Видео с ютуба Lafora's Disease

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

A devastating Lafora Disease diagnosis | Fighting the Rare

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

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

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

Lafora Disease Sibling Support Group Information | Living with Lafora

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

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

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

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

Meet Emi | Living with Lafora Disease

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

Lafora Disease Explained

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

What are treatment options for Lafora Disease? | Lafora Disease Therapeutic Overview

Ultra-Rare Epilepsy: Lafora Disease - José Serratosa

The smiling faces of our Lafora disease warriors