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@JTHjournal

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JTH will no longer have an active presence on X. While this account will remain available as an archive, we will no longer monitor comments or post new content.

Joined November 2016
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@JTHjournal
JTH
2 months
JTH will no longer have an active presence on X. While this account will remain available as an archive, we will no longer post new content or monitor engagement. To continue receiving updates, follow us on: .LinkedIn: BlueSky:
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RT @MarcCarrier1: The Repeat Study addressed a really important knowledge gap!.The incidence of recurrent events following an ante- or post….
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RT @GendronNico: 🚨How to deal with interference on heparin anti-Xa activity caused by oral factor FXa inhibitors: Communication from the @i….
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RT @SETH__Oficial: 📰How we treat severe inherited antithrombin deficiency: lessons from cases homozygous for the Budapest 3 variant👉 https:….
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This study provides new insights into VWF regulation in complement-mediated diseases, opening avenues for targeted therapies in TMA and atypical HUS!. ✅ W1183R-CFH enhances VWF cleavage by ADAMTS-13, potentially reducing large prothrombotic multimers.✅ Identifies strong binding
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RT @AngLi_MD: Preventing arterial #thromboembolism (ATE) in high-risk cancer patients should focus on modifiable CV risk factors. Kim et al….
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🔍 What are the key design and feasibility challenges in pediatric DOAC trials, and how can future antithrombotic studies be improved to ensure robust and clinically meaningful results?. This Study.✅ Identifies common feasibility barriers, such as sample size adjustments and
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🔍 How can we accurately measure FVIII activity in hemophilia A patients receiving efanesoctocog, particularly in those also on long-term emicizumab therapy?. ✅ Efanesoctocog, an ultra-extended half-life FVIII, can now be accurately measured even with emicizumab present.✅
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In this meta-Analysis of 16 studies (2300+ patients),.✅ Peak & trough concentrations of apixaban and rivaroxaban established 📉.✅ Age & kidney function impact drug levels—highlighting the need for personalized dosing.✅ Findings align with known pharmacokinetic studies
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A PAR4 genetic variant (rs2227376) reduces venous thromboembolism (VTE) risk by decreasing platelet activation & thrombin generation.🐁 Mice with the PAR4-P322L mutation had smaller venous clots & fewer procoagulant platelets. 💡 Could targeting PAR4 signaling be a future
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🤖 AI Meets Coagulation Genetics! 🧬. Machine learning (ML) is revolutionizing genetic variant interpretation for coagulation factor deficiencies, with increasing focus on hemophilia A & B. 🔍 Key Insights:.✅ AI tools like Hema-Class improve variant classification &
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RT @TomReiser: Interested in the fundamentals of key topics in #thrombosis and #hemoastasis? .Don't miss the BRAND NEW Educational Review S….
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Individuals with a new cancer diagnosis and no stroke history have an increased risk of ischemic stroke which varies according to site and stage. Future research is needed to identify individuals at highest risk who may benefit from preventative treatment.@DebSiegal
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RT @ZHeart11768530: 🔴Venous thromboembolism and Duration of Anticoagulation ⤵️ #2025Review @JTHjournal. 🔹Basics of diagnosis and trea….
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RT @kolja_pantic: Something we really needed! Comprehensive and understandable review which can be useful to all early career professionals….
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💡 Could Roxadustat be the next big thing in ITP treatment? . 🔬 Roxadustat, a HIF-1α stabilizer, shows promising therapeutic potential for ITP by enhancing megakaryocyte development & immune modulation!.📊 Key Findings:.✅ Reduced ITP risk (OR 0.79, P=0.01).✅ No significant
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🦠 Gut microbiota & progesterone play a crucial role in bone marrow mesenchymal stem cell (BM-MSC) dysfunction in PITP. 🧬 Increased progesterone leads to BM-MSC senescence & apoptosis, impairing immune regulation. 🔗
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How do structural changes in the A1 domain of von Willebrand factor (VWF) lead to type 2M von Willebrand disease? 🧬🔬.This study reveals that both misfolding and hyperstabilization of A1 disrupt platelet adhesion—offering new insights into VWF function!
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A single amino acid replacement (D189A) switches thrombin specificity from trypsin-like to chymotrypsin-like. The observation establishes a new paradigm in the field of trypsin-like proteases. 🔗
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