Rebeca Ridings Figueroa

Charity & Research Manager at @CureCLCN4. All views are my own.

[Cure CLCN4 @CureCLCN4]

From animal & cell models to a patient registry, our aim is to equip researchers with the resources to drive the research on #clcn4-condition forward 🔬To this end, we have funded the generation of three CLCN4-rat models, available to researchers via the INFRAFRONTIER repository

[Rebeca Ridings Figueroa @rebecaridfig]

Super excited to share the details of Cure CLCN4's Pilot Grant Program! 🙌 Whether you're already involved in research on CLCN4-NDC or are interested in #rarediseases #neurodevelopmentaldisorders and want to join the #clcn4 field, this is a great opportunity!
#cureclcn4

[Cure CLCN4 @CureCLCN4]

We are thrilled to announce that applications for Cure CLCN4’s Pilot Grant Program are now open!🔬
💰 Award: £150,000 (2-3 grants of £50-75k each).
🚨Deadline: 15th December 2023
For further details and application 👉 https://t.co/etI5XNTbUG
#cureclcn4 #clcn4grant #research

[Cure CLCN4 @CureCLCN4]

We are thrilled to announce that applications for Cure CLCN4’s Pilot Grant Program are now open!🔬
💰 Award: £150,000 (2-3 grants of £50-75k each).
🚨Deadline: 15th December 2023
For further details and application 👉 https://t.co/etI5XNTbUG
#cureclcn4 #clcn4grant #research

[Cure CLCN4 @CureCLCN4]

🚨 Study Alert! The Translational Centre of Research Excellence for Speech Disorders (Australia) has launched an online study on speech & language in CLCN4-related condition. 🌟 Details here: https://t.co/BUJkApKfio
#cureclcn4 #clcn4 #speech

[RARE Revolution Magazine® @RareRevolutionM]

Symptoms of #CLCN4-NDC: developmental delays, intellectual disability, #seizures, and movement disorders. For more info, check out our website's section for families 👪 https://t.co/gZ4hsqTOla and professionals ��‍⚕️ https://t.co/PfDgBZzzgT #cureclcn4 #tuesdaytakeover @CureCLCN4

[RARE Revolution Magazine® @RareRevolutionM]

👋 Welcome to @CureCLCN4’s #tuesdaytakeover of @RareRevolutionM! Today, we're shining a spotlight on CLCN4-related neurodevelopmental condition, a rare genetic condition that can cause intellectual disability, seizures, behavioural and movement disorders. https://t.co/TOD016b11v

[Cure CLCN4 @CureCLCN4]

Only four weeks left to register for in-person attendance at the @CureCLCN4 Scientific Conference 2023, happening on 16th & 17th June! Check out the incredible line-up of speakers that you won't want to miss 🙌 For further details visit our website: https://t.co/p9FPjwYa16

[Cure CLCN4 @CureCLCN4]

Exciting news! Two #Clcn4 rat models, produced by PHENOMIN-ICS and funded by @CureCLCN4, are now available for research on the #EMMArepository of @InfrafrontierEU🔬! 👉🏻https://t.co/SZdJn4W8xV
Many thanks to families and friends who helped raise the funds to make it possible🙏

[Bain Brain Lab @BainBrainLab]

Why become a child neurologist? Care for sweet kiddos like Alessia and alongside fierce parent advocates for rare diseases! @CureCLCN4 @s_searchlight

[Cure CLCN4 @CureCLCN4]

We are proud to announce the first Cure CLCN4 webinar, coming in October! 🥳 Stay tuned for details on when and how to watch this episode #cureclcn4 #clcn4 #specialparenting #webinar

[EURORDIS-Rare Diseases Europe @eurordis]

Welcome to the 2022 #EURORDISSummerSchool's 2️⃣8️⃣ participants from 1️⃣8️⃣ countries, and our amazing speakers!

Today we kicked off to a good start with sessions on 🔬therapeutic development in rare diseases, and the methodology and design of clinical trials.
Happy learning to all!

[Rebeca Ridings Figueroa @rebecaridfig]

And it's finally happening! After so many months of work, the @CureCLCN4 Scientific Conference starts today at 1pm! 🥳 #london #cureclcn4 #clcn4 #raredisease

[Rebeca Ridings Figueroa @rebecaridfig]

@RareRevolutionM #CLCN4 neurodevelopmental condition
@CureCLCN4

[Cure CLCN4 @CureCLCN4]

Don't forget to sign up for Cure CLCN4's scientific conference happening on May 27th and 28th! For more details, including the list of speakers and registration details, visit our website: https://t.co/TKMiH0wMbw

#cureclcn4 #clcn4 #raredisease #ionchannel