Atlas of Inherited Metabolic Diseases Authors (Record no. 7527)

MARC details
000 -LEADER
fixed length control field 02666nam a22002777a 4500
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20240305192509.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 220716b |||||||| |||| 00| 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 1138196606
International Standard Book Number 9781138196605
040 ## - CATALOGING SOURCE
Transcribing agency dlc
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 616.3/9 NYH
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name William L Nyhan
9 (RLIN) 10818
245 ## - TITLE STATEMENT
Title Atlas of Inherited Metabolic Diseases Authors
250 ## - EDITION STATEMENT
Edition statement 4, illustrated
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. London
Name of publisher, distributor, etc. CRC Press
Date of publication, distribution, etc. 2020
300 ## - PHYSICAL DESCRIPTION
Extent 872 pages
520 ## - SUMMARY, ETC.
Summary, etc. In a field where even experts may find that years have elapsed since they last encountered a child with a given disorder, it is essential for the clinician to have a comprehensive source of practical and highly illustrated information covering the whole spectrum of metabolic disease to refer to.<br/><br/>The content is divided into sections of related disorders, including disorders of amino acid metabolism, lipid storage disorders, and mitochondrial diseases for ease of reference, with an introductory outline where appropriate summarizing the biochemical features and general management issues. Within the sections, each chapter deals with an individual disease, opening with a useful summary of major phenotypic expression including clear and helpful biochemical pathways, identifying for the reader exactly where the defect occurs.<br/><br/>Throughout the book, plentiful photographs, often showing extremely rare disorders, are an invaluable aid to diagnosis.<br/><br/>Key Features<br/><br/>• Fully updated to incorporate all new developments in the field<br/><br/>• Brand new chapters cover methylmalonic aciduria of ACSF3 deficiency, branched chain keto acid dehydrogenase deficiency, serine deficiencies, purine nucleoside phosphorylase deficiency, antiquitin deficiency, and others<br/><br/>• Excellent and detailed clinical descriptions, with numerous valuable hints and suggestions for management<br/><br/>• Helpful explanatory algorithms and decision trees, and high-quality illustrative material including biochemical pathways and an unrivaled photographic collection, which enhance clinical applicability<br/><br/>The fourth edition of this highly regarded book, authored by two of the foremost authorities in pediatric metabolic medicine, continues to provide incomparable insight into the problems associated with metabolic diseases and remains invaluable to pediatricians, geneticists, and general clinicians worldwide.
600 ## - SUBJECT ADDED ENTRY--PERSONAL NAME
General subdivision Medical / Pediatrics
9 (RLIN) 26838
General subdivision Medical / Genetics
9 (RLIN) 26881
General subdivision Medical / General
9 (RLIN) 26821
General subdivision Medical / Endocrinology & Metabolism
9 (RLIN) 27222
General subdivision Medical › General
9 (RLIN) 27115
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 10816
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme ddc
Koha item type E-BOOKS
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Collection Home library Current library Shelving location Date acquired Total checkouts Full call number Barcode Date last seen Price effective from Koha item type
            MWALIMU NYERERE LEARNING RESOURCES CENTRE-CUHAS BUGANDO MWALIMU NYERERE LEARNING RESOURCES CENTRE-CUHAS BUGANDO   07/16/2022   616.3/9 NYH EBS11919 07/16/2022 07/16/2022 E-BOOKS
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