know more about our lab! 🧑🔬🧪🥼
🇵🇹 Laboratório de Biomedicina Mitocondrial e Teranóstica / 🇬🇧 Mitochondrial Biomedicine and Theranostics Laboratory (LBioMiT)
💻follow us https://t.co/O1AqYSelaA
💻more info https://t.co/l1ayqoOsUr
read our mission statement [thread]⬇️
#DidYouKnow that regardless of which #RareCondition a person has, the following remains true?
The average #RareDisease patient waits 4 years before receiving a final #Diagnosis
Source: Rare disease statistics based on data collected by @rarediseaseuk
https://t.co/Md46cIyxJH
Mito Foundation’s Quarterly #Grant Round is now open!
Applications close 5pm AEST Friday 23 June 2023.
These grants are designed to support the best clinical work and research into primary #mitochondrial disease.
Apply today!
#research#mito
Opps at @cnc_uc @UnivdeCoimbra#MSCA#MSCAPF#postdoc
if you're interested in a MSCA in our lab, see contacts in our profile and visit CNC's page for more info
LIVRO VERMELHO DOS MAMÍFEROS DE PORTUGAL CONTINENTAL
Apresentação Pública
18 abr | 17h30 - Entrada livre!
Programa completo aqui https://t.co/ofyo29fm8y
Starting today, twice a month, you will learn about #mitochondria and the diseases associated to the lack of cellular energy!
This initiative is part of Mit.OnOff, between us/@cnc_uc and @UiB, & sponsored by @EEAGrantsPT!
Stay tuned!
#CNCResearch#CNCResearchers#SciComm
Have you ever heard of BIO Art?
It's where Biomedical Science meets Art.
Send in your creations and maybe win first prize - a Travel Grant worth € 500 to the ASM 2024.
https://t.co/oQBKvGiyRH
https://t.co/pSiaGg9QIR
A Faculdade de Medicina da Universidade de Coimbra faz parte da história da instituição desde a sua fundação, em 1290.
Ao longo dos tempos, a FMUC manteve o seu foco na disponibilização de uma formação académica e clínica de excelência. 🧑⚕️🩺
#UCoimbra
What a grandiose final with the Americas joining our Global Chain of Lights ✨!
With the #LightUpForRare movement, let’s continue to raise awareness for people living with a rare disease.
👉https://t.co/LRb1IGhZBZ
This #RareDiseaseDay, we call for action to eliminate barriers preventing people living with a rare disease's full participation in society.
Share our Official Rare Disease Day video, translated into over 40 languages, to spread our call for equity!
👉 https://t.co/G7A9lJSkMU
#RareDiseaseDay went like this for LBioMiT!
We talked with over 100 students of medicine, dentistry and other health and biomedicine areas about our research work: #mito, #LHON and #mitonoff project 💚🪫🔋
thank you to @befmuc for granting us the space for the day
Tomorrow it's #RareDiseaseDay 2023!
💡 Light up at 7 pm wherever you are to raise awareness for people living with a rare disease!
🏛️ Find a monument being lit up near you: https://t.co/LRb1IGhZBZ
🏠 Find out how to light up your home: https://t.co/S0PNzbafDo
#LightUpForRare
Proud to be talking about our research activity at the #Genetics#Matters event today at the Discovery Museum in Newcastle with @MitoResearch team as part of our public & patient engagement strategy. #ProjectPearl Without Research, there will never be a Cure.
@befmuc 💚💪
"Cada um de nós, sozinho, é raro. Juntos, seremos mais e melhor, e chegaremos mais longe! Nenhuma doença é tão rara que não mereça que se descubra a sua causa e se encontre o tratamento!" - MG