DANIELI ANDRADE
@daniandradeaps
Reumatologist, Prof University of Sao Paulo, Antiphospholipid, Auto-immunity
You might like
PANLAR talk about What have we learned so far from the 2023 ACR EULAR APS Criteria?
#WTDay24 is excited to continue highlighting the strong Olympic athletes that have been affected by blood clots 💪. Swipe to see these inspiring individuals and click here to read more about them: bit.ly/3WAFaed
Our Most Recent Publication Investigating "Damage" measured by DIAPS (damage index for antiphospholipid syndrome) in antiphospholipid antibody-positive patients . pubmed.ncbi.nlm.nih.gov/37307082/. We Want to Thank All APS ACTION Members for Their Contributions
Watching a talk by one of my scientific heroes Jane Salmon from the stage itself 🤯 #ACR22
Great talk by Jason Knight at ACR covering APS and COVID.
Encuentro histórico en #SAR2022 @carlostororeuma @daniandradeaps @alibafer_miguel @gponsestel y @Lupusreference #GLADEL #PANLAR @gladelweb @PanlarLeague @SLEuroSociety
Wonderful to be back in Cordoba to talk about APS in the National Argentina Meeting…… especially before World Soccer Cup so that we keep our frienship!
Sharing our recently published experience with COVID vaccination in APS patients.
What a power couple! Amazing educative session by @daniandradeaps & @jasonsknight #ICAPA2022
Very excited to hear the good feedback about my talks at ICAPA. Congrats to Guillermo Pons Stel, Paula Alba and Maria Laura Bertolaccini for all they did facing Pandemics.
Natural history of PF4 antibodies in vaccine induced immune thrombocytopenia in UK cohort - 72% remain + for PF4 antibodies at 100 days - 12.6% relapsed, predominantly with thrombocytopenia & < 90 days Thanks to Brian Craven for leading this work pubmed.ncbi.nlm.nih.gov/35263420/
Cardiovascular disease risk in APS: Thrombo-inflammation and atherothrombosis. (free access) access. authors.elsevier.com/a/1egU3_KP4rfb…
TODAY is #RareDiseaseDay! All around the world, the rare disease community is coming together to share their colours, raise awareness, and demand equity for people living with a rare disease. As a global community, we have a powerful voice! How are you sharing your colours?
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