02464nam 2200553 450 991079067680332120230120011144.00-444-53494-6(CKB)2550000001123662(EBL)1429408(OCoLC)862831601(SSID)ssj0000629806(PQKBManifestationID)11380086(PQKBTitleCode)TC0000629806(PQKBWorkID)10743882(PQKB)11092233(MiAaPQ)EBC1429408(EXLCZ)99255000000112366220101105d2012 uy| 0engur|n|---|||||txtccrAtaxic disorders /volume editors, Sankara H. Subramony and Alexandria DürrEdinburgh :Elsevier,2012.1 online resource (682 p.)Handbook of clinical neurology ;3rd series, volume 103Description based upon print version of record.0-444-51892-4 1-299-94128-1 Includes bibliographical references and index.section 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.This 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 nHandbook of clinical neurology ;3rd ser., v. 103.AtaxiaMovement disordersAtaxia.Movement disorders.616.8/3Subramony Sankara H1489534Dürr Alexandra1489535MiAaPQMiAaPQMiAaPQBOOK9910790676803321Ataxic disorders3710266UNINA