
Gaia Colasante
@ColasanteGaia
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Excited and honored to have our latest paper published in Brain @Brain1878, alongside the research contributions of two giants in Dravet Syndrome and DEEs @LoriLIsom1 @Go3than !
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RT @FundacionDravet: 🧪🧠#EDSC2024 nos trae la primera sesión de charlas sobre investigación en el SÃndrome de Dravet. Desde tratamientos in….
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RT @MartinaMainard1: Thrilled to receive the best poster award at the #EDSC2024! Thanks to the Dravet Sindrome Foundation for these two ama….
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RT @DNS_Retreat: 📢 The inaugural @DNS_Retreat will take place on January 18-19, 2024, at the splendid venue located @LaStatale Via Festa de….
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Happy to carry on exciting and challenging research funded by @Telethonitalia !.
Bando Multi-round di Fondazione Telethon: assegnati ulteriori 4,36 milioni di euro. Fondazione Telethon annuncia i vincitori del secondo round del bando, 24 i progetti di eccellenza finanziati sulle malattie genetiche rare in tutta Italia.
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RT @AleParziAle: Dear friends, I have a position for working in my team in Milan on the modeling of rare neurological diseases. 👇Please RT….
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Hope for Dravet syndrome! Thanks to @Telethonitalia @AssociazioneGruppoFamiglieDravet @SwissDravet SyndromeAssociation
nature.com
Nature Communications - Dravet syndrome is a devastating epileptic encephalopathy caused by Scn1a gene haploinsufficiency. Exploiting a novel knock-in mouse model, here the authors show that...
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RT @LignaniLab_UCL: 🔥Check out the last paper led by @gaiacolasante in which is shown how Scn1a reactivation after symptoms onset rescues e….
nature.com
Nature Communications - Dravet syndrome is a devastating epileptic encephalopathy caused by Scn1a gene haploinsufficiency. Exploiting a novel knock-in mouse model, here the authors show that...
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RT @LignaniLab_UCL: Great work by @ColasanteGaia @sophieqyc_q @broccoli_lab @s_schorge @BrainEditorial and all the other co-authors! @EU_Co….
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