BONZANNI, MATTIA

BONZANNI, MATTIA  

Dipartimento di Bioscienze  

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Titolo Data di pubblicazione Autori Tipo File Abstract
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability 2018 Campostrini, GiuliaCastellotti, BarbaraMilanesi, RaffaellaBonzanni, MattiaBucchi, AnnalisaBaruscotti, MirkoBarbuti, AndreaDi Francesco, Dario + Article (author) -
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability 2018 Bonzanni, MattiaMilanesi, RaffaellaCampostrini, GiuliaCastellotti, BarbaraBucchi, AnnalisaBaruscotti, MirkoBarbuti, AndreaDi Francesco, Dario + Article (author) -
The expression of the rare caveolin-3 variant T78M alters cardiac ion channels function and membrane excitability 2017 CampostriniGiulia; BonzanniAlessio; BazziniClaudia; MilanesiRaffaella; VezzoliElena; FrancoliniMaura; BaruscottiMirko; BucchiPeter J.; Di FrancescoDario; Barbuti + Article (author) -
THE EXPRESSION OF THE RARE CAVEOLIN-3 VARIANT T78M ALTERS CARDIAC ION CHANNELS FUNCTION AND MEMBRANE EXCITABILITY. 2018 BONZANNI, MATTIA Doctoral Thesis -