ERN-ITHACA
@ERNIthaca
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European Reference Network on congenital malformations and rare intellectual disability (ERN-ITHACA).
Joined September 2017
Yesterday was the first day of the 35th Eurodysmorpho conference in Vilnius. A beautiful morning workshop on Bayesian risk calculation was held by Emilia Bijlsma, a session strongly encouraged by @eshg_young and @ERNIthaca
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🌟Save the date – 2nd International Conference on Clinical Research Networks for Rare Diseases🌟 💡“Mobilising the Global Rare Disease Clinical Research Ecosystem” 🗓️9-10 December 2025 🌍Co-organized by @ERDERA_org, RDI & IRDiRC 📩Register now: https://t.co/EWDLvRpPar
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Nominations are open for the Leena Peltonen Prize (€10,000). candidates: outstanding young researchers, Early career stage, no age or graduation limit Awardee will give the Leena Peltonen Lecture at #eshg2026 in Gothenburg. 📅 Deadline: 31 Oct 2025 🔗
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Outstanding rare disease care goes beyond treatment — it embraces the whole person and their support system. Help us spotlight the champions of holistic care in the rare disease community! Submit your nominations for the #EURORDISAwards2026! 👇 🌟 https://t.co/PwHeNlhNnG
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Met with @eurordis to discuss how we can accelerate innovation and deliver new treatments faster to all Europeans living with rare diseases. Moving forward decisively on the #BiotechAct, #ERNs, and #CMA will be key to making this a reality. #RareDiseases
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In the latest episode of #EurordisRareOnAir, @TomaszGrybek shares his journey across two continents for a treatment for his son and how this led him to advocate for patient involvement in medicines regulation. 👉 Tomasz & Boris’s story: https://t.co/Hppr9lOynL
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My #TEDx talk about #rarediseases and #undiagnoseddiseases. I truly belive that by raising public and healthcare awareness about RDs, by supporting treatment and of course by global collaboration we can save lives of individuals with RARE DISEASES! https://t.co/zl0pIlmLBo
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Make your voice heard!🗣️ #ERDERA has launched a survey to explore how #RareDisease patients can contribute to EU-funded research. 🔐 Confidential & created with patients 🔗 Take the survey: https://t.co/g32SAtlhRD (open until mid-July) 📄 More: https://t.co/V3B80kzFUg
@eurordis
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📣 ERDERA is happy to announce a new facilitation period for the MOOC: “Diagnosing Rare Diseases: From the Clinic to Research and Back”! 📅 12 May – 4 July 👉 Get expert support, ask questions & boost your knowledge in #RareDiseases 🔗 More at https://t.co/VSxkddTSn3
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@euro_nmd, @ERN_RND, @Metab_ERN, @ERNIthaca, and EpiCARE will be present at the 2025 EPNS Munich Congress from July 8–12. Visit us at the joint booth at Intercongress GmbH!
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🧬Submit your abstract for the 2025 Eurodysmorpho in Vilnius 16th-19th Sept 2025🗓️The new deadline for abstract submission is Friday 6th June 2025 ⏰( https://t.co/gfi297uSzD) Registration fee 30€. Presentation of a clinical case necessary to participate @eshg_young @ERNIthaca
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5 days left to submit your abstract for EuroDysmorpho! This workshop a great opportunity to showcase your dysmorpho cases, receive feedback, and connect with peers in a collegial atmosphere. Don't miss out, especially if you're a young geneticist! https://t.co/PCDhi4ZzVp
ern-ithaca.eu
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Our turn to present our network to the Board of Members States and to show how impactful ERNs are! Next step is heading to Milan for the @eshgsociety Congress🧬where we'll be sharing a booth with @euro_nmd, ERN EYEs and Genturis. See you there!
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📣 ERDERA is happy to announce a new facilitation period for the MOOC: “Diagnosing Rare Diseases: From the Clinic to Research and Back”! 📅 From 12 May – 4 July, get expert support, ask questions & boost your knowledge in #RareDiseases 🔗 More at https://t.co/VSxkddTSn3
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🚨 We're hiring at #ERDERA! Join us to make a difference in the rare disease field. We're looking for: 🟣 Office Manager (Bilingual) 🟣 Senior Policy and Liaison Manager Apply now 👉 https://t.co/k0qBD3eeSQ 📣 Spread the word and help us find the right talent! #Jobs #RareDiseases
erdera.org
About ERDERA ERDERA – the European Rare Diseases Research Alliance – is a European partnership uniting over 170 public and private organisations across 37 countries around a single goal: turning […]
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🧬Abstract submission for EuroDysmorpho 2025 is available on our website until may 31st! EuroDysmorpho is a 30+ year meeting open to any presentation in the field of human development. 🗓️17-20 Sept. 2025 📍Vilnius, Lithuania To know more:
ern-ithaca.eu
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Don't miss out our MOOC on #RareDiseases diagnosis ! 🎯Public: primarily medical students and Phd but also ePAG, paramedics - anyone interested 🚨 May 12 - July 4, a new facilitation period where mentors will be available to answers students questions https://t.co/qo778cixsP
futurelearn.com
Develop your understanding of rare genetic diseases and their diagnosis, and discover more about the role of technology in medical research with this free online course.
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It's official! ✨Abstract submissions now open for #ASHG25 🧬 Share your latest research in human genetics and genomics on a world-class stage 🗓️ Deadline: June 9, 2025, at 5 PM U.S. ET 🔗 Submit here: https://t.co/rWC9XKW0q3
#humangenetics
#genomics
#ASHG
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First organised by Prof. Dian Donnai in 1984, the MDC is now a leading biennial international event for experts in 🧬 #Dysmorphology #CongenitalMalformations
#NeurodevelopmentalDisorders
#GenomicMedicine #RareConditions Looking forward to welcoming friends from around the 🌍
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