wmb, Autore presso GNAO1

30 September 2021

ENG – GNAO1: partono i primi progetti di ricerca sostenuti dall’associazione italiana

In soli due anni, la onlus “Famiglie GNAO1” è diventata un punto di riferimento per i pazienti e la comunità scientifica. La malattia correlata a GNAO1 è una patologia genetica molto rara che colpisce il neurosviluppo e con esordio in età pediatrica. Ad oggi, sono noti poco più di 200 pazienti al mondo affetti da questa malattia, i […]

4 October 2020

Events Past

ENG – Run 4 GNAO1 Warriors

On GNAO1 Awareness Day, Famiglie GNAO1 invites all its supporters to participate in the RUN 4 GNAO1 WARRIORS awareness initiative. A virtual run / walk, to support research on disease and help all our little, great warriors.

1 October 2020

Events Past

ENG – GNAO1 EU Conference 2020

Famiglie GNAO1 hosted the second GNAO1 European Conference online from 1-3 October 2020. The principal objectives of this conference were: facilitate cross-pollination of research ideas and developments across the globe, continue to build a centre of innovative GNAO1 research and practice in the European Union and generate awareness, so that GNAO1 patients are able to […]

16 November 2019

Events Past

ENG – GNAO1 EU Conference 2019

Famiglie GNAO1 hosted the first European GNAO1 conference in Rome, Italy on 16 November 2019. The goal of this conference was to engage the medical, research, rehabilitation and health policy community in Italy and Europe to: begin the foundations of a strong center of innovative GNAO1 research and practice in the European Union and facilitate […]