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

SOLDOVIERI, Maria Virginia
 Distribuzione geografica
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Continente #
NA - Nord America 4.557
EU - Europa 4.216
AS - Asia 1.547
SA - Sud America 369
AF - Africa 153
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 12
AN - Antartide 1
Totale 10.868
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Nazione #
US - Stati Uniti d'America 4.449
RU - Federazione Russa 2.087
IE - Irlanda 630
SG - Singapore 628
CN - Cina 415
BR - Brasile 290
DE - Germania 213
IT - Italia 198
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 66
CA - Canada 61
PL - Polonia 42
JP - Giappone 40
AR - Argentina 31
BD - Bangladesh 30
MX - Messico 27
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
MY - Malesia 10
PH - Filippine 10
AU - Australia 9
IL - Israele 9
JO - Giordania 9
EU - Europa 8
JM - Giamaica 8
MA - Marocco 7
SA - Arabia Saudita 7
TN - Tunisia 7
UZ - Uzbekistan 7
KR - Corea 6
KZ - Kazakistan 6
PY - Paraguay 6
AE - Emirati Arabi Uniti 5
KE - Kenya 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 10.864
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Città #
Dallas 885
Moscow 689
Dublin 627
Chandler 459
San Jose 438
Jacksonville 386
Singapore 292
Ashburn 211
Beijing 178
Ann Arbor 163
Vienna 147
New York 132
Wilmington 127
Helsinki 123
Abidjan 98
The Dalles 91
Woodbridge 91
Brussels 86
Frankfurt am Main 75
Los Angeles 73
San Mateo 73
Boardman 67
Hong Kong 66
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
Toronto 20
Santa Clara 19
Stockholm 19
Montreal 17
Poplar 17
Hanoi 16
San Francisco 16
Falls Church 15
Redwood City 15
Da Nang 14
Boston 13
Brooklyn 13
Johannesburg 13
Munich 13
Napoli 13
Phoenix 13
Hefei 12
Jakarta 12
Nanjing 12
Amsterdam 11
Atlanta 11
Baghdad 10
Kunming 10
Mexico City 10
Mumbai 10
Naples 10
Amman 9
Chicago 9
Council Bluffs 9
Denver 9
Falkenstein 9
Mountain View 9
Norwalk 9
Auburn Hills 8
Augusta 8
Lahore 8
Ankara 7
Buenos Aires 7
Manchester 7
Querétaro 7
Zhengzhou 7
Brasília 6
Buffalo 6
Calgary 6
City of London 6
Clearwater 6
Fortaleza 6
Milan 6
Nuremberg 6
Ottawa 6
Porto Alegre 6
Quito 6
Rio de Janeiro 6
Seattle 6
Tashkent 6
Bologna 5
Charlotte 5
Curitiba 5
Nairobi 5
New Delhi 5
Paris 5
Pune 5
Totale 6.686
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Nome #
Activation and Desensitization of Trpv1 Channels in Sensory Neurons by the Peroxisome Proliferator-Activated Receptor α Agonist Palmitoylethanolamide 288
Activation of Kv7 potassium channels inhibits intracellular Ca2+ increases triggered by TRPV1-mediated pain-inducing stimuli in F11 immortalized sensory neurons 284
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 241
Epilepsy-causing mutations in kv7.2 c-terminus affect binding and functional modulation by calmodulin. 227
Autism and developmental disability caused by KCNQ3 gain-of-function variants 220
A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes 214
Effects of natural and synthetic isothiocyanate-based H2S-releasers against chemotherapy-induced neuropathic pain: Role of Kv7 potassium channels 213
Pharmacological Targeting Of Neuronal Kv7.2/3 Channels: A Focus On Chemotypes And Receptor Sites 211
Characterization of two de novo KCNT1 mutations in children with malignant migrating partial seizures in infancy 210
Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels 207
The occurrence of a Kv7.4 potassium channel in neuronal mitochondria 207
A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy 205
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation 203
Expression and function of Kv7.4 channels in Rat cardiac mitochondria: possible targets for cardioprotection 203
Early-Onset Epileptic Encephalopathy Caused by Gain-of-Function Mutations in the Voltage Sensor of Kv7.2 and Kv7.3 Potassium Channel Subunits. 201
Epileptic encephalopathy in a patientwith a novel variant in the Kv7.2 S2 transmembrane segment: Clinical, genetic, and functional features 200
Early-onset epileptic encephalopathy caused by a reduced sensitivity of Kv7.2 potassium channels to phosphatidylinositol 4,5-bisphosphate 197
Differential Regulation of PI(4,5)P2Sensitivity of Kv7.2 and Kv7.3 Channels by Calmodulin 197
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 197
Addressing the use of PDIF-CN(2) molecules in the development of n-type organic field-effect transistors for biosensing applications 193
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability. 191
De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy 190
Cardiotoxic effects of antihistamines: From basics to clinics (... and back) 186
Calcium cytotoxicity sensitizes prostate cancer cells to standard-of-care treatments for locally advanced tumors 179
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 179
Identification of a Potent Tryptophan-Based TRPM8 Antagonist with in Vivo Analgesic Activity 178
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant 177
Expression, Localization, and Pharmacological Role of K(v)7 Potassium Channels in Skeletal Muscle Proliferation, Differentiation, and Survival after Myotoxic Insults 168
β-Adrenergic response is counteracted by extremely-low-frequency pulsed electromagnetic fields in beating cardiomyocytes 164
A new Italian FHM2 family: Clinical aspects and functional analysis of the disease-associated mutation 164
Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions 161
Kv7.3 Compound Heterozygous Variants in Early Onset Encephalopathy Reveal Additive Contribution of C-Terminal Residues to PIP2-Dependent K+Channel Gating 161
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 160
Molecular pharmacology and therapeutic potential of neuronal Kv7-modulating drugs 160
Neuronal potassium channel openers in the management of epilepsy: role and potential of retigabine 160
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine 159
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism 158
Critical role of large-conductance calcium- and voltage-activated potassium channels in leptin-induced neuroprotection of N-methyl-d-aspartate-exposed cortical neurons. 157
CORRELATING THE CLINICAL AND GENETIC FEATURES OF BENIGN FAMILIAL NEONATAL SEIZURES (BFNS) WITH THE FUNCTIONAL CONSEQUENCES OF THE UNDERLYING MUTATIONS 153
Tryptamine-Based Derivatives as Transient Receptor Potential Melastatin Type 8 (TRPM8) Channel Modulators 153
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy 152
Erratum to: Towards the realization of label-free biosensors through impedance spectroscopy integrated with IDES technology 152
Kv7.4 channels regulate potassium permeability in neuronal mitochondria 148
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 147
Driving with no brakes: molecular pathophysiology of kv7 potassium channels 145
Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction 143
Functional Characterization of Two Variants at the Intron 6-Exon 7 Boundary of the KCNQ2 Potassium Channel Gene Causing Distinct Epileptic Phenotypes 141
Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits 138
De novo variants in KCNA3 cause developmental and epileptic encephalopathy 137
The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants 135
Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathy 132
Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with KCNT1-related drug-resistant focal epilepsy 130
Human neoplastic mesothelial cells express voltage-gated sodium channels involved in cell motility 129
Isoxazole derivatives as potent transient receptor potential melastatin type 8 (TRPM8) agonists. 124
Fluoxetine Treatment in Epilepsy of Infancy with Migrating Focal Seizures Due to KCNT1 Variants: An Open Label Study. 122
Functional and biochemical interaction between PPARα receptors and TRPV1 channels: Potential role in PPARα agonists-mediated analgesia. 122
Lysinuric protein intolerance: identification and functional analysis of mutations of the SLC7A7 gene 118
The ever changing moods of calmodulin: how structural plasticity entails transductional adaptability. 116
In Silico Assisted Identification, Synthesis, and In Vitro Pharmacological Characterization of Potent and Selective Blockers of the Epilepsy-Associated KCNT1 Channel 112
Distinct epilepsy phenotypes and response to drugs in KCNA1 gain- and loss-of function variants 110
Gating consequences of charge neutralization of arginine residues in the S-4 segment of K(v)7.2, an epilepsy-linked K+ channel subunit 106
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC) 105
KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological Properties 103
Synthesis and Pharmacological Characterization of Conformationally Restricted Retigabine Analogues as Novel Neuronal Kv7 Channel Activators 103
Towards the realization of label-free biosensors through impedance spectroscopy integrated with IDES technology 100
Pharmacological approaches in drug-resistant pediatric epilepsies caused by pathogenic variants in potassium channel genes. 82
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 11.065
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Categoria #
all - tutte 44.351
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 44.351
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202114 0 0 0 0 0 0 0 0 0 0 0 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
2025/20265.466 178 522 590 376 1.427 1.012 443 180 174 442 87 35
Totale 11.065