Human pathobiochemistry : (Record no. 107619)
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000 -LEADER | |
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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 |
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 |
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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 |