Top Tweets for #cureShank
Big news from CureSHANK!
π Meet our new Chief Scientific Officer
𧬠Discover #PMSDDS highlights
π¬ Clinical trial updates
π© Get it all here: https://t.co/lxqVPhJ9b7
#CureSHANK
π§ Prof. @haitham_amal, CSO @NeuroNOS, explains how NO dysregulation drives PhelanβMcDermidβ―Syndrome (PMS) & how our FDAβorphan small molecule advances to firstβinβhuman trials inβ―2026. Watch βΆοΈ https://t.co/9JT8589bzl
#PMSF #CureSHANK #RareDisease #Autism #DrugDiscovery
Mark your calendars for our Spring Community Webinar to learn how CureSHANK is accelerating treatments for Phelan-McDermid syndrome in 2023!
Registration info coming soon.
#CureSHANK #shank3 #phelanmcdermidsyndrome #raredisease
The #CureSHANK Biomarkers and Outcome Measures Consortium holds a Kick Off Meeting next week to prioritize 2023 projects!
Companies interested in joining can contact Project Manager Trish Davidson at [email protected].
#SHANK3 #PhelanMcDermidsyndrome #RareDisease
Learn more about how the FDA helps the development of treatments at https://t.co/YNRIfWdMwE.
#showyourstripes #shareyourcolors #careaboutrare #raredisease #rarediseaseday #rarediseaseday2023 #rarediseaseawareness #rarediseaseweek #phelanmcdermidsyndrome #cureshank
At CureSHANK and PMSF, we are working to make life better for those with Phelan-McDermid syndrome. To paraphrase our close friend, Sue Lomas, founder of @PhelanMcDermidsyndromeFoundation: #showyourstripes #careaboutrare #rarediseaseday2023 #rarediseaseawareness #cureshank
Did you know that 1 in 15,000 people have Phelan-McDermid syndrome? Among the highest single-gene causes of autism + intellectual disability, this genetic disorder also results in myriad other health issues. #showyourstripes #rarediseaseday2023 #phelanmcdermidsyndrome #cureshank
At CureSHANK and @PhelanMcDermidSyndromeFoundation, we are working to make life better for those with Phelan-McDermid syndrome. #showyourstripes #careaboutrare #raredisease #rarediseaseday2023 #rarediseaseawareness #rarediseaseweek #phelanmcdermidsyndrome #cureshank
Webinar #1 of #CureSHANK Biomarkers and Outcome Measures Consortium's "Resources for Researchers" series, provided information to industry about #iPSC resources at #NIMH and the most up-to-date research on #SHANK3 using iPSC.
We invite you to watch!
https://t.co/0ssPot8RG9
We are thrilled to have Ms. Emery Silva join us, as she brings much enthusiasm, passion and creativity to our executive committee!
#anythingforasa #phelanmcdermidsyndrome #CureSHANK
CureSHANK will consider proposals that explore mechanisms of epilepsy in SHANK3 haplo-insufficiency or clinical research studies of epilepsy in Phelan-McDermid syndrome.
#CureSHANK #epilepsy #phelanmcdermidsyndrome #neurodevelopmentaldisorders #autism #NeuroTwitter
Synaptic Shank polymerizes via SAM domains, and binds SAPAP/GKAP via PDZ domains. Is this important for human health? Find out in our new paper in Mol Psychiatry. Thanks to SPC@EMBL Hamburg and AG Lohr (Biology, Uni Hamburg). https://t.co/gfv1DIjRek. #cureShank
Our Externally-Led Patient-Focused Drug Development (EL-PFDD) meeting with the FDA is underway! Join us between 10am-3pmEST by going to https://t.co/VgW9KY1hZj to access the live stream!
#pmspfdd #cureshank #PMSF #shank3 #phelanmcdermidsyndrome #phelanlucky
AGENDA for our EL-PFDD meeting for Phelan-McDermid syndrome (PMS) w/ FDA this Tuesday, November 8 (10am-3pmEST).
Heartbreaking stories with hope for the future.
To attend: https://t.co/W0aJqn6rFM
Download Agenda PDF: https://t.co/5Cg7IJKnOK
#pmspfdd #shank3 #cureshank #pmsf
Learn more about Charles' and Geraldine's story below, and why our upcoming meeting with the FDA on November 8th is so important!
#pmspfdd #epilepsy #pmsf #cureshank #phelanmcdermidsyndrome #lgs
https://t.co/xXQnETjdWA
Great to have the focused support from @ChanZuckerberg for the entire rare disease community #cureSHANK #shank3 #phelanmcdermid
#RareDisease affects over 400 million individuals and their families worldwide. Weβre proud to support the patients, researchers and clinicians working to dramatically accelerate the pace of scientific research: https://t.co/ZdRtgs23fo #RareAsOne #RareDiseaseDay
Last day of February every year is #RareDiseaseDay. Our children, our families, our Phelan-McDermid Syndrome community are together on this day with 300 million people around the world, living their best lives with a #RareDisease. #CureSHANK #SHANK3 #phelanmcdermidsyndrome
A truly important day for the worldwide community of people and families living with rare disease. I hope this inspires many to pay attention and find ways to get involved. #cureshank #shank3 #phelanmcdermid #RareDiseaseDay
TOMORROW IS #RareDiseaseDay!
What do you have planned for the day? Visit https://t.co/54vIkznn6J to find out what others are up to!
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