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Neuromuscular disordersa comprehensive review with illustrative cases /

Record Type:	Electronic resources : Monograph/item
Title/Author:	Neuromuscular disordersby Satish V. Khadilkar, Rakhil S. Yadav, Bhagyadhan A. Patel.
Reminder of title:	a comprehensive review with illustrative cases /
Author:	Khadilkar, Satish V.
other author:	Yadav, Rakhil S.
Published:	Singapore :Springer Nature Singapore :2024.
Description:	xxxvi, 838 p. :ill. (some col.), digital ;24 cm.
Contained By:	Springer Nature eBook
Subject:	Neuromuscular diseases.
Online resource:	https://doi.org/10.1007/978-981-97-9010-4
ISBN:	9789819790104$q(electronic bk.)

Neuromuscular disordersa comprehensive review with illustrative cases /
Khadilkar, Satish V.

Neuromuscular disordersa comprehensive review with illustrative cases /[electronic resource] :by Satish V. Khadilkar, Rakhil S. Yadav, Bhagyadhan A. Patel. - Second edition. - Singapore :Springer Nature Singapore :2024. - xxxvi, 838 p. :ill. (some col.), digital ;24 cm.

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.

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.

ISBN: 9789819790104$q(electronic bk.)

Standard No.: 10.1007/978-981-97-9010-4doiSubjects--Topical Terms:

281134
Neuromuscular diseases.

LC Class. No.: RC925.5

Dewey Class. No.: 616.744

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