Literature DB >> 9509255

Advances in the medical treatment of epilepsy.

C W Bazil1, T A Pedley.   

Abstract

Treatment options for epilepsy, especially using antiepileptic drugs, have increased substantially in the past five years. Since 1993, four novel antiepileptic drugs have been approved and marketed in the United States: felbamate, gabapentin, lamotrigine, and topiramate. Two others, tiagabine and vigabatrin, are likely to be approved in the near future. For many patients, these agents offer the realistic promise of improved seizure control, often with fewer adverse effects and less significant drug interactions compared with older agents. In addition, fosphenytoin, a water-soluble phenytoin prodrug with a number of advantages over intravenous phenytoin, has been released. There are new administration options for carbamazepine, diazepam, and valproic acid. For drug-resistant or -intolerant patients, there has been renewed interest in alternative therapies, especially the ketogenic diet. Taken together, these represent significant therapeutic advances that are benefiting patients with epilepsy. At the same time, improved understanding of the basic mechanisms of epileptogenesis, and of the cellular and molecular actions of available antiepileptic drugs, creates a framework for designing unique therapeutic strategies that are targeted at key sites of vulnerability involved in the development and maintenance of the epileptic state.

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Year:  1998        PMID: 9509255     DOI: 10.1146/annurev.med.49.1.135

Source DB:  PubMed          Journal:  Annu Rev Med        ISSN: 0066-4219            Impact factor:   13.739


  11 in total

Review 1.  New antiepileptic drugs.

Authors:  C W Bazil
Journal:  Curr Neurol Neurosci Rep       Date:  2001-07       Impact factor: 5.081

Review 2.  Pharmacological and biochemical aspects of GABAergic neurotransmission: pathological and neuropsychobiological relationships.

Authors:  Renê Oliveira Beleboni; Ruither Oliveira Gomes Carolino; Andrea Baldocchi Pizzo; Lissandra Castellan-Baldan; Joaquim Coutinho-Netto; Wagner Ferreira dos Santos; Norberto Cysne Coimbra
Journal:  Cell Mol Neurobiol       Date:  2004-12       Impact factor: 5.046

3.  Ultrastructure of Purkinje cell perikarya and their dendritic processes in the rat cerebellar cortex in experimental encephalopathy induced by chronic application of valproate.

Authors:  M E Sobaniec-Lotowska
Journal:  Int J Exp Pathol       Date:  2001-12       Impact factor: 1.925

4.  Low frequency stimulation decreases seizure activity in a mutation model of epilepsy.

Authors:  Kara Buehrer Kile; Nan Tian; Dominique M Durand
Journal:  Epilepsia       Date:  2010-07-26       Impact factor: 5.864

Review 5.  Tetrazoles via Multicomponent Reactions.

Authors:  Constantinos G Neochoritis; Ting Zhao; Alexander Dömling
Journal:  Chem Rev       Date:  2019-02-01       Impact factor: 60.622

6.  3-Amino-5-methyl-5-(4-pyrid-yl)hydantoin.

Authors:  Hristo Varbanov; Rossen Buyukliev; Adriana Bakalova; Alexander Roller
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-04-02

7.  DNA topoisomerase I inhibitors ameliorate seizure-like behaviors and paralysis in a Drosophila model of epilepsy.

Authors:  J Song; L Parker; L Hormozi; M A Tanouye
Journal:  Neuroscience       Date:  2008-07-23       Impact factor: 3.590

8.  Synthesis and antiproliferative activity of substituted diazaspiro hydantoins: a structure-activity relationship study.

Authors:  C S Ananda Kumar; S B Benaka Prasad; K Vinaya; S Chandrappa; N R Thimmegowda; S R Ranganatha; Sanjay Swarup; K S Rangappa
Journal:  Invest New Drugs       Date:  2008-07-08       Impact factor: 3.850

9.  3-(4-Bromo-phen-yl)-1-butyl-5-[1-(2-chloro-6-methyl-phen-yl)-1H-tetra-zol-5-yl]imidazolidine-2,4-dione.

Authors:  Gabriel B Hall; Federico Medda; Sue A Roberts; Christopher Hulme
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-06-15

10.  Propyl-2-(8-(3,4-difluorobenzyl)-2',5'-dioxo-8-azaspiro[bicyclo[3.2.1] octane-3,4'-imidazolidine]-1'-yl) acetate induces apoptosis in human leukemia cells through mitochondrial pathway following cell cycle arrest.

Authors:  Chandagirikoppal V Kavitha; Mridula Nambiar; Pavan B Narayanaswamy; Elizabeth Thomas; Ujjwal Rathore; Channapillekoppalu S Ananda Kumar; Bibha Choudhary; Kanchugarakoppal S Rangappa; Sathees C Raghavan
Journal:  PLoS One       Date:  2013-07-26       Impact factor: 3.240

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