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Accelerating Diagnosis for Rare Disease Patients Through Genetic Newborn Screening and Artificial Intelligence

ID: 1446116518182277249

linkhttps://screen4care.eu/ calendar_today07-10-2021 14:14:30

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EUScience&Innovation🇪🇺 (@euscienceinnov) 's Twitter Profile Photo

Early genetic checks being developed by researchers with EU and industry funding will accelerate treatments for illnesses that affect millions of people in Europe. Read more ➡️ europa.eu/!wRCmQ8 #ResearchImpactEU #HorizonMagazine

Screen4Care (@screen4care) 's Twitter Profile Photo

Have you checked out the second issue of our #newsletter yet? 📰 If not, feel free to dive in using the link below. And don't forget to subscribe so you don't miss future issues! 📬✨ 🔗 screen4care.eu/newsletter/Scr… #Screen4Care #RareDisease #NBS #NewbornScreening #EUResearch

Have you checked out the second issue of our #newsletter yet? 📰 If not, feel free to dive in using the link below. And don't forget to subscribe so you don't miss future issues! 📬✨

🔗 screen4care.eu/newsletter/Scr…

#Screen4Care #RareDisease #NBS #NewbornScreening #EUResearch
Screen4Care (@screen4care) 's Twitter Profile Photo

🧬 September is Newborn Screening Awareness Month and we’re all in! This year we’re focusing on providing soon-to-be parents with key insights on #RareDisease screening. Stay tuned!🌟 #Screen4Facts #Screen4Care

🧬 September is Newborn Screening Awareness Month and we’re all in! This year we’re focusing on providing soon-to-be parents with key insights on #RareDisease screening. Stay tuned!🌟
 
#Screen4Facts #Screen4Care
Screen4Care (@screen4care) 's Twitter Profile Photo

🧬 82% of parents of children with rare diseases wish for a birth diagnosis, according to the latest #RareBarometer survey. Early diagnosis can improve treatment and help children prepare for adulthood. 🌱 Let’s support #NBS for better futures. 🙏 #Screen4Care #Screen4Facts

🧬 82% of parents of children with rare diseases wish for a birth diagnosis, according to the latest #RareBarometer survey. Early diagnosis can improve treatment and help children prepare for adulthood. 🌱

Let’s support #NBS for better futures. 🙏

#Screen4Care #Screen4Facts
EURORDIS-Rare Diseases Europe (@eurordis) 's Twitter Profile Photo

No child should be deprived of early diagnosis and care that can improve or save lives. Support a harmonised European approach to newborn screening. Read the 11 Key Principles, available in 13 languages: go.eurordis.org/Jakheu #NewbornScreening #RareDiseases #EqualCare

No child should be deprived of early diagnosis and care that can improve or save lives.

Support a harmonised European approach to newborn screening.

Read the 11 Key Principles, available in 13 languages: go.eurordis.org/Jakheu 

#NewbornScreening #RareDiseases #EqualCare
Screen4Care (@screen4care) 's Twitter Profile Photo

🩺 Calling all clinicians! Contribute to developing a clinical decision-support model for rare diseases by taking our #survey, in collaboration with BAPEMED, by Sept 30. 👉 screen4c.limesurvey.net/643664?lang=en Thank you for participating and sharing—your support matters! 🙏 #Screen4Care

🩺 Calling all clinicians!

Contribute to developing a clinical decision-support model for rare diseases by taking our #survey, in collaboration with <a href="/bapemed/">BAPEMED</a>, by Sept 30.

👉 screen4c.limesurvey.net/643664?lang=en

Thank you for participating and sharing—your support matters! 🙏

#Screen4Care
Screen4Care (@screen4care) 's Twitter Profile Photo

✨ What a great time we had at #AOMCJMS2024 in Nara, Japan! 🔬 Our Sci Coordinator Alessandra Ferlini was honoured to speak on genetic diagnosis of neuromuscular diseases, exploring #Screen4Care’s mission to advance #GenomicMedicine. 🧬 Thanks to Ichizo Nishino for the opportunity! 🙏

✨ What a great time we had at #AOMCJMS2024 in Nara, Japan!

🔬 Our Sci Coordinator Alessandra Ferlini was honoured to speak on genetic diagnosis of neuromuscular diseases, exploring #Screen4Care’s mission to advance #GenomicMedicine. 🧬

Thanks to <a href="/one333/">Ichizo Nishino</a> for the opportunity! 🙏
EURORDIS-Rare Diseases Europe (@eurordis) 's Twitter Profile Photo

Today we hosted Screen4Care’s Newborn Screening (NBS) Forum, brining together experts to explore the implications of genetic NBS. As a core partner in #Screen4Care, we are ensuring that the patient voice is at the forefront of these vital discussions.⏬ go.eurordis.org/4qpRco

Today we hosted <a href="/Screen4Care/">Screen4Care</a>’s Newborn Screening (NBS) Forum, brining together experts to explore the implications of genetic NBS.

As a core partner in #Screen4Care, we are ensuring that the patient voice is at the forefront of these vital discussions.⏬
go.eurordis.org/4qpRco
Screen4Care (@screen4care) 's Twitter Profile Photo

Have a minute? ⏰Watch "60 Seconds with Alessandra Ferlini" to learn how our Scientific Coordinator is playing a key role in exploring the potential of next-generation sequencing and digital tools to improve outcomes for people living with rare diseases.👇 #Screen4Care Roche