Search filters

List of works by Paolo Scalmani

Action potential initiation in neocortical inhibitory interneurons.

scientific article

Effects in neocortical neurons of mutations of the Na(v)1.2 Na+ channel causing benign familial neonatal-infantile seizures.

scientific article published in October 2006

Epileptogenic ion channel mutations: From bedside to bench and, hopefully, back again ⬇️

scientific article published on September 15, 2010

Hippocampal hyperexcitability and specific epileptiform activity in a mouse model of Dravet syndrome

scientific article published on 10 May 2013

Interneuronal Network Activity at the Onset of Seizure-Like Events in Entorhinal Cortex Slices.

scientific article

Layer-specific properties of the persistent sodium current in sensorimotor cortex.

scientific article published on 8 February 2006

Modeling NaV1.1/SCN1A sodium channel mutations in a microcircuit with realistic ion concentration dynamics suggests differential GABAergic mechanisms leading to hyperexcitability in epilepsy and hemiplegic migraine

scientific article published on 27 July 2021

Modulatory proteins can rescue a trafficking defective epileptogenic Nav1.1 Na+ channel mutant

scientific article published on 01 October 2007

Pharmacological enhancement of mGlu5 receptors rescues behavioral deficits in SHANK3 knock-out mice

scientific article

Pharmacological enhancement of mGlu5 receptors rescues behavioral deficits in SHANK3 knock-out mice

scientific article published on 26 April 2016

Phosphorylation of sodium channels mediated by protein kinase-C modulates inhibition by topiramate of tetrodotoxin-sensitive transient sodium current

scientific article

Pure haploinsufficiency for Dravet syndrome Na(V)1.1 (SCN1A) sodium channel truncating mutations

scientific article published on 9 December 2011

SULT4A1 modulates synaptic development and function by promoting the formation of PSD-95/NMDAR complex

scientific article published on 12 August 2020

Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel

scientific article

Paulina is supported by:

About Paulina

Help