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Over 1200 families are caring for a loved one with the rare disease ”SynGAP” resulting from a variant of the SYNGAP1 gene. This 10 minute weekly podcast is for them. A quick summary of the latest news in the space. The host is Mike Graglia, co-founder & managing director of the SynGAP Research Fund. SRF is a parent-led, all volunteer public charity in the US that strives to accelerate research into treatments for SYNGAP1 so that we can help our loved ones in a timeframe that matters. Learn more at https://www.syngapresearchfund.org/
Episodes
Friday Aug 18, 2023
Stanford Grant, CSC, UCSF Study, SYNGAP1 Case Report, Conference - #s10e112
Friday Aug 18, 2023
Friday Aug 18, 2023
Congratulations to Dr. Knowles, read our press release.
Check out the CSC Clinic at Stanford
Don’t miss #S10e111 to learn about Dr. Helbig
https://www.youtube.com/watch?v=i6EZUrqsn2g
In you are coming to or near SF, please go to the Willsey Lab and do the breathing test with your SYNGAPian
Congratulations to Dr. Kadam for the SRF supported Case Study
Publication: https://www.frontiersin.org/articles/10.3389/fneur.2023.1221161/full
Tweet: https://twitter.com/cureSYNGAP1/status/1692227117126439099
Register for the conference, it’s going to be fabulous.
- Registration link: https://Syngap.Fund/Orlando
- Hotels ASAP: https://Syngap.Fund/2023hotel
- Merch https://www.bonfire.com/srf-syngap1-conference-2023/
Volunteer with SRF!
- https://www.syngapresearchfund.org/volunteer-with-syngap-research-fund
This is a podcast: subscribe to and rate this 10 minute #podcast #SYNGAP10
- https://www.syngapresearchfund.org/syngap10-podcast
Apple podcasts:
- https://podcasts.apple.com/us/podcast/syngap10-weekly-10-minute-updates-on-syngap1-video/id1560389818
Episode 112 of #Syngap10 - August 18, 2023
#epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #GeneChat
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