Loading…
Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene
Saved in:
Published in: | Pediatrics International 2005, Vol.47 (1), p.105-108 |
---|---|
Main Authors: | , , , , , , , |
Format: | Report |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 108 |
container_issue | 1 |
container_start_page | 105 |
container_title | Pediatrics International |
container_volume | 47 |
creator | Shibayama, Keiko Ohyama, Yoshihide Hishinuma, Akira Yokota, Yukifumi Kazahari, Koji Kazahari, Mayumi Ieiri, Tamio Matsuura, Nobuo |
description | |
doi_str_mv | 10.1111/j.1442-200x.2005.02020.x |
format | report |
fullrecord | <record><control><sourceid>istex</sourceid><recordid>TN_cdi_istex_primary_ark_67375_WNG_WLGK4T3F_D</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_WLGK4T3F_D</sourcerecordid><originalsourceid>FETCH-istex_primary_ark_67375_WNG_WLGK4T3F_D3</originalsourceid><addsrcrecordid>eNqViu0KgjAYhUcU9HkP7w245kfp_8qCIoIE-zemrZypk22C3n0SdQGdA-ccOA9CYBNs91rm2PY8x3IIaXEfK0yc3rgdoMnvuA377TqBFZC1P0ZTrXNCSOAH3gRdrk2SFqISKSsg62ppsk5JcRe6hJQ1mt8h6YBB2RhmhKxAPsBkHD6YUbIWFSie8tpIBU9e8TkaPVih-eLbM2SFu2hzsIQ2vKW1EiVTHWXqRde-669ofN7T-LQ_epEb0q37L_8GQvhPHw</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>report</recordtype></control><display><type>report</type><title>Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene</title><source>Wiley</source><creator>Shibayama, Keiko ; Ohyama, Yoshihide ; Hishinuma, Akira ; Yokota, Yukifumi ; Kazahari, Koji ; Kazahari, Mayumi ; Ieiri, Tamio ; Matsuura, Nobuo</creator><creatorcontrib>Shibayama, Keiko ; Ohyama, Yoshihide ; Hishinuma, Akira ; Yokota, Yukifumi ; Kazahari, Koji ; Kazahari, Mayumi ; Ieiri, Tamio ; Matsuura, Nobuo</creatorcontrib><identifier>ISSN: 1328-8067</identifier><identifier>EISSN: 1442-200X</identifier><identifier>DOI: 10.1111/j.1442-200x.2005.02020.x</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Pty</publisher><subject>subclinical hypothyroidism ; thyrotropin receptor mutation</subject><ispartof>Pediatrics International, 2005, Vol.47 (1), p.105-108</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,784,4490,27925</link.rule.ids></links><search><creatorcontrib>Shibayama, Keiko</creatorcontrib><creatorcontrib>Ohyama, Yoshihide</creatorcontrib><creatorcontrib>Hishinuma, Akira</creatorcontrib><creatorcontrib>Yokota, Yukifumi</creatorcontrib><creatorcontrib>Kazahari, Koji</creatorcontrib><creatorcontrib>Kazahari, Mayumi</creatorcontrib><creatorcontrib>Ieiri, Tamio</creatorcontrib><creatorcontrib>Matsuura, Nobuo</creatorcontrib><title>Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene</title><title>Pediatrics International</title><subject>subclinical hypothyroidism</subject><subject>thyrotropin receptor mutation</subject><issn>1328-8067</issn><issn>1442-200X</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2005</creationdate><recordtype>report</recordtype><recordid>eNqViu0KgjAYhUcU9HkP7w245kfp_8qCIoIE-zemrZypk22C3n0SdQGdA-ccOA9CYBNs91rm2PY8x3IIaXEfK0yc3rgdoMnvuA377TqBFZC1P0ZTrXNCSOAH3gRdrk2SFqISKSsg62ppsk5JcRe6hJQ1mt8h6YBB2RhmhKxAPsBkHD6YUbIWFSie8tpIBU9e8TkaPVih-eLbM2SFu2hzsIQ2vKW1EiVTHWXqRde-669ofN7T-LQ_epEb0q37L_8GQvhPHw</recordid><startdate>200502</startdate><enddate>200502</enddate><creator>Shibayama, Keiko</creator><creator>Ohyama, Yoshihide</creator><creator>Hishinuma, Akira</creator><creator>Yokota, Yukifumi</creator><creator>Kazahari, Koji</creator><creator>Kazahari, Mayumi</creator><creator>Ieiri, Tamio</creator><creator>Matsuura, Nobuo</creator><general>Blackwell Science Pty</general><scope>BSCLL</scope></search><sort><creationdate>200502</creationdate><title>Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene</title><author>Shibayama, Keiko ; Ohyama, Yoshihide ; Hishinuma, Akira ; Yokota, Yukifumi ; Kazahari, Koji ; Kazahari, Mayumi ; Ieiri, Tamio ; Matsuura, Nobuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-istex_primary_ark_67375_WNG_WLGK4T3F_D3</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2005</creationdate><topic>subclinical hypothyroidism</topic><topic>thyrotropin receptor mutation</topic><toplevel>online_resources</toplevel><creatorcontrib>Shibayama, Keiko</creatorcontrib><creatorcontrib>Ohyama, Yoshihide</creatorcontrib><creatorcontrib>Hishinuma, Akira</creatorcontrib><creatorcontrib>Yokota, Yukifumi</creatorcontrib><creatorcontrib>Kazahari, Koji</creatorcontrib><creatorcontrib>Kazahari, Mayumi</creatorcontrib><creatorcontrib>Ieiri, Tamio</creatorcontrib><creatorcontrib>Matsuura, Nobuo</creatorcontrib><collection>Istex</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shibayama, Keiko</au><au>Ohyama, Yoshihide</au><au>Hishinuma, Akira</au><au>Yokota, Yukifumi</au><au>Kazahari, Koji</au><au>Kazahari, Mayumi</au><au>Ieiri, Tamio</au><au>Matsuura, Nobuo</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene</atitle><jtitle>Pediatrics International</jtitle><date>2005-02</date><risdate>2005</risdate><volume>47</volume><issue>1</issue><spage>105</spage><epage>108</epage><pages>105-108</pages><issn>1328-8067</issn><eissn>1442-200X</eissn><cop>Oxford, UK</cop><pub>Blackwell Science Pty</pub><doi>10.1111/j.1442-200x.2005.02020.x</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1328-8067 |
ispartof | Pediatrics International, 2005, Vol.47 (1), p.105-108 |
issn | 1328-8067 1442-200X |
language | eng |
recordid | cdi_istex_primary_ark_67375_WNG_WLGK4T3F_D |
source | Wiley |
subjects | subclinical hypothyroidism thyrotropin receptor mutation |
title | Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T20%3A48%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.atitle=Subclinical%20hypothyroidism%20caused%20by%20a%20mutation%20of%20the%20thyrotropin%20receptor%20gene&rft.jtitle=Pediatrics%20International&rft.au=Shibayama,%20Keiko&rft.date=2005-02&rft.volume=47&rft.issue=1&rft.spage=105&rft.epage=108&rft.pages=105-108&rft.issn=1328-8067&rft.eissn=1442-200X&rft_id=info:doi/10.1111/j.1442-200x.2005.02020.x&rft_dat=%3Cistex%3Eark_67375_WNG_WLGK4T3F_D%3C/istex%3E%3Cgrp_id%3Ecdi_FETCH-istex_primary_ark_67375_WNG_WLGK4T3F_D3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |