A Novel Mutation of the Calcium-Sensing Receptor Gene Causing Familial Hypocalciuric Hypercalcemia Complicates Medical Followup after Roux-en-Y Gastric Bypass: A Case Report and a Summary of Mutations Found in the Same Hospital Laboratory

A Novel Mutation of the Calcium-Sensing Receptor Gene Causing Familial Hypocalciuric Hypercalcemia Complicates Medical Followup after Roux-en-Y Gastric Bypass: A Case Report and a Summary of Mutations Found in the Same Hospital Laboratory

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Case reports in endocrinology 2019, Vol.2019, p.9468252-9468252
Hauptverfasser: Carlsson, Elin Rebecka, Toft Nielsen, Mai-Britt, Høgh, Anne Mette, Veggerby Grønlund, Rikke, Fenger, Mogens, Ambye, Louise
Format: Report
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 9468252
container_issue
container_start_page 9468252
container_title Case reports in endocrinology
container_volume 2019
creator Carlsson, Elin Rebecka
Toft Nielsen, Mai-Britt
Høgh, Anne Mette
Veggerby Grønlund, Rikke
Fenger, Mogens
Ambye, Louise
description
doi_str_mv 10.1155/2019/9468252
format Report
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_2195259538</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2195259538</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_21952595383</originalsourceid><addsrcrecordid>eNqVTrtSAkEQ3ECrpJTMD5jQ5GTvjqU4M6QEAjEAEyNqPAZda1_uQ72f9hvco_QDnGSmp2e6m7HLkl-XpRCjipfNqBlPppWoTtig4g0vJoKXZ2wYwhvPNeFVXY8H7HsGD_aDFKxTxCitAXuA-EowR9XKpIstmSDNC2yoJRethyWZnk3H7QK1VBIVrDpn2-OLl22PyPeQtESYW-2UbDFSgDXt86RgYZWyn8kBHiJ52Nj0VZApnmCJIfYSt53DEG5glr0CZXtnfQQ0e0DYJq3Rd33Uv9ghK6ZMSnNMv0VNsLLByZjN7vHZeszhuwt2ekAVaPjbz9nV4u5xviqct--JQtxpGVpSCg3ZFHZV2YhKNKKe1v84_QFMhIAX</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>report</recordtype><pqid>2195259538</pqid></control><display><type>report</type><title>A Novel Mutation of the Calcium-Sensing Receptor Gene Causing Familial Hypocalciuric Hypercalcemia Complicates Medical Followup after Roux-en-Y Gastric Bypass: A Case Report and a Summary of Mutations Found in the Same Hospital Laboratory</title><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central Open Access</source><source>Wiley-Blackwell Open Access Titles</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Carlsson, Elin Rebecka ; Toft Nielsen, Mai-Britt ; Høgh, Anne Mette ; Veggerby Grønlund, Rikke ; Fenger, Mogens ; Ambye, Louise</creator><creatorcontrib>Carlsson, Elin Rebecka ; Toft Nielsen, Mai-Britt ; Høgh, Anne Mette ; Veggerby Grønlund, Rikke ; Fenger, Mogens ; Ambye, Louise</creatorcontrib><identifier>ISSN: 2090-6501</identifier><identifier>DOI: 10.1155/2019/9468252</identifier><language>eng</language><ispartof>Case reports in endocrinology, 2019, Vol.2019, p.9468252-9468252</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,784,864,4490,27925</link.rule.ids></links><search><creatorcontrib>Carlsson, Elin Rebecka</creatorcontrib><creatorcontrib>Toft Nielsen, Mai-Britt</creatorcontrib><creatorcontrib>Høgh, Anne Mette</creatorcontrib><creatorcontrib>Veggerby Grønlund, Rikke</creatorcontrib><creatorcontrib>Fenger, Mogens</creatorcontrib><creatorcontrib>Ambye, Louise</creatorcontrib><title>A Novel Mutation of the Calcium-Sensing Receptor Gene Causing Familial Hypocalciuric Hypercalcemia Complicates Medical Followup after Roux-en-Y Gastric Bypass: A Case Report and a Summary of Mutations Found in the Same Hospital Laboratory</title><title>Case reports in endocrinology</title><issn>2090-6501</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2019</creationdate><recordtype>report</recordtype><recordid>eNqVTrtSAkEQ3ECrpJTMD5jQ5GTvjqU4M6QEAjEAEyNqPAZda1_uQ72f9hvco_QDnGSmp2e6m7HLkl-XpRCjipfNqBlPppWoTtig4g0vJoKXZ2wYwhvPNeFVXY8H7HsGD_aDFKxTxCitAXuA-EowR9XKpIstmSDNC2yoJRethyWZnk3H7QK1VBIVrDpn2-OLl22PyPeQtESYW-2UbDFSgDXt86RgYZWyn8kBHiJ52Nj0VZApnmCJIfYSt53DEG5glr0CZXtnfQQ0e0DYJq3Rd33Uv9ghK6ZMSnNMv0VNsLLByZjN7vHZeszhuwt2ekAVaPjbz9nV4u5xviqct--JQtxpGVpSCg3ZFHZV2YhKNKKe1v84_QFMhIAX</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Carlsson, Elin Rebecka</creator><creator>Toft Nielsen, Mai-Britt</creator><creator>Høgh, Anne Mette</creator><creator>Veggerby Grønlund, Rikke</creator><creator>Fenger, Mogens</creator><creator>Ambye, Louise</creator><scope>7X8</scope></search><sort><creationdate>20190101</creationdate><title>A Novel Mutation of the Calcium-Sensing Receptor Gene Causing Familial Hypocalciuric Hypercalcemia Complicates Medical Followup after Roux-en-Y Gastric Bypass: A Case Report and a Summary of Mutations Found in the Same Hospital Laboratory</title><author>Carlsson, Elin Rebecka ; Toft Nielsen, Mai-Britt ; Høgh, Anne Mette ; Veggerby Grønlund, Rikke ; Fenger, Mogens ; Ambye, Louise</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_21952595383</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Carlsson, Elin Rebecka</creatorcontrib><creatorcontrib>Toft Nielsen, Mai-Britt</creatorcontrib><creatorcontrib>Høgh, Anne Mette</creatorcontrib><creatorcontrib>Veggerby Grønlund, Rikke</creatorcontrib><creatorcontrib>Fenger, Mogens</creatorcontrib><creatorcontrib>Ambye, Louise</creatorcontrib><collection>MEDLINE - Academic</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carlsson, Elin Rebecka</au><au>Toft Nielsen, Mai-Britt</au><au>Høgh, Anne Mette</au><au>Veggerby Grønlund, Rikke</au><au>Fenger, Mogens</au><au>Ambye, Louise</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>A Novel Mutation of the Calcium-Sensing Receptor Gene Causing Familial Hypocalciuric Hypercalcemia Complicates Medical Followup after Roux-en-Y Gastric Bypass: A Case Report and a Summary of Mutations Found in the Same Hospital Laboratory</atitle><jtitle>Case reports in endocrinology</jtitle><date>2019-01-01</date><risdate>2019</risdate><volume>2019</volume><spage>9468252</spage><epage>9468252</epage><pages>9468252-9468252</pages><issn>2090-6501</issn><doi>10.1155/2019/9468252</doi></addata></record>
fulltext fulltext
identifier ISSN: 2090-6501
ispartof Case reports in endocrinology, 2019, Vol.2019, p.9468252-9468252
issn 2090-6501
language eng
recordid cdi_proquest_miscellaneous_2195259538
source DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; Wiley-Blackwell Open Access Titles; PubMed Central; Alma/SFX Local Collection
title A Novel Mutation of the Calcium-Sensing Receptor Gene Causing Familial Hypocalciuric Hypercalcemia Complicates Medical Followup after Roux-en-Y Gastric Bypass: A Case Report and a Summary of Mutations Found in the Same Hospital Laboratory
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T16%3A28%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.atitle=A%20Novel%20Mutation%20of%20the%20Calcium-Sensing%20Receptor%20Gene%20Causing%20Familial%20Hypocalciuric%20Hypercalcemia%20Complicates%20Medical%20Followup%20after%20Roux-en-Y%20Gastric%20Bypass:%20A%20Case%20Report%20and%20a%20Summary%20of%20Mutations%20Found%20in%20the%20Same%20Hospital%20Laboratory&rft.jtitle=Case%20reports%20in%20endocrinology&rft.au=Carlsson,%20Elin%20Rebecka&rft.date=2019-01-01&rft.volume=2019&rft.spage=9468252&rft.epage=9468252&rft.pages=9468252-9468252&rft.issn=2090-6501&rft_id=info:doi/10.1155/2019/9468252&rft_dat=%3Cproquest%3E2195259538%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2195259538&rft_id=info:pmid/&rfr_iscdi=true