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Oxford textbook of neuromuscular disorders /

Part of the Oxford Textbooks in Clinical Neurology series, the Oxford Textbook of Neuromuscular Disorders covers the scientific basis, clinical diagnosis, and treatment of neuromuscular disorders with a particular focus on the most clinically relevant disorders. The book is organized into seven sect...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Hilton-Jones, David (Editor ), Turner, Martin R. (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Oxford : Oxford University Press, 2014.
Edición:First edition.
Colección:Oxford textbooks in clinical neurology.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 0 |a Oxford textbook of neuromuscular disorders /  |c edited by David Hilton-Jones, Martin R. Turner. 
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505 0 |a Cover; Oxford Textbook of Neuromuscular Disorders; Series; Copyright; Preface; Contents; Abbreviations; Contributors; section 1Approach to the Patient; CHAPTER 1 Eliciting the history; CHAPTER 2 Genetic considerations; CHAPTER 3 Examination; SECTION 2Anterior Horn; CHAPTER 4 Amyotrophic lateral sclerosis; CHAPTER 5 Spinal muscular atrophy and hereditary motor neuropathy; CHAPTER 6 Kennedy disease; CHAPTER 7 Poliomyelitis; SECTION 3Peripheral Nerve: Inherited; CHAPTER 8 Charcot-Marie-Tooth disease; CHAPTER 9 Hereditary sensory and autonomic neuropathies. 
505 8 |a CHAPTER 10 Familial amyloid polyneuropathyCHAPTER 11 Inherited metabolic neuropathies; SECTION 4Peripheral Nerve: Acquired; Chapter 12 Mononeuropathy; CHAPTER 13 Multiple mononeuropathies; CHAPTER 14 Plexopathy; CHAPTER 15 Polyneuropathies: axonal; CHAPTER 16 Polyneuropathies: demyelinating; CHAPTER 17 Diabetic neuropathy; CHAPTER 18 Peripheral nerve hyperexcitability disorders; SECTION 5Neuromuscular Junction: Inherited and Acquired; CHAPTER 19 Inherited myasthenic syndromes; CHAPTER 20 Myasthenia gravis; CHAPTER 21 The Lambert-Eaton myasthenic syndrome; SECTION 6Muscle. 
505 8 |a CHAPTER 22 The dystrophinopathiesCHAPTER 23 Limb-girdle muscular dystrophies; CHAPTER 24 The congenital muscular dystrophies; CHAPTER 25 The myotonic dystrophies; CHAPTER 26 Facioscapulohumeral muscular dystrophy; CHAPTER 27 Distal and myofibrillar myopathies; CHAPTER 28 Congenital/ultrastructural myopathies; CHAPTER 29 Metabolic myopathies; CHAPTER 30 Mitochondrial cytopathies; CHAPTER 31 Skeletal muscle channelopathies; CHAPTER 32 Idiopathic inflammatory myopathies; CHAPTER 33 Drug-induced neuromuscular disorders; CHAPTER 34 Endocrine myopathies; SECTION 7Acute Neuromuscular Consults. 
505 8 |a CHAPTER 35 The neuromuscular emergency consultCHAPTER 36 Critical care of neuromuscular disorders; Index. 
520 |a Part of the Oxford Textbooks in Clinical Neurology series, the Oxford Textbook of Neuromuscular Disorders covers the scientific basis, clinical diagnosis, and treatment of neuromuscular disorders with a particular focus on the most clinically relevant disorders. The book is organized into seven sections, starting with the general approach to the patient with neuromuscular disorders and then focusing on specific neuromuscular conditions affecting theperipheral nervous system from its origins at the spinal cord anterior horn on its outward course to their effector muscles and the inbound sensory. 
504 |a Includes bibliographical references and index. 
546 |a English. 
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650 0 |a Diseases. 
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700 1 |a Turner, Martin R.,  |e editor. 
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