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Hereditary angioedema : (Record no. 8576)

MARC details
000 -LEADER
fixed length control field 00954nam a22002057a 4500
003 - CONTROL NUMBER IDENTIFIER
control field OCT
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20230306142105.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 230306b ph ||||| |||| 00| 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 03604039
040 ## - CATALOGING SOURCE
Transcribing agency OCT
240 ## - UNIFORM TITLE
Uniform title Nursing 2022 /
Medium December 2022
245 ## - TITLE STATEMENT
Title Hereditary angioedema :
Remainder of title a rare but serious and commonly misdiagnosed disease
Statement of responsibility, etc. Lisa Zacek
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Hagerstown, MD :
Name of publisher, distributor, etc. Wolters Kluwer :
Date of publication, distribution, etc. 2022
300 ## - PHYSICAL DESCRIPTION
Extent Volume 52(12) : pages 44-50
500 ## - GENERAL NOTE
General note Hereditary angiodema is a rare and commonly misdiagnosed disease characterized by recurrent, painful, nonnurticarial, and nonpruritic deep tissue swelling attacks, including potentially life-threatening asphyxiation. Nurses can assist in identifying disease hallmarks and provide emergency care. patient support, and education about inject able or infused medications
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Angiodema
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element C1 inhibitor
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Hereditary angiodema
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Continuing Resources
Suppress in OPAC No

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