Видео с ютуба Lafora Disease

Innovative Approach to Halt Lafora Disease: A New Hope for Epilepsy

Niki's Update on Angelina | Living with Lafora Disease | February 2025

Family's son dies of Lafora disease, learns his brother also has it

A devastating Lafora Disease diagnosis | Fighting the Rare

Подросток из Лонг-Айленда борется с редкой болезнью, от которой страдают менее 100 человек во все...

Young Woman is Only 1 in AL Currently Diagnosed with Lafora Disease | News 19 at 4:30 p.m.

Dr. Berge Minassian explaining Lafora Disease symptoms | Fighting the Rare

"What is going on?" | Angelina's first Lafora Disease symptoms | Fighting the Rare

A family's fight for the drugs they say can change their children's lives

Lafora Disease Sibling Support Group Information | Living with Lafora

Genetic Epilepsy - Lafora Disease - Challenges & Hopes - Berge Minassian

Let’s talk #Lafora - part 1/2

Meet Emi | Living with Lafora Disease

Survivor's Guilt | Merriam Family Story | Living with Lafora Disease

Girl fighting rare disease gets big surprise

Lafora Disease Explained

Exciting Research Into The Ultra-Rare Epilepsy: Lafora Disease - Jordi Duran

Ultra-Rare Epilepsy: Lafora Disease - José Serratosa