LEADER 02214nam 2200553 450 001 9910811990803321 005 20230617003600.0 010 $a1-4698-7738-4 035 $a(CKB)2430000000022362 035 $a(EBL)3418712 035 $a(SSID)ssj0000353309 035 $a(PQKBManifestationID)11264820 035 $a(PQKBTitleCode)TC0000353309 035 $a(PQKBWorkID)10288550 035 $a(PQKB)10118067 035 $a(MiAaPQ)EBC2032532 035 $a(Au-PeEL)EBL2032532 035 $a(CaPaEBR)ebr10865274 035 $a(OCoLC)880453787 035 $a(EXLCZ)992430000000022362 100 $a20140508h20052005 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aMyoclonic epilepsies /$fPierre Genton [and six others], editors ; Anne M. Sydor, acquisition editor ; Scott Scheidt, developmental editor 205 $aFirst edition. 210 1$aPhiladelphia, Pennsylvania :$cLippincott Williams & Wilkins,$d2005. 210 4$dİ2005 215 $a1 online resource (304 p.) 225 1 $aAdvances in Neurology,$x0091-3952 300 $aDescription based upon print version of record. 311 $a0-7817-5248-5 330 $a This volume is the first comprehensive text and clinical reference on idiopathic myoclonic epilepsies of infancy, childhood, adolescence, and adulthood. The world's foremost experts describe the phenotypes and subtypes of myoclonic epilepsies and the underlying molecular defects and summarize cutting-edge advances in molecular genetics that shed new light on the etiologies of these syndromes. The book offers clinicians much-needed assistance in recognizing and diagnosing idiopathic myoclonic epilepsies and selecting appropriate treatment. Each chapter includes diagnostic and treatment algor 410 0$aAdvances in neurology. 606 $aEpilepsy 615 0$aEpilepsy. 676 $a616.853 702 $aGenton$b Pierre 702 $aSydor$b Anne M 702 $aScheidt$b Scott 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910811990803321 996 $aMyoclonic epilepsies$94110923 997 $aUNINA