Human pathobiochemistry : (Record no. 107619)

MARC details
000 -LEADER
fixed length control field 02247nam a22002775i 4500
001 - CONTROL NUMBER
control field 20843367
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20201127165550.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 190207s2019 nyu 000 0 eng
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9789811329760 (hbk.)
040 ## - CATALOGING SOURCE
Original cataloging agency DLC
Language of cataloging eng
Description conventions rda
Transcribing agency DLC
042 ## - AUTHENTICATION CODE
Authentication code pcc
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 612.015 HUM
245 10 - TITLE STATEMENT
Title Human pathobiochemistry :
Remainder of title from clinical studies to molecular mechanisms /
Statement of responsibility, etc. Toshitaka Oohashi, Hirokazu Tsukahara, Francesco Ramirez, Chad L. Barber, Fumio Otsuka, editors.
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture New York, NY :
Name of producer, publisher, distributor, manufacturer Springer,
Date of production, publication, distribution, manufacture, or copyright notice 2019.
300 ## - PHYSICAL DESCRIPTION
Extent xi, 349 pages : illustrations, 26 cm.
500 ## - GENERAL NOTE
General note Euro : 119.99/-<br/>TBH86/102
505 ## - FORMATTED CONTENTS NOTE
Formatted contents note Part1. Metabolic Disorders.- 1. Citrin Deficiency.- 2. Aspartoacylase Deficiency (Canavan Disease, N-Acetylaspartic Aciduria).- 3. Prominent Insulin Resistance in Congenital Generalized Lipoatrophy.- 4. Fabry Disease.- 5. Familial Hypercholesterolemia.- 6. Gaucher Disease.- 7. Heme Oxygenase-1 Deficiency.- 8. The Homocystinurias.- 9. Hypophosphatasia.- 10. Phenylketonuria.- 11. Triglyceride Deposit Cardiomyovasculopathy.- 12. Urea Cycle Disorders.- 13. Wilson Disease.- Part2. Genetics.- 14. Achondroplasia.- 15. Acute Myeloid Leukemia: Mutations Blocking Differentiation Lead to Distinct Leukemic Subtypes.- 16. 1-Antitrypsin Deficiency.- 17. Hereditary Anticoagulant Deficiencies.- 18. Cherubism.- 19. Cancer and Excess Iron.- 20. Fukuyama Congenital Muscular Dystrophy and Related Diseases.- 21. Hereditary Proteinuric Glomerular Disorders.- 22. Marfan Syndrome.- 23. When Materials Are at Fault: The Skeletal Collagens, Osteogenesis Imperfecta and Chondrodysplasias.- Part3. Others.- 24. Acute Kidney Injury: Transition to Chronic Kidney Disease.- 25. Type I Interferonopathies: Common Pathological Features Between Congenital Infections and Genetic Disorders.- 26. Epilepsy.- 27. Hemophagocytic Lymphohistiocytosis.- 28. Hepatitis C Virus Infection.- 29. Substance Abuse Emergencies.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Source of heading or term Clinical biochemistry
Topical term or geographic name entry element Biochemistry
Form subdivision Human physiology
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Oohashi, Toshitaka;
Relator term Editor
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Tsukahara, Hirokazu;
Relator term Editor
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Ramirez, Francesco;
Relator term Editor
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Barber, Chad L.;
Relator term Editor
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Otsuka, Fumio;
Relator term Editor
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Books
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Collection code Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
    Dewey Decimal Classification     SIAS Collection H.T. Parekh Library H.T. Parekh Library 27/11/2020   612.015 HUM K3674 09/11/2020 09/11/2020 Books

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