IRIS
STRIANO, PASQUALE
 Distribuzione geografica
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Continente #
EU - Europa 67.879
AS - Asia 7.918
NA - Nord America 4.923
SA - Sud America 696
AF - Africa 148
OC - Oceania 27
Continente sconosciuto - Info sul continente non disponibili 3
Totale 81.594
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Nazione #
IT - Italia 66.683
US - Stati Uniti d'America 4.574
SG - Singapore 3.168
CN - Cina 2.012
VN - Vietnam 1.030
BD - Bangladesh 826
FR - Francia 570
BR - Brasile 446
HK - Hong Kong 298
DE - Germania 144
CA - Canada 140
AR - Argentina 99
FI - Finlandia 97
MX - Messico 97
JP - Giappone 88
IN - India 84
GB - Regno Unito 78
IQ - Iraq 66
ID - Indonesia 54
NL - Olanda 48
CH - Svizzera 41
EC - Ecuador 38
PK - Pakistan 34
ZA - Sudafrica 33
PH - Filippine 31
JM - Giamaica 30
ES - Italia 29
AU - Australia 26
CL - Cile 22
CO - Colombia 22
RU - Federazione Russa 22
KR - Corea 21
VE - Venezuela 21
IE - Irlanda 20
TN - Tunisia 20
MA - Marocco 18
SA - Arabia Saudita 18
TH - Thailandia 18
TR - Turchia 18
JO - Giordania 17
RO - Romania 17
AT - Austria 15
PE - Perù 15
PL - Polonia 15
UZ - Uzbekistan 15
EG - Egitto 14
NP - Nepal 14
DZ - Algeria 13
KE - Kenya 13
SV - El Salvador 12
UA - Ucraina 12
AE - Emirati Arabi Uniti 11
BO - Bolivia 11
CR - Costa Rica 11
UY - Uruguay 11
GT - Guatemala 10
AZ - Azerbaigian 9
KG - Kirghizistan 9
LB - Libano 9
MY - Malesia 9
PY - Paraguay 9
KZ - Kazakistan 8
PR - Porto Rico 8
SE - Svezia 8
TW - Taiwan 8
AL - Albania 7
IL - Israele 7
OM - Oman 7
TT - Trinidad e Tobago 7
HU - Ungheria 6
LT - Lituania 6
PS - Palestinian Territory 6
PT - Portogallo 6
BE - Belgio 5
BY - Bielorussia 5
CI - Costa d'Avorio 5
DO - Repubblica Dominicana 5
GR - Grecia 5
HN - Honduras 5
RS - Serbia 5
BH - Bahrain 4
CZ - Repubblica Ceca 4
KW - Kuwait 4
SK - Slovacchia (Repubblica Slovacca) 4
SY - Repubblica araba siriana 4
AM - Armenia 3
BA - Bosnia-Erzegovina 3
BB - Barbados 3
BS - Bahamas 3
DK - Danimarca 3
ET - Etiopia 3
GE - Georgia 3
LV - Lettonia 3
MD - Moldavia 3
NI - Nicaragua 3
NO - Norvegia 3
QA - Qatar 3
SI - Slovenia 3
AO - Angola 2
AW - Aruba 2
Totale 81.537
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Città #
Genova 39.689
Genoa 17.146
Rapallo 4.658
Vado Ligure 4.355
San Jose 1.439
Singapore 1.349
Ashburn 673
Lauterbourg 539
Beijing 333
Ho Chi Minh City 314
Hong Kong 284
New York 265
Hanoi 230
Council Bluffs 220
Santa Clara 148
Los Angeles 126
Frankfurt am Main 115
Helsinki 85
Bordighera 82
Tokyo 72
Rome 65
Buffalo 59
Milan 58
Da Nang 57
Mexico City 56
Haiphong 53
Chicago 51
Dallas 50
Tianjin 44
Naples 37
Zurich 35
San Francisco 31
São Paulo 31
Orem 30
Toronto 30
Turin 30
Montreal 28
Phoenix 26
Shanghai 26
Amsterdam 25
Guangzhou 22
Baghdad 21
Biên Hòa 21
Quito 21
Atlanta 20
City of London 19
Dublin 19
Boardman 18
Bologna 18
Cardiff 18
Hải Dương 18
Bari 17
Florence 17
Kingston 17
Can Tho 16
Chennai 16
Madrid 16
Amman 15
Mumbai 14
Palermo 14
Brooklyn 13
Houston 13
Nairobi 13
Quảng Ngãi 13
Tashkent 13
Verona 13
Bogotá 12
Charlotte 12
Lima 12
Nuremberg 12
Rio de Janeiro 12
Thái Nguyên 12
Des Moines 11
London 11
San Salvador 11
Seattle 11
Aurora 10
Jeddah 10
Johannesburg 10
Lahore 10
Lappeenranta 10
Memphis 10
Montevideo 10
Paris 10
Baku 9
Belo Horizonte 9
Brasília 9
Buenos Aires 9
Cape Town 9
Dhaka 9
Ninh Bình 9
San José 9
Santiago 9
Sydney 9
Thái Bình 9
Warsaw 9
Cagliari 8
Caracas 8
Guayaquil 8
Jakarta 8
Totale 73.715
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Nome #
(1)H-MR spectroscopy indicates prominent cerebellar dysfunction in benign adult familial myoclonic epilepsy. 1.405
A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms. 253
"Comorbidity" between epilepsy and headache/migraine: the other side of the same coin! 247
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 239
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features 232
A 3-year-old boy with drug-resistant complex partial seizures 231
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. 230
22-year-old girl with status epilepticus and progressive neurological symptoms. 219
A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures. 219
A novel SCN2A mutation in family with benign familial infantile seizures. 216
A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2. 213
Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype. 206
'Autoimmune epilepsy' or exasperated search for the etiology of seizures of unknown origin? 205
Whole-genome linkage scan for epilepsy-related photosensitivity: a mega-analysis. 198
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy. 198
A clinical and genetic study of 33 new cases with early-onset absence epilepsy. 197
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability 197
Pyridoxine-dependent epilepsy: An under-recognised cause of intractable seizures. 193
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy 192
A pilot open-label trial of zonisamide in Unverricht-Lundborg disease. 192
Idiopathic focal epilepsies: the "lost tribe" 191
Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development 191
Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach? 188
Do regulatory regions matter in FOXG1 duplications? 187
ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma Elasticum 187
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome 187
Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndrome. 186
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome). 186
Anxiolytic and Analgesic Effects of Melatonin in Paediatric Dentistry 186
Similar but not identical: clinical implications for molecular studies in monozygotic discordant twins with epilepsy. 186
Lumping encephalopathies with inflammation-mediated status epilepticus: is there enough evidence? 186
A t(4;9)(q34;p22) translocation associated with partial epilepsy, mental retardation, and dysmorphism. 185
GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features. 185
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies—An Italian observational multicenter study 185
Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations 185
Epilepsy associated with supratentorial brain tumors under 3 years of life. 184
Clinical and genetic findings in 26 Italian patients with Lafora disease. 184
End-of-life: still an Italian dilemma. 184
Health-related quality of life in epilepsy: findings obtained with a new Italian instrument. 184
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome. 184
Recurrent hypothermia with hyperhidrosis in two siblings: familial Shapiro syndrome variant. 183
Dramatic response to levetiracetam in post-ischaemic Holmes' tremor. 183
Temporal lobe epilepsy and anti glutamic acid decarboxylase autoimmunity. 181
LGI1 microdeletion in autosomal dominant lateral temporal epilepsy. 181
The gelastic seizures-hypothalamic hamartoma syndrome: Facts, hypotheses, and perspectives. 181
The genetics of monogenic idiopathic epilepsies and epileptic encephalopathies. 180
Levetiracetam in patients with cortical myoclonus: a clinical and electrophysiological study. 180
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy 180
NovelAMPD2mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalities 180
Epileptogenesis due to peripheral injury as a cause of focal epilepsy. 179
Clinical features of Sturge-Weber syndrome without facial nevus: Five novel cases. 179
"Ictal epileptic headache": Beyond the epidemiological evidence. 179
TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsy 179
Long-term follow-up in two siblings with pyridoxine-dependent seizures associated with a novel ALDH7A1 mutation. 178
Suppression of myoclonus in SCA2 by piracetam. 178
'Ictal epileptic headache': Recent concepts for new classifications criteria. 178
A proof-of-concept trial of the whey protein alfa-lactalbumin in chronic cortical myoclonus. 178
Evaluation of presumably disease causing SCN1A variants in a cohort of common epilepsy syndromes 178
Idiopathic mesial temporal lobe epilepsy: don't sow the tares with the wheat! 177
Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy. 177
From migralepsy to ictal epileptic headache: the story so far. 177
Sudden death in Unverricht-Lundborg patients: is serotonin the key? 176
Epileptic myoclonus as ciprofloxacin-associated adverse effect. 176
Long-term evolution of EEG in Unverricht-Lundborg disease. 176
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy 176
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases. 176
Comment to: overlap cases of eyelid myoclonia with absences and juvenile myoclonic epilepsy. 175
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 174
Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy. 173
Comment to: Diabetic hyperglycemia is associated with the severity of epileptic seizures in adults. 173
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. 173
What have we learned about ictal epileptic headache? A review of well-documented cases. 173
Autosomal recessive progressive myoclonus epilepsy due to impaired ceramide synthesis 173
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families. 173
Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients 173
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. 172
De novo mutations in HCN1 cause early infantile epileptic encephalopathy 172
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture 171
Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 171
Autoantibodies to glutamic acid decarboxylase (GAD) in focal and generalized epilepsy: A study on 233 patients. 171
Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication 171
TBC1D24 genotype-phenotype correlation 170
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations. 169
Lateralizing value of the auditory aura in partial seizures. 169
Metabolic and endocrine effects of valproic acid chronic treatment. 169
Epilepsy: old drugs do the trick in childhood absence epilepsy. 168
CHD2 mutations are a rare cause of generalized epilepsy with myoclonic-atonic seizures 168
Functional changes in hypothalamic hamartoma neurons and gelastic epilepsy. 167
Life-threatening status epilepticus following gabapentin administration in a patient with benign adult familial myoclonic epilepsy. 167
Reflex seizures and reflex epilepsies: Old models for understanding mechanisms of epileptogenesis. 167
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 167
Galloway-Mowat syndrome: an early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature. 166
New terminology for headache/migraine as the sole ictal epileptic manifestation: the downsides. Reply to Cianchetti et al. 166
Migralepsy, hemicrania epileptica, post-ictal headache and "ictal epileptic headache": a proposal for terminology and classification revision. 166
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. 166
Erratum to: Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 165
Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome. 165
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families. 165
Posterior reversible encephalopathy syndrome (PRES) in critically ill obstetric patients. 164
Rhombencephalosynapsis in a patient with mental retardation, epilepsy, and dysmorphisms. 164
Totale 19.605
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Categoria #
all - tutte 290.327
article - articoli 286.239
book - libri 272
conference - conferenze 607
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.209
Totale 580.654
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021533 0 0 0 0 0 0 0 0 0 0 0 533
2021/20226.787 298 281 1.012 439 234 353 338 1.512 381 664 431 844
2022/20235.776 746 257 68 457 876 1.067 40 475 1.159 50 478 103
2023/20243.509 229 476 106 334 262 488 161 148 288 170 282 565
2024/202510.984 325 910 275 611 1.570 1.123 1.067 1.395 594 703 1.029 1.382
2025/202621.910 2.131 677 2.094 1.709 2.369 2.049 2.988 1.056 1.635 1.838 1.658 1.706
Totale 82.825