Loading…
Partial HELLP syndrome (ELLP) in a woman heterozygous for the prothrombin G20210A mutation
Saved in:
Published in: | The journal of maternal-fetal & neonatal medicine 2009-01, Vol.22 (8), p.714-716 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c325t-6aff0446398fe1b6d663fd33fe24c4d2e9d00868ada0e655731466bf4f2651413 |
container_end_page | 716 |
container_issue | 8 |
container_start_page | 714 |
container_title | The journal of maternal-fetal & neonatal medicine |
container_volume | 22 |
creator | Politou, Marianna Gialeraki, Argyri Salamalekis, Georgios Markatos, Christos Merkouri, Efrosyni Travlou, Anthi Salamalekis, Emmanouil Skarpas, Panagiotis |
description | |
doi_str_mv | 10.1080/14767050802609783 |
format | article |
fullrecord | <record><control><sourceid>informahealthcare_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1080_14767050802609783</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1080_14767050802609783</sourcerecordid><originalsourceid>FETCH-LOGICAL-c325t-6aff0446398fe1b6d663fd33fe24c4d2e9d00868ada0e655731466bf4f2651413</originalsourceid><addsrcrecordid>eNp9kE9LwzAYxoMobk4_gBfJUQ_VpEnTFr2MMTeh4A568VLSJrEdbTOSlNF9ejM2EBF2ev_w_B7e9wHgFqNHjBL0hGnMYhT5NmQojRNyBsb7XUDTiJ4fey9IRuDK2jVCIaYougQjnNI4ZRSNwdeKG1fzBi7nWbaCduiE0a2E9_vxAdYd5HCrW97BSjpp9G741r2FShvoKgk3RrvKA4UXLkLvj6aw7R13te6uwYXijZU3xzoBn6_zj9kyyN4Xb7NpFpQkjFzAuFKIUkbSRElcMMEYUYIQJUNaUhHKVCCUsIQLjiSLophgylihqApZhCkmE4APvqXR1hqp8o2pW26GHKN8n1P-LyfP3B2YTV-0UvwSx2C84OUgqDv_a8u32jQid3xotFGGd2Vtc3LK__kPXkneuKrkRuZr3ZvO53Hiuh-GroZx</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Partial HELLP syndrome (ELLP) in a woman heterozygous for the prothrombin G20210A mutation</title><source>Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list)</source><creator>Politou, Marianna ; Gialeraki, Argyri ; Salamalekis, Georgios ; Markatos, Christos ; Merkouri, Efrosyni ; Travlou, Anthi ; Salamalekis, Emmanouil ; Skarpas, Panagiotis</creator><creatorcontrib>Politou, Marianna ; Gialeraki, Argyri ; Salamalekis, Georgios ; Markatos, Christos ; Merkouri, Efrosyni ; Travlou, Anthi ; Salamalekis, Emmanouil ; Skarpas, Panagiotis</creatorcontrib><identifier>ISSN: 1476-7058</identifier><identifier>EISSN: 1476-4954</identifier><identifier>DOI: 10.1080/14767050802609783</identifier><identifier>PMID: 19479640</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Adult ; Cesarean Section ; Female ; Gestational Age ; HELLP Syndrome - diagnosis ; HELLP Syndrome - genetics ; HELLP Syndrome - therapy ; Heparin, Low-Molecular-Weight - therapeutic use ; Heterozygote ; Humans ; Mutation ; Pregnancy ; Prothrombin - genetics ; Twins</subject><ispartof>The journal of maternal-fetal & neonatal medicine, 2009-01, Vol.22 (8), p.714-716</ispartof><rights>2009 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c325t-6aff0446398fe1b6d663fd33fe24c4d2e9d00868ada0e655731466bf4f2651413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19479640$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Politou, Marianna</creatorcontrib><creatorcontrib>Gialeraki, Argyri</creatorcontrib><creatorcontrib>Salamalekis, Georgios</creatorcontrib><creatorcontrib>Markatos, Christos</creatorcontrib><creatorcontrib>Merkouri, Efrosyni</creatorcontrib><creatorcontrib>Travlou, Anthi</creatorcontrib><creatorcontrib>Salamalekis, Emmanouil</creatorcontrib><creatorcontrib>Skarpas, Panagiotis</creatorcontrib><title>Partial HELLP syndrome (ELLP) in a woman heterozygous for the prothrombin G20210A mutation</title><title>The journal of maternal-fetal & neonatal medicine</title><addtitle>J Matern Fetal Neonatal Med</addtitle><subject>Adult</subject><subject>Cesarean Section</subject><subject>Female</subject><subject>Gestational Age</subject><subject>HELLP Syndrome - diagnosis</subject><subject>HELLP Syndrome - genetics</subject><subject>HELLP Syndrome - therapy</subject><subject>Heparin, Low-Molecular-Weight - therapeutic use</subject><subject>Heterozygote</subject><subject>Humans</subject><subject>Mutation</subject><subject>Pregnancy</subject><subject>Prothrombin - genetics</subject><subject>Twins</subject><issn>1476-7058</issn><issn>1476-4954</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kE9LwzAYxoMobk4_gBfJUQ_VpEnTFr2MMTeh4A568VLSJrEdbTOSlNF9ejM2EBF2ev_w_B7e9wHgFqNHjBL0hGnMYhT5NmQojRNyBsb7XUDTiJ4fey9IRuDK2jVCIaYougQjnNI4ZRSNwdeKG1fzBi7nWbaCduiE0a2E9_vxAdYd5HCrW97BSjpp9G741r2FShvoKgk3RrvKA4UXLkLvj6aw7R13te6uwYXijZU3xzoBn6_zj9kyyN4Xb7NpFpQkjFzAuFKIUkbSRElcMMEYUYIQJUNaUhHKVCCUsIQLjiSLophgylihqApZhCkmE4APvqXR1hqp8o2pW26GHKN8n1P-LyfP3B2YTV-0UvwSx2C84OUgqDv_a8u32jQid3xotFGGd2Vtc3LK__kPXkneuKrkRuZr3ZvO53Hiuh-GroZx</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Politou, Marianna</creator><creator>Gialeraki, Argyri</creator><creator>Salamalekis, Georgios</creator><creator>Markatos, Christos</creator><creator>Merkouri, Efrosyni</creator><creator>Travlou, Anthi</creator><creator>Salamalekis, Emmanouil</creator><creator>Skarpas, Panagiotis</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20090101</creationdate><title>Partial HELLP syndrome (ELLP) in a woman heterozygous for the prothrombin G20210A mutation</title><author>Politou, Marianna ; Gialeraki, Argyri ; Salamalekis, Georgios ; Markatos, Christos ; Merkouri, Efrosyni ; Travlou, Anthi ; Salamalekis, Emmanouil ; Skarpas, Panagiotis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c325t-6aff0446398fe1b6d663fd33fe24c4d2e9d00868ada0e655731466bf4f2651413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Cesarean Section</topic><topic>Female</topic><topic>Gestational Age</topic><topic>HELLP Syndrome - diagnosis</topic><topic>HELLP Syndrome - genetics</topic><topic>HELLP Syndrome - therapy</topic><topic>Heparin, Low-Molecular-Weight - therapeutic use</topic><topic>Heterozygote</topic><topic>Humans</topic><topic>Mutation</topic><topic>Pregnancy</topic><topic>Prothrombin - genetics</topic><topic>Twins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Politou, Marianna</creatorcontrib><creatorcontrib>Gialeraki, Argyri</creatorcontrib><creatorcontrib>Salamalekis, Georgios</creatorcontrib><creatorcontrib>Markatos, Christos</creatorcontrib><creatorcontrib>Merkouri, Efrosyni</creatorcontrib><creatorcontrib>Travlou, Anthi</creatorcontrib><creatorcontrib>Salamalekis, Emmanouil</creatorcontrib><creatorcontrib>Skarpas, Panagiotis</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>The journal of maternal-fetal & neonatal medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Politou, Marianna</au><au>Gialeraki, Argyri</au><au>Salamalekis, Georgios</au><au>Markatos, Christos</au><au>Merkouri, Efrosyni</au><au>Travlou, Anthi</au><au>Salamalekis, Emmanouil</au><au>Skarpas, Panagiotis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Partial HELLP syndrome (ELLP) in a woman heterozygous for the prothrombin G20210A mutation</atitle><jtitle>The journal of maternal-fetal & neonatal medicine</jtitle><addtitle>J Matern Fetal Neonatal Med</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>22</volume><issue>8</issue><spage>714</spage><epage>716</epage><pages>714-716</pages><issn>1476-7058</issn><eissn>1476-4954</eissn><cop>England</cop><pub>Informa UK Ltd</pub><pmid>19479640</pmid><doi>10.1080/14767050802609783</doi><tpages>3</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1476-7058 |
ispartof | The journal of maternal-fetal & neonatal medicine, 2009-01, Vol.22 (8), p.714-716 |
issn | 1476-7058 1476-4954 |
language | eng |
recordid | cdi_crossref_primary_10_1080_14767050802609783 |
source | Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list) |
subjects | Adult Cesarean Section Female Gestational Age HELLP Syndrome - diagnosis HELLP Syndrome - genetics HELLP Syndrome - therapy Heparin, Low-Molecular-Weight - therapeutic use Heterozygote Humans Mutation Pregnancy Prothrombin - genetics Twins |
title | Partial HELLP syndrome (ELLP) in a woman heterozygous for the prothrombin G20210A mutation |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T21%3A44%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-informahealthcare_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Partial%20HELLP%20syndrome%20(ELLP)%20in%20a%20woman%20heterozygous%20for%20the%20prothrombin%20G20210A%20mutation&rft.jtitle=The%20journal%20of%20maternal-fetal%20&%20neonatal%20medicine&rft.au=Politou,%20Marianna&rft.date=2009-01-01&rft.volume=22&rft.issue=8&rft.spage=714&rft.epage=716&rft.pages=714-716&rft.issn=1476-7058&rft.eissn=1476-4954&rft_id=info:doi/10.1080/14767050802609783&rft_dat=%3Cinformahealthcare_cross%3E10_1080_14767050802609783%3C/informahealthcare_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c325t-6aff0446398fe1b6d663fd33fe24c4d2e9d00868ada0e655731466bf4f2651413%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/19479640&rfr_iscdi=true |