CACNA1A Foundation
The CACNA1A Foundation aims to find specific treatment options for CACNA1A patients by building a supportive and collaborative network of patients, families, clinicians, and scientists to raise awareness and accelerate the understanding, diagnosis and treatment of CACNA1A-linked diseases.
Find us on Instagram, Facebook, and Twitter!
Praxis Medicines Emerald Study Community Meeting for the CACNA1A Community
About the ICD-10 code for CACNA1A
Pharmacotherapy of cerebellar disorders, including CACNAIA
Special Education Survival Guide
Special Education Survival Guide
Vocational Rehabilitation: Assisting People with Disabilities Toward Gainful Employment
Understanding Your Child’s Neurodevelopmental or Neuropsychological Evaluation
Closing
Effective Speech and Language Therapy Strategies for Children with CACNA1A-related Disorders
Mastering the Art of Advocacy in a Healthcare Setting
Empowering Change: The Impact of Community Engagement
Welcome to Day 2 of the CACNA1A Foundation's 2024 Creating Connections Conference
Movement Disorders (ataxia, dystonia, eye movements): Ask the Experts Anything Panel
Ask the Experts Anything Panel about Hemiplegic Migraines and Epilepsy
Science is Better Together - Insights from the 2024 Research Roundtable
Clinical Trial Readiness Initiatives
CACNA1A 101: The Genetics of CACNA1A
Welcome to Day 1 of the CACNA1A Creating Connections Community Conference
Fikri Birey, PhD Interview with Pangkong Fox, PhD from the CACNA1A Foundation
Estate and Special Needs Planning Webinar, Kathleen Hayes, Esq.
CACNA1A Foundation Grant Interview: Jen Pan, PhD, December, 2024
CACNA1A Foundation 2024 Overview: Join us on our mission to find a cure.
CACNA1A Foundation Global Genes poster 2024
Summary of Kessi et al. 2023 paper on genotype-phenotype correlations of CACNA1A-related disorders
CACNA1A Foundation Grant Recipient Interview w/Dr. van de Warrenburg & Marina Hommersom, Radboud UMC
CACNA1A related Hemiplegic Migraine What it is and What is being Done