Neurophysiol. 1991 Jul;8(3):261-74. J Clin Neurophysiol. 1991. PMID: 1918332 Review.
Diagnosis and management of the progressive myoclonus epilepsies (PMEs) provides a challenge to the clinician and neurophysiologist. ...The major causes are PME of the Unverricht-Lundborg type, Lafora disease, neuronal ceroid lipofuscinoses (three forms), MER …
Diagnosis and management of the progressive myoclonus epilepsies (PMEs) provides a challenge to the clinician and neurophysiol …
[Differential diagnosis of chorea].
Shimohata T, Nishizawa M. Shimohata T, et al. Brain Nerve. 2009 Aug;61(8):963-71. Brain Nerve. 2009. PMID: 19697886 Review. Japanese.
Recent studies have demonstrated that such disorders include dentatorubral pallidoluysian atrophy (DRPLA), spinocerebellar ataxia type 17 (SCA17), Huntington disease like 1 (HDL1), Huntington disease like 2 (HDL2), and benign hereditary chorea (BHC). We recently identified …
Recent studies have demonstrated that such disorders include dentatorubral pallidoluysian atrophy (DRPLA), spinocerebellar ataxia type