STRIANO, SALVATORE
 Distribuzione geografica
Continente #
AS - Asia 7.944
NA - Nord America 6.735
EU - Europa 5.022
SA - Sud America 931
AF - Africa 165
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 5
Totale 20.811
Nazione #
US - Stati Uniti d'America 6.420
SG - Singapore 3.780
RU - Federazione Russa 2.433
VN - Vietnam 1.423
CN - Cina 1.305
BR - Brasile 758
HK - Hong Kong 727
IT - Italia 499
FR - Francia 298
SE - Svezia 293
FI - Finlandia 281
DE - Germania 255
NL - Olanda 232
UA - Ucraina 221
CA - Canada 195
IE - Irlanda 184
GB - Regno Unito 152
JP - Giappone 141
IN - India 136
MX - Messico 87
AR - Argentina 73
ZA - Sudafrica 51
BD - Bangladesh 49
IQ - Iraq 46
PH - Filippine 39
TH - Thailandia 36
PL - Polonia 32
KR - Corea 29
EC - Ecuador 28
TR - Turchia 27
ES - Italia 26
PK - Pakistan 25
ID - Indonesia 24
CI - Costa d'Avorio 21
AT - Austria 19
TW - Taiwan 19
IR - Iran 18
UZ - Uzbekistan 16
CO - Colombia 15
MA - Marocco 15
CL - Cile 14
PY - Paraguay 14
NP - Nepal 13
BE - Belgio 12
EG - Egitto 12
KE - Kenya 12
LT - Lituania 12
SA - Arabia Saudita 12
TN - Tunisia 11
UY - Uruguay 11
AE - Emirati Arabi Uniti 10
DZ - Algeria 10
JO - Giordania 10
VE - Venezuela 10
AZ - Azerbaigian 8
KZ - Kazakistan 8
RO - Romania 8
AL - Albania 7
AU - Australia 7
BG - Bulgaria 6
DK - Danimarca 6
JM - Giamaica 6
MN - Mongolia 6
TT - Trinidad e Tobago 6
ET - Etiopia 5
HN - Honduras 5
LV - Lettonia 5
PS - Palestinian Territory 5
RS - Serbia 5
CH - Svizzera 4
CZ - Repubblica Ceca 4
EU - Europa 4
GR - Grecia 4
IS - Islanda 4
LB - Libano 4
MR - Mauritania 4
MY - Malesia 4
PE - Perù 4
TL - Timor Orientale 4
BO - Bolivia 3
CR - Costa Rica 3
HU - Ungheria 3
IL - Israele 3
KW - Kuwait 3
MG - Madagascar 3
MK - Macedonia 3
NO - Norvegia 3
AM - Armenia 2
AO - Angola 2
BB - Barbados 2
BH - Bahrain 2
CG - Congo 2
CV - Capo Verde 2
DO - Repubblica Dominicana 2
GD - Grenada 2
GT - Guatemala 2
KH - Cambogia 2
LU - Lussemburgo 2
LY - Libia 2
MD - Moldavia 2
Totale 20.774
Città #
Singapore 1.730
San Jose 1.023
Hong Kong 696
Moscow 576
Chandler 534
Ho Chi Minh City 419
Ashburn 341
Beijing 332
Hanoi 310
Millbury 251
Jacksonville 247
Santa Clara 239
Princeton 235
Lauterbourg 216
The Dalles 204
Nanjing 186
Amsterdam 181
Los Angeles 178
Boston 155
Tokyo 125
Buffalo 117
Woodbridge 116
Wilmington 109
New York 98
Ottawa 98
São Paulo 76
Naples 71
Haiphong 68
Hefei 67
Ann Arbor 63
Norwalk 61
Houston 60
Nanchang 59
Boardman 57
Da Nang 53
Munich 53
Falls Church 52
Kronberg 52
Redondo Beach 49
Dallas 44
Milan 41
Napoli 40
Chennai 39
Jiaxing 37
Mexico City 37
Shenyang 37
Hebei 36
Chicago 34
Denver 34
Orem 34
Toronto 34
Tianjin 33
Montreal 32
Seattle 32
Stockholm 29
Warsaw 29
Brooklyn 27
Atlanta 26
Rome 26
Frankfurt am Main 25
Johannesburg 25
London 25
Nuremberg 25
Biên Hòa 24
Changsha 24
Council Bluffs 24
Rio de Janeiro 23
Thái Nguyên 20
Baghdad 19
Belo Horizonte 19
Hải Dương 18
Thái Bình 18
Can Tho 17
Poplar 17
Coyoacán 16
Phoenix 16
San Mateo 16
Helsinki 15
Kunming 15
Ninh Bình 15
San Francisco 15
Turku 15
Mumbai 14
Ardabil 13
Manchester 13
Porto Alegre 13
Shanghai 13
Tashkent 13
Tân Tiến 13
Ankara 12
Bangkok 12
Des Moines 12
Nairobi 12
Ribeirão Preto 12
Seoul 12
Bến Tre 11
Dhaka 11
Leawood 11
Salvador 11
Amman 10
Totale 10.902
Nome #
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. 200
(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). 160
Epileptic seizures in multiple sclerosis: clinical and EEG correlations. 151
A pilot open-label trial of zonisamide in Unverricht-Lundborg disease. 151
GLUTAMIC ACID DECARBOXYLASE ANTIBODIES IN IDIOPATHIC GENERALIZED EPILEPSY AND TYPE 1 DIABETES. 149
Levetiracetam for cerebellar tremor in multiple sclerosis: an open-label pilot tolerability and efficacy study. 149
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
Characterization of reproductive endocrine disorders in women with epilepsy. 143
Diagnostic implications of genetic copy number variation in epilepsy plus 141
Inherited neuromyotonia: A clinical and genetic study of a family. 140
Epileptic myoclonus as ciprofloxacin-associated adverse effect. 139
Posterior reversible encephalopathy syndrome in intensive care medicine. 138
22-year-old girl with status epilepticus and progressive neurological symptoms. 137
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. 134
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy. 133
Limited place for plasma monitoring of new antiepileptic drugs in clinical practice. 132
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing 131
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families. 128
Serum MHD monitoring may be useful in the management of side effects in epileptic patients on high doses of oxcarbazepine. 126
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases. 125
Life-threatening status epilepticus following gabapentin administration in a patient with benign adult familial myoclonic epilepsy. 124
Abnormal pattern of luteinizing hormone pulsatility in women with epilepsy. 124
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 124
Reflex seizures and reflex epilepsies: old models for understanding mechanisms of epileptogenesis. 124
The syndrome gelastic seizures-hypothalamic hamartoma: severe, potentially reversible encephalopathy. 123
The clinical spectrum and natural history of gelastic epilepsy-hypothalamic hamartoma syndrome 121
Autoantibodies to glutamic acid decarboxylase (GAD) in focal and generalized epilepsy: A study on 233 patients. 121
Dramatic response to levetiracetam in post-ischaemic Holmes' tremor. 121
A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms. 121
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 120
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization. 120
Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion. 120
Aspetti clinico-neuroradiologici e terapeutici dell’encefalopatia posteriore reversibile (PRES) 119
Refractory, life-threatening status epilepticus in a 3-year-old girl. 118
Unfavourable outcome of Hashimoto encephalopathy due to status epilepticus. One autopsy case. 117
Gelastic epilepsy: symptomatic and cryptogenic cases. 117
Children grow-up... 117
Insulinoma presenting as refractory late-onset epilepsy. 116
Posterior reversible encephalopathy syndrome (PRES) in critically ill obstetric patients. 114
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 114
Sudden death in Unverricht-Lundborg patients: is serotonin the key? 113
CHD2 mutations: Only epilepsy? Description of cognitive and behavioral profile in a case with a new mutation 112
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations 111
Paroxysmal dystonia in Behcet's disease. 111
Severe pulmonary congestion in a near miss at the first seizure: Further evidence for respiratory dysfunction in sudden unexpected death in epilepsy 111
A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy. 111
Use of Levetiracetam in patients with epilepsy and chronic liver disease | [Uso di Levetiracetam nei pazienti con epilessia ed epatopatia cronica: dati preliminari]. 111
Use of Levetiracetam plasma levels monitoring in the management of patients with epilepsy. 110
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations. 110
Levetiracetam in patients with epilepsy and chronic liver disease: observations in a case series. 109
Is epilepsy a real problem in multiple sclerosis patients? 109
Comment to: Diabetic hyperglycemia is associated with the severity of epileptic seizures in adults. 109
Hyperhomocysteinemia and retinal vascular changes in patients with epilepsy. 108
Suppression of myoclonus in SCA2 by piracetam. 108
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. 107
Re: Fame 3: a novel form of progressive myoclonus and epilepsy. 107
Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME. 106
Response to: 'Cortical tremor or cortical pseudotremor?'. 106
A unique case of "masturbatory" seizures in primary generalized epilepsy. 106
Eyelid myoclonia with absences: an overlooked epileptic syndrome? 105
A pilot open-label trial of zonisamide inUnverricht-Lundborg disease. 105
Benign intracranial hypertension of obese women. A twenty cases report. 105
Epilepsy, cerebral calcifications, and gluten-related disorders: Are anti-transglutaminase 6 antibodies the missing link? 105
Tiagabine in glial tumors. 104
Posterior reversible encephalopathy syndrome (PRES) in critically ill obstetric patients. 104
Frontotemporal dementia presenting as Gescwind's syndrome 104
New and investigational antiepileptic drugs. 104
Neurological features and long-term follow-up in 15q11.2-13.1 duplication. 104
Epilepsia partialis continua as a first symptom of multiple sclerosis: electrophysiological study of one case. 103
Is retinal assessment useful in epileptic patients with hyperhomocysteinemia? 103
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families. 102
Epileptogenesis due to peripheral injury as a cause of focal epilepsy. 101
Small hypothalamic hamartomas and gelastic seizures. 101
Progressive myoclonic ataxia associated to epileptic seizures, opsoclonus and optical atrophy. 101
Do gonadotropins play a role in catamenial epilepsy? | [Le gonadotropine ipofisarie hanno un ruolo nella patogenesi delle crisi catameniali?]. 101
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
Reproductive endocrine disorders in women with primary generalized epilepsy. 98
Chitosan may decrease serum valproate and increase the risk of seizure reappearance. 98
Cerebellar ataxia and hypogonadism. A clinicopathological report. 98
Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sisters. 97
Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy. 97
Lesional reflex epilepsy associated with the thought of food. 96
A proof-of-concept trial of the whey protein alfa-lactalbumin in chronic cortical myoclonus. 95
A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures 94
Cutis verticis gyrata--mental deficiency syndrome: a patient with drug-resistant epilepsy and polymicrogyria. 94
Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome. 93
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 93
Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome. 93
Facial myoclonus presenting as epilepsia partialis continua in a patient with an opercular lesion | [Epilessia Parziale Continua con mioclono faciale da lesione opercolare stabilizzata]. 93
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations. 93
Epilepsia partialis continua as a first symptom of multiple sclerosis: electrophysiological study of one case. 92
Disorders in cortical development and epilepsy - 13 years of experience 92
Topiramate-associated worsening symptoms in a patient with familial hemiplegic migraine 91
Familial cortical tremor and epilepsy: A well-defined syndrome with genetic heterogeneity waiting for nosological placement in the ILAE classification. 91
Posterior reversible encephalopathy syndrome in intensive care medicine. 91
Paroxysmal dystonia in Behçet's disease. 91
Gelastic seizures-hypothalamic hamartoma syndrome: study on five patients | [Sindrome crisi gelastiche-amartoma ipotalamico: studio di cinque casi]. 91
Neuroimaging follow-up in a case of Rasmussen's encephalitis with dyskinesias. 89
Fronto-temporal dementia presenting as Geschwind's syndrome. 89
Totale 11.400
Categoria #
all - tutte 66.976
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 66.976


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021153 0 0 0 0 0 0 0 0 0 0 142 11
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
2025/20269.753 1.193 662 898 945 1.808 440 1.222 557 1.346 587 95 0
Totale 20.950