IRIS
STRIANO, SALVATORE
 Distribuzione geografica
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Continente #
AS - Asia 7.980
NA - Nord America 7.092
EU - Europa 5.067
SA - Sud America 946
AF - Africa 165
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 5
Totale 21.264
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Nazione #
US - Stati Uniti d'America 6.754
SG - Singapore 3.782
RU - Federazione Russa 2.433
VN - Vietnam 1.424
CN - Cina 1.314
BR - Brasile 767
HK - Hong Kong 729
IT - Italia 529
FR - Francia 300
SE - Svezia 293
FI - Finlandia 281
DE - Germania 255
NL - Olanda 232
UA - Ucraina 223
CA - Canada 209
IE - Irlanda 185
GB - Regno Unito 153
JP - Giappone 142
IN - India 136
MX - Messico 89
AR - Argentina 75
BD - Bangladesh 66
ZA - Sudafrica 51
IQ - Iraq 46
PH - Filippine 39
TH - Thailandia 36
PL - Polonia 32
ES - Italia 29
KR - Corea 29
EC - Ecuador 28
TR - Turchia 27
ID - Indonesia 25
PK - Pakistan 25
CI - Costa d'Avorio 21
AT - Austria 19
TW - Taiwan 19
IR - Iran 18
CO - Colombia 17
UZ - Uzbekistan 16
CL - Cile 15
MA - Marocco 15
NP - Nepal 14
PY - Paraguay 14
LT - Lituania 13
BE - Belgio 12
EG - Egitto 12
KE - Kenya 12
SA - Arabia Saudita 12
TN - Tunisia 11
UY - Uruguay 11
VE - Venezuela 11
AE - Emirati Arabi Uniti 10
DZ - Algeria 10
JO - Giordania 10
JM - Giamaica 9
AZ - Azerbaigian 8
KZ - Kazakistan 8
RO - Romania 8
AL - Albania 7
AU - Australia 7
BG - Bulgaria 7
DK - Danimarca 6
HN - Honduras 6
MN - Mongolia 6
MY - Malesia 6
TT - Trinidad e Tobago 6
CZ - Repubblica Ceca 5
ET - Etiopia 5
GR - Grecia 5
LV - Lettonia 5
PS - Palestinian Territory 5
RS - Serbia 5
CH - Svizzera 4
EU - Europa 4
IS - Islanda 4
LB - Libano 4
MR - Mauritania 4
PE - Perù 4
TL - Timor Orientale 4
BO - Bolivia 3
CR - Costa Rica 3
GT - Guatemala 3
HU - Ungheria 3
IL - Israele 3
KW - Kuwait 3
MG - Madagascar 3
MK - Macedonia 3
NO - Norvegia 3
PT - Portogallo 3
AM - Armenia 2
AO - Angola 2
BB - Barbados 2
BH - Bahrain 2
CG - Congo 2
CV - Capo Verde 2
DM - Dominica 2
DO - Repubblica Dominicana 2
GD - Grenada 2
KH - Cambogia 2
LU - Lussemburgo 2
Totale 21.224
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Città #
Singapore 1.731
San Jose 1.073
Hong Kong 698
Moscow 576
Chandler 534
Ho Chi Minh City 419
Ashburn 371
Beijing 333
Hanoi 311
Millbury 251
Jacksonville 250
Santa Clara 243
Princeton 235
Lauterbourg 216
The Dalles 204
Los Angeles 190
Nanjing 186
Amsterdam 181
Boston 156
Tokyo 125
Buffalo 122
Woodbridge 116
Wilmington 110
New York 109
Ottawa 98
São Paulo 77
Naples 75
Haiphong 68
Hefei 67
Houston 66
Council Bluffs 65
Ann Arbor 63
Norwalk 61
Nanchang 59
Boardman 57
Dallas 56
Da Nang 53
Munich 53
Falls Church 52
Kronberg 52
Redondo Beach 49
Milan 43
Napoli 40
Chennai 39
Denver 38
Chicago 37
Jiaxing 37
Mexico City 37
Orem 37
Shenyang 37
Hebei 36
Montreal 35
Toronto 34
Tianjin 33
Seattle 32
Brooklyn 31
Rome 30
Atlanta 29
Stockholm 29
Warsaw 29
Frankfurt am Main 25
Johannesburg 25
London 25
Nuremberg 25
Rio de Janeiro 25
Biên Hòa 24
Changsha 24
Thái Nguyên 20
Baghdad 19
Belo Horizonte 19
Hải Dương 18
Phoenix 18
Thái Bình 18
Can Tho 17
Poplar 17
Coyoacán 16
San Francisco 16
San Mateo 16
Helsinki 15
Kunming 15
Ninh Bình 15
Turku 15
Mumbai 14
Ardabil 13
Manchester 13
Porto Alegre 13
Shanghai 13
Tashkent 13
Tân Tiến 13
Ankara 12
Bangkok 12
Charlotte 12
Des Moines 12
Nairobi 12
Ribeirão Preto 12
Seoul 12
Bến Tre 11
Dhaka 11
Leawood 11
Salvador 11
Totale 11.121
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Nome #
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. 203
(1)H-MR spectroscopy indicates prominent cerebellar dysfunction in benign adult familial myoclonic epilepsy. 177
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome). 162
Epileptic seizures in multiple sclerosis: clinical and EEG correlations. 152
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing 151
A pilot open-label trial of zonisamide in Unverricht-Lundborg disease. 151
Levetiracetam for cerebellar tremor in multiple sclerosis: an open-label pilot tolerability and efficacy study. 150
GLUTAMIC ACID DECARBOXYLASE ANTIBODIES IN IDIOPATHIC GENERALIZED EPILEPSY AND TYPE 1 DIABETES. 149
Characterization of reproductive endocrine disorders in women with epilepsy. 146
The spectrum and the natural history of gelastic seizures-hypothalamic hamartoma syndrome | [Lo spettro e la storia naturale della sindrome epilessia gelastica-amartoma ipotalamico]. 145
Diagnostic implications of genetic copy number variation in epilepsy plus 144
Epileptic myoclonus as ciprofloxacin-associated adverse effect. 140
Inherited neuromyotonia: A clinical and genetic study of a family. 140
Posterior reversible encephalopathy syndrome in intensive care medicine. 140
22-year-old girl with status epilepticus and progressive neurological symptoms. 140
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. 136
Limited place for plasma monitoring of new antiepileptic drugs in clinical practice. 134
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy. 133
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families. 131
Abnormal pattern of luteinizing hormone pulsatility in women with epilepsy. 130
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases. 129
Life-threatening status epilepticus following gabapentin administration in a patient with benign adult familial myoclonic epilepsy. 127
Serum MHD monitoring may be useful in the management of side effects in epileptic patients on high doses of oxcarbazepine. 127
The syndrome gelastic seizures-hypothalamic hamartoma: severe, potentially reversible encephalopathy. 126
Reflex seizures and reflex epilepsies: old models for understanding mechanisms of epileptogenesis. 126
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 125
The clinical spectrum and natural history of gelastic epilepsy-hypothalamic hamartoma syndrome 123
Autoantibodies to glutamic acid decarboxylase (GAD) in focal and generalized epilepsy: A study on 233 patients. 122
Refractory, life-threatening status epilepticus in a 3-year-old girl. 122
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 122
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization. 122
A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms. 122
Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion. 122
Dramatic response to levetiracetam in post-ischaemic Holmes' tremor. 121
Aspetti clinico-neuroradiologici e terapeutici dell’encefalopatia posteriore reversibile (PRES) 120
Unfavourable outcome of Hashimoto encephalopathy due to status epilepticus. One autopsy case. 119
Gelastic epilepsy: symptomatic and cryptogenic cases. 119
Children grow-up... 119
Do gonadotropins play a role in catamenial epilepsy? | [Le gonadotropine ipofisarie hanno un ruolo nella patogenesi delle crisi catameniali?]. 118
Insulinoma presenting as refractory late-onset epilepsy. 117
Use of Levetiracetam plasma levels monitoring in the management of patients with epilepsy. 117
Use of Levetiracetam in patients with epilepsy and chronic liver disease | [Uso di Levetiracetam nei pazienti con epilessia ed epatopatia cronica: dati preliminari]. 117
Paroxysmal dystonia in Behcet's disease. 116
Sudden death in Unverricht-Lundborg patients: is serotonin the key? 116
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 116
CHD2 mutations: Only epilepsy? Description of cognitive and behavioral profile in a case with a new mutation 116
Posterior reversible encephalopathy syndrome (PRES) in critically ill obstetric patients. 115
Levetiracetam in patients with epilepsy and chronic liver disease: observations in a case series. 115
Severe pulmonary congestion in a near miss at the first seizure: Further evidence for respiratory dysfunction in sudden unexpected death in epilepsy 113
Re: Fame 3: a novel form of progressive myoclonus and epilepsy. 113
A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy. 113
Hyperhomocysteinemia and retinal vascular changes in patients with epilepsy. 113
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations 111
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations. 111
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. 110
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
Suppression of myoclonus in SCA2 by piracetam. 110
Response to: 'Cortical tremor or cortical pseudotremor?'. 108
Epilepsy, cerebral calcifications, and gluten-related disorders: Are anti-transglutaminase 6 antibodies the missing link? 108
Neurological features and long-term follow-up in 15q11.2-13.1 duplication. 107
Tiagabine in glial tumors. 106
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families. 106
Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME. 106
New and investigational antiepileptic drugs. 106
A pilot open-label trial of zonisamide inUnverricht-Lundborg disease. 106
A unique case of "masturbatory" seizures in primary generalized epilepsy. 106
Posterior reversible encephalopathy syndrome (PRES) in critically ill obstetric patients. 105
Eyelid myoclonia with absences: an overlooked epileptic syndrome? 105
Benign intracranial hypertension of obese women. A twenty cases report. 105
Epilepsia partialis continua as a first symptom of multiple sclerosis: electrophysiological study of one case. 104
Frontotemporal dementia presenting as Gescwind's syndrome 104
Is retinal assessment useful in epileptic patients with hyperhomocysteinemia? 104
Epileptogenesis due to peripheral injury as a cause of focal epilepsy. 104
Reproductive endocrine disorders in women with primary generalized epilepsy. 102
Small hypothalamic hamartomas and gelastic seizures. 102
Progressive myoclonic ataxia associated to epileptic seizures, opsoclonus and optical atrophy. 101
Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sisters. 100
Chitosan may decrease serum valproate and increase the risk of seizure reappearance. 100
Depression in epilepsy: prevalence in a group of out-patients of the Epilepsy Center of the University of Naples | [LA DEPRESSIONE NEI PAZIENTI CON EPILESSIA: PREVALENZA IN UNA POPOLAZIONE DI PAZIENTI AMBULATORIALI DEL CENTRO PER L'EPILESSIA DELL'UNIVERSITA' DI NAPOLI] 100
Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy. 99
Cerebellar ataxia and hypogonadism. A clinicopathological report. 99
Cutis verticis gyrata--mental deficiency syndrome: a patient with drug-resistant epilepsy and polymicrogyria. 98
Lesional reflex epilepsy associated with the thought of food. 98
A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures 96
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations. 96
A proof-of-concept trial of the whey protein alfa-lactalbumin in chronic cortical myoclonus. 95
Familial cortical tremor and epilepsy: A well-defined syndrome with genetic heterogeneity waiting for nosological placement in the ILAE classification. 94
Posterior reversible encephalopathy syndrome in intensive care medicine. 94
Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome. 94
Facial myoclonus presenting as epilepsia partialis continua in a patient with an opercular lesion | [Epilessia Parziale Continua con mioclono faciale da lesione opercolare stabilizzata]. 94
Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome. 93
Epilepsia partialis continua as a first symptom of multiple sclerosis: electrophysiological study of one case. 93
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 93
Gelastic seizures-hypothalamic hamartoma syndrome: study on five patients | [Sindrome crisi gelastiche-amartoma ipotalamico: studio di cinque casi]. 93
Disorders in cortical development and epilepsy - 13 years of experience 93
Topiramate-associated worsening symptoms in a patient with familial hemiplegic migraine 92
Lateralizing value of the auditory aura in partial seizures. 91
Paroxysmal dystonia in Behçet's disease. 91
Comment on "Factors influencing clinical features of absence seizures". 90
Totale 11.625
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Categoria #
all - tutte 71.260
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 71.260
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.232 35 9 1 2 9 85 23 49 231 64 161 563
2022/20231.352 250 89 32 120 167 156 1 102 178 160 66 31
2023/2024855 41 145 112 44 40 31 32 82 6 19 235 68
2024/20255.426 354 455 17 41 99 165 588 264 526 590 1.878 449
2025/202610.080 1.193 662 898 945 1.808 440 1.222 557 1.346 587 188 234
2026/2027126 126 0 0 0 0 0 0 0 0 0 0 0
Totale 21.403