IRIS  Catalogo Istituzionale della Ricerca dell'Università degli Studi del Molise

SOLDOVIERI, Maria Virginia
 Distribuzione geografica
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Continente #
NA - Nord America 4.881
EU - Europa 4.254
AS - Asia 1.587
SA - Sud America 406
Continente sconosciuto - Info sul continente non disponibili 209
AF - Africa 153
OC - Oceania 13
AN - Antartide 1
Totale 11.504
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Nazione #
US - Stati Uniti d'America 4.752
RU - Federazione Russa 2.087
IE - Irlanda 631
SG - Singapore 631
CN - Cina 418
BR - Brasile 300
IT - Italia 224
DE - Germania 214
UA - Ucraina 171
FI - Finlandia 166
AT - Austria 152
GB - Regno Unito 140
SE - Svezia 135
VN - Vietnam 115
FR - Francia 110
CI - Costa d'Avorio 98
IN - India 90
BE - Belgio 86
CA - Canada 70
HK - Hong Kong 67
PL - Polonia 42
JP - Giappone 40
AR - Argentina 35
BD - Bangladesh 35
MX - Messico 30
CO - Colombia 24
NL - Olanda 24
ES - Italia 22
ID - Indonesia 22
IQ - Iraq 21
ZA - Sudafrica 19
EC - Ecuador 17
TR - Turchia 16
CL - Cile 14
PH - Filippine 14
PK - Pakistan 14
LT - Lituania 13
MY - Malesia 13
IR - Iran 12
AU - Australia 9
IL - Israele 9
JM - Giamaica 9
JO - Giordania 9
EU - Europa 8
MA - Marocco 7
SA - Arabia Saudita 7
TN - Tunisia 7
UZ - Uzbekistan 7
KR - Corea 6
KZ - Kazakistan 6
PY - Paraguay 6
VE - Venezuela 6
AE - Emirati Arabi Uniti 5
KE - Kenya 5
RO - Romania 5
CH - Svizzera 4
CZ - Repubblica Ceca 4
ET - Etiopia 4
GR - Grecia 4
HN - Honduras 4
KG - Kirghizistan 4
LB - Libano 4
MD - Moldavia 4
NP - Nepal 4
NZ - Nuova Zelanda 4
AL - Albania 3
DO - Repubblica Dominicana 3
DZ - Algeria 3
QA - Qatar 3
RS - Serbia 3
TH - Thailandia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AZ - Azerbaigian 2
CR - Costa Rica 2
DK - Danimarca 2
GE - Georgia 2
LK - Sri Lanka 2
LV - Lettonia 2
NI - Nicaragua 2
OM - Oman 2
PA - Panama 2
PT - Portogallo 2
SN - Senegal 2
SV - El Salvador 2
TT - Trinidad e Tobago 2
XK - ???statistics.table.value.countryCode.XK??? 2
AO - Angola 1
AQ - Antartide 1
BG - Bulgaria 1
BM - Bermuda 1
BO - Bolivia 1
GF - Guiana Francese 1
GM - Gambi 1
GT - Guatemala 1
KW - Kuwait 1
LY - Libia 1
MK - Macedonia 1
ML - Mali 1
MQ - Martinica 1
MU - Mauritius 1
Totale 11.297
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Città #
Dallas 887
Moscow 689
Dublin 628
San Jose 497
Chandler 459
Jacksonville 388
Singapore 293
Ashburn 225
Beijing 180
Ann Arbor 163
Vienna 147
New York 133
Wilmington 128
Helsinki 123
Abidjan 98
The Dalles 91
Woodbridge 91
Brussels 86
Frankfurt am Main 75
Los Angeles 75
San Mateo 73
Boardman 67
Hong Kong 67
Council Bluffs 64
Princeton 57
Rome 56
Lauterbourg 53
Houston 42
Ho Chi Minh City 38
São Paulo 38
Warsaw 33
Chennai 32
Tokyo 31
Santa Clara 30
Columbus 27
Molise 27
Dearborn 24
Orem 24
Hillsboro 23
London 23
Phoenix 23
Toronto 22
Stockholm 19
Hanoi 17
Montreal 17
Poplar 17
Brooklyn 16
Naples 16
San Francisco 16
Da Nang 15
Falls Church 15
Redwood City 15
Boston 14
Jakarta 13
Johannesburg 13
Munich 13
Napoli 13
Atlanta 12
Chicago 12
Hefei 12
Nanjing 12
Amsterdam 11
Mexico City 11
Baghdad 10
Kunming 10
Mumbai 10
Amman 9
Brasília 9
Denver 9
Falkenstein 9
Mountain View 9
Norwalk 9
Auburn Hills 8
Augusta 8
Lahore 8
Milan 8
Quito 8
Ankara 7
Buenos Aires 7
Charlotte 7
Manchester 7
Querétaro 7
Seattle 7
Zhengzhou 7
Bogotá 6
Buffalo 6
Calgary 6
City of London 6
Clearwater 6
Fortaleza 6
Medellín 6
New Delhi 6
Nuremberg 6
Ottawa 6
Porto Alegre 6
Rio de Janeiro 6
Tashkent 6
Bologna 5
Curitiba 5
Nairobi 5
Totale 6.895
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Nome #
Activation and Desensitization of Trpv1 Channels in Sensory Neurons by the Peroxisome Proliferator-Activated Receptor α Agonist Palmitoylethanolamide 295
Activation of Kv7 potassium channels inhibits intracellular Ca2+ increases triggered by TRPV1-mediated pain-inducing stimuli in F11 immortalized sensory neurons 289
Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S-4 region of KCNQ2 causing benign familial neonatal convulsions 248
Epilepsy-causing mutations in kv7.2 c-terminus affect binding and functional modulation by calmodulin. 234
Autism and developmental disability caused by KCNQ3 gain-of-function variants 224
A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes 221
Effects of natural and synthetic isothiocyanate-based H2S-releasers against chemotherapy-induced neuropathic pain: Role of Kv7 potassium channels 219
The occurrence of a Kv7.4 potassium channel in neuronal mitochondria 217
Pharmacological Targeting Of Neuronal Kv7.2/3 Channels: A Focus On Chemotypes And Receptor Sites 216
Characterization of two de novo KCNT1 mutations in children with malignant migrating partial seizures in infancy 215
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation 214
Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels 212
A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy 211
Early-Onset Epileptic Encephalopathy Caused by Gain-of-Function Mutations in the Voltage Sensor of Kv7.2 and Kv7.3 Potassium Channel Subunits. 208
Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy 207
Epileptic encephalopathy in a patientwith a novel variant in the Kv7.2 S2 transmembrane segment: Clinical, genetic, and functional features 206
Expression and function of Kv7.4 channels in Rat cardiac mitochondria: possible targets for cardioprotection 206
Differential Regulation of PI(4,5)P2Sensitivity of Kv7.2 and Kv7.3 Channels by Calmodulin 204
Addressing the use of PDIF-CN(2) molecules in the development of n-type organic field-effect transistors for biosensing applications 203
Early-onset epileptic encephalopathy caused by a reduced sensitivity of Kv7.2 potassium channels to phosphatidylinositol 4,5-bisphosphate 202
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability. 199
Cardiotoxic effects of antihistamines: From basics to clinics (... and back) 194
De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy 194
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant 186
A Novel Kv7.3 Variant in the Voltage-Sensing S4 Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and in vitro Rescue by β-Hydroxybutyrate 183
Identification of a Potent Tryptophan-Based TRPM8 Antagonist with in Vivo Analgesic Activity 182
Calcium cytotoxicity sensitizes prostate cancer cells to standard-of-care treatments for locally advanced tumors 181
A new Italian FHM2 family: Clinical aspects and functional analysis of the disease-associated mutation 175
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism 175
Expression, Localization, and Pharmacological Role of K(v)7 Potassium Channels in Skeletal Muscle Proliferation, Differentiation, and Survival after Myotoxic Insults 174
Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions 173
Kv7.3 Compound Heterozygous Variants in Early Onset Encephalopathy Reveal Additive Contribution of C-Terminal Residues to PIP2-Dependent K+Channel Gating 170
Neuronal potassium channel openers in the management of epilepsy: role and potential of retigabine 170
Molecular pharmacology and therapeutic potential of neuronal Kv7-modulating drugs 168
β-Adrenergic response is counteracted by extremely-low-frequency pulsed electromagnetic fields in beating cardiomyocytes 167
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 165
Critical role of large-conductance calcium- and voltage-activated potassium channels in leptin-induced neuroprotection of N-methyl-d-aspartate-exposed cortical neurons. 164
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine 163
Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction 162
CORRELATING THE CLINICAL AND GENETIC FEATURES OF BENIGN FAMILIAL NEONATAL SEIZURES (BFNS) WITH THE FUNCTIONAL CONSEQUENCES OF THE UNDERLYING MUTATIONS 161
Tryptamine-Based Derivatives as Transient Receptor Potential Melastatin Type 8 (TRPM8) Channel Modulators 159
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy 156
Erratum to: Towards the realization of label-free biosensors through impedance spectroscopy integrated with IDES technology 155
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 153
Kv7.4 channels regulate potassium permeability in neuronal mitochondria 153
Driving with no brakes: molecular pathophysiology of kv7 potassium channels 152
Functional Characterization of Two Variants at the Intron 6-Exon 7 Boundary of the KCNQ2 Potassium Channel Gene Causing Distinct Epileptic Phenotypes 147
The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants 145
Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits 144
De novo variants in KCNA3 cause developmental and epileptic encephalopathy 140
Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with KCNT1-related drug-resistant focal epilepsy 135
Human neoplastic mesothelial cells express voltage-gated sodium channels involved in cell motility 134
Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathy 134
Functional and biochemical interaction between PPARα receptors and TRPV1 channels: Potential role in PPARα agonists-mediated analgesia. 131
Isoxazole derivatives as potent transient receptor potential melastatin type 8 (TRPM8) agonists. 131
Fluoxetine Treatment in Epilepsy of Infancy with Migrating Focal Seizures Due to KCNT1 Variants: An Open Label Study. 125
Lysinuric protein intolerance: identification and functional analysis of mutations of the SLC7A7 gene 125
The ever changing moods of calmodulin: how structural plasticity entails transductional adaptability. 122
In Silico Assisted Identification, Synthesis, and In Vitro Pharmacological Characterization of Potent and Selective Blockers of the Epilepsy-Associated KCNT1 Channel 118
Gating consequences of charge neutralization of arginine residues in the S-4 segment of K(v)7.2, an epilepsy-linked K+ channel subunit 113
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC) 113
Distinct epilepsy phenotypes and response to drugs in KCNA1 gain- and loss-of function variants 113
KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological Properties 112
Synthesis and Pharmacological Characterization of Conformationally Restricted Retigabine Analogues as Novel Neuronal Kv7 Channel Activators 107
Towards the realization of label-free biosensors through impedance spectroscopy integrated with IDES technology 105
Pharmacological approaches in drug-resistant pediatric epilepsies caused by pathogenic variants in potassium channel genes. 88
The long and winding road to personalized medicine in KCNMA1-linked channelopathies revealed by novel variants associated with the Liang-Wang syndrome 79
null 58
Totale 11.504
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Categoria #
all - tutte 46.878
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 46.878
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022324 0 0 4 13 42 44 12 35 75 43 26 30
2022/20231.807 225 80 30 181 133 169 11 79 780 59 42 18
2023/2024357 72 40 16 7 8 95 10 17 12 11 10 59
2024/20251.239 111 49 147 51 252 56 72 66 106 28 122 179
2025/20265.481 178 522 590 376 1.427 1.012 443 180 174 442 87 50
2026/2027424 76 122 226 0 0 0 0 0 0 0 0 0
Totale 11.504