Pyruvate kinase deficiency / (Record no. 96842)

MARC details
000 -LEADER
fixed length control field 01867nam a2200385 i 4500
001 - CONTROL NUMBER
control field 2133328
003 - CONTROL NUMBER IDENTIFIER
control field StDuBDS
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20231010110650.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS--GENERAL INFORMATION
fixed length control field m|||||o||d||||||||
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field cr |||||||||||
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 230117s2018 enka fob 001|0|eng|d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9781910797891 (PDF ebook) :
Terms of availability No price
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 9781910797884 (pbk.) :
Terms of availability No price
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 9781910797891
040 ## - CATALOGING SOURCE
Original cataloging agency StDuBDS
060 #4 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER
Classification number WH 322
100 1# - MAIN ENTRY--PERSONAL NAME
Personal author Glader, Bertil E.,
Relator term author.
245 10 - TITLE STATEMENT
Title Pyruvate kinase deficiency /
Medium [e-book]
250 ## - EDITION
Edition statement First edition.
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Abingdon, Oxford :
Name of producer, publisher, distributor, manufacturer Karger,
Date of production, publication, distribution, manufacture, or copyright notice 2018.
300 ## - PHYSICAL DESCRIPTION
Physical description 1 online resource (64 pages) :
Other physical details illustrations (colour).
490 1# - SERIES TITLE
Series statement Fast facts
500 ## - GENERAL NOTE
General note Also issued in print: 2018.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references and index.
520 8# - ABSTRACT
Abstract You may be unfamiliar with pyruvate kinase (PK) deficiency. It is a rare inherited enzyme disorder that affects the glycolytic pathway used by red blood cells to generate energy, manifesting as hemolytic anemia. The symptoms vary greatly between individuals, making diagnosis difficult, and management primarily comprises supportive treatments. Written by experts in the field, this book provides a comprehensive introduction to the condition.
650 #0 - SUBJECT HEADINGS
Subject term Blood
General subdivision Diseases.
650 #0 - SUBJECT HEADINGS
Subject term Metabolism
General subdivision Disorders.
650 #2 - SUBJECT HEADINGS
Subject term Hematologic Diseases.
700 1# - ADDED PERSONAL NAME
Added personal author Barcellini, Wilma,
Relator term author.
700 1# - ADDED PERSONAL NAME
Added personal author Grace, Rachael,
Relator term author.
830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE
Uniform title Fast facts.
856 40 - ONLINE RESOURCE
Uniform Resource Identifier <a href="https://app.kortext.com/Shibboleth.sso/Login?entityID=https://idp.eng.nhs.uk/openathens&target=https://app.kortext.com/borrow/2133328">https://app.kortext.com/Shibboleth.sso/Login?entityID=https://idp.eng.nhs.uk/openathens&target=https://app.kortext.com/borrow/2133328</a>
Link text Eligible NHS OpenAthens account holders click here for access
588 ## - SOURCE OF DESCRIPTION NOTE
Source of description note Description based on online resource; title from PDF title page (viewed on January 17, 2023).
Holdings
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