LEADER 04264nam 2200793Ia 450 001 9910821845003321 005 20200520144314.0 010 $a9786613274106 010 $a9781119973317 010 $a1119973317 010 $a9781283274104 010 $a1283274108 010 $a9781119973331 010 $a1119973333 010 $a9781119973300 010 $a1119973309 035 $a(CKB)2550000000054292 035 $a(EBL)819241 035 $a(OCoLC)760105222 035 $a(SSID)ssj0000622298 035 $a(PQKBManifestationID)12223757 035 $a(PQKBTitleCode)TC0000622298 035 $a(PQKBWorkID)10655013 035 $a(PQKB)10617156 035 $a(SSID)ssj0000612394 035 $a(PQKBManifestationID)11424242 035 $a(PQKBTitleCode)TC0000612394 035 $a(PQKBWorkID)10569436 035 $a(PQKB)11006311 035 $a(MiAaPQ)EBC819241 035 $a(Au-PeEL)EBL819241 035 $a(CaPaEBR)ebr10501330 035 $a(CaONFJC)MIL327410 035 $a(Perlego)1013075 035 $a(EXLCZ)992550000000054292 100 $a20110411d2011 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aNeuromuscular disorders /$fedited by Rabi N. Tawil, Shannon Venance 205 $a1st ed. 210 $aChichester, West Sussex, UK $cWiley-Blackwell$d2011 215 $a1 online resource (285 p.) 225 1 $aNeurology in practice 300 $aDescription based upon print version of record. 311 08$a9780470654569 311 08$a0470654562 320 $aIncludes bibliographical references and index. 327 $aNeuromuscular Disorders; Contents; Contributor List; Acknowledgment; Series Preface; Preface; 1: Neuromuscular Diseases: Approach to Clinical Diagnosis; Part I: Myopathies; 2: Approach to Diseases of Muscle; 3: Inflammatory Myopathies; 4: Toxic Myopathies; 5: Metabolic Myopathies; 6: Mitochondrial Myopathies; 7: Dystrophinopathies; 8: Limb-Girdle Dystrophies; 9: Facioscapulohumeral Dystrophy; 10: Myotonic Dystrophies; 11: Oculopharyngeal Muscular Dystrophy; 12: Distal Myopathies; 13: Muscle Channelopathies; 14: Congenital Myopathies; Part II: Disorders of the Neuromuscular Junction 327 $a15: Approach to Diseases of the Neuromuscular Junction16: Myasthenia Gravis; 17: Botulism; 18: Lambert-Eaton Myasthenic Syndrome; 19: Congenital Myasthenic Syndromes; Part III: Disorders of Peripheral Nerve; 20: Approach to Diagnosis of Peripheral Nerve Disease; 21: Hereditary Motor Sensory Neuropathies (Charcot-Marie-Tooth Disease); 22: Diabetic Neuropathies; 23: Toxic and Metabolic Neuropathies; 24: Acute Inflammatory Demyelinating Neuropathies and Variants; 25: Chronic Immune-mediated Demyelinating Polyneuropathies; 26: Vasculitic Neuropathies; 27: Paraneoplastic Neuropathies 327 $a28: Brachial and Lumbosacral PlexopathiesPart IV: Disorders of Motor Neurons; 29: Approach to Diseases of the Motor Neurons; 30: Spinal Muscular Atrophy; 31: Amyotrophic Lateral Sclerosis; 32: Neuromuscular Disorders in the Intensive Care Unit; Index; colour plate 330 $aA new addition to the Neurology in Practice series, Neuromuscular Disorders provides a clinical guide to the challenging diagnosis and management of neuromuscular disorders. As a part of the series, various feature boxes are highlighted throughout. ""Tips and Tricks"" give suggestions on how to improve outcomes through practical technique or patient questioning. In addition, ""Caution"" warning boxes supply helpful advice on how to avoid problems and 'Science Revisited' boxes offer quick reminders of the basic science principles necessary for understanding the presented concepts. 410 0$aNeurology in practice. 606 $aNeuromuscular diseases 606 $aMusculoskeletal system$xDiseases 615 0$aNeuromuscular diseases. 615 0$aMusculoskeletal system$xDiseases. 676 $a616.7/44 701 $aTawil$b Rabi N$01601804 701 $aVenance$b Shannon Lee$f1959-$01601805 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910821845003321 996 $aNeuromuscular disorders$93925570 997 $aUNINA