NHS Logo

Neuromuscular disease : (Record no. 91027)

MARC details
000 -LEADER
fixed length control field 07228cam a2200781Ia 4500
001 - CONTROL NUMBER
control field ocn828628173
003 - CONTROL NUMBER IDENTIFIER
control field OCoLC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20240729131117.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS--GENERAL INFORMATION
fixed length control field m d
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field cr cnu---unuuu
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 130227s2013 nyu ob 001 0 eng d
010 ## - LIBRARY OF CONGRESS CONTROL NUMBER
Canceled/invalid LC control number 2012035669
040 ## - CATALOGING SOURCE
Original cataloging agency N$T
019 ## -
-- 829459853
-- 835236031
-- 1071772777
-- 1107716610
-- 1109946093
-- 1117878447
-- 1171563306
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9781107336148
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 1107336147
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9780511735905
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 0511735901
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9781107332829
Qualifying information (EBL)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 1107332826
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 9780521171854
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 0521171857
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9781107334489
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 1107334489
035 ## - SYSTEM CONTROL NUMBER
System control number 539302
-- (N$T)
035 ## - SYSTEM CONTROL NUMBER
System control number (OCoLC)828628173
Canceled/invalid control number (OCoLC)829459853
-- (OCoLC)835236031
-- (OCoLC)1071772777
-- (OCoLC)1107716610
-- (OCoLC)1109946093
-- (OCoLC)1117878447
-- (OCoLC)1171563306
060 #4 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER
Classification number 2013 F-795
060 #4 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER
Classification number WE 550
072 #7 - SUBJECT CATEGORY CODE
Subject category code HEA
Subject category code subdivision 039110
Source bisacsh
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED
Subject category code subdivision 056000
Source bisacsh
049 ## - LOCAL HOLDINGS (OCLC)
Holding library MAIN
245 00 - TITLE STATEMENT
Title Neuromuscular disease :
Subtitle a case-based approach
Statement of responsibility, etc
Medium [E-Book]
260 ## - PUBLICATION INFORMATION
Place of publication New York :
Publisher Cambridge University Press,
Date 2013.
300 ## - PHYSICAL DESCRIPTION
Physical description 1 online resource
336 ## - CONTENT TYPE
Content type term text
Content type code txt
Source rdacontent
337 ## - MEDIA TYPE
Media type term computer
Media type code c
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term online resource
Carrier type code cr
Source rdacarrier
490 1# - SERIES TITLE
Series statement Cambridge medicine
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references and index.
520 ## - ABSTRACT
Abstract "There are over 600 neuromuscular disorders and the variability of these syndromes can leave clinicians feeling as if they are lost in a maze as they seek to diagnose and manage patients. This book addresses this problem by using the case-history and symptom manifestation as a starting point for the diagnostic process in adult patients, mimicking the situation in the consultation room. For each case, diagnostic tools, disease pathogenesis, prognosis and treatment options are discussed, along with rare manifestations and differential diagnoses. Symptoms, signs and syndromes are cross-linked to help the reader navigate the variety of disorders. Accompanying tables give a broader picture of the manifestations of a particular disease within the landscape of neuromuscular disorders. This highly-illustrated book, with accompanying videos, will aid neurologists at all levels, internists, geneticists, rehabilitation physicians and researchers in the field, as they seek to familiarize themselves with this complex range of disorders"--Provided by publisher.
505 0# - CONTENTS
Contents Introduction: approach to the patient -- Part I. Motor neurone diseases. Case 1. Classical amyotrophic lateral sclerosis ; Case 2. ALS with frontotemporal dementia ; Case 3. Primary lateral sclerosis ; Case 4. Progressive muscular atrophy ; Case 5. Kennedy disease ; Case 6. Spinal muscular atrophy type III, Kugelberg-Welander disease ; Case 7. Post-polio syndrome ; Case 8. Spinal dural fistula -- Part II. Neuropathies. Case 9. Charcot-Marie-Tooth disease type 1A ; Case 10. Hereditary neuropathy with liability to pressure palsy ; Case 11. Charcot-Marie-Tooth disease type 2A, mitofusinopathy ; Case 12. X-linked Charcot-Marie-Tooth disease ; Case 13. Hereditary sensory and autonomic neuropathy type 4 ; Case 14. Guillain-Barre; syndrome ; Case 15. Miller-Fisher syndrome ; Case 16. Chronic inflammatory demyelinating polyneuropathy ; Case 17. Multifocal motor neuropathy ; Case 18. Peripheral nerve hyperexcitability syndrome, Morvan's syndrome ; Case 19. Vasculitic neuropathy ; Case 20. Neuropathy and ataxia caused by IgM gammopathy ; Case 21. Polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes ; Case 22. Subacute sensory paraneoplastic neuropathy and ganglionopathy ; Case 23. Neurolymphomatosis ; Case 24. Diabetic neuropathy ; Case 25. Alcohol neuropathy ; Case 26. HIV neuropathy ; Case 27. Lyme radiculoneuritis ; Case 28. Lepromatous neuropathy ; Case 29. Toxic iatrogenic neuropathy ; Case 30. Idiopathic neuralgic amyotrophy ; Case 31. Small nerve fibre neuropathy ; Case 32. Critical illness polyneuropathy ; Case 33. Chronic idiopathic axonal polyneuropathy -- Part III. Neuromuscular junction disorders. Case 34. Classic myasthenia gravis ; Case 35. Myasthenia gravis with autoantibodies to MuSK ; Case 36. Lambert-Eaton myasthenic syndrome ; Case 37. Congenital myasthenic syndrome: slow channel syndrome -- Part IV. Myopathies. Case 38. Becker muscular dystrophy ; Case 39. Caveolinopathy, including limb girdle muscular dystrophy type 1C ; Case 40. Limb girdle muscular dystrophy type 2A, calpainopathy ; Case 41. Limb girdle muscular dystrophy type 2I, fukutin-related protein deficiency ; Case 42. Emery-Dreifuss muscular dystrophy ; Case 43. Facio-scapulo-humeral dystrophy ; Case 44. Miyoshi myopathy, dysferlinopathy, limb girdle muscular dystrophy type 2B ; Case 45. Distal myopathy with rimmed vacuoles, hereditary inclusion body myopathy ; Case 46. Oculopharyngeal muscular dystrophy ; Case 47. A woman with a family history of muscle weakness and severe cardiac complaints, desminopathy ; Case 48. Late-onset congenital myopathy caused by a mutation in the RYR1 gene, central core disease ; Case 49. Bethlem myopathy ; Case 50. Myotonic dystrophy type 1, Curschmann-Steinert disease ; Case 51. Myotonic dystrophy type 2, proximal myotonic myopathy ; Case 52. Becker myotonia, chloride channelopathy ; Case 53. Glycogen storage disease type 2, Pompe disease ; Case 54. Glycogen storage disease type 5, McArdle disease ; Case 55. Mitochondrial disease: progressive ophthalmoplegia ; Case 56. Myositis ; Case 57. Sporadic inclusion body myositis ; Case 58. Sarcoid myopathy ; Case 59. Hypothyroid myopathy -- Video legends -- Index.
590 ## - LOCAL NOTE (RLIN)
Local note WorldCat record variable field(s) change: 650
650 #0 - SUBJECT HEADINGS
Subject term Neuromuscular diseases
650 #0 - SUBJECT HEADINGS
Subject term Neuromuscular diseases.
650 #0 - SUBJECT HEADINGS
Subject term Diagnosis, Differential.
9 (RLIN) 5871
650 #2 - SUBJECT HEADINGS
Subject term Neuromuscular Diseases
650 #2 - SUBJECT HEADINGS
Subject term Diagnosis, Differential
9 (RLIN) 5871
650 12 - SUBJECT HEADINGS
Subject term Neuromuscular Diseases
General subdivision diagnosis
650 12 - SUBJECT HEADINGS
Subject term Neuromuscular Diseases
General subdivision therapy
700 1# - ADDED PERSONAL NAME
Added personal author Wokke, John H. J.,
830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE
Uniform title Cambridge medicine (Series)
856 ## - ONLINE RESOURCE
Uniform Resource Identifier <a href="#gotoholdings">#gotoholdings</a>
Link text Access resource
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Suppress in OPAC Do not Suppress in OPAC
347 ## - DIGITAL FILE CHARACTERISTICS
File type data file
Source rda
588 0# - SOURCE OF DESCRIPTION NOTE
Source of description note Print version record.
938 ## -
-- Askews and Holts Library Services
-- ASKH
-- AH24993710
938 ## -
-- Askews and Holts Library Services
-- ASKH
-- AH28319369
938 ## -
-- Coutts Information Services
-- COUT
-- 24881837
-- 47.00 GBP
938 ## -
-- EBSCOhost
-- EBSC
-- 539302
938 ## -
-- ProQuest MyiLibrary Digital eBook Collection
-- IDEB
-- cis24881837
938 ## -
-- YBP Library Services
-- YANK
-- 10249349
938 ## -
-- YBP Library Services
-- YANK
-- 10256762
938 ## -
-- YBP Library Services
-- YANK
-- 10350364
938 ## -
-- YBP Library Services
-- YANK
-- 10381185
938 ## -
-- ProQuest Ebook Central
-- EBLB
-- EBL1139545
994 ## -
-- 92
-- N$T
Holdings
Withdrawn status Lost status Damaged status Not for loan Home library Current library Shelving location Date acquired Source of acquisition Total Checkouts Date last seen Uniform Resource Identifier Price effective from Koha item type
        Stenhouse Library (Kingston Hospital) Stenhouse Library (Kingston Hospital) Online 28/11/2022 eBook EBSCO clinical collection   28/11/2022 https://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=539302 28/11/2022 Electronic book
London Health Libraries Consortium Privacy notice and Membership terms and conditions