LEADER 02464nam 2200553 450 001 9910790676803321 005 20230120011144.0 010 $a0-444-53494-6 035 $a(CKB)2550000001123662 035 $a(EBL)1429408 035 $a(OCoLC)862831601 035 $a(SSID)ssj0000629806 035 $a(PQKBManifestationID)11380086 035 $a(PQKBTitleCode)TC0000629806 035 $a(PQKBWorkID)10743882 035 $a(PQKB)11092233 035 $a(MiAaPQ)EBC1429408 035 $a(EXLCZ)992550000001123662 100 $a20101105d2012 uy| 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aAtaxic disorders /$fvolume editors, Sankara H. Subramony and Alexandria Du?rr 210 1$aEdinburgh :$cElsevier,$d2012. 215 $a1 online resource (682 p.) 225 1 $aHandbook of clinical neurology ;$v3rd series, volume 103 300 $aDescription based upon print version of record. 311 $a0-444-51892-4 311 $a1-299-94128-1 320 $aIncludes bibliographical references and index. 327 $asection 1. Basic aspects -- section 2. Acquired ataxias -- section 3. Degenerative ataxias -- section 4. Degenerative ataxias : mitochondrial, autosomal, recessive and x-linked -- section 5. Degenerative ataxias : autosomal dominant -- section 6. Other issues. 330 $aThis volume's primary goal is to provide a comprehensive understanding of recent developments and advancements in the study of ataxic disorders. Beginning with an examination of the cerebellar region, and then progressing to a fresh perspective on the clinical aspects of the various forms of ataxia, this handbook gives clinicians a state-of-the-art reference for the management of the many etiologies and neurological manifestations of ataxic disorders. Clinicians will gain a broader understanding of generative ataxias and the genetic disorders associated with them. In addition, new n 410 0$aHandbook of clinical neurology ;$v3rd ser., v. 103. 606 $aAtaxia 606 $aMovement disorders 615 0$aAtaxia. 615 0$aMovement disorders. 676 $a616.8/3 701 $aSubramony$b Sankara H$01489534 701 $aDu?rr$b Alexandra$01489535 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910790676803321 996 $aAtaxic disorders$93710266 997 $aUNINA