IRIS
STRIANO, SALVATORE
 Distribuzione geografica
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Continente #
NA - Nord America 3.617
EU - Europa 1.767
AS - Asia 1.712
AF - Africa 20
SA - Sud America 14
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 7.136
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Nazione #
US - Stati Uniti d'America 3.501
SG - Singapore 778
CN - Cina 536
IT - Italia 408
HK - Hong Kong 337
SE - Svezia 266
FI - Finlandia 263
UA - Ucraina 195
NL - Olanda 181
IE - Irlanda 178
DE - Germania 131
CA - Canada 112
GB - Regno Unito 70
IN - India 21
RU - Federazione Russa 21
CI - Costa d'Avorio 17
IR - Iran 17
FR - Francia 14
BR - Brasile 12
BE - Belgio 9
RO - Romania 7
BG - Bulgaria 6
ES - Italia 5
TR - Turchia 5
VN - Vietnam 5
EU - Europa 4
JP - Giappone 4
KR - Corea 4
MX - Messico 4
CH - Svizzera 3
KE - Kenya 3
AE - Emirati Arabi Uniti 2
AR - Argentina 2
AU - Australia 2
CZ - Repubblica Ceca 2
HU - Ungheria 2
RS - Serbia 2
SM - San Marino 2
GR - Grecia 1
ID - Indonesia 1
JO - Giordania 1
LV - Lettonia 1
TH - Thailandia 1
Totale 7.136
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Città #
Singapore 654
Chandler 533
Hong Kong 335
Millbury 251
Jacksonville 246
Princeton 235
Nanjing 184
Santa Clara 182
Amsterdam 170
Boston 131
Woodbridge 116
Wilmington 109
Ottawa 97
Ashburn 83
Beijing 78
Ann Arbor 63
Norwalk 61
Naples 60
Nanchang 59
Boardman 55
Falls Church 52
Kronberg 52
Houston 45
Napoli 40
Shenyang 37
Hebei 36
Jiaxing 35
Milan 31
Seattle 24
Tianjin 22
Changsha 19
Rome 19
San Mateo 16
Kunming 15
Helsinki 14
Ardabil 13
Toronto 12
Des Moines 11
Leawood 11
Fairfield 10
Augusta 8
Indiana 8
Redmond 7
Bologna 6
Falkenstein 6
Lanzhou 6
Munich 6
New York 6
Sofia 6
Atripalda 5
Guangzhou 5
Hangzhou 5
Orange 5
Shanghai 5
Columbus 4
Dong Ket 4
Fremont 4
London 4
Monmouth Junction 4
Mumbai 4
Oviedo 4
Padova 4
Piemonte 4
San Francisco 4
Sheffield 4
Tappahannock 4
Timisoara 4
Turin 4
Waanrode 4
West Jordan 4
Brussels 3
Caserta 3
Castel San Giorgio 3
Cecina 3
Changchun 3
Dalmine 3
Göteborg 3
Lawrence 3
Los Angeles 3
Moscow 3
Mountain View 3
Nairobi 3
Redwood City 3
Tokyo 3
Valdagno 3
Zhengzhou 3
Avigliano 2
Belgrade 2
Bronte 2
Buenos Aires 2
Buffalo 2
Caldogno 2
Cambridge 2
Castelnuovo Rangone 2
Clifton 2
Cologne 2
Courcelles 2
Dorking 2
Dublin 2
Fort Worth 2
Totale 4.440
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Nome #
(1)H-MR spectroscopy indicates prominent cerebellar dysfunction in benign adult familial myoclonic epilepsy. 127
GLUTAMIC ACID DECARBOXYLASE ANTIBODIES IN IDIOPATHIC GENERALIZED EPILEPSY AND TYPE 1 DIABETES. 107
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome). 73
The spectrum and the natural history of gelastic seizures-hypothalamic hamartoma syndrome | [Lo spettro e la storia naturale della sindrome epilessia gelastica-amartoma ipotalamico]. 70
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. 66
22-year-old girl with status epilepticus and progressive neurological symptoms. 65
A unique case of "masturbatory" seizures in primary generalized epilepsy. 57
Diagnostic implications of genetic copy number variation in epilepsy plus 56
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy. 53
A pilot open-label trial of zonisamide in Unverricht-Lundborg disease. 53
Characterization of reproductive endocrine disorders in women with epilepsy. 51
Limited place for plasma monitoring of new antiepileptic drugs in clinical practice. 51
CHD2 mutations: Only epilepsy? Description of cognitive and behavioral profile in a case with a new mutation 51
A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures 50
Children grow-up... 50
Comment to: Diabetic hyperglycemia is associated with the severity of epileptic seizures in adults. 50
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. 49
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families. 49
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families. 49
Insulinoma presenting as refractory late-onset epilepsy. 49
A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2. 48
Severe pulmonary congestion in a near miss at the first seizure: Further evidence for respiratory dysfunction in sudden unexpected death in epilepsy 48
A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms. 48
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations 47
Epileptic seizures in multiple sclerosis: clinical and EEG correlations. 47
Use of Levetiracetam plasma levels monitoring in the management of patients with epilepsy. 47
Inherited neuromyotonia: A clinical and genetic study of a family. 45
Sudden death in Unverricht-Lundborg patients: is serotonin the key? 45
Hyperhomocysteinemia and retinal vascular changes in patients with epilepsy. 45
22-year-old girl with status epilepticus and progressive neurological symptoms. 45
Epileptic myoclonus as ciprofloxacin-associated adverse effect. 44
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. 44
Lateralizing value of the auditory aura in partial seizures. 44
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins. 44
Eyelid myoclonia with absences: an overlooked epileptic syndrome? 44
ACTH treatment in electrical status epilepticus during sleep (ESES) | [L'ACTH NEL TRATTAMENTO DELLO STATO DI MALE ELETTRICO DURANTE IL SONNO]. 44
Characterization of reproductive endocrine disorders in women with epilepsy. 43
Comment to: Status epilepticus induced by star fruit intoxication in patients with chronic renal disease. 43
Response to: 'Cortical tremor or cortical pseudotremor?'. 43
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 43
Familial cortical tremor and epilepsy: A well-defined syndrome with genetic heterogeneity waiting for nosological placement in the ILAE classification. 42
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy. 41
A t(4;9)(q34;p22) translocation associated with partial epilepsy, mental retardation, and dysmorphism. 41
Posterior reversible encephalopathy syndrome in intensive care medicine. 41
Refractory, life-threatening status epilepticus in a 3-year-old girl. 41
Gelastic seizures-hypothalamic hamartoma syndrome: study on five patients | [Sindrome crisi gelastiche-amartoma ipotalamico: studio di cinque casi]. 41
IDIOPATHIC PARTIAL EPILEPSY WITH AUDITORY FEATURES (IPEAF): A CLINICAL AND GENETIC STUDY OF 53 SPORADIC CASES 40
Abnormal pattern of luteinizing hormone pulsatility in women with epilepsy. 40
Levetiracetam in patients with epilepsy and chronic liver disease: observations in a case series. 40
Is epilepsy a real problem in multiple sclerosis patients? 40
Small hypothalamic hamartomas and gelastic seizures. 40
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations. 40
A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2. 40
Aspetti clinico-neuroradiologici e terapeutici dell’encefalopatia posteriore reversibile (PRES) 40
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations. 39
Prolonged Q-T interval syndrome presenting as idiopathic epilepsy. 39
New and investigational antiepileptic drugs. 39
A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy. 39
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases. 39
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 39
Relationship between serum mono-hydroxy-carbazepine concentrations and adverse effects in patients with epilepsy on high-dose oxcarbazepine therapy. 38
Re: Fame 3: a novel form of progressive myoclonus and epilepsy. 38
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 38
Adult onset Rasmussen’s Encephalitis: a case report. 38
Clinical and genetic findings in 26 Italian patients with Lafora disease. 37
Electroclinical and genetic findings in a family with cortical tremor, myoclonus, and epilepsy. 37
Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype. 37
Autoantibodies to glutamic acid decarboxylase (GAD) in focal and generalized epilepsy: A study on 233 patients. 37
The syndrome gelastic seizures-hypothalamic hamartoma: severe, potentially reversible encephalopathy. 37
A proof-of-concept trial of the whey protein alfa-lactalbumin in chronic cortical myoclonus. 37
Epileptic seizures can follow high doses of oral vardenafil. 36
Frontotemporal dementia presenting as Gescwind's syndrome 36
Hyperhomocysteinemia in epileptic patients on new antiepileptic drugs. 36
Chitosan may decrease serum valproate and increase the risk of seizure reappearance. 36
Clinical spectrum and critical care management of Posterior Reversible Encephalopathy Syndrome (PRES) 36
Unfavourable outcome of Hashimoto encephalopathy due to status epilepticus. One autopsy case. 35
Efficacy of levetiracetam in the treatment of drug-resistant Rett syndrome. 35
Epilepsy Syndromes in Development. Introduction. 35
An Unusual Case of Kleine-levin Syndrome Associated With Sleep Terrors 35
Cerebellar ataxia and hypogonadism. A clinicopathological report. 35
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 35
Posterior reversible encephalopathy syndrome (PRES) in critically ill obstetric patients. 34
The clinical spectrum and natural history of gelastic epilepsy-hypothalamic hamartoma syndrome 34
Conventional EEG in the differential diagnosis of dementia syndromes. 34
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 34
ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy. 34
Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy. 34
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing 33
Levetiracetam for cerebellar tremor in multiple sclerosis: an open-label pilot tolerability and efficacy study. 33
PRES: a dramatic but potentially reversible syndrome needing a prompt diagnosis. 33
Migraine and benign focal epilepsy with occipital paroxysms (BFEOP): two distinct nosographic entities or a pathological continuum? 33
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations. 33
Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion. 33
Typical progression of myoclonic epilepsy of the Lafora type: a case report 32
Epileptogenesis due to peripheral injury as a cause of focal epilepsy. 32
Progressive myoclonic ataxia associated to epileptic seizures, opsoclonus and optical atrophy. 32
Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome. 32
Suppression of myoclonus in SCA2 by piracetam. 32
Benign intracranial hypertension of obese women. A twenty cases report. 32
Vigabatrin in add-on therapy in partial, drug-resistant epilepsies. Are there any predictive criteria for its efficacy? 32
Totale 4.318
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Categoria #
all - tutte 35.518
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 35.518
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020195 0 0 0 0 0 0 2 1 3 35 91 63
2020/2021783 38 60 111 62 61 141 45 13 63 36 142 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
2024/20251.504 354 455 17 41 99 165 373 0 0 0 0 0
Totale 7.275