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

SOLDOVIERI, Maria Virginia
 Distribuzione geografica
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Continente #
NA - Nord America 4.362
EU - Europa 4.211
AS - Asia 1.473
SA - Sud America 366
AF - Africa 153
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 12
AN - Antartide 1
Totale 10.591
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Nazione #
US - Stati Uniti d'America 4.266
RU - Federazione Russa 2.087
IE - Irlanda 630
SG - Singapore 583
CN - Cina 397
BR - Brasile 287
DE - Germania 213
IT - Italia 193
UA - Ucraina 169
FI - Finlandia 166
AT - Austria 152
GB - Regno Unito 139
SE - Svezia 135
FR - Francia 109
VN - Vietnam 107
CI - Costa d'Avorio 98
IN - India 88
BE - Belgio 86
HK - Hong Kong 61
CA - Canada 54
PL - Polonia 42
JP - Giappone 40
AR - Argentina 31
BD - Bangladesh 27
MX - Messico 26
NL - Olanda 22
ES - Italia 21
IQ - Iraq 21
ID - Indonesia 19
ZA - Sudafrica 19
TR - Turchia 15
PK - Pakistan 14
LT - Lituania 13
CL - Cile 12
IR - Iran 12
EC - Ecuador 11
CO - Colombia 10
PH - Filippine 10
AU - Australia 9
IL - Israele 9
JO - Giordania 9
EU - Europa 8
MY - Malesia 8
MA - Marocco 7
SA - Arabia Saudita 7
TN - Tunisia 7
UZ - Uzbekistan 7
KZ - Kazakistan 6
PY - Paraguay 6
AE - Emirati Arabi Uniti 5
JM - Giamaica 5
KE - Kenya 5
KR - Corea 5
RO - Romania 5
VE - Venezuela 5
CH - Svizzera 4
ET - Etiopia 4
KG - Kirghizistan 4
LB - Libano 4
MD - Moldavia 4
NZ - Nuova Zelanda 4
AL - Albania 3
CZ - Repubblica Ceca 3
DO - Repubblica Dominicana 3
DZ - Algeria 3
GR - Grecia 3
RS - Serbia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AZ - Azerbaigian 2
DK - Danimarca 2
GE - Georgia 2
HN - Honduras 2
LK - Sri Lanka 2
LV - Lettonia 2
NP - Nepal 2
OM - Oman 2
PA - Panama 2
PT - Portogallo 2
SN - Senegal 2
TH - Thailandia 2
TT - Trinidad e Tobago 2
XK - ???statistics.table.value.countryCode.XK??? 2
AO - Angola 1
AQ - Antartide 1
BG - Bulgaria 1
BO - Bolivia 1
CR - Costa Rica 1
GF - Guiana Francese 1
GM - Gambi 1
GT - Guatemala 1
KW - Kuwait 1
LY - Libia 1
ML - Mali 1
MU - Mauritius 1
NG - Nigeria 1
NO - Norvegia 1
PE - Perù 1
PS - Palestinian Territory 1
SK - Slovacchia (Repubblica Slovacca) 1
SL - Sierra Leone 1
Totale 10.588
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Città #
Dallas 883
Moscow 689
Dublin 627
Chandler 459
Jacksonville 386
San Jose 315
Singapore 285
Ashburn 201
Beijing 176
Ann Arbor 163
Vienna 147
New York 131
Wilmington 127
Helsinki 123
Abidjan 98
The Dalles 91
Woodbridge 91
Brussels 86
Frankfurt am Main 75
San Mateo 73
Los Angeles 70
Boardman 67
Hong Kong 61
Princeton 57
Lauterbourg 53
Rome 52
Houston 40
Ho Chi Minh City 35
São Paulo 35
Warsaw 33
Chennai 32
Tokyo 31
Molise 27
Columbus 25
Dearborn 24
Orem 24
Hillsboro 23
London 23
Stockholm 19
Toronto 18
Montreal 17
Poplar 17
Hanoi 16
Falls Church 15
Redwood City 15
San Francisco 15
Da Nang 14
Santa Clara 14
Brooklyn 13
Johannesburg 13
Munich 13
Napoli 13
Phoenix 13
Boston 12
Hefei 12
Jakarta 12
Nanjing 12
Amsterdam 11
Atlanta 11
Baghdad 10
Kunming 10
Mumbai 10
Amman 9
Chicago 9
Council Bluffs 9
Denver 9
Falkenstein 9
Mexico City 9
Mountain View 9
Naples 9
Norwalk 9
Auburn Hills 8
Augusta 8
Lahore 8
Ankara 7
Buenos Aires 7
Manchester 7
Querétaro 7
Brasília 6
Calgary 6
City of London 6
Clearwater 6
Fortaleza 6
Milan 6
Nuremberg 6
Porto Alegre 6
Quito 6
Seattle 6
Tashkent 6
Bologna 5
Charlotte 5
Curitiba 5
Nairobi 5
New Delhi 5
Ottawa 5
Paris 5
Pune 5
Rio de Janeiro 5
Shenyang 5
Turku 5
Totale 6.517
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Nome #
Activation and Desensitization of Trpv1 Channels in Sensory Neurons by the Peroxisome Proliferator-Activated Receptor α Agonist Palmitoylethanolamide 286
Activation of Kv7 potassium channels inhibits intracellular Ca2+ increases triggered by TRPV1-mediated pain-inducing stimuli in F11 immortalized sensory neurons 281
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 239
Epilepsy-causing mutations in kv7.2 c-terminus affect binding and functional modulation by calmodulin. 219
Autism and developmental disability caused by KCNQ3 gain-of-function variants 216
A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes 211
Characterization of two de novo KCNT1 mutations in children with malignant migrating partial seizures in infancy 209
Pharmacological Targeting Of Neuronal Kv7.2/3 Channels: A Focus On Chemotypes And Receptor Sites 207
Effects of natural and synthetic isothiocyanate-based H2S-releasers against chemotherapy-induced neuropathic pain: Role of Kv7 potassium channels 204
Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels 203
Early-Onset Epileptic Encephalopathy Caused by Gain-of-Function Mutations in the Voltage Sensor of Kv7.2 and Kv7.3 Potassium Channel Subunits. 200
The occurrence of a Kv7.4 potassium channel in neuronal mitochondria 200
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation 199
Epileptic encephalopathy in a patientwith a novel variant in the Kv7.2 S2 transmembrane segment: Clinical, genetic, and functional features 198
Expression and function of Kv7.4 channels in Rat cardiac mitochondria: possible targets for cardioprotection 198
A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy 197
Early-onset epileptic encephalopathy caused by a reduced sensitivity of Kv7.2 potassium channels to phosphatidylinositol 4,5-bisphosphate 195
Differential Regulation of PI(4,5)P2Sensitivity of Kv7.2 and Kv7.3 Channels by Calmodulin 192
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 191
De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy 189
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability. 188
Addressing the use of PDIF-CN(2) molecules in the development of n-type organic field-effect transistors for biosensing applications 187
Cardiotoxic effects of antihistamines: From basics to clinics (... and back) 183
Calcium cytotoxicity sensitizes prostate cancer cells to standard-of-care treatments for locally advanced tumors 177
Identification of a Potent Tryptophan-Based TRPM8 Antagonist with in Vivo Analgesic Activity 175
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant 172
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 169
Expression, Localization, and Pharmacological Role of K(v)7 Potassium Channels in Skeletal Muscle Proliferation, Differentiation, and Survival after Myotoxic Insults 164
β-Adrenergic response is counteracted by extremely-low-frequency pulsed electromagnetic fields in beating cardiomyocytes 162
A new Italian FHM2 family: Clinical aspects and functional analysis of the disease-associated mutation 161
Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions 159
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 159
Molecular pharmacology and therapeutic potential of neuronal Kv7-modulating drugs 158
Neuronal potassium channel openers in the management of epilepsy: role and potential of retigabine 158
Critical role of large-conductance calcium- and voltage-activated potassium channels in leptin-induced neuroprotection of N-methyl-d-aspartate-exposed cortical neurons. 156
CORRELATING THE CLINICAL AND GENETIC FEATURES OF BENIGN FAMILIAL NEONATAL SEIZURES (BFNS) WITH THE FUNCTIONAL CONSEQUENCES OF THE UNDERLYING MUTATIONS 152
Kv7.3 Compound Heterozygous Variants in Early Onset Encephalopathy Reveal Additive Contribution of C-Terminal Residues to PIP2-Dependent K+Channel Gating 151
Tryptamine-Based Derivatives as Transient Receptor Potential Melastatin Type 8 (TRPM8) Channel Modulators 149
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine 147
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy 147
Erratum to: Towards the realization of label-free biosensors through impedance spectroscopy integrated with IDES technology 146
Kv7.4 channels regulate potassium permeability in neuronal mitochondria 146
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 141
Driving with no brakes: molecular pathophysiology of kv7 potassium channels 139
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism 138
Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction 137
Functional Characterization of Two Variants at the Intron 6-Exon 7 Boundary of the KCNQ2 Potassium Channel Gene Causing Distinct Epileptic Phenotypes 135
De novo variants in KCNA3 cause developmental and epileptic encephalopathy 135
Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits 134
The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants 129
Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathy 129
Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with KCNT1-related drug-resistant focal epilepsy 127
Human neoplastic mesothelial cells express voltage-gated sodium channels involved in cell motility 124
Isoxazole derivatives as potent transient receptor potential melastatin type 8 (TRPM8) agonists. 123
Functional and biochemical interaction between PPARα receptors and TRPV1 channels: Potential role in PPARα agonists-mediated analgesia. 119
Fluoxetine Treatment in Epilepsy of Infancy with Migrating Focal Seizures Due to KCNT1 Variants: An Open Label Study. 117
Lysinuric protein intolerance: identification and functional analysis of mutations of the SLC7A7 gene 116
The ever changing moods of calmodulin: how structural plasticity entails transductional adaptability. 113
Distinct epilepsy phenotypes and response to drugs in KCNA1 gain- and loss-of function variants 109
In Silico Assisted Identification, Synthesis, and In Vitro Pharmacological Characterization of Potent and Selective Blockers of the Epilepsy-Associated KCNT1 Channel 108
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC) 104
KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological Properties 101
Gating consequences of charge neutralization of arginine residues in the S-4 segment of K(v)7.2, an epilepsy-linked K+ channel subunit 100
Synthesis and Pharmacological Characterization of Conformationally Restricted Retigabine Analogues as Novel Neuronal Kv7 Channel Activators 100
Towards the realization of label-free biosensors through impedance spectroscopy integrated with IDES technology 93
Pharmacological approaches in drug-resistant pediatric epilepsies caused by pathogenic variants in potassium channel genes. 81
The long and winding road to personalized medicine in KCNMA1-linked channelopathies revealed by novel variants associated with the Liang-Wang syndrome 78
null 58
Totale 10.788
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Categoria #
all - tutte 42.590
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 42.590
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021103 0 0 0 0 0 0 0 0 0 10 79 14
2021/2022402 13 65 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
2025/20265.189 178 522 590 376 1.427 1.012 443 180 174 287 0 0
Totale 10.788