MARC details
000 -LEADER |
fixed length control field |
02439nam a22003737a 4500 |
003 - CONTROL NUMBER IDENTIFIER |
control field |
CUTN |
005 - DATE AND TIME OF LATEST TRANSACTION |
control field |
20210707123556.0 |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
fixed length control field |
210707b ||||| |||| 00| 0 eng d |
020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
International Standard Book Number |
9780195393514 (hbk.) |
020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
International Standard Book Number |
0195393511 (hbk.) |
041 ## - LANGUAGE CODE |
Language |
English |
042 ## - AUTHENTICATION CODE |
Authentication code |
pcc |
060 10 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER |
Classification number |
WL 390 |
Item number |
D5695 2011 |
082 00 - DEWEY DECIMAL CLASSIFICATION NUMBER |
Classification number |
616.83 |
Edition number |
22 |
Item number |
WAL |
100 ## - MAIN ENTRY--PERSONAL NAME |
Personal name |
Walker, Ruth H. |
245 04 - TITLE STATEMENT |
Title |
The differential diagnosis of chorea / |
Statement of responsibility, etc |
edited by Ruth H. Walker. |
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT) |
Place of publication, distribution, etc |
Oxford : |
Name of publisher, distributor, etc |
Oxford University Press, |
Date of publication, distribution, etc |
2011. |
300 ## - PHYSICAL DESCRIPTION |
Extent |
xxi, 452 p. : |
Other physical details |
ill. ; |
Dimensions |
24 cm. |
500 ## - GENERAL NOTE |
General note |
R.C.C<br/>HB |
505 ## - FORMATTED CONTENTS NOTE |
Title |
1. Introduction : an approach to the patient with chorea<br/> |
-- |
2. Functional anatomy of chorea |
-- |
3. Huntington disease<br/> |
-- |
4. Benign hereditary chorea<br/> |
-- |
5. Huntington's disease-like 2 |
-- |
6. Chorea-acanthocytosis<br/> |
-- |
7. McLeod syndrome<br/> |
-- |
8. Neurodegeneration with brain iron accumulation |
-- |
9. Neuroferritinopathy |
-- |
10. Aceruloplasminemia / Frank Skidmore. Chorea in prion diseases |
-- |
11. Chorea in inherited ataxias |
-- |
12. Inherited metabolic diseases causing chorea in childhood<br/> |
-- |
13. Medication-induced chorea<br/> |
-- |
14. Metabolic causes of chorea |
-- |
15. Structural causes of chorea |
-- |
16. Sydenham chorea |
-- |
17. Paraneoplastic and other autoimmune choreas<br/> |
-- |
18. Paroxysmal chorea<br/> |
-- |
19. Psychiatric aspects of the neurodegenerative choreas<br/> |
-- |
20. Psychogenic chorea |
-- |
21. Treatment of chorea |
520 ## - SUMMARY, ETC. |
Summary, etc |
<br/>The involuntary movement disorder known as chorea can be due to a wide variety of neurological conditions, both genetic and acquired. This volume provides a comprehensive account of these conditions. While Huntington's disease is the prototypic inherited chorea, with the development of the genetic test for this disorder it has become apparent that a small but significant proportion of patients with this phenotype do not have this diagnosis. Although less common than Huntington's disease, it is vital to correctly diagnose these patients with advances in molecular medicine, it is now easier to i. |
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Chorea |
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Diagnosis, Differential. |
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) |
Department Name |
Department of Applied Psychology |
942 ## - ADDED ENTRY ELEMENTS (KOHA) |
Source of classification or shelving scheme |
Dewey Decimal Classification |
Koha item type |
General Books |
504 ## - BIBLIOGRAPHY, ETC. NOTE |
Bibliography, etc |
Includes bibliographical references and index. |
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
General subdivision |
Diagnosis. |
650 #2 - SUBJECT ADDED ENTRY--TOPICAL TERM |
General subdivision |
diagnosis. |
650 #2 - SUBJECT ADDED ENTRY--TOPICAL TERM |
General subdivision |
complications. |
650 #2 - SUBJECT ADDED ENTRY--TOPICAL TERM |
General subdivision |
etiology. |