Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report. (Record no. 27173615)

MARC details
000 -LEADER
fixed length control field 01508 a2200445 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250517153609.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201805s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1668-3501
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.5546/aap.2017.eng.e153
Source of number or code doi
040 ## - CATALOGING SOURCE
Original cataloging agency NLM
Language of cataloging eng
Transcribing agency NLM
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Katipoğlu, Nagehan
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20180511
245 00 - TITLE STATEMENT
Title Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Archivos argentinos de pediatria
Date of publication, distribution, etc. 06 2017
300 ## - PHYSICAL DESCRIPTION
Extent e153-e156 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Case Reports; Journal Article
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Anemia, Megaloblastic
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Diabetes Mellitus
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Female
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Hearing Loss, Sensorineural
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Humans
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Infant
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Membrane Transport Proteins
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Mutation
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Thiamine Deficiency
General subdivision congenital
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Karapinar, Tuba H
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Demir, Korean
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Aydin Köker, Sultan
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Nalbantoğlu, Özlem
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Ay, Yılmaz
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Korkmaz, Hüseyin A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Oymak, Yeşim
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Yıldız, Melek
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Tunç, Selma
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Hazan, Filiz
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Vergin, Canan
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Ozkan, Behzat
773 0# - HOST ITEM ENTRY
Title Archivos argentinos de pediatria
Related parts vol. 115
-- no. 3
-- p. e153-e156
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.5546/aap.2017.eng.e153">https://doi.org/10.5546/aap.2017.eng.e153</a>
Public note Available from publisher's website

No items available.