{"product_id":"neuromuscular-disease-a-case-based-approach-paperback-softback-9781108744188","title":"Neuromuscular Disease; A Case-Based Approach (Paperback \/ softback) 9781108744188","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eNeuromuscular Disease\u003c\/font\u003e\u003cbr\u003e\r\n\u003cfont size=\"5\"\u003eA Case-Based Approach\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cem\u003e66 highly-illustrated adult and paediatric neuromuscular cases, with state-of-the-art diagnostic investigations and treatment and care plans.\u003c\/em\u003e\u003c\/p\u003e\r\n\r\n\r\n\u003cp\u003e\u003cfont size=\"4\"\u003eJessica E. Hoogendijk (Author), Marianne de Visser (Author), Pieter A. van Doorn (Author), Erik H. Niks (Author)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9781108744188, Cambridge University Press\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003ePaperback \/ softback, published 19 December 2024\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e294 pages\u003cbr\u003e25.5 x 17.9 x 1.5 cm, 0.62 kg\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\u003eThere are over 800 neuromuscular disorders and this can leave clinicians feeling lost as they try to diagnose and manage patients. On the basis of 66 adult and paediatric neuromuscular case vignettes, readers will be walked through using case histories and clinical manifestations as a starting point for diagnosis. For each case, diagnostic tools, disease pathogenesis, prognosis and treatment options are discussed. Symptoms, signs and syndromes are cross-linked to help the reader navigate the array of disorders. Accompanying tables explain differential diagnoses and 30 videos demonstrate clinical features. This second edition has been thoroughly updated as the neuromuscular subspecialty has developed from clinically and pathologically descriptive to making use of new diagnostic technologies and therapies. Neurologists at all levels, paediatricians, internists, geneticists, rehabilitation physicians, physiotherapists and researchers in the field will find this an invaluable guide, as they seek to familiarise themselves with this complex range of disorders.\u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003ePart I. Evaluation and Treatment of Patients with a Neuromuscular Disorder: 1. Neuromuscular diseases: anterior horn cell disorders, peripheral neuropathies, neuromuscular junction disorders, myopathies\u003cbr\u003e 2. History taking and clinical examination\u003cbr\u003e 3. Differential diagnosis by presenting or prominent clinical feature\u003cbr\u003e 4. Electrodiagnostic studies\u003cbr\u003e 5. Imaging\u003cbr\u003e 6. Muscle and nerve pathology\u003cbr\u003e 7. Genetic testing\u003cbr\u003e 8. Management\u003cbr\u003e Part II. Neuromuscular Cases\u003cbr\u003e Disorders of the Anterior Horn Cell: 1. Amyotrophic lateral sclerosis\u003cbr\u003e 2. Primary lateral sclerosis, 3. Progressive muscular atrophy)\u003cbr\u003e 4. Segmental spinal muscular atrophy\u003cbr\u003e 5. Spinal and bulbar muscular atrophy (SBMA\u003cbr\u003e Kennedy disease)\u003cbr\u003e 6. Spinal muscular atrophy type I\u003cbr\u003e 7. Spinal muscular atrophy type 3\u003cbr\u003e 8. Post-polio syndrome\u003cbr\u003e poliomyelitis anterior acuta, West Nile virus poliomyelitis, acute flaccid weakness in children\u003cbr\u003e Peripheral Neuropathies: 9. Guillain-Barré syndrome and Miller-Fisher syndrome\u003cbr\u003e 10. Chronic inflammatory demyelinating polyneuropathy\u003cbr\u003e 11. IgM anti-MAG polyneuropathy\u003cbr\u003e 12. Polyneuropathy, organomegaly, endocrine manifestations, monoclonal protein, and skin changes syndrome\u003cbr\u003e 13. Vasculitic neuropathy\u003cbr\u003e 14. Small fibre neuropathy\u003cbr\u003e 15. Paraneoplastic sensory neuronopathy (SNN, ganglionopathy)\u003cbr\u003e 16. Wartenberg migrant sensory neuropathy\u003cbr\u003e 17. Multifocal motor neuropathy\u003cbr\u003e 18. Peripheral nerve hyperexcitability syndromes: Morvan syndrome\u003cbr\u003e 19. Idiopathic brachial plexus neuropathy, neuralgic amyotrophy\u003cbr\u003e 20. Diabetic polyneuropathy\u003cbr\u003e 21. Alcoholic polyneuropathy\u003cbr\u003e 22. Chronic idiopathic axonal polyneuropathy\u003cbr\u003e 23. Critical illness polyneuropathy and myopathy\u003cbr\u003e 24. Drug-induced polyneuropathies: Amiodarone polyneuropathy\u003cbr\u003e 25. Lyme radiculopathy\u003cbr\u003e 26. Leprosy\u003cbr\u003e 27. Charcot-Marie-Tooth disease type 1a\/Hereditary neuropathy with liability to pressure palsies\u003cbr\u003e 28. Charcot-Marie-Tooth disease type 2a and 2b\u003cbr\u003e 29. Hereditary sensory and autonomic neuropathy type 4\u003cbr\u003e 30. Hereditary transthyretin amyloidosis\u003cbr\u003e Disorders of the Neuromuscular Junction: 31. Myasthenia gravis with acetylcholine receptor antibodies\u003cbr\u003e 32. Myasthenia gravis with MuSK antibodies\u003cbr\u003e 33. Drug-induced myasthenia gravis: Immune checkpoint inhibitor-related\u003cbr\u003e 34. Lambert-Eaton myasthenic syndrome\u003cbr\u003e 35. Congenital myasthenic syndromes: Dok7\u003cbr\u003e Myopathies: 36. Duchenne muscular dystrophy\u003cbr\u003e 37. Becker muscular dystrophy\u003cbr\u003e 38. Facioscapulohumeral muscular dystrophy\u003cbr\u003e 39. Myotonic dystrophy type 1\u003cbr\u003e 40. Myotonic dystrophy type 2\u003cbr\u003e 41. Limb girdle muscular dystrophy R1, calpain-related\u003cbr\u003e 42. Limb girdle muscular dystrophy R9, FKRP-related\u003cbr\u003e 43. Bethlem myopathy, a collagen VI-related myopathy\u003cbr\u003e Ullrich congenital muscular dystrophy\u003cbr\u003e 44. Oculopharyngeal muscular dystrophy\u003cbr\u003e 45. Emery-Dreifuss muscular dystrophy\u003cbr\u003e 46. Caveolinopathy, rippling muscle disease\u003cbr\u003e 47. Distal myopathies: Miyoshi myopathy, dysferlinopathy\u003cbr\u003e anoctaminopathy\u003cbr\u003e 48. Distal myopathies: GNE myopathy\u003cbr\u003e 49. Myofibrillar myopathies: Desminopathy\u003cbr\u003e 50. Skeletal muscle channelopathies: non-dystrophic myotonia\u003cbr\u003e myotonia congenita (Becker)\u003cbr\u003e 51. Skeletal muscle channelopathies: hypokalaemic periodic paralysis\u003cbr\u003e 52. Pompe Disease (glycogen storage disease type II\u003cbr\u003e α-glucosidase deficiency)\u003cbr\u003e 53. McArdle Disease (glycogen storage disease type V)\u003cbr\u003e myophosphorylase deficiency), rhabdomyolysis\u003cbr\u003e 54. Carnitine palmitoyltransferase-II deficiency\u003cbr\u003e 55. Mitochondrial myopathies: chronic progressive external ophthalmoplegia\u003cbr\u003e 56. Ryanodine receptor 1-related disorders\u003cbr\u003e 57. Congenital myopathies: X-linked myotubular myopathy\u003cbr\u003e 58. Congenital myopathies: nemaline myopathy\u003cbr\u003e 59. Juvenile dermatomyositis\u003cbr\u003e 60. Dermatomyositis\u003cbr\u003e 61. Immune-mediated necrotising myopathy\u003cbr\u003e 62. Inclusion body myositis\u003cbr\u003e 63. Endocrine myopathy: Hypothyroid myopathy\u003cbr\u003e hyperthyroid myopathy\u003cbr\u003e 64. Drug-induced myopathies: hydroxychloroquine myopathy\u003cbr\u003e 65. A- or paucisymptomatic hyperCKaemia\u003cbr\u003e 66. Exertional rhabdomyolysis.\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eSubject Areas: Neurology \u0026amp; clinical neurophysiology [\u003ca title=\"See our other books on Neurology \u0026amp; clinical neurophysiology\" href=\"https:\/\/freshlyprintedbooks.co.uk\/search?q=%22Neurology%20\u0026amp;%20clinical%20neurophysiology%20%5BMJN%5D%22\"\u003eMJN\u003c\/a\u003e]\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\u003c\/font\u003e","brand":"Cambridge University Press","offers":[{"title":"Brand New","offer_id":52460702400792,"sku":"9781108744188","price":45.59,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9781108744188i.jpg?v=1785458993","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/neuromuscular-disease-a-case-based-approach-paperback-softback-9781108744188","provider":"Freshly Printed Books","version":"1.0","type":"link"}