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Listen to SCN2A Insights to keep up to date with the latest research in SCN2A, genetic epilepsy and rare genetic disorders. Hosted by Ms Kris Pierce, RARE Global Advocacy Leadership Council member, and Dr David Cunnington, parents of Will, who has SCN2A.
Episode | Date |
---|---|
Transition
|
Feb 20, 2022 |
Living With Epilepsy
|
Jan 29, 2022 |
Quality of Life Measures
|
Mar 27, 2021 |
Ciitizen
|
Mar 09, 2021 |
Sleep in Autism
|
Aug 22, 2020 |
Simons Searchlight
|
Jul 17, 2020 |
SFARI
|
Jul 17, 2020 |
Angel Aid
|
Jul 13, 2020 |
Lennox-Gastaut Syndrome
|
May 30, 2020 |
Supporting Children
|
Apr 18, 2020 |
Strategies for Carers
|
Apr 18, 2020 |
COVID-19
|
Mar 17, 2020 |
Global Genes
|
Feb 28, 2020 |
Family Stories
|
Feb 23, 2020 |
Exploring Families' Needs
|
Feb 16, 2020 |
Loss of Function & Autism
|
Jan 11, 2020 |
Models in Rare Diseases
|
Jan 03, 2020 |
Genetic Epilepsy Clinics
|
Dec 23, 2019 |
Antisense Oligonucleotides
|
Dec 22, 2019 |
Genetic Testing
|
Nov 09, 2019 |
Sleep in Children with Developmental Disabilities
|
Nov 09, 2019 |
CURE Epilepsy
|
Nov 09, 2019 |
Working Together
|
Nov 09, 2019 |
Developing Treatments
|
Nov 09, 2019 |
Parents on a Mission
|
Nov 09, 2019 |
Natural History Study
|
Nov 09, 2019 |
SCN2A Overview
|
Nov 09, 2019 |
Introducing 'SCN2A Insights'
|
Sep 10, 2019 |