Glenn Pierce
@gfp55
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🚨 Time's running out to submit your #BleedingDisorders research to the #WFHCongress2024! Don't miss this opportunity to showcase your work on a global stage, win prestigious awards, and connect with global experts. Deadline: Nov 15, 2023. Submit now: https://t.co/lIzneA35Ei 🩸
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World Federation of Hemophilia (@wfhemophilia) and (@EHC_Haemophilia) statement on vaccine thrombosis thrombocytopenia. Persons with bleeding disorders not at increased risk from very rare event, should get vaccinated. Risks of COVID-19 greater
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Come watch the arguments, assessments and suggestions for evaluating gene therapies for hemophilia
On Dec 11 at 10 a.m. the WFH will host a session to explore patient perspectives related to the scientific inquiry of gene therapy. The panelists will discuss the quest to answer the unknowns around safety, variability and durability of response. Register: https://t.co/hkxW49wk2C
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The #WFHVirtualSummit Committee understands the importance of sharing knowledge of #VWD and the Summit program reflects this. Glenn Pierce, MD, PhD, WFH Vice-President, Medical, highlights the importance of bringing awareness to VWD. Watch the video here: https://t.co/pmlq7cWXst
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The High Price of Hemophilia https://t.co/CcE2z1B6iN via @ASH Clinical News
ashclinicalnews.org
The High Price of Hemophilia - Bleeding Disorders, Feature Articles, Spotlight - ASH Clinical News
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The hemophilia gene therapy race faces a critical year in 2020 https://t.co/j1T3G1wgjG via @BioPharmaDive
biopharmadive.com
While BioMarin looks poised to reach market in hemophilia A first, Sangamo and Spark are advancing rival gene therapies to tackle the blood disorder.
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assuming specific activity of the transgene protein is same as pd or recombinant. Ag levels are not the solution unless specific activity is previously validated.
At least they can be compared properly with antigen estimation?
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The WFH WBDR has reached another milestone – over 2,500 patients! We are well on our way to our goal of enrolling 10,000 patients #patientvoice.The WFH would like to thank everyone involved for helping us to grow the WBDR #bleedingdisorders #hemophilia
https://t.co/opUeL4zEUz
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Join us at #WFH2020WorldCongress for the largest congress for the #bleedingdisorders community! While there, take the time to explore the Batu Caves, said to be around 400 million years old. https://t.co/AejeRbpwUe
#TreatmentforAll
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Bayer Makes Global Impact Through World Federation of Hemophilia Humanitarian Aid Program | BioSpace https://t.co/5o2C0ZvJtp
#jobs
biospace.com
In addition to education and training, it will offer Bayer’s complete portfolio of recombinant Factor VIII treatments to healthcare providers in more than 60 countries.
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St. Jude Children’s Research Hospital and the World Federation of Hemophilia announce collaboration New arrangement will establish gene therapy clinical trial for hemophilia patients in low- and middle-income countries https://t.co/YBI5QgRe0y
#genetherapy #WorldHemophiliaDay2019
stjude.org
Collaboration will improve the understanding of how advanced technologies, such as gene therapy for hemophilia B, can move rapidly to countries with limited resources.
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April 17 is the day!
This #WorldHemophiliaDay, Boston will stand out again as 2 of its most famous landmarks will #LightItUpRed. Can you guess which ones? #WHD2019
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We are pleased to announce our acquisition of @Bioverativ, a biopharma company focused on therapies for hemophilia and other rare blood disorders, expanding our presence in specialty care and strengthening our leadership in rare diseases #Bioverativ
https://t.co/BDraaabnDf
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Critics claim I only tweet about Trump's incompetence and horrific policies. Untrue. I also tweet about his lies and his appalling ego.
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Continued...you are a disgrace to honesty and truth, and a failure to your constituents. Apparently all other commenters to your op-ed agree
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