NALCN News/Blog - Page 3 of 5 - Libellas Foundation

Fundación Libellas is a Proud REN and EURORDIS member!

Post published:January 18, 2021

Rare diseases and rare epilepsies collaborating! As part of REN, we look forward to learning from and sharing our knowledge with a whole patient engagement community. https://www.rareepilepsynetwork.org/ By joining forces,…

An unexplored sodium channel and its implication in rare and not so rare diseases

Post published:January 17, 2021

Spanish to english Google translate POSTED ON JANUARY 11, 2021 GENOTIPIA Angel Aledo Serrano, Antonio Gil-Nagel Rein Neurology Service, Hospital Ruber Internacional. MADRID Researchers from a French-Spanish consortium, together with the…

“Iguales y Diferentes”. La condena de tener una enfermedad ultrarara / con Isabel Pastor

Post published:December 8, 2020

By Hub de salud https://hubdesalud.es/programas/iguales%20y%20diferentes/ Diciembre 8, 2020. Isabel es una de las pocas niñas en el mundo que tiene el Síndrome de CLIFAHDD. Su patología es tan rara que…