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Webinar #131 – CAMP4’s SYNGAP1 Ascend Phase 1/2 Trial: What You Need To Know
Webinar #130 – Family Meeting with CAMP4 Therapeutics (In Person or Virtual)
TAKE ACTION: Six Ways U.S. Families Can Help Advance SYNGAP1 Research
SYNGAP1 CENSUS 2026 Update: +45 in Q2 – Total = 1,806
CURE SYNGAP1 Announces $111,960 Investment in RARE-X Partnership to Advance ProMMIS Patient-Reported Outcome Measure Data Collection – PR46
Webinar #125 – Three SYNGAP1 studies at the Seaver Autism Center at Mount Sinai
Webinar #124 – CURE ID: A Treatment Registry of Repurposed Drugs for SYNGAP1
Webinario #123 – Ensayos clínicos con nuevas terapias en SYNGAP1 y otras encefalopatías genéticas
SYNGAP1 CENSUS 2026 Update: +54 in Q1 – Total = 1,761
Four Stories, One Purpose: Our Visits to CHOP
Cuatro historias, un mismo propósito: Nuestras Visitas a CHOP
Preparing for SYNGAP1 Clinical Trials: What Families Need to Know
Emerging Medicines to Treat SYNGAP1-Related Disorders: Primer, Comparison, Glossary
Complete the ProMMiS SYNGAP1 Natural History Study by Filling out RARE-X Surveys
Webinar #121 – CURE SYNGAP1 Conference 2025 Family Day Presentations
Webinario #122 – Celebrando el Día de las Enfermedades Poco Frecuentes: Hablemos de las Novedades en SYNGAP1
CURE SYNGAP1 Grant Funding Programs
Webinar #120 – CURE SYNGAP1 Conference 2025 Science Day Presentations