Commentary from Sara Mariotto Università di Verona: What is the potential role of autologous hematopoietic stem cell transplantation as rescue treatment in refractory #MOGAD cases?

Serum Biomarker Profiles Discriminate AQP4 Seropositive and Double Seronegative Neuromyelitis Optica Spectrum Disorder
neurology.org/doi/10.1212/NX…
AleDinoto Sara Mariotto Romain Marignier Marco Capobianco Eoin Flanagan Alvaro Cobo Calvo Georgina Arrambide

Introducing our TSF Beanie, designed to keep you cozy & shine a light on #NMOSD , #MOGAD and other rare neuroimmune conditions. It's available in 11 colors & ships globally🌎 the-sumaira-foundation.square.site

All proceeds benefit research funded through TSF🌺

A novel cell-based immunofluorescence assay for the detection of autoantibodies to myelin-associated glycoprotein

frontiersin.org/articles/10.33…

Thanks to all who joined and made these 3 amazing events possible! AleDinoto Sara Carta The Sumaira Foundation Elia Sechi Romain Marignier Dr Ava Easton, CEO - Encephalitis International Raffaele Iorio Luigi Zuliani

🇮🇹 Incontra i relatori!

Siamo onorati di essere affiancati da neurologi ed esperti italiani alla prima Giornata del Paziente Italiano del TSF per #NMOSD , #MOGAD e #EA - giornata di formazione, unione e divertimento.

Registrazione: eventbrite.com/e/biglietti-gi…

TSF è lieta di invitare tutti i pazienti italiani con NMOSD, MOGAD o encefalite, i loro caregivers, ed i medici interessati a queste patologie a partecipare a questa giornata di formazione, unione e divertimento.
Questo è il link per registrarvi:
eventbrite.com/e/biglietti-gi…

You are all welcome to join us! 🩺🔬

🇮🇹 TSF è lieta di invitare tutti i pazienti italiani con #NMOSD , #MOGAD o #encefalite , i loro caregivers, ed i medici interessati a queste patologie a partecipare a questa giornata di formazione, unione e divertimento.

Registrazione: eventbrite.com/e/biglietti-gi…

🧠👀🔬 We’ve extended the 2023 TSF Grant application deadline to October 23rd so folks have the weekend to submit.

We encourage researchers from anywhere in the 🌎 to apply for grants (up to $25,000) for research focused on #NMOSD and/or #MOGAD : sumairafoundation.org/tsf-funded-res…

Everything is possibile when you have a great team! AleDinoto Sara Carta ECTRIMS

Slightly biased but this might possibly be the most iconic photo of #MSMilan2023 🩷💕💗

#NMOSD #MOGAD #ECTRIMS #NeuroTwitter #girlpower

In 2023, TSF funded publication fees for 12 #MOGAD papers from 9 countries in Frontiers - Neurology.

Congratulations to the authors & thank you for your great work!

Access the publications here:
frontiersin.org/research-topic…

#NeuroTwitter

1⃣ month left to apply for a $25,000 TSF research grant for #NMOSD and/or #MOGAD 🌎🌍🌏

View our research portfolio & apply here: sumairafoundation.org/tsf-funded-res…

#SpreadTheWord #NeuroTwitter

us02web.zoom.us/webinar/regist…

🇮🇹 Partecipa al nostro prossimo Webinar dal titolo: Trattamenti per #NMOSD e #MOGAD in Italia - martedì 27 agosto alle 16:00 con il dott. Raffaele Iorio Raffaele Iorio, neurologo del Policlinico Gemelli.

us02web.zoom.us/webinar/regist…

🎙️Sara Mariotto explains a major obstacle to research & finding treatment for double seronegative #NMOSD is the small patient population, making participating critical.

Listen to the full Demystifying NMO/MOG Podcast podcast episode here: podcasts.apple.com/us/podcast/epi…

Thanks Elia Sechi for organysing this interesting meeting and for the invitation, always happy to contribute!

In this episode, Nicole Helton, Sara Mariotto &
Sumaira Flower 🍉, join us to talk about Double Seronegative NMO. From the patient experience, science & advocacy, they cover it all.

#DoubleSeronegativeNMO #NMO #neurotwitter
The Sumaira Foundation Genentech

podcasts.apple.com/us/podcast/epi…

Non-demyelinating disorders mimicking or misdiagnosed as NMOSD
doi.org/10.1111/ene.15… Pietro Zara Adrian Budhram Sara Mariotto Sara Carta LavaleFló AleDinoto Sebastian López Eoin Flanagan