Видео с ютуба Lafora

Let’s talk #Lafora - part 1/2

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

Matthew Gentry Studies Lafora's Disease.

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

Let’s talk #Lafora disease - part 2

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

Genetic #epilepsyawarenessday - #Lafora Disease - Challenges & Hopes - Berge Minassian

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

Lafora Disease Sibling Support Group Information | Living with Lafora

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

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

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

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

Meet Emi | Living with Lafora Disease

More Clips from Lafora Disease Science Symposium 2022

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

Un viaggio di speranza verso la cura della Lafora - per Federico

Gene-Based Therapy for Lafora Disease