Massimo Mantegazza
@MantegazzaMassi
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Pathophysiology of neuronal excitability in epilepsy, migraine and neurodevelopmental diseases.
Nice (Sophia Antipolis) France
Joined August 2013
RT @LampertLabRWTH: After the seminar is before the seminar! Following the very successful start mark your calendars for the next #WWSCS gi…
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RT @LampertLabRWTH: In the first talk of the is series @MantegazzaMassi will not only share exciting new data on Nav1.1 and its role in pat…
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RT @LalDennis: 🚀 Join our study & please retweet Refine semi-automated tools for genetic variant classification. 👩⚕️ Who? Medical pros…
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RT @NeuroMod2020: ⏳Applications for our MSc program Mod4NeuCog are open until July 15!💡 What we offer: ➡️An interdisciplinary training in…
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New lab's paper. NaV1.1/Scn1a phenotype: homozygous patient's gain-of-function variant causes life-threatening apneas and brainstem depolarization; responds to sodium channel blockers. With S.Cestele, E.Tolner, @a_brunklaus , A.van den Maagdenberg, et al.
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RT @SwissIonChannel: Deadline for abstract submission to the #Grindelwald meeting on #SodiumChannels is very soon: 18 Nov. You don't want t…
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RT @DSFeu: 🗓️ Next March, @MadridCODEM will host the European Dravet Syndrome Conference 2024 🧬🔬, an international event 🌍 for experts in #…
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@SwissIonChannel @LampertLabRWTH 👍 Hi Hugues, that’s for sure interesting… and I guess you will also provide the snow!
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RT @FiladelfiaGene1: Registration for the 2nd #Channelopathy Meeeting in Tübingen is now open 👇 Genetic epilepsies and other neuronal ion…
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