Description
The Nile on eBay FREE SHIPPING UK WIDE Neuromuscular Disorders by Satish V. Khadilkar, Rakhil S. Yadav, Bhagyadhan A. Patel This book provides a concise overview of the diagnosis, therapy, and recent updates of various neuromuscular disorders in tabulated form and with illustrative cases. Treating neuromuscular disorders requires a sound, step-by-step clinical approach based on differential diagnosis and laboratory investigations. FORMAT Hardcover CONDITION Brand New Publisher Description This book provides a concise overview of the diagnosis, therapy, and recent updates of various neuromuscular disorders in tabulated form and with illustrative cases. Treating neuromuscular disorders requires a sound, step-by-step clinical approach based on differential diagnosis and laboratory investigations. Yet to date, no single, compact book offers all the relevant information about managing these disorders. This book fills that gap, presenting the state of the art in the field and addressing practical problems with their solutions. Each chapter covers disorder characteristics, clinical differentiating points, relevant investigations, and their interpretation, available genetic testing, best management approaches, and counseling. Illustrative cases provide valuable insights, while extensive tables and illustrations will be helpful for the Neurologist, neuromuscular specialist, Neurology resident, Physician, and physiotherapist. Table of Contents Part I Approach to a Neuromuscular Case.- 1. Neuromuscular disorders: A clinical approach.- Part II Basic principles.- 2. Electrophysiology.- 3. Histopathology.- 4. Genetics.- 5. Immunotherapy.- 6. Rehabilitation.- Part III Motor weakness: Asymmetric: UMN and LMN signs and fasciculation.- 7. Motor Neuron Diseases (Amyotrophic Lateral Sclerosis).- Part IV Motor weakness: Asymmetric: LMN only.- 8. Polio / Post-polio syndrome.- 9. Hirayama disease and Other Focal Amyotrophies.- 10. Progressive muscular atrophy (PMA).- 11. Acute motor axonal neuropathy (AMAN).- 12. Multifocal motor neuropathy (MMN).- 13. Fascio-scapular muscular dystrophy (FSHD).- Part V Motor weakness: Symmetric: Proximal.- 14. Spinal Muscular atrophy (SMA).- 15. Porphyria.- 16. Congenital Myasthenic syndromes (CMS).- 17. Dystrophinopathies: Duchenne and Becker Muscular Dystrophies.- 18. Limb-Girdle Muscular Dystrophies (LGMD).- 19. Emery Dreifuss Muscular dystrophy (EDMD).- 20. Oculopharyngeal muscular dystrophy (OPMD).- 21. Congenital muscular dystrophies (CMD).- 22. Congenital myopathies.- 23. Inflammatory myopathies.- Part VI Motor weakness: Symmetric: Distal.- 24. Distal Hereditary Motor Neuropathy (dHMN).- 25. Distal myopathies.- 26. Myotonic dystrophies.- 27. Brown-Vialetto-Van Laere syndrome (BVVL).- Part VII Motor weakness: Fluctuating weakness.- 28. Myasthenia Gravis (MG).- 29. Lambert-Eaton myasthenic syndrome (LEMS) and myasthenia gravis Lambert-Eaton overlap syndrome (MLOS).- 30. Periodic paralysis.- Part VIII Motor weakness: Exercise intolerance.- 31. Metabolic myopathies.- Part IX Motor weakness: Muscle stiffness, cramps, spasms, rigidity, or contracture.- 32. Peripheral nerve hyperexcitability disorder: Neuromyotonia and Satoyoshi syndrome.- 33. Stiff person syndrome.- 34. Non dystrophic myotonias.- Part X Sensory motor weakness: asymmetric.- 35. Individual Mononeuropathies.- 36. Mononeuritis multiplex: Vasculitis (systemic, non-systemic) Neuropathies.- 37. Mononeuritis multiplex: Multifocal acquired demyelinating sensory and motor neuropathy (MADSAM).- 38. Mononeuritis multiplex: Hansen disease (leprosy).- 39. Chronic immune polyradiculopathy -Sensory (CISP), Motor (CIMP), Sensory-motor (CISMP).- 40. Compressive Radiculopathies.- 41. Brachial plexopathy.- 42. Lumbosacral plexopathy.- 43. Hereditary neuropathy with pressure palsy (HNPP).- Part XI Sensory motor weakness: Symmetric.- 44. Hereditary motor sensory neuropathies (HMSN)/ Charcot-Marie-Tooth disease (CMT).- 45. Guillain-Barré syndrome (GBS).- 46. Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP).- 47. X-linked form of Charcot-Marie-Tooth disease (CMT X).- 48. Other Hereditary neuropathies 1.- 49. Other Hereditary neuropathies 2.- 50.Neuropathy secondary to systemic diseases.- Part XII Sensory.- 51. Miller Fisher syndrome (MFS).- 52. Distal acquired demyelinating symmetric (DADS) neuropathy.- 53. Paraproteinemic neuropathy.- 54.Sensory ganglionopathies. Details ISBN 9819790093 Author Bhagyadhan A. Patel Publisher Springer Verlag, Singapore ISBN-13 9789819790098 Format Hardcover Country of Publication Singapore Replaces 9789811053603 Audience Professional & Vocational Subtitle A Comprehensive Review with Illustrative Cases Edition Description Second Edition 2024 Pages 838 Year 2024 Publication Date 2024-12-29 DEWEY 616.8 Country of Origin NL Product Class Description Clinical Medicine: Professional ISBN-10 9819790093 UK Release Date 2024-12-29 Imprint Springer Verlag, Singapore Place of Publication Singapore Alternative 9789819790104 Illustrations 101 Illustrations, color; 59 Illustrations, black and white We've got this At The Nile, if you're looking for it, we've got it. With fast shipping, low prices, friendly service and well over a million items - you're bound to find what you want, at a price you'll love! 30 DAY RETURN POLICY No questions asked, 30 day returns! FREE DELIVERY No matter where you are in the UK, delivery is free. 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Would reccomend this seller 110%! messaged me to verify I was certain and happy with what I was buying and checked in regularly to ensure I was never confused on when the package was due or shipped! When I was out during the delivery, the seller went out of their way to ensure I was kept up to date on the redelivery and tracking info! Recieved safely and all products were pristine condition! Securely packed and good value for money - even came with freebies :) very high quality would buy again!
I had a ‘90s copy. I was excited about the new edition. With a new forward by J Wasserman and intro by LM DuQuette. The book was excellent value and it arrived in perfect condition as it was sold new. A gorgeous looking tome.I gave 5 stars for the description, I had no communication with the seller and only gave 4 stars for Dispatch Time. Dispatched on Nov 4th with the last day being tomorrow. The process was great. Highly recommended. I’ve done business with these guys and will continue to.
I love these diaries but they can be a little expensive. However this was a good price from this seller and I would definitely use this seller again. Excellent communication. The delivery time was a little longer than stated but it wasn’t the seller’s fault. They were very supportive. I was worried the item would arrive bent or folded if it was taking so long in transit but it was really well packaged and in perfect condition.
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