Maria V. Soldovieri

Via De Sanctis
Campobasso, 86100, Italy

Last Updated: 09/26/2026

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Found 50 publications

Phenotypic Biodiversity and Niche-Associated Functional Traits in Lactiplantibacillus plantarum.

Phenotypic Biodiversity and Niche-Associated Functional Traits in Lactiplantibacillus plantarum.

Journal: Current issues in molecular biology
Published: June 08, 2026

Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2-developmental encephalopathy.

Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2-developmental encephalopathy.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: November 27, 2024

Fluoxetine Treatment in Epilepsy of Infancy with Migrating Focal Seizures Due to KCNT1 Variants: An Open Label Study.

Fluoxetine Treatment in Epilepsy of Infancy with Migrating Focal Seizures Due to KCNT1 Variants: An Open Label Study.

Journal: Annals of neurology
Published: October 17, 2024

Pharmacological approaches in drug-resistant pediatric epilepsies caused by pathogenic variants in potassium channel genes.

Pharmacological approaches in drug-resistant pediatric epilepsies caused by pathogenic variants in potassium channel genes.

Journal: Frontiers in cellular neuroscience
Published: October 16, 2024

In Silico Assisted Identification, Synthesis, and In Vitro Pharmacological Characterization of Potent and Selective Blockers of the Epilepsy-Associated KCNT1 Channel.

In Silico Assisted Identification, Synthesis, and In Vitro Pharmacological Characterization of Potent and Selective Blockers of the Epilepsy-Associated KCNT1 Channel.

Journal: Journal of medicinal chemistry
Published: May 23, 2024

Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with KCNT1-related drug-resistant focal epilepsy.

Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with KCNT1-related drug-resistant focal epilepsy.

Journal: Frontiers in cellular neuroscience
Published: January 09, 2024

De novo variants in KCNA3 cause developmental and epileptic encephalopathy.

De novo variants in KCNA3 cause developmental and epileptic encephalopathy.

Journal: Annals of neurology
Published: January 16, 2023

A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine.

A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine.

Journal: Epilepsia
Published: January 05, 2023

KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological Properties.

KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological Properties.

Journal: Annals of neurology
Published: August 02, 2022

The long and winding road to personalized medicine in KCNMA1-linked channelopathies revealed by novel variants associated with the Liang-Wang syndrome.

The long and winding road to personalized medicine in KCNMA1-linked channelopathies revealed by novel variants associated with the Liang-Wang syndrome.

Journal: Acta physiologica (Oxford, England)
Published: June 09, 2022

Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathy.

Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathy.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 04, 2022

Functional Characterization of Two Variants at the Intron 6-Exon 7 Boundary of the KCNQ2 Potassium Channel Gene Causing Distinct Epileptic Phenotypes.

Functional Characterization of Two Variants at the Intron 6-Exon 7 Boundary of the KCNQ2 Potassium Channel Gene Causing Distinct Epileptic Phenotypes.

Journal: Frontiers in pharmacology
Published: February 09, 2022
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Last Updated: 09/26/2026