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Quoted phrase not found in phrase index: "Epilepsy, childhood absence, susceptibility to, 5"
Page 1
Genetic testing in the epilepsies-developments and dilemmas.
Poduri A, Sheidley BR, Shostak S, Ottman R. Poduri A, et al. Nat Rev Neurol. 2014 May;10(5):293-9. doi: 10.1038/nrneurol.2014.60. Epub 2014 Apr 15. Nat Rev Neurol. 2014. PMID: 24733164 Free PMC article. Review.
In the past two decades, the number of genes recognized to have a role in the epilepsies has dramatically increased. The availability of testing for epilepsy-related genes is potentially helpful for clarification of the diagnosis and prognosis, selection of optimal treatme …
In the past two decades, the number of genes recognized to have a role in the epilepsies has dramatically increased. The availability of tes …
Childhood Absence Epilepsy evolving to Eyelid Myoclonia with Absence Epilepsy.
Galli J, Micheletti S, Malerba L, Fazzi E, Giordano L. Galli J, et al. Seizure. 2018 Oct;61:1-3. doi: 10.1016/j.seizure.2018.07.009. Epub 2018 Jul 18. Seizure. 2018. PMID: 30029089 Free article.
PURPOSE: Children with Childhood Absence Epilepsy (CAE) may develop generalized tonic-clonic seizure or juvenile myoclonic epilepsy. A possible evolution to Eyelid Myoclonia with Absence Epilepsy (EMA) hasn't been documented yet. We repor …
PURPOSE: Children with Childhood Absence Epilepsy (CAE) may develop generalized tonic-clonic seizure or juvenile myoclo …
Photosensitivity in idiopathic generalized epilepsies.
Covanis A. Covanis A. Epilepsia. 2005;46 Suppl 9:67-72. doi: 10.1111/j.1528-1167.2005.00315.x. Epilepsia. 2005. PMID: 16302877 Free article. Review.
Photosensitivity is an abnormal visual sensitivity of the brain in reaction to flickering light sources or patterns and is expressed in the electroencephalogram as generalized spike-and-wave discharge and in more susceptible individuals as clinical seizures. The most commo …
Photosensitivity is an abnormal visual sensitivity of the brain in reaction to flickering light sources or patterns and is expressed in the …
Advances in lafora progressive myoclonus epilepsy.
Delgado-Escueta AV. Delgado-Escueta AV. Curr Neurol Neurosci Rep. 2007 Sep;7(5):428-33. doi: 10.1007/s11910-007-0066-7. Curr Neurol Neurosci Rep. 2007. PMID: 17764634 Review.
Abstract Lafora progressive myoclonus epilepsy is an autosomal recessive, fatal, generalized polyglucosan storage disorder that occurs in childhood or adolescence with stimulus sensitive epilepsy (resting and action myoclonias, grand mal, and absence), …
Abstract Lafora progressive myoclonus epilepsy is an autosomal recessive, fatal, generalized polyglucosan storage disorder that occur …
Prevalence of idiopathic epilepsy among school children in Gharbia Governorate, Egypt.
Alshahawy AK, Darwish AH, Elsaid Shalaby S, Mawlana W. Alshahawy AK, et al. Brain Dev. 2018 Apr;40(4):278-286. doi: 10.1016/j.braindev.2017.12.009. Epub 2017 Dec 30. Brain Dev. 2018. PMID: 29295801
Higher prevalence was reported in males (7.7/1000) and in children from urban areas (8.25/1000). Generalized seizures were observed in 56.5% of the children with epilepsy, whereas focal seizures were present in 43.5%. Thirty-four (49.27%) children were diagno …
Higher prevalence was reported in males (7.7/1000) and in children from urban areas (8.25/1000). Generalized seizures were observed in 56. …
Magnetic susceptibility as a 1-year predictor of outcome in familial cerebral cavernous malformations: a pilot study.
Incerti I, Fusco M, Contarino VE, Siggillino S, Conte G, Lanfranconi S, Bertani GA, Gaudino C, d'Orio P, Pallini R, D'Alessandris QG, Meessen JMTA, Nicolis EB, Vasamì A, Dejana E, Bianchi AM, Triulzi FM, Latini R, Scola E. Incerti I, et al. Eur Radiol. 2023 Jun;33(6):4158-4166. doi: 10.1007/s00330-022-09366-2. Epub 2023 Jan 5. Eur Radiol. 2023. PMID: 36602570
OBJECTIVES: To test whether quantitative susceptibility mapping (QSM) of cerebral cavernous malformations (CCMs) assessed at baseline may predict the presence or absence of haemorrhagic signs at 1-year follow-up. ...KEY POINTS: QSM in semi-automatically segmented CC …
OBJECTIVES: To test whether quantitative susceptibility mapping (QSM) of cerebral cavernous malformations (CCMs) assessed at baseline …
EEG features and epilepsy in MECP2-mutated patients with the Zappella variant of Rett syndrome.
Buoni S, Zannolli R, De Felice C, De Nicola A, Guerri V, Guerra B, Casali S, Pucci B, Corbini L, Mari F, Renieri A, Zappella M, Hayek J. Buoni S, et al. Clin Neurophysiol. 2010 May;121(5):652-7. doi: 10.1016/j.clinph.2010.01.003. Epub 2010 Feb 12. Clin Neurophysiol. 2010. PMID: 20153689
OBJECTIVE: To assess the presence/absence of peculiar EEG features and epilepsy in MECP2-mutated Rett patients with the Zappella-Rett variant (Z-RTT) also known as preserved speech variant. ...CONCLUSIONS: EEG electrophysiological patterns and epileptogenic susce …
OBJECTIVE: To assess the presence/absence of peculiar EEG features and epilepsy in MECP2-mutated Rett patients with the Zappel …
Pattern-sensitive epilepsy: electroclinical characteristics, natural history, and delineation of the epileptic syndrome.
Radhakrishnan K, St Louis EK, Johnson JA, McClelland RL, Westmoreland BF, Klass DW. Radhakrishnan K, et al. Epilepsia. 2005 Jan;46(1):48-58. doi: 10.1111/j.0013-9580.2005.26604.x. Epilepsia. 2005. PMID: 15660768 Free article.
During a median follow-up period of 15.7 years, 25 (45.5%) of 55 patients who were followed up for > or =5 years achieved complete seizure remission. The median age at remission was 24.4 years. The absence of progressive neurologic disease was corre …
During a median follow-up period of 15.7 years, 25 (45.5%) of 55 patients who were followed up for > or =5 years achieved c …
Incidence of epilepsies and epileptic syndromes among children in Navarre, Spain: 2002 through 2005.
Durá-Travé T, Yoldi-Petri ME, Gallinas-Victoriano F. Durá-Travé T, et al. J Child Neurol. 2008 Aug;23(8):878-82. doi: 10.1177/0883073808314898. J Child Neurol. 2008. PMID: 18660472
Based on International League Against Epilepsy criteria, 191 patients were diagnosed as having epilepsy. ...Among school-aged children, focal benign epilepsies (27.8%) and cryptogenic and absence epilepsies (18.5% for both) are the most prevalent, with …
Based on International League Against Epilepsy criteria, 191 patients were diagnosed as having epilepsy. ...Among school-aged …
Operant conditioning of EEG rhythms and ritalin in the treatment of hyperkinesis.
Shouse MN, Lubar JF. Shouse MN, et al. Biofeedback Self Regul. 1979 Dec;4(4):299-312. doi: 10.1007/BF00998960. Biofeedback Self Regul. 1979. PMID: 526475
The clinical effectiveness of SMR operant conditioning has been claimed for epilepsy, insomnia, and hyperkinesis concurrent with seizure disorders. The present report attempts to follow up and replicate preliminary findings that suggested the technique's successful applica …
The clinical effectiveness of SMR operant conditioning has been claimed for epilepsy, insomnia, and hyperkinesis concurrent with seiz …
24 results