IRIS
STRIANO, PASQUALE
 Distribuzione geografica
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Continente #
AS - Asia 4.064
NA - Nord America 3.544
EU - Europa 2.444
SA - Sud America 474
Continente sconosciuto - Info sul continente non disponibili 135
AF - Africa 92
OC - Oceania 5
Totale 10.758
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Nazione #
US - Stati Uniti d'America 3.377
SG - Singapore 1.869
RU - Federazione Russa 1.205
CN - Cina 783
VN - Vietnam 664
BR - Brasile 388
IT - Italia 340
HK - Hong Kong 313
SE - Svezia 185
DE - Germania 175
FR - Francia 131
CA - Canada 109
FI - Finlandia 90
NL - Olanda 76
JP - Giappone 75
IN - India 70
BD - Bangladesh 69
GB - Regno Unito 60
IE - Irlanda 57
KR - Corea 34
MX - Messico 31
AR - Argentina 30
AT - Austria 29
ZA - Sudafrica 25
IQ - Iraq 24
ID - Indonesia 22
UA - Ucraina 22
PH - Filippine 21
TH - Thailandia 19
ES - Italia 18
EC - Ecuador 16
TR - Turchia 16
CI - Costa d'Avorio 15
PL - Polonia 15
MA - Marocco 14
PK - Pakistan 13
CL - Cile 9
PY - Paraguay 9
EG - Egitto 8
TW - Taiwan 8
CO - Colombia 7
TN - Tunisia 7
AZ - Azerbaigian 6
JO - Giordania 6
MN - Mongolia 6
MY - Malesia 6
AE - Emirati Arabi Uniti 5
BE - Belgio 5
GT - Guatemala 5
JM - Giamaica 5
NP - Nepal 5
UY - Uruguay 5
UZ - Uzbekistan 5
VE - Venezuela 5
BY - Bielorussia 4
DZ - Algeria 4
ET - Etiopia 4
LB - Libano 4
LV - Lettonia 4
PE - Perù 4
TT - Trinidad e Tobago 4
AU - Australia 3
DK - Danimarca 3
GR - Grecia 3
IS - Islanda 3
LT - Lituania 3
RS - Serbia 3
SY - Repubblica araba siriana 3
AO - Angola 2
BB - Barbados 2
CR - Costa Rica 2
CZ - Repubblica Ceca 2
HN - Honduras 2
MK - Macedonia 2
NI - Nicaragua 2
NO - Norvegia 2
OM - Oman 2
PT - Portogallo 2
SA - Arabia Saudita 2
TL - Timor Orientale 2
AF - Afghanistan, Repubblica islamica di 1
AG - Antigua e Barbuda 1
AM - Armenia 1
BH - Bahrain 1
BJ - Benin 1
BO - Bolivia 1
BW - Botswana 1
CG - Congo 1
CU - Cuba 1
CV - Capo Verde 1
DO - Repubblica Dominicana 1
EE - Estonia 1
GD - Grenada 1
GE - Georgia 1
GH - Ghana 1
HR - Croazia 1
HU - Ungheria 1
IL - Israele 1
IR - Iran 1
KE - Kenya 1
Totale 10.605
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Città #
Singapore 927
San Jose 630
Chandler 313
Moscow 303
Hong Kong 299
Ashburn 256
Ho Chi Minh City 199
Beijing 183
Hefei 173
Santa Clara 155
Hanoi 144
The Dalles 126
Los Angeles 97
Lauterbourg 91
Boston 71
Amsterdam 64
Tokyo 62
Ottawa 58
Millbury 57
Princeton 57
Nanjing 56
New York 55
Buffalo 53
São Paulo 53
Naples 52
Dallas 44
Jacksonville 44
Frankfurt am Main 39
Kronberg 38
Milan 38
Boardman 37
Council Bluffs 37
Wilmington 36
Redondo Beach 31
Haiphong 30
Munich 29
Da Nang 28
Seoul 28
Des Moines 25
Houston 25
Rome 25
Nanchang 23
Nuremberg 21
Ann Arbor 20
Helsinki 20
Lawrence 20
Norwalk 20
Chennai 19
Chicago 19
Falls Church 19
Woodbridge 19
Denver 18
Brooklyn 17
Napoli 17
Seattle 17
Atlanta 16
Dong Ket 16
Jiaxing 16
Düsseldorf 15
London 15
Montreal 15
Orem 15
Vienna 15
Toronto 14
Johannesburg 13
Rio de Janeiro 13
Tianjin 13
Can Tho 12
Hải Dương 12
Lappeenranta 12
Stockholm 12
Fairfield 11
Mexico City 11
Kunming 10
Shenyang 10
Thái Nguyên 10
Baghdad 9
San Francisco 9
Warsaw 9
Bologna 8
Philadelphia 8
Shanghai 8
Ankara 7
Falkenstein 7
Hebei 7
Long Xuyen 7
Manchester 7
Phoenix 7
Poplar 7
Amman 6
Bangkok 6
Belo Horizonte 6
Brasília 6
Dhaka 6
Kuala Lumpur 6
Miami 6
Ninh Bình 6
Porto Alegre 6
Queens 6
Quito 6
Totale 5.779
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Nome #
Diagnosis and management of type 1 sialidosis: Clinical insights from long-term care of four unrelated patients 171
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome). 163
Effects of three-months folate supplementation on early vascular abnormalities in hyperhomocysteinemic patients with epilepsy 160
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing 156
Epileptic seizures in multiple sclerosis: clinical and EEG correlations. 153
A pilot open-label trial of zonisamide in Unverricht-Lundborg disease. 152
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 149
Clinical features and genotype–phenotype correlations in epilepsy patients with de novo DYNC1H1 variants 148
Diagnostic implications of genetic copy number variation in epilepsy plus 144
Genotype-phenotype spectrum and correlations in Xia-Gibbs syndrome: Report of five novel cases and literature review 143
Posterior reversible encephalopathy syndrome in intensive care medicine. 142
22-year-old girl with status epilepticus and progressive neurological symptoms. 141
Novel biallelic variants expand the phenotype of NAA20-related syndrome 139
Limited place for plasma monitoring of new antiepileptic drugs in clinical practice. 136
Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants 134
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases. 130
Cyclic Vomiting Syndrome in Children 130
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox-Gastaut Syndrome. 129
Spectrum of epilepsy with eyelid myoclonia: Delineation of disease subtypes from a large multicenter study 127
The syndrome gelastic seizures-hypothalamic hamartoma: severe, potentially reversible encephalopathy. 127
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus 126
Refractory, life-threatening status epilepticus in a 3-year-old girl. 124
Temporal-parietal-occipital epilepsy in GEFS+ associated with SCN1A mutation 124
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy 123
Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion. 122
Epilepsy Course and Developmental Trajectories in STXBP1 -DEE 119
Children grow-up... 119
An Italian consensus on the management of Lennox-Gastaut syndrome 118
Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia 117
Insulinoma presenting as refractory late-onset epilepsy. 117
Sudden death in Unverricht-Lundborg patients: is serotonin the key? 117
Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations 116
Clinical efficacy of low-dose Perampanel correlates with neurophysiological changes in familial adult myoclonus epilepsy 2 115
Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors 115
KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum. 115
National scale full-resolution P-SBAS processing for the investigation of critical infrastructure deformations related to the built-up environment  114
Myoclonus: Differential diagnosis and current management 114
Severe pulmonary congestion in a near miss at the first seizure: Further evidence for respiratory dysfunction in sudden unexpected death in epilepsy 114
A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy. 114
Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical Development 113
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. 113
Re: Fame 3: a novel form of progressive myoclonus and epilepsy. 113
Hyperhomocysteinemia and retinal vascular changes in patients with epilepsy. 113
Is epilepsy a real problem in multiple sclerosis patients? 110
Comment to: Diabetic hyperglycemia is associated with the severity of epileptic seizures in adults. 110
Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME. 108
Response to: 'Cortical tremor or cortical pseudotremor?'. 108
Neurological features and long-term follow-up in 15q11.2-13.1 duplication. 107
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies. 107
Perampanel as precision therapy in rare genetic epilepsies 106
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families. 106
New and investigational antiepileptic drugs. 106
Eyelid myoclonia with absences: an overlooked epileptic syndrome? 106
Chitosan may decrease serum valproate and increase the risk of seizure reappearance. 105
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 105
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 105
Is retinal assessment useful in epileptic patients with hyperhomocysteinemia? 104
Epileptogenesis due to peripheral injury as a cause of focal epilepsy. 104
Small hypothalamic hamartomas and gelastic seizures. 102
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing 100
Lesional reflex epilepsy associated with the thought of food. 100
Epilepsy, EEG and chromosomal rearrangements 98
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations. 97
Familial cortical tremor and epilepsy: A well-defined syndrome with genetic heterogeneity waiting for nosological placement in the ILAE classification. 95
Topiramate-associated worsening symptoms in a patient with familial hemiplegic migraine 93
Lateralizing value of the auditory aura in partial seizures. 93
The spectrum of intermediate SCN8A-related epilepsy 91
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. 90
Comment on "Factors influencing clinical features of absence seizures". 90
Abnormal sensorimotor cortex and thalamo-cortical networks in familial adult myoclonic epilepsy type 2: pathophysiology and diagnostic implications 90
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins. 89
Transient epileptic amnesia: a new epileptic syndrome in development? 88
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 88
Efficacy of levetiracetam in the treatment of drug-resistant Rett syndrome. 87
Eyelid fluttering, typical EEG pattern, and impaired intellectual function: a homogeneous epileptic condition among the patients presenting with eyelid myoclonia. 85
Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy. 85
Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbidities 84
Familial Adult Myoclonus Epilepsy: A Non-Coding Repeat Expansion Disorder of Cerebellar-Thalamic-Cortical Loop 84
A solved puzzle: Familial adult myoclonus epilepsy is a new expansion repeats disorder 83
First and Second Generation Cosmo-Skymed Advanced Dinsar Processing for Investigating Deformations Affecting The Built-up Environment 83
Comment to: Status epilepticus induced by star fruit intoxication in patients with chronic renal disease. 83
Cortical tremor: a tantalizing conundrum between cortex and cerebellum 83
Epileptic myoclonus as ciprofloxacin-associated adverse effect [8] 81
LGI1 microdeletion in autosomal dominant lateral temporal epilepsy. 77
Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences 77
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis 76
Electroencephalographic features in dravet syndrome: five-year follow-up study in 22 patients 72
Typical progression of myoclonic epilepsy of the Lafora type: a case report. 71
Cannabidiol in Pharmacoresistant Epilepsy: Clinical Pharmacokinetic Data From an Expanded Access Program 69
Gabapentin: a Ca2+ channel alpha 2-delta ligand far beyond epilepsy therapy. 68
Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death. 68
Psychiatric features in gelastic epilepsy and hypothalamic hamartoma: long-term psychodiagnostic observations. 68
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients 68
Erratum: Posterior reversible encephalopathy syndrome and spinal epidural haematoma in a hypertensive patient (European Journal of Anaesthesiology (2007) 21 (1065-1067)) 68
Epilepsy and multiple sclerosis: Review of literature and our epilepsy center's experience 67
Clinical spectrum and critical care management of posterior reversible encephalopathy syndrome (PRES) 66
Reflex myoclonic epilepsy in infancy: A multicenter clinical study. 63
West syndrome associated with 14q12 duplications harboring FOXG1 62
Unfavourable outcome of Hashimoto encephalopathy due to status epilepticus: One autopsy case [1] 57
Cortico-muscular coherence and brain networks in familial adult myoclonic epilepsy and progressive myoclonic epilepsy 56
Totale 10.561
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Categoria #
all - tutte 34.843
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 34.843
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022466 0 11 3 0 6 15 11 13 102 62 64 179
2022/2023716 83 40 19 90 96 91 0 74 96 66 42 19
2023/2024405 21 71 35 16 17 23 4 53 4 17 107 37
2024/20252.686 151 150 11 25 72 167 304 179 168 272 975 212
2025/20265.584 538 434 573 548 987 229 659 282 676 313 130 215
2026/2027182 142 40 0 0 0 0 0 0 0 0 0 0
Totale 10.758