IRIS
STRIANO, PASQUALE
 Distribuzione geografica
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Continente #
EU - Europa 67.367
AS - Asia 6.924
NA - Nord America 2.790
SA - Sud America 677
AF - Africa 148
OC - Oceania 25
Continente sconosciuto - Info sul continente non disponibili 2
Totale 77.933
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Nazione #
IT - Italia 66.211
SG - Singapore 3.108
US - Stati Uniti d'America 2.617
CN - Cina 1.870
VN - Vietnam 1.027
FR - Francia 567
BR - Brasile 439
HK - Hong Kong 284
DE - Germania 141
FI - Finlandia 97
AR - Argentina 95
MX - Messico 90
JP - Giappone 87
IN - India 82
GB - Regno Unito 74
IQ - Iraq 66
BD - Bangladesh 63
ID - Indonesia 54
CA - Canada 47
NL - Olanda 41
CH - Svizzera 34
EC - Ecuador 34
PK - Pakistan 33
ZA - Sudafrica 33
PH - Filippine 31
AU - Australia 24
ES - Italia 24
RU - Federazione Russa 22
CL - Cile 21
CO - Colombia 21
IE - Irlanda 20
TN - Tunisia 20
KR - Corea 19
VE - Venezuela 19
MA - Marocco 18
TH - Thailandia 18
TR - Turchia 18
JO - Giordania 17
RO - Romania 17
SA - Arabia Saudita 17
AT - Austria 15
PE - Perù 15
UZ - Uzbekistan 15
EG - Egitto 14
PL - Polonia 14
DZ - Algeria 13
KE - Kenya 13
NP - Nepal 12
UA - Ucraina 12
BO - Bolivia 11
UY - Uruguay 11
AE - Emirati Arabi Uniti 10
AZ - Azerbaigian 9
KG - Kirghizistan 9
LB - Libano 9
PY - Paraguay 9
KZ - Kazakistan 8
SE - Svezia 8
TW - Taiwan 8
AL - Albania 7
IL - Israele 7
MY - Malesia 7
OM - Oman 7
JM - Giamaica 6
LT - Lituania 6
PS - Palestinian Territory 6
PT - Portogallo 6
CI - Costa d'Avorio 5
CR - Costa Rica 5
DO - Repubblica Dominicana 5
GR - Grecia 5
RS - Serbia 5
BE - Belgio 4
BH - Bahrain 4
CZ - Repubblica Ceca 4
KW - Kuwait 4
SK - Slovacchia (Repubblica Slovacca) 4
SY - Repubblica araba siriana 4
AM - Armenia 3
BY - Bielorussia 3
DK - Danimarca 3
ET - Etiopia 3
GE - Georgia 3
LV - Lettonia 3
NO - Norvegia 3
QA - Qatar 3
SI - Slovenia 3
TT - Trinidad e Tobago 3
AO - Angola 2
BA - Bosnia-Erzegovina 2
BB - Barbados 2
BG - Bulgaria 2
GA - Gabon 2
GH - Ghana 2
GT - Guatemala 2
HR - Croazia 2
HU - Ungheria 2
LC - Santa Lucia 2
MG - Madagascar 2
MT - Malta 2
Totale 77.890
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Città #
Genova 39.689
Genoa 17.125
Rapallo 4.658
Vado Ligure 4.355
Singapore 1.299
San Jose 1.035
Lauterbourg 539
Ashburn 400
Ho Chi Minh City 313
Hong Kong 271
Beijing 239
Hanoi 229
Council Bluffs 212
New York 134
Frankfurt am Main 112
Santa Clara 104
Helsinki 85
Bordighera 82
Tokyo 72
Da Nang 56
Haiphong 53
Los Angeles 53
Mexico City 52
Tianjin 42
Zurich 31
Rome 30
São Paulo 30
Orem 29
Chicago 28
Milan 28
Amsterdam 25
Shanghai 25
Guangzhou 22
Baghdad 21
Biên Hòa 21
City of London 19
Dublin 19
Cardiff 18
Hải Dương 18
Quito 18
Can Tho 16
Chennai 16
Amman 15
Montreal 15
Madrid 14
Mumbai 14
Nairobi 13
Quảng Ngãi 13
Tashkent 13
Bogotá 12
Florence 12
Lima 12
Nuremberg 12
Rio de Janeiro 12
Thái Nguyên 12
Atlanta 10
Buffalo 10
Johannesburg 10
Lappeenranta 10
Montevideo 10
Paris 10
Turin 10
Baku 9
Belo Horizonte 9
Brasília 9
Buenos Aires 9
Cape Town 9
Des Moines 9
Dhaka 9
Jeddah 9
Lahore 9
Ninh Bình 9
Santiago 9
Thái Bình 9
Warsaw 9
Bologna 8
Dallas 8
Guayaquil 8
Jakarta 8
London 8
Toronto 8
Tunis 8
Bari 7
Bishkek 7
Caracas 7
Denver 7
Long Xuyen 7
Quezon City 7
Salvador 7
San Francisco 7
Santo André 7
Shenzhen 7
Tirana 7
Bandung 6
Bangkok 6
Basra 6
Bucharest 6
Curitiba 6
Guarulhos 6
Houston 6
Totale 72.154
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Nome #
(1)H-MR spectroscopy indicates prominent cerebellar dysfunction in benign adult familial myoclonic epilepsy. 1.402
A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms. 247
"Comorbidity" between epilepsy and headache/migraine: the other side of the same coin! 244
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 233
A 3-year-old boy with drug-resistant complex partial seizures 228
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. 228
22-year-old girl with status epilepticus and progressive neurological symptoms. 217
A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures. 216
A novel SCN2A mutation in family with benign familial infantile seizures. 214
A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2. 210
Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype. 202
'Autoimmune epilepsy' or exasperated search for the etiology of seizures of unknown origin? 201
Whole-genome linkage scan for epilepsy-related photosensitivity: a mega-analysis. 195
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability 195
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy. 195
A clinical and genetic study of 33 new cases with early-onset absence epilepsy. 190
Pyridoxine-dependent epilepsy: An under-recognised cause of intractable seizures. 189
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy 189
A pilot open-label trial of zonisamide in Unverricht-Lundborg disease. 189
Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development 188
Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach? 185
Do regulatory regions matter in FOXG1 duplications? 185
Idiopathic focal epilepsies: the "lost tribe" 185
ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma Elasticum 185
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome). 184
Similar but not identical: clinical implications for molecular studies in monozygotic discordant twins with epilepsy. 184
Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndrome. 183
End-of-life: still an Italian dilemma. 183
Health-related quality of life in epilepsy: findings obtained with a new Italian instrument. 183
Clinical and genetic findings in 26 Italian patients with Lafora disease. 182
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome. 182
Lumping encephalopathies with inflammation-mediated status epilepticus: is there enough evidence? 182
A t(4;9)(q34;p22) translocation associated with partial epilepsy, mental retardation, and dysmorphism. 181
Epilepsy associated with supratentorial brain tumors under 3 years of life. 180
Recurrent hypothermia with hyperhidrosis in two siblings: familial Shapiro syndrome variant. 180
Dramatic response to levetiracetam in post-ischaemic Holmes' tremor. 180
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome 180
GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features. 179
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies—An Italian observational multicenter study 179
Temporal lobe epilepsy and anti glutamic acid decarboxylase autoimmunity. 178
Epileptogenesis due to peripheral injury as a cause of focal epilepsy. 178
Levetiracetam in patients with cortical myoclonus: a clinical and electrophysiological study. 178
LGI1 microdeletion in autosomal dominant lateral temporal epilepsy. 178
NovelAMPD2mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalities 178
'Ictal epileptic headache': Recent concepts for new classifications criteria. 177
"Ictal epileptic headache": Beyond the epidemiological evidence. 177
The genetics of monogenic idiopathic epilepsies and epileptic encephalopathies. 176
Sudden death in Unverricht-Lundborg patients: is serotonin the key? 175
Epileptic myoclonus as ciprofloxacin-associated adverse effect. 175
From migralepsy to ictal epileptic headache: the story so far. 175
A proof-of-concept trial of the whey protein alfa-lactalbumin in chronic cortical myoclonus. 175
Idiopathic mesial temporal lobe epilepsy: don't sow the tares with the wheat! 174
Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy. 174
Suppression of myoclonus in SCA2 by piracetam. 174
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy 174
Evaluation of presumably disease causing SCN1A variants in a cohort of common epilepsy syndromes 174
Long-term follow-up in two siblings with pyridoxine-dependent seizures associated with a novel ALDH7A1 mutation. 173
Long-term evolution of EEG in Unverricht-Lundborg disease. 173
TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsy 173
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy 173
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases. 173
What have we learned about ictal epileptic headache? A review of well-documented cases. 172
The gelastic seizures-hypothalamic hamartoma syndrome: Facts, hypotheses, and perspectives. 172
Clinical features of Sturge-Weber syndrome without facial nevus: Five novel cases. 171
Comment to: overlap cases of eyelid myoclonia with absences and juvenile myoclonic epilepsy. 171
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features 171
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 171
Comment to: Diabetic hyperglycemia is associated with the severity of epileptic seizures in adults. 170
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. 170
De novo mutations in HCN1 cause early infantile epileptic encephalopathy 170
Autosomal recessive progressive myoclonus epilepsy due to impaired ceramide synthesis 169
Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 168
Lateralizing value of the auditory aura in partial seizures. 168
Anxiolytic and Analgesic Effects of Melatonin in Paediatric Dentistry 168
Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy. 167
Autoantibodies to glutamic acid decarboxylase (GAD) in focal and generalized epilepsy: A study on 233 patients. 167
Metabolic and endocrine effects of valproic acid chronic treatment. 167
TBC1D24 genotype-phenotype correlation 167
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. 167
Functional changes in hypothalamic hamartoma neurons and gelastic epilepsy. 166
Epilepsy: old drugs do the trick in childhood absence epilepsy. 166
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families. 166
Migralepsy, hemicrania epileptica, post-ictal headache and "ictal epileptic headache": a proposal for terminology and classification revision. 165
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations. 164
Reflex seizures and reflex epilepsies: Old models for understanding mechanisms of epileptogenesis. 164
Erratum to: Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 164
Galloway-Mowat syndrome: an early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature. 163
Life-threatening status epilepticus following gabapentin administration in a patient with benign adult familial myoclonic epilepsy. 163
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 163
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. 163
Willful modulation of brain activity in disorders of consciousness. 162
Comment to: addition of verapamil in the treatment of severe myoclonic epilepsy in infancy (Iannetti et al.). 162
New terminology for headache/migraine as the sole ictal epileptic manifestation: the downsides. Reply to Cianchetti et al. 162
Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome. 162
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families. 162
Posterior reversible encephalopathy syndrome (PRES) in critically ill obstetric patients. 161
Lennox-Gastaut syndrome with late-onset and prominent reflex seizures in trisomy 21 patients. 161
Rhombencephalosynapsis in a patient with mental retardation, epilepsy, and dysmorphisms. 161
Commentary to: "Evaluation of serum lipids and carotid artery intima media thickness in epileptic children treated with valproic acid". 160
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. 160
Totale 19.155
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Categoria #
all - tutte 272.685
article - articoli 268.812
book - libri 254
conference - conferenze 571
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.048
Totale 545.370
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.468 0 0 0 0 0 0 0 0 0 1.175 760 533
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
2025/202618.218 2.131 677 2.094 1.709 2.369 2.049 2.988 1.056 1.635 1.510 0 0
Totale 79.133