CRIS Current Research Information System

LICCHETTA, LAURA
 Distribuzione geografica
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Continente #
NA - Nord America 6.822
AS - Asia 5.605
EU - Europa 4.689
SA - Sud America 375
AF - Africa 345
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 4
Totale 17.851
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Nazione #
US - Stati Uniti d'America 6.676
SG - Singapore 1.792
CN - Cina 1.558
IT - Italia 1.141
VN - Vietnam 1.009
GB - Regno Unito 920
DE - Germania 671
SE - Svezia 572
HK - Hong Kong 487
BR - Brasile 291
NL - Olanda 260
IN - India 255
RU - Federazione Russa 235
KR - Corea 215
IE - Irlanda 178
FR - Francia 172
UA - Ucraina 133
CI - Costa d'Avorio 115
CA - Canada 102
ZA - Sudafrica 86
FI - Finlandia 80
JO - Giordania 65
JP - Giappone 59
EE - Estonia 55
AT - Austria 50
BG - Bulgaria 49
TG - Togo 48
AR - Argentina 43
CH - Svizzera 41
SC - Seychelles 39
ID - Indonesia 38
MX - Messico 32
ES - Italia 25
NG - Nigeria 24
BE - Belgio 21
PL - Polonia 21
PK - Pakistan 17
TR - Turchia 17
UZ - Uzbekistan 16
GR - Grecia 15
BD - Bangladesh 14
EC - Ecuador 14
CO - Colombia 8
IQ - Iraq 8
MY - Malesia 8
RO - Romania 8
IR - Iran 7
LB - Libano 7
AU - Australia 6
EG - Egitto 6
PY - Paraguay 6
CL - Cile 5
IL - Israele 5
LT - Lituania 5
PH - Filippine 5
TN - Tunisia 5
DK - Danimarca 4
DO - Repubblica Dominicana 4
HU - Ungheria 4
KE - Kenya 4
MA - Marocco 4
NO - Norvegia 4
PE - Perù 4
PT - Portogallo 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AE - Emirati Arabi Uniti 3
CM - Camerun 3
CZ - Repubblica Ceca 3
HR - Croazia 3
KZ - Kazakistan 3
LV - Lettonia 3
NZ - Nuova Zelanda 3
RS - Serbia 3
SA - Arabia Saudita 3
AL - Albania 2
AZ - Azerbaigian 2
CG - Congo 2
DZ - Algeria 2
HN - Honduras 2
MT - Malta 2
PA - Panama 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
TW - Taiwan 2
VE - Venezuela 2
AD - Andorra 1
AM - Armenia 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BO - Bolivia 1
BT - Bhutan 1
EU - Europa 1
GA - Gabon 1
GD - Grenada 1
GH - Ghana 1
JM - Giamaica 1
KG - Kirghizistan 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
Totale 17.840
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Città #
Singapore 1.212
Ashburn 840
Southend 708
Fairfield 700
Hefei 500
Chandler 498
Hong Kong 481
Woodbridge 338
Seattle 324
Houston 311
Wilmington 293
Santa Clara 262
Cambridge 253
Ann Arbor 237
Ho Chi Minh City 228
Beijing 220
Seoul 209
Princeton 206
Hanoi 189
Bologna 185
Dublin 178
Boardman 137
Dallas 128
Abidjan 115
Dong Ket 114
Turin 108
Los Angeles 104
New York 87
Redmond 79
Westminster 78
Munich 76
Jacksonville 71
Berlin 69
Nanjing 68
Montréal 67
Amman 65
Florence 64
Milan 63
Redondo Beach 63
Padova 57
Tokyo 56
Buffalo 52
Rome 50
Sofia 49
Lomé 48
Saint Petersburg 48
Mcallen 46
Jinan 42
Modena 42
Bengaluru 41
Nuremberg 39
Helsinki 38
Amsterdam 35
San Diego 35
Bern 32
Council Bluffs 32
Shenyang 32
Vienna 32
Frankfurt am Main 31
Lappeenranta 31
Chicago 29
Haiphong 28
São Paulo 27
Jakarta 26
Nanchang 26
Castel Maggiore 24
Falls Church 24
Abeokuta 22
Changsha 22
Tianjin 22
Dearborn 21
Brussels 20
Da Nang 20
Düsseldorf 20
London 20
Des Moines 19
Mülheim 19
Zhengzhou 19
Medford 18
Redwood City 18
Shanghai 18
Falkenstein 17
Yubileyny 17
Biên Hòa 16
Hebei 16
Bühl 15
Guangzhou 15
Ha Long 15
Hải Dương 15
Warsaw 15
Naples 14
Orem 14
Paris 14
Mexico City 13
Quận Bình Thạnh 13
Boydton 12
Jiaxing 12
Phoenix 12
San Jose 12
Tongling 12
Totale 11.527
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Nome #
Clinical features and pathophysiology of disorders of arousal in adults: A window into the sleeping brain 440
Prognostic value of pathogenic variants in Lafora Disease: systematic review and meta-analysis of patient-level data 335
LGI1 microdeletions are not a frequent cause of partial epilepsy with auditory features (PEAF). 231
Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies 225
Adult patients with intellectual disability and epilepsy: clinical and genetic study of 114 cases 218
A seizure response dog: video recording of reacting behaviour during repetitive prolonged seizures. 212
Auditory aura in nocturnal frontal lobe epilepsy: a red flag to suspect an extra-frontal epileptogenic zone 208
The Arousal Disorders Questionnaire: a new and effective screening tool for confusional arousals, Sleepwalking and Sleep Terrors in epilepsy and sleep disorders units 202
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy 200
Accurate Detection of Hot-Spot MTOR Somatic Mutations in Archival Surgical Specimens of Focal Cortical Dysplasia by Molecular Inversion Probes 198
Autosomal dominant partial epilepsy with auditory features: A new locus on chromosome 19q13.11-q13.31. 197
Emilia-Romagna Study on Pregnancy and Exposure to Antiepileptic drugs (ESPEA): a population-based study on prescription patterns, pregnancy outcomes and fetal health 192
GATOR1 complex: the common genetic actor in focal epilepsies 190
Profile of neuropsychological impairment in Sleep-related Hypermotor Epilepsy 185
Behçet disease presenting with movement disorders and antibasal ganglia antibodies 183
Polysomnographic features differentiating disorder of arousals from sleep-related hypermotor epilepsy 183
Incidence of sudden unexpected death in nocturnal frontal lobe epilepsy: a cohort study. 178
Cerebral areas involved in music perception: studying musicogenic epilepsy. 177
Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy 176
Effect of valproic acid on perampanel pharmacokinetics in patients with epilepsy. 176
Response to the letter "New avenues to prevent sudden unexpected death in nocturnal frontal lobe epilepsy: follow the route established by omega-3 polyunsaturated fatty acids". 175
Fattori prognostici in 170 pazienti con epilessia temporale mesiale 175
Epilepsy with auditory features: Long-term outcome and predictors of terminal remission 172
Epilepsy with auditory features: Contribution of known genes in 112 patients 171
Encephalopathy in COVID-19 Presenting With Acute Aphasia Mimicking Stroke 170
FDG-PET findings and alcohol-responsive myoclonus in a patient with Unverricht-Lundborg disease 167
Definition and diagnostic criteria of sleep-related hypermotor epilepsy 167
Epilepsy with auditory features: A heterogeneous clinico-molecular disease 165
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy 164
Characteristics of a large population of patients with refractory epilepsy attending tertiary referral centers in Italy. 162
Juvenile absence epilepsy relapsing as recurrent absence status, mimicking transient global amnesia, in an elderly patient 158
Specific motor patterns of arousal disorders in adults: A video-polysomnographic analysis of 184 episodes 157
Phenotype variability of GLUT1 deficiency syndrome: Description of a case series with novel SLC2A1 gene mutations 156
Prevalence of Nocturnal Frontal Lobe Epilepsy in the Adult Population of Bologna and Modena, Emilia-Romagna Region, Italy. 154
Ictal characteristics of psychogenic nonepileptic seizures: what we have learned from video/EEG recordings - a literature review. 149
Health-related quality of life in epilepsy: findings obtained with a new Italian instrument. 148
FDG-PET assessment and metabolic patterns in Lafora disease 148
Ictal vasodepressive syncope in temporal lobe epilepsy 148
Relationship between plasma concentrations and clinical effects of perampanel: A prospective observational study 148
Cortical myoclonic tremor induced by fixation-off sensitivity: An unusual cause of insomnia 147
Tailored surgery for drug-resistant epilepsy due to temporal pole encephalocele and microdysgenesis. 146
Proton MR spectroscopy in patients with sleep-related hypermotor epilepsy (SHE): Evidence of altered cingulate cortex metabolism 146
A case of clinical worsening after stereo-electroencephalographic-guided radiofrequency thermocoagulation in a patient with polymicrogyria 145
Nocturnal motor behaviors with unexpected EEG and brain MRI findings 144
Increased frequency of arousal parasomnias in families with nocturnal frontal lobe epilepsy: a common mechanism? 144
Epilepsy in MT-ATP6 - related mils/NARP: correlation of elettroclinical features with heteroplasmy 144
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals 143
A prospective study of direct medical costs in a large cohort of consecutively enrolled patients with refractory epilepsy in Italy 143
Epilepsy in ring chromosome 20 syndrome 141
Epilepsy in coeliac disease: not just a matter of calcifications. 141
Treatment with metformin in twelve patients with Lafora disease 141
Risk of hospitalization and death for COVID-19 in persons with epilepsy over a 20-month period: The EpiLink Bologna cohort, Italy 138
Seizures with paroxysmal arousals in sleep-related hypermotor epilepsy (SHE): Dissecting epilepsy from NREM parasomnias 138
Neuropsychological impairment in patients with early onset nocturnal frontal lobe epilepsy. 136
Health-related quality of life in patients with Nocturnal Frontal Lobe Epilepsy. 135
Progressive myoclonic epilepsies: definitive and still undetermined causes 133
Epilepsy With Auditory Features: From Etiology to Treatment 133
Patterns of prescription of antiepileptic drugs in patients with refractory epilepsy at tertiary referral centres in Italy. 129
Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients 129
Whole-exome sequencing in adult patients with developmental and epileptic encephalopathy: It is never too late 129
Relationship between adverse effects of antiepileptic drugs, number of coprescribed drugs, and drug load in a large cohort of consecutive patients with drug-refractory epilepsy. 129
Biallelic pathogenic variants of PARS2 cause developmental and epileptic encephalopathy with spike-and-wave activation in sleep 128
Epilepsy and inborn errors of metabolism in adults: The diagnostic odyssey of a young woman with medium-chain acyl-coenzyme A dehydrogenase deficiency 128
Limbic encephalitis with anti-GAD antibodies and Thomsen myotonia: A casual or causal association? 128
A stereo EEG study in a patient with sleep-related hypermotor epilepsy due to DEPDC5 mutation 126
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2 125
Polygenic burden in focal and generalized epilepsies 125
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K(+) channel properties 124
Epilepsy with Bilateral Hippocampal Hyperintensity and Celiac Disease: Comorbidity or a real association? 124
Progressive Myoclonus Epilepsies Diagnostic Yield with Next-Generation Sequencing in Previously Unsolved Cases 124
Quantitative dried blood spot microsampling for therapeutic drug monitoring of -antiseizure medications by design of experiment and UHPLC-MS/MS 123
The landscape of epilepsy-related GATOR1 variants 123
Tobacco habits in nocturnal frontal lobe epilepsy 122
Super refractory status epilepticus in Lafora disease interrupted by vagus nerve stimulation: A case report 121
DEPDC5 mutations in epilepsy with auditory features 120
MECP2 duplication syndrome: The electroclinical features of a case with long-term evolution 119
Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease) 119
Prognostic factors in patients with Mesial Temporal Lobe Epilepsy (MTLE): A preliminary study. 119
The Impact of the COVID-19 Pandemic on People With Epilepsy. An Italian Survey and a Global Perspective 119
Erratum: Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals (The American Journal of Human Genetics (2021) 108(6) (965–982), (S0002929721001403), (10.1016/j.ajhg.2021.04.009)) 118
Complete Agenesis of Corpus Callosum in KCNQ2-Related Neonatal Epileptic Encephalopathy 117
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study 114
Mutations in DEPDC5 cause familial focal epilepsy with variable foci. 114
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations 114
An Italian multicentre study of perampanel in progressive myoclonus epilepsies 114
Clinical Reasoning: Young woman with orbital pain and diplopia 114
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy 113
If seizures left speechless: CA-P-S C-A-R-E, a proposal of a new ictal language evaluation protocol 112
A Novel Mutation af Cln3 Associated with Delayed-Classic Juvenile Ceroid Lipofucinois and Autophagic Vacuolar Myopathy 111
Incidence of sudden unexpected death in epilepsy in sleep-related hypermotor epilepsy, formerly named nocturnal frontal lobe epilepsy 111
Neuropsychological assessment in patients with early onset nocturnal frontal lobe epilepsy. 111
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 111
Clinical characterization of non-ketotic hyperglycemia-related seizures: A systematic review and individual participant data meta-analysis 111
Expanding the therapeutic role of highly purified cannabidiol in monogenic epilepsies: A multicenter real-world study 110
Secondary sclerosing cholangitis in critically ill patients with febrile infection-related epilepsy syndrome (FIRES): a case series 109
Ictal Bradycardia and Asystole in Sleep-Related Hypermotor Epilepsy: A Study of 200 Patients 109
Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy 108
Epilepsy with eyelid myoclonias and Sotos syndrome features in a patient with compound heterozygous missense variants in APC2 gene 107
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants 106
Identification of genes responsible for Nocturnal Frontal Lobe Epilepsy (NFLE): role of DEPDC5 mutations 106
Totale 14.971
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Categoria #
all - tutte 51.611
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 51.611
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021983 0 0 0 0 0 101 59 113 139 122 89 360
2021/20222.119 164 62 111 206 191 104 57 147 109 265 402 301
2022/20232.300 227 290 105 254 175 165 78 117 409 104 281 95
2023/2024821 56 118 54 100 59 147 31 71 31 68 36 50
2024/20253.197 96 458 209 244 394 134 155 103 49 342 212 801
2025/20264.977 1.073 1.022 819 820 873 370 0 0 0 0 0 0
Totale 18.325