Ya Hui Hung

Today is Niemann-Pick Disease Awareness Day, a time to support those affected by conditions such as Niemann-Pick Disease Type C (NP-C). Supported by @NiemannPickOz, Dr @HungYaHui's team is working on an innovative mRNA gene therapy for NP-C. Learn more: florey.edu.au/research-proje…

In honour of Niemann-Pick Disease Awareness Day, we spoke with Mandy Whitechurch, Founder of @NiemannPickOz Foundation and mother of Timothy and Matthew. With volunteers and families, @NiemannPickOz supports our research into a new gene therapy for NP-C: bit.ly/3YpTBTg

@TheFlorey, my team and I are joining @Child_Dementia to #FACEit, to raise Childhood Dementia Awareness and help to make a difference through our research for effective treatments. Learn more 👉 childhooddementia.org

Emotions like Joy, Sadness, Anger, Anxiety, Fear, and Disgust, all contribute to the creation of memories.  For those living with childhood dementia, these emotions and memories slip away. They become confused and disoriented.  #ChildhoodDementiaAwarenessDay #ChildhoodDementia

We are grateful to the Australian NPC Disease Foundation (@niemannpickoz) for supporting our research at The Florey to improve the health and wellbeing of those living with NP-C. Learn more: florey.edu.au/research-proje… #TheFlorey #impact #neuroscience #NiemannPickC @HungYaHui

It's an honour to take part in the 2024 NPC Conference held by the Australian NPC Disease Foundation this week, with Dr @HungYaHui from The Florey presenting her team's research in developing an effective mRNA gene therapy for #NiemannPickC.

It's great to see our partners from the Australian NPC Disease Foundation (@NiemannPickOz) featured in the Herald Sun this morning. Thank you @NiemannPickOz for supporting Florey's research to help Noah and other children with NPC disease. Read here: heraldsun.com.au/lifestyle/heal…

Please join us for this important event #YOD

This International Women's Day, hear from some of our Florey scientists who have shared their perspectives and stories being women in science. Read the story in full: florey.edu.au/news/2024/03/i… #TheFlorey #IWD2024 #InspireInclusion

Today is 29th February - a day that occurs only every 1,461 days. A rare day, making it is extra special to celebrate #RareDiseaseDay today to raise awareness and support for 300 million people living with a #RareDisease. Learn more about our rare disease research @TheFlorey 👇

We love Renee's intro to her kids. She's one of the parents raising awareness to create change. Sadly, Hudson, Holly and Austin all have #childhooddementia caused by Niemann-Pick disease type C. You can see Renee’s full interview here: bit.ly/3SuyYRz

Promoting understanding and offering support, the @NiemannPickOz is dedicated to improving lives affected by Niemann-Pick disease. Learn more on their website: npcd.org.au . #RareDiseaseDay2024 #LightUpForRare #ShareYourColours #RareDiseaseDay #raredisease

Very pleased to see the launch of this short comedy/drama on the importance of increasing the number of conditions included in newborn heelprick tests - please watch and share! @fragilexuk @M4RareDiseases @GeneticAll_UK @camraredisease #rareconditions youtube.com/watch?v=oVKBVE…

What are Lysosomal Storage Diseases? youtu.be/gW6_QWbQLCs via @YouTube Neat intro video from a collab with Platt lab team @PharmOxford @NiemannPickUK

@kariisssaaa Congratulations!

Really pleased to share that two of my grant applications have been funded! I'm absolutely thrilled and excited to see my research program of comparing different adult- and childhood onset dementias developing 😍1/3

Today is the Global #NiemannPickDisease Awareness Day. If you have not heard of Niemann-Pick Disease, learn more about this rare and devastating condition and how you can help to support the #NiemannPick community 👉 npcd.org.au

It's #ChildhoodDementia Day today! My team at @theflorey is helping to raise Childhood Dementia awareness by putting stickers on our faces to #FACEit. Learn more 👉 @Child_Dementia childhooddementia.org

More details about the Lysosomal Disease Summit can be found here: bit.ly/LDSummit2023

Join me at the #LysosomalDisease Summit in Melbourne, 27-29 October 2023. There are student scholarships available, sponsored by @FabryAustralia. Apply here: lysosomaldiseasesummit.org/scholarship/ Deadline has been extended to 22 September, 2023.

@AshenafiBetrie @EamonnDickson @NatureComms Congratulations @EamonnDickson!

@EamonnDickson @NatureComms @HungYaHui

Happy Friday everyone! Delighted to share our latest work out today @naturecommunications led by an amazing postdoc in our group, @mcasasprat. rdcu.be/dh0zw Below is a brief summary: