Видео с ютуба Lafora's Disease

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

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

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

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

Lafora Disease Sibling Support Group Information | Living with Lafora

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

Lafora Disease Explained

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

Ultra-Rare Epilepsy: Lafora Disease - José Serratosa

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

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

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

URGENT CALL: Fully Fund the ION283 Safety Study | Lafora Disease Treatment

Girl fighting rare disease gets big surprise

Dr. Berge Minassian explains Lafora Disease in Miniature Wirehaired Dachshunds

Pre-clinical treatments for Lafora disease - a childhood dementia driven by perturbed metabolism

Scientists at IRB Barcelona discover the cause of neurodegeneration in Lafora disease

EYE ON HEALTH: Raising awareness of Lafora disease