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020 _a9789819790104
_9978-981-97-9010-4
024 7 _a10.1007/978-981-97-9010-4
_2doi
050 4 _aRC346-429.2
072 7 _aPSAN
_2bicssc
072 7 _aSCI089000
_2bisacsh
072 7 _aPSAN
_2thema
100 1 _aKhadilkar, Satish V.
_eauthor.
_4aut
_4http://id.loc.gov/vocabulary/relators/aut
_989857
245 1 0 _aNeuromuscular Disorders
_h[electronic resource] :
_bA Comprehensive Review with Illustrative Cases /
_cby Satish V. Khadilkar, Rakhil S. Yadav, Bhagyadhan A. Patel.
250 _a2nd ed. 2024.
264 1 _aSingapore :
_bSpringer Nature Singapore :
_bImprint: Springer,
_c2024.
300 _aXXXVI, 838 p. 160 illus., 101 illus. in color.
_bonline resource.
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
347 _atext file
_bPDF
_2rda
505 0 _aPart 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.
520 _aThis 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.
650 0 _aNervous system
_xDiseases.
_964036
650 0 _aNeurology .
_966816
650 0 _aNervous system
_xRadiography.
_974040
650 0 _aNeurophysiology.
_973730
650 1 4 _aNeurological Disorders.
_974042
650 2 4 _aNeurology.
_966816
650 2 4 _aNeuroradiology.
_974043
650 2 4 _aNeurophysiology.
_973730
700 1 _aYadav, Rakhil S.
_eauthor.
_4aut
_4http://id.loc.gov/vocabulary/relators/aut
_989858
700 1 _aPatel, Bhagyadhan A.
_eauthor.
_4aut
_4http://id.loc.gov/vocabulary/relators/aut
_989859
710 2 _aSpringerLink (Online service)
773 0 _tSpringer Nature eBook
776 0 8 _iPrinted edition:
_z9789819790098
776 0 8 _iPrinted edition:
_z9789819790111
776 0 8 _iPrinted edition:
_z9789819790128
856 4 0 _uhttps://doi.org/10.1007/978-981-97-9010-4
912 _aZDB-2-SME
912 _aZDB-2-SXM
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