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Neuromuscular Disorders of Infancy, Childhood, and Adolescence
A Clinician's Approach
9780750671903
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Description
Childhood neuromuscular disorders differ from adult diseases and require much experience to evaluate. However, most neurologists trained in EMG have little experience evaluating children or infants. This book, written by a stellar list of world-class experts in paediatric neuromuscular diseases, provides clinicians with the knowledge they need to successfully diagnose and treat their paediatric patients.
Product Details
34551
9780750671903
9780750671903
Data sheet
- Publication date
- 2002
- Issue number
- 1
- Cover
- hard cover
- Pages count
- 1344
- Dimensions (mm)
- 216 x 279
- Weight (g)
- 3996
- I. Clinical and Laboratory Approach to the Infant and Child with a Neuromuscular Problem
1. Introduction: Historical Perspectives
2. Genetics
3. EMG
4. Muscle Biopsy
5. Nerve Biopsy
II. Infantile Hypotonia and Arthrogryposis
6. Neonatal Hypotonia
7. Arthrogryposis
III. Anterior Horn Cell Disorders
8. Spinal Muscular Atrophies
9. Juvenile Muscular Atrophy of Unilateral Upper Extremity (Hirayama Disease)
10. Juvenile ALS vs. Other Motor Neuron Disorders
11. Infantile Poliomyelitis and Other Enteropathic Motor Neuron Diseases
IV. Radiculopathies and Plexopathies
12. Radiculopathies
13. Plexopathies Rabies
Peripheral Nerve Disorders
14. Vaccine Associated Poliomyelitis
15. Tetanus
16. Rabies
Mononeuropathies
17. Facial Palsies: Congenital and acquired
18. Upper Extremities
19. Lower Extremities
Polyneuropathies
20. Overview of the Neuropathies
21. Congenital and Early Infantile Neuropathies
22. Hereditary Charcot - Marie - Tooth and Other Genetic Neuropathies
23. Guillain - Barre Syndrome
24. Acute Moter Axonal Neuropathy in Childhood
25. Tick Paralysis
26. Chronic Inflammatory Demyelinating and Recurrent Neuropathies
27. Peripheral Neuropathy in Inherited Metabolic Disease
28. Neuropathies Secondary to Systemic Disorders
29. Childhood Hansens Disease
30. Toxic Neuropathies
31. Autonomic Neuropathies
V. Neuromuscular Junction Disorders
32. Infantile Botulism
33. Congential Miyasthenia Gravis
34. Acquired Miyasthenia Gravis in Childhood
VI. Myopathies
35. Clinical Syndromes of Congenital Myopathies
36. Congenital Muscular Dystrophies
37. Dystrophinopathies
38. Facioscapulohumeral Dystrophy, Scapuloperoneal Syndromes and Distal Myopathies
39. The Limb Girdle Muscular Dystrophies
40. Emery - Dreifuss Muscular Dystrophy
41. Myopathies of Systemic Disease
42. Channelopathies Affecting Skeletal Muscle in Childhood
43. Glycogen Storage Diseases of Muscle
44. Lipid Storage Muscular Disorders
45. Myoadenylate Deaminase Deficiency
46. Metabolic : Mitochondrial
47. Juvenile Dermatomyositis and other Inflammatory Myopathies in Children
48. Other Inflammatory Myopathies: Viral Trichinosis, and Pyomyositis
49. Rigid Spine Syndromes
VII. Special Clinical Problems
50. Neuromuscular Problems of the Critically III Neonate and Child
51. HyperCKemia and Rhabdomyolysis
52. Malignant Hyperthermia
53. Continuous Muscle Fiber Activity Including the Stiff Person
54. Disorder of the Ocular Motor Cranial Nerves and Extraocular Muscles
55. Neurogenic Dysphagia in Newborns and Infants
56. Friedreichs Ataxis, Vitamin E. Deficiency
57. Dominantly Inherited Spinocerebellar Syndromes
58. Reflex Sympathetic Dystrophy
VIII. General Therapeutic Principles
59. Autoimmune Pharmacotherapeutic Intervention in Children
60. Androgen and Corticosteroid Therapy of Muscular Dystrophies: New Therapeutic Modalities
61. The Principles and Practice of Molecular Therapies
62. Intensive Care Management
63. Orthopedic Treatment
64. Rehabilitation of the Pediatric Patient with a Neuromuscular Disease
65. Bioethical Issues
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