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231226s2023 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2023.109804
|2 doi
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|a pubmed24n1210.xml
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|a (DE-627)NLM363311718
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|a (NLM)37838215
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|a (PII)S1521-6616(23)00567-3
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Ding, Zetao
|e verfasserin
|4 aut
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|a Beyond the classics
|b The emerging value of anti-phosphatidylserine/prothrombin antibodies in antiphospholipid syndrome
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|c 2023
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 06.11.2023
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|a Date Revised 28.11.2023
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2023. Published by Elsevier Inc.
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|a Antiphospholipid syndrome (APS) is an autoimmune disorder characterized by the presence of antiphospholipid antibodies (aPLs), which can lead to thrombosis and pregnancy complications. Within the diverse range of aPLs, anti-phosphatidylserine/prothrombin antibodies (aPS/PT) have gained significance in clinical practice. The detection of aPS/PT has proven valuable in identifying APS patients and stratifying their risk, especially when combined with other aPL tests like lupus anticoagulant (LA) and anti-β2-glycoprotein I (aβ2GPI). Multivariate analyses have confirmed aPS/PT as an independent risk factor for vascular thrombosis and obstetric complications, with its inclusion in the aPL score and the Global Anti-Phospholipid Syndrome Score (GAPSS) aiding in risk evaluation. However, challenges remain in the laboratory testing of aPS/PT, including the need for assay standardization and its lower sensitivity in certain patient populations. Further research is necessary to validate the clinical utility of aPS/PT antibodies in APS diagnosis, risk stratification, and management
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Anti-phosphatidylserine/prothrombin antibody
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|a Antiphospholipid syndrome
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|a Obstetric complications
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|a Risk stratification
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|a Thrombosis
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|a Prothrombin
|2 NLM
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|a 9001-26-7
|2 NLM
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|a Phosphatidylserines
|2 NLM
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|a Antibodies, Antiphospholipid
|2 NLM
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|a beta 2-Glycoprotein I
|2 NLM
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1 |
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|a Pan, Haoyu
|e verfasserin
|4 aut
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1 |
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|a Yang, Zhixia
|e verfasserin
|4 aut
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1 |
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|a Yang, Chengde
|e verfasserin
|4 aut
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|a Shi, Hui
|e verfasserin
|4 aut
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0 |
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 256(2023) vom: 15. Nov., Seite 109804
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:256
|g year:2023
|g day:15
|g month:11
|g pages:109804
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|u http://dx.doi.org/10.1016/j.clim.2023.109804
|3 Volltext
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|d 256
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