List of works - Maria Virginia Soldovieri

A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutation.

scientific article

A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability

scientific article published on 19 December 2014

Activation of Kv7 Potassium Channels Inhibits Intracellular Ca2+ Increases Triggered By TRPV1-Mediated Pain-Inducing Stimuli in F11 Immortalized Sensory Neurons

scientific article published on 04 September 2019

Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions.

scientific article published on May 2007

Cardiotoxic effects of antihistamines: from basics to clinics (...and back).

scientific article published on 29 April 2008

Critical role of large-conductance calcium- and voltage-activated potassium channels in leptin-induced neuroprotection of N-methyl-d-aspartate-exposed cortical neurons.

scientific article

Driving with no brakes: molecular pathophysiology of Kv7 potassium channels

scientific article

Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits.

scientific article

Epilepsy-causing mutations in Kv7.2 C-terminus affect binding and functional modulation by calmodulin.

scientific article published on 12 June 2015

Epileptic Encephalopathy In A Patient With A Novel Variant In The Kv7.2 S2 Transmembrane Segment: Clinical, Genetic, and Functional Features

scientific article published on 10 July 2019

Functional and biochemical interaction between PPARα receptors and TRPV1 channels: Potential role in PPARα agonists-mediated analgesia.

scientific article published on 8 July 2014

Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits

scientific article published on 25 February 2013

Isoxazole derivatives as potent transient receptor potential melastatin type 8 (TRPM8) agonists

scientific article published on 20 September 2013

Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels

scientific article

Neuronal potassium channel openers in the management of epilepsy: role and potential of retigabine.

scientific article published on 7 December 2010

Neutralization of a unique, negatively-charged residue in the voltage sensor of K V 7.2 subunits in a sporadic case of benign familial neonatal seizures

scientific article published on April 2009

Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A.

scientific article published on 13 January 2014

The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants.

scientific article published on February 2011

The ever changing moods of calmodulin: how structural plasticity entails transductional adaptability.

scientific article published on 22 May 2014

Towards the realization of label-free biosensors through impedance spectroscopy integrated with IDES technology

scientific article published on 12 January 2012

List of works by Maria Virginia Soldovieri

A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutation.

A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability

Activation of Kv7 Potassium Channels Inhibits Intracellular Ca2+ Increases Triggered By TRPV1-Mediated Pain-Inducing Stimuli in F11 Immortalized Sensory Neurons

Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions.

Cardiotoxic effects of antihistamines: from basics to clinics (...and back).

Critical role of large-conductance calcium- and voltage-activated potassium channels in leptin-induced neuroprotection of N-methyl-d-aspartate-exposed cortical neurons.

Driving with no brakes: molecular pathophysiology of Kv7 potassium channels

Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits.

Epilepsy-causing mutations in Kv7.2 C-terminus affect binding and functional modulation by calmodulin.

Epileptic Encephalopathy In A Patient With A Novel Variant In The Kv7.2 S2 Transmembrane Segment: Clinical, Genetic, and Functional Features

Functional and biochemical interaction between PPARα receptors and TRPV1 channels: Potential role in PPARα agonists-mediated analgesia.

Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits

Isoxazole derivatives as potent transient receptor potential melastatin type 8 (TRPM8) agonists

Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels

Neuronal potassium channel openers in the management of epilepsy: role and potential of retigabine.

Neutralization of a unique, negatively-charged residue in the voltage sensor of K V 7.2 subunits in a sporadic case of benign familial neonatal seizures

Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A.

The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants.

The ever changing moods of calmodulin: how structural plasticity entails transductional adaptability.

Towards the realization of label-free biosensors through impedance spectroscopy integrated with IDES technology