Introduction to SLC13A5 Epilepsy

Mom Mondays - What Do You Wish People Know About SLC13A5 Epilepsy?Подробнее

An SLC13A5 Epilepsy Family's Story - TESS Research FoundationПодробнее

What is TESS Research Foundation? (Subtítulos en Español)Подробнее

SLC13A5 and epilepsyПодробнее

Raising a Child With SLC13A5 Deficiency - Nicole Windisch - SLC13A5 Deficiency Family Day 2020Подробнее

Living With Seizures - Dr. Brenda Porter, MD, PhD - SLC13A5 Deficiency Family Day 2020Подробнее

Mom Mondays - What Does SLC13A5 Epilepsy Look Like for a Child?Подробнее

Introduction to SLC13A5 Genetics with Elli Brimble, MS - Ask the Expert Webinars (07/25/2020)Подробнее

Mom Mondays - Why Don't We Have a Treatment for SLC13A5 Epilepsy?Подробнее

Webinar for SLC13A5 Families with Dr. Brenda Porter (10/05/2019) - Ask the Expert WebinarsПодробнее

Genetics: Everything You Need To KnowПодробнее

One family's journey to an SLC13A5 Deficiency diagnosisПодробнее

Dr. Anne Murphy's Research Overview - SLC13A5 Research Roundtable 2018Подробнее

Naillaret & Her Little Brother, Yavi - SLC13A5 Sibling Interviews with MaggieПодробнее

Welcome & Introduction to TESS Research Foundation - Kimberly Nye - Research Roundtable 2020Подробнее

The Davis Family - A Day in the Life of a Family Living with SLC13A5 EpilepsyПодробнее

Davis Family (1 Minute Ver.) - A Day in the Life of a Family with SLC13A5 EpilepsyПодробнее

Moderator: Kimberly Nye, Founder of Tess Research Foundation (SLC13A5)Подробнее

Pediatric Epilepsy: An Introduction, by Lurie Children's Priyamvada Tatachar, MDПодробнее