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:
Neuromuscular diseases.
Nervous system > Diseases.
Diseases.
Nervous System Diseases
Disease
Neuromuscular Diseases
Maladies neuromusculaires.
Système nerveux > Maladies.
Maladies.
disease.
illness.
HEALTH & FITNESS > Diseases > General.
MEDICAL > Clinical Medicine.
MEDICAL > Diseases.
MEDICAL > Evidence-Based Medicine.
MEDICAL > Internal Medicine.
Nervous system > Diseases
Diseases
Neuromuscular diseases
Acceso en línea:Texto completo
Tabla de Contenidos:
  • 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.
  • 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.
  • 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.
  • CHAPTER 35 The neuromuscular emergency consultCHAPTER 36 Critical care of neuromuscular disorders; Index.

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