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

Year Number of Results
1999 1
2000 1
2002 1
2005 2
2008 1
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2015 1
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14 results

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Page 1
The current status of neuroimaging for epilepsy.
Duncan J. Duncan J. Curr Opin Neurol. 2009 Apr;22(2):179-84. doi: 10.1097/WCO.0b013e328328f260. Curr Opin Neurol. 2009. PMID: 19300096 Review.
Functional MRI of language and memory are becoming used as a predictor of deficits as a result of temporal lobe resection.Increased uptake of the PET tracer 11C-alpha-methyl tryptophan shows promise for localizing epileptogenic malformations of cortical development. ...
Functional MRI of language and memory are becoming used as a predictor of deficits as a result of temporal lobe resection.Increased u …
New insights into the clinical management of partial epilepsies.
Hirsch E, de Saint-Martin A, Arzimanoglou A. Hirsch E, et al. Epilepsia. 2000;41 Suppl 5:S13-17. doi: 10.1111/j.1528-1157.2000.tb06042.x. Epilepsia. 2000. PMID: 11045435 Free article. Review.
The diagnosis, treatment, and prognosis of seizure disorders depend on the correct identification of epileptic syndromes. ...
The diagnosis, treatment, and prognosis of seizure disorders depend on the correct identification of epileptic syndromes. ...
Variants in CHRNB2 and CHRNA4 Identified in Patients with Insular Epilepsy.
Cadieux-Dion M, Meneghini S, Villa C, Toffa DH, Wickstrom R, Bouthillier A, Sandvik U, Gustavsson B, Mohamed I, Cossette P, Combi R, Becchetti A, Nguyen DK. Cadieux-Dion M, et al. Can J Neurol Sci. 2020 Nov;47(6):800-809. doi: 10.1017/cjn.2020.126. Epub 2020 Jun 15. Can J Neurol Sci. 2020. PMID: 32536355
RESULTS: We localized the epileptic foci to the left insula in the first case (now seizure-free following epilepsy surgery) and to both insulae in the second case. Based on tools predicting the possible impact of amino acid substitutions on the structure and function of pr …
RESULTS: We localized the epileptic foci to the left insula in the first case (now seizure-free following epilepsy surgery) and to both insu …
Genetic focal epilepsies: state of the art and paths to the future.
Andermann F, Kobayashi E, Andermann E. Andermann F, et al. Epilepsia. 2005;46 Suppl 10:61-7. doi: 10.1111/j.1528-1167.2005.00361.x. Epilepsia. 2005. PMID: 16359475 Free article. Review.
At present, we can provide genetic counseling and a more accurate prognosis for most of the familial focal epilepsies. Greater awareness of the genetic basis in this group of disorders by the treating physicians is essential for identification of new families. ...
At present, we can provide genetic counseling and a more accurate prognosis for most of the familial focal epilepsies. Greater awaren …
Debate: Does genetic information in humans help us treat patients? PRO--genetic information in humans helps us treat patients. CON--genetic information does not help at all.
Delgado-Escueta AV, Bourgeois BF. Delgado-Escueta AV, et al. Epilepsia. 2008 Dec;49 Suppl 9:13-24. doi: 10.1111/j.1528-1167.2008.01922.x. Epilepsia. 2008. PMID: 19087113 Free article. Review.
Genotyping also portends a brighter future, helping us to reassess the true course, severity, and progressive nature of Dravet's syndrome and Unverricht-Lundborg PME and helping us craft a future curative treatment for Dravet's syndrome and Lafora disease. ...In addition, …
Genotyping also portends a brighter future, helping us to reassess the true course, severity, and progressive nature of Dravet's synd …
Mutations in familial nocturnal frontal lobe epilepsy might be associated with distinct neurological phenotypes.
Steinlein OK, Hoda JC, Bertrand S, Bertrand D. Steinlein OK, et al. Seizure. 2012 Mar;21(2):118-23. doi: 10.1016/j.seizure.2011.10.003. Epub 2011 Oct 28. Seizure. 2012. PMID: 22036597 Free article.
ADNFLE was initially described as a "pure" seizure disorder with a mostly benign course. We have analysed the clinical features of 19 ADNFLE families from 12 countries with a total of 150 patients and grouped them with respect to their nAChR mutations. ...The functional da …
ADNFLE was initially described as a "pure" seizure disorder with a mostly benign course. We have analysed the clinical features of 19 …
Autosomal dominant nocturnal frontal lobe epilepsy: an electroclinical study of a Norwegian family with ten affected members.
Nakken KO, Magnusson A, Steinlein OK. Nakken KO, et al. Epilepsia. 1999 Jan;40(1):88-92. doi: 10.1111/j.1528-1157.1999.tb01993.x. Epilepsia. 1999. PMID: 9924907 Free article.
Although the seizure susceptibility varied among the affected individuals, the epilepsy course was mostly benign. CONCLUSIONS: Patients with ADNFLE, either with the 776ins3 mutation or the Ser248Phe mutation, and those without any recognized mutation in the acetylcholine r …
Although the seizure susceptibility varied among the affected individuals, the epilepsy course was mostly benign. CONCLUSIONS: Patien …
Molecular modelling of the interactions of carbamazepine and a nicotinic receptor involved in the autosomal dominant nocturnal frontal lobe epilepsy.
Ortells MO, Barrantes GE. Ortells MO, et al. Br J Pharmacol. 2002 Jul;136(6):883-95. doi: 10.1038/sj.bjp.0704786. Br J Pharmacol. 2002. PMID: 12110613 Free PMC article.
Phe248 residues are the main component of CBZ binding sites in the mutant, while this is not true for Ser248 in the normal receptor. 4. A higher number of blocking binding sites and a predicted higher affinity found for CBZ in the mutant account for its differential sensit …
Phe248 residues are the main component of CBZ binding sites in the mutant, while this is not true for Ser248 in the normal receptor. 4. A hi …
A case of autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) coexisting with pervasive developmental disorder harboring SCN1A mutation in addition to CHRNB2 mutation.
Sone D, Sugawara T, Sakakibara E, Tomioka Y, Taniguchi G, Murata Y, Watanabe M, Kaneko S. Sone D, et al. Epilepsy Behav. 2012 Oct;25(2):192-5. doi: 10.1016/j.yebeh.2012.07.027. Epub 2012 Sep 29. Epilepsy Behav. 2012. PMID: 23032131
However, the relation between SCN1A and ADNFLE is unknown. We report the clinical course and symptomatic characteristics of this case although the relationship between ADNFLE mutation and SCN1A mutation remains to be elucidated....
However, the relation between SCN1A and ADNFLE is unknown. We report the clinical course and symptomatic characteristics of this case …
14 results