Neuromuscular Disorders
portes grátis
Neuromuscular Disorders
A Comprehensive Review with Illustrative Cases
Khadilkar, Satish V.; Yadav, Rakhil S.; Patel, Bhagyadhan A.
Springer Verlag, Singapore
01/2025
836
Dura
9789819790098
Pré-lançamento - envio 15 a 20 dias após a sua edição
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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-Barre 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.
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Neuromuscular disorders;Neuropathy;Myopathy;Motor neuron disease;Radiculopathy
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-Barre 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.
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