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Peripheral nerve disorders [electronic resource]

Peripheral nerve disorders [electronic resource]

자료유형
E-Book(소장)
개인저자
Said, G. (Gerard). Krarup, Christian.
서명 / 저자사항
Peripheral nerve disorders [electronic resource] / edited by Gérard Said, Christian Krarup.
발행사항
Edinburgh :   Elsevier,   2013.  
형태사항
1 online resource (xv, 987 p.) : ill. (some col.).
총서사항
Handbook of clinical neurology ;v. 115
ISBN
0444529020 9780444529022 9780444633552 0444633553
요약
Disorders of the peripheral nervous system (PNS) are the cause of prominent neurological symptoms including weakness, sensory loss, pain and autonomic dysfunction associated with deficits, morbidity and mortality. These disorders may be primary hereditary or cryptogenic neurologic disorders confined to the PNS or part of the pathology of both the central nervous system and the PNS. Most PNS disorders are secondary to other system disorders and may be responsive to treatment of the primary disease. Important advances have been obtained in several areas including molecular genetics, biochemistry, immunology, morphology and physiology that have enhanced our understanding of the causes and consequences of damage to peripheral nerve. Understanding of both these groups of PNS diseases has greatly expanded over recent years and has led to important advances of treatment both to protect and to repair damages of peripheral nerve. This volume provides an overview of the state-of-the-art of examination, diagnosis and treatment of these very diverse disorders and will be of interest to both the research and clinical neuroscience and neurology communities. *Cover both hereditary and cryptogenic neurologic disorders *Includes advances in the basic science of PNS from molecular genetics, biochemistry, immunology, morphology and physiology *Detailed coverage of neuropathy in connective tissue disorders, infectious disorders, metabolic disorders and malignancy.
일반주기
Title from e-Book title page.  
내용주기
Prelude to the peripheral neuropathies -- Microscopic anatomy: normal structure -- Gross anatomy and development of the peripheral nervous system -- Physiology and pathophysiology of myelinated nerve fibers -- Biology of Schwann cells -- Neurophysiological approach to disorders of peripheral nerve -- Testing the autonomic nervous system -- Imaging of the peripheral nervous system -- The nerve biopsy: indications, technical aspects, and contribution -- The cutaneous nerve biopsy: technical aspects, indications, and contribution -- Antibody testing in peripheral nerve disorders -- DNA testing in hereditary neuropathies -- Examination and clinical care of the patient with neuropathy -- How to explore a patient with a chronic axonal polyneuropathy -- Evaluation of a patient with suspected chronic demyelinating polyneuropathy -- Sensory-motor assessment in clinical research trials -- Management of painful neuropathies -- Diagnosis of brachial and lumbosacral plexus lesions -- Compression and entrapment neuropathies -- Facial nerve palsy and hemifacial spasm -- The Guillain-Barre syndrome -- Chronic inflammatory demyelinative polyneuropathy -- Treatment of chronic inflammatory demyelinating polyradiculoneuropathy -- Multifocal motor neuropathy -- Neuropathy and monoclonal gammopathy -- Vasculitic neuropathy -- Sarcoidosis of the peripheral nervous system -- Leprous neuropathy -- HIV peripheral neuropathy -- Human T-cell leukemia virus (HTLV)-associated neuropathy -- Herpes virus infection in the peripheral nervous system -- Lyme neuroborreliosis -- Diabetic neuropathy -- Biology of diabetic neuropathy -- Uremic neuropathy -- Porphyric neuropathy -- Fabry disease -- Transthyretin familial amyloid polyneuropathy -- Hereditary gelsolin amyloidosis -- Malignant cell infiltration in the peripheral nervous system -- Paraneoplastic neuropathy -- Drug-induced neuropathies -- Late radiation injury to peripheral nerves -- Neuromuscular complications of critical illness -- The surgery of peripheral nerves (including tumors) -- Peripheral neuropathy in the elderly -- Dominant Charcot-Marie-Tooth syndrome and cognate disorders -- Recessively transmitted predominantly motor neuropathies -- Early onset (childhood) monogenic neuropathies -- Hereditary sensory and autonomic neuropathies -- Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders -- Giant axonal neuropathy -- Neurofibromatosis type 1 (NF1): diagnosis and management -- Neurofibromatosis type 2 (NF2): diagnosis and management.
서지주기
Includes bibliographical references and index.
이용가능한 다른형태자료
Issued also as a book.  
일반주제명
Nerves, Peripheral --Diseases. Peripheral Nervous System Diseases.
바로가기
ScienceDirect   URL
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245 0 0 ▼a Peripheral nerve disorders ▼h [electronic resource] / ▼c edited by Gérard Said, Christian Krarup.
260 ▼a Edinburgh : ▼b Elsevier, ▼c 2013.
300 ▼a 1 online resource (xv, 987 p.) : ▼b ill. (some col.).
490 1 ▼a Handbook of clinical neurology ; ▼v v. 115
500 ▼a Title from e-Book title page.
504 ▼a Includes bibliographical references and index.
505 0 ▼a Prelude to the peripheral neuropathies -- Microscopic anatomy: normal structure -- Gross anatomy and development of the peripheral nervous system -- Physiology and pathophysiology of myelinated nerve fibers -- Biology of Schwann cells -- Neurophysiological approach to disorders of peripheral nerve -- Testing the autonomic nervous system -- Imaging of the peripheral nervous system -- The nerve biopsy: indications, technical aspects, and contribution -- The cutaneous nerve biopsy: technical aspects, indications, and contribution -- Antibody testing in peripheral nerve disorders -- DNA testing in hereditary neuropathies -- Examination and clinical care of the patient with neuropathy -- How to explore a patient with a chronic axonal polyneuropathy -- Evaluation of a patient with suspected chronic demyelinating polyneuropathy -- Sensory-motor assessment in clinical research trials -- Management of painful neuropathies -- Diagnosis of brachial and lumbosacral plexus lesions -- Compression and entrapment neuropathies -- Facial nerve palsy and hemifacial spasm -- The Guillain-Barre syndrome -- Chronic inflammatory demyelinative polyneuropathy -- Treatment of chronic inflammatory demyelinating polyradiculoneuropathy -- Multifocal motor neuropathy -- Neuropathy and monoclonal gammopathy -- Vasculitic neuropathy -- Sarcoidosis of the peripheral nervous system -- Leprous neuropathy -- HIV peripheral neuropathy -- Human T-cell leukemia virus (HTLV)-associated neuropathy -- Herpes virus infection in the peripheral nervous system -- Lyme neuroborreliosis -- Diabetic neuropathy -- Biology of diabetic neuropathy -- Uremic neuropathy -- Porphyric neuropathy -- Fabry disease -- Transthyretin familial amyloid polyneuropathy -- Hereditary gelsolin amyloidosis -- Malignant cell infiltration in the peripheral nervous system -- Paraneoplastic neuropathy -- Drug-induced neuropathies -- Late radiation injury to peripheral nerves -- Neuromuscular complications of critical illness -- The surgery of peripheral nerves (including tumors) -- Peripheral neuropathy in the elderly -- Dominant Charcot-Marie-Tooth syndrome and cognate disorders -- Recessively transmitted predominantly motor neuropathies -- Early onset (childhood) monogenic neuropathies -- Hereditary sensory and autonomic neuropathies -- Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders -- Giant axonal neuropathy -- Neurofibromatosis type 1 (NF1): diagnosis and management -- Neurofibromatosis type 2 (NF2): diagnosis and management.
520 8 ▼a Disorders of the peripheral nervous system (PNS) are the cause of prominent neurological symptoms including weakness, sensory loss, pain and autonomic dysfunction associated with deficits, morbidity and mortality. These disorders may be primary hereditary or cryptogenic neurologic disorders confined to the PNS or part of the pathology of both the central nervous system and the PNS. Most PNS disorders are secondary to other system disorders and may be responsive to treatment of the primary disease. Important advances have been obtained in several areas including molecular genetics, biochemistry, immunology, morphology and physiology that have enhanced our understanding of the causes and consequences of damage to peripheral nerve. Understanding of both these groups of PNS diseases has greatly expanded over recent years and has led to important advances of treatment both to protect and to repair damages of peripheral nerve. This volume provides an overview of the state-of-the-art of examination, diagnosis and treatment of these very diverse disorders and will be of interest to both the research and clinical neuroscience and neurology communities. *Cover both hereditary and cryptogenic neurologic disorders *Includes advances in the basic science of PNS from molecular genetics, biochemistry, immunology, morphology and physiology *Detailed coverage of neuropathy in connective tissue disorders, infectious disorders, metabolic disorders and malignancy.
530 ▼a Issued also as a book.
538 ▼a Mode of access: World Wide Web.
650 0 ▼a Nerves, Peripheral ▼x Diseases.
650 1 2 ▼a Peripheral Nervous System Diseases. ▼0 (DNLM)D010523.
700 1 ▼a Said, G. ▼q (Gerard).
700 1 ▼a Krarup, Christian.
830 0 ▼a Handbook of clinical neurology ; ▼v 3rd ser., v. 115.
856 4 0 ▼3 ScienceDirect ▼u https://oca.korea.ac.kr/link.n2s?url=http://www.sciencedirect.com/science/book/9780444529022
945 ▼a KLPA
991 ▼a E-Book(소장)

소장정보

No. 소장처 청구기호 등록번호 도서상태 반납예정일 예약 서비스
No. 1 소장처 중앙도서관/e-Book 컬렉션/ 청구기호 CR 616.808 2013 등록번호 E14004749 도서상태 대출불가(열람가능) 반납예정일 예약 서비스 M

컨텐츠정보

목차

Section 1 Introduction 1. Prelude to the peripheral neuropathies Section 2 Structure and function 2. Microscopic anatomy: normal structures; 3. Gross anatomy and development of the peripheral nervous system; 4. Physiology and pathophysiology of myelinated nerve fibers; 5. Biology of Schwann cells; 6. Neurophysiological approach to disorders of peripheral nerve; 7. Testing autonomic functions; 8. Imaging of the peripheral nervous system; 9. The nerve biopsy: indications, technical aspects and contribution; 10. The cutaneous nerve biopsy: Technical aspects, indications, and contribution; 11. Antibody testing in peripheral nerve disorders; 12. DNA testing in hereditary neuropathies Section 3 Clinical aspects 13. Examination and clinical care of the patient with neuropathy; 14. How to explore a patient with chronic axonal neuropathy; 15. Evaluation of a patient with suspected chronic demyelinating polyneuropathy; 16. Sensory-motor assessment in clinical research trials; 17. Management of painful neuropathies Section 4 Plexus and compression lesions 18. Diagnosis of brachial and lumbosacral plexus lesions; 19. Compression and entrapment neuropathies; 20. Facial nerve palsy and hemifacial spasm Section 5 Inflammatory root and nerve lesions 21. The Guillain-Barre syndrome; 22. Chronic inflammatory demyelinating polyneuropathy; 23. Treatment of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP); 24. Multifocal motor neuropathy? 25. Neuropathy and monoclonal gammopathy Section 6 Neuropathy in connective tissue disorders 26. Vasculitic neuropathy; 27. Sarcoidosis of the peripheral nervous system Section 7 Neuropathy in infectious disorders 28. Leprous neuropathy; 29. HIV peripheral neuropathy; 30. Human t-cell leukemia virus (HTLV) associated neuropathy; 31. Herpes virus infection of the peripheral nervous system; 32. Lyme neuroborreliosis Section 8 Neuropathy and metabolic disorders 33. Diabetic neuropathy; 34. Biology of diabetic neuropathy; 35. Uremic neuropathy; 36. Porphyric neuropathy; 37. Fabry’s disease; 38. Transthyretin familial amyloid polyneuropathy; 39. Hereditary gelsolin amyloidosis Section 9 Neuropathy and malignancy 40. Malignant cell infiltration in the peripheral nervous system; 41. Paraneoplastic neuropathy Section 10 Cryptogenic, Traumatic and Iatrogenic neuropathies 42. Drug induced neuropathies; 43. Late radiation injury to peripheral nerves; 44. Neuromuscular complications of critical illness; 45. The surgery of peripheral nerves (including tumours); 46. Neuropathy in the elderly Section 11. Familial neuropathies 47. Dominant Charcot-Marie-Tooth syndrome and cognate disorders; 48. Recessively transmitted predominantly motor neuropathies; 49. Early onset childhood monogenic neuropathies; 50. Hereditary sensory and autonomic neuropathies; 51. Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders; 52. Giant axonal neuropathy; 53. Neurofibromatosis 1(NF1), diagnosis and management; 54. Neurofibromatosis type 2 (NF2) diagnosis and management ?


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