IRIS
STRIANO, SALVATORE
 Distribuzione geografica
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Continente #
NA - Nord America 3.069
EU - Europa 1.649
AS - Asia 578
AF - Africa 20
SA - Sud America 12
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 5.334
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Nazione #
US - Stati Uniti d'America 2.959
CN - Cina 517
IT - Italia 349
SE - Svezia 266
FI - Finlandia 254
UA - Ucraina 195
IE - Irlanda 178
NL - Olanda 178
DE - Germania 120
CA - Canada 108
GB - Regno Unito 64
IN - India 19
CI - Costa d'Avorio 17
IR - Iran 16
BR - Brasile 10
FR - Francia 10
RO - Romania 7
BE - Belgio 6
BG - Bulgaria 6
SG - Singapore 5
TR - Turchia 5
VN - Vietnam 5
EU - Europa 4
KR - Corea 4
CH - Svizzera 3
KE - Kenya 3
RU - Federazione Russa 3
AE - Emirati Arabi Uniti 2
AR - Argentina 2
AU - Australia 2
HK - Hong Kong 2
HU - Ungheria 2
MX - Messico 2
RS - Serbia 2
SM - San Marino 2
CZ - Repubblica Ceca 1
ES - Italia 1
GR - Grecia 1
ID - Indonesia 1
JP - Giappone 1
LV - Lettonia 1
TH - Thailandia 1
Totale 5.334
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Città #
Chandler 533
Millbury 251
Jacksonville 246
Princeton 235
Nanjing 184
Amsterdam 170
Boston 131
Woodbridge 116
Wilmington 109
Ottawa 96
Ashburn 80
Beijing 78
Ann Arbor 63
Norwalk 61
Nanchang 59
Naples 56
Boardman 55
Falls Church 52
Kronberg 52
Houston 45
Napoli 40
Shenyang 37
Hebei 36
Jiaxing 35
Tianjin 22
Changsha 19
Milan 17
San Mateo 16
Kunming 15
Ardabil 13
Des Moines 11
Leawood 11
Rome 11
Fairfield 10
Seattle 10
Toronto 9
Augusta 8
Indiana 8
Redmond 7
Bologna 6
Lanzhou 6
New York 6
Sofia 6
Atripalda 5
Guangzhou 5
Helsinki 5
Orange 5
Dong Ket 4
Fremont 4
Hangzhou 4
London 4
Monmouth Junction 4
Padova 4
Piemonte 4
Tappahannock 4
Timisoara 4
Turin 4
Waanrode 4
West Jordan 4
Caserta 3
Castel San Giorgio 3
Cecina 3
Changchun 3
Dalmine 3
Göteborg 3
Lawrence 3
Los Angeles 3
Mountain View 3
Mumbai 3
Nairobi 3
Redwood City 3
San Francisco 3
Shanghai 3
Avigliano 2
Belgrade 2
Buenos Aires 2
Buffalo 2
Caldogno 2
Cambridge 2
Castelnuovo Rangone 2
Cologne 2
Courcelles 2
Dorking 2
Dublin 2
Fort Worth 2
Geneva 2
Hong Kong 2
Jinan 2
Mexico 2
Moscow 2
Munich 2
Ningbo 2
Palermo 2
Parma 2
Philadelphia 2
Pomezia 2
Potenza 2
Pune 2
Ravenna 2
Salerno 2
Totale 3.195
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Nome #
(1)H-MR spectroscopy indicates prominent cerebellar dysfunction in benign adult familial myoclonic epilepsy. 121
GLUTAMIC ACID DECARBOXYLASE ANTIBODIES IN IDIOPATHIC GENERALIZED EPILEPSY AND TYPE 1 DIABETES. 65
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome). 64
22-year-old girl with status epilepticus and progressive neurological symptoms. 59
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. 52
The spectrum and the natural history of gelastic seizures-hypothalamic hamartoma syndrome | [Lo spettro e la storia naturale della sindrome epilessia gelastica-amartoma ipotalamico]. 48
A pilot open-label trial of zonisamide in Unverricht-Lundborg disease. 45
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy. 44
CHD2 mutations: Only epilepsy? Description of cognitive and behavioral profile in a case with a new mutation 44
Diagnostic implications of genetic copy number variation in epilepsy plus 44
Characterization of reproductive endocrine disorders in women with epilepsy. 43
Severe pulmonary congestion in a near miss at the first seizure: Further evidence for respiratory dysfunction in sudden unexpected death in epilepsy 43
Limited place for plasma monitoring of new antiepileptic drugs in clinical practice. 43
Children grow-up... 43
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families. 42
A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2. 41
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations 40
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. 40
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. 40
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families. 40
Comment to: Diabetic hyperglycemia is associated with the severity of epileptic seizures in adults. 40
A unique case of "masturbatory" seizures in primary generalized epilepsy. 40
Insulinoma presenting as refractory late-onset epilepsy. 39
Sudden death in Unverricht-Lundborg patients: is serotonin the key? 39
Hyperhomocysteinemia and retinal vascular changes in patients with epilepsy. 39
ACTH treatment in electrical status epilepticus during sleep (ESES) | [L'ACTH NEL TRATTAMENTO DELLO STATO DI MALE ELETTRICO DURANTE IL SONNO]. 39
Epileptic seizures in multiple sclerosis: clinical and EEG correlations. 38
Comment to: Status epilepticus induced by star fruit intoxication in patients with chronic renal disease. 38
Response to: 'Cortical tremor or cortical pseudotremor?'. 38
22-year-old girl with status epilepticus and progressive neurological symptoms. 38
Epileptic myoclonus as ciprofloxacin-associated adverse effect. 37
A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures 37
Inherited neuromyotonia: A clinical and genetic study of a family. 36
Characterization of reproductive endocrine disorders in women with epilepsy. 36
Familial cortical tremor and epilepsy: A well-defined syndrome with genetic heterogeneity waiting for nosological placement in the ILAE classification. 36
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins. 36
Levetiracetam in patients with epilepsy and chronic liver disease: observations in a case series. 35
Lateralizing value of the auditory aura in partial seizures. 35
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 35
A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms. 35
Abnormal pattern of luteinizing hormone pulsatility in women with epilepsy. 34
New and investigational antiepileptic drugs. 34
Refractory, life-threatening status epilepticus in a 3-year-old girl. 34
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy. 33
Prolonged Q-T interval syndrome presenting as idiopathic epilepsy. 33
Eyelid myoclonia with absences: an overlooked epileptic syndrome? 33
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 33
Use of Levetiracetam plasma levels monitoring in the management of patients with epilepsy. 33
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations. 32
IDIOPATHIC PARTIAL EPILEPSY WITH AUDITORY FEATURES (IPEAF): A CLINICAL AND GENETIC STUDY OF 53 SPORADIC CASES 32
Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype. 32
Relationship between serum mono-hydroxy-carbazepine concentrations and adverse effects in patients with epilepsy on high-dose oxcarbazepine therapy. 32
Posterior reversible encephalopathy syndrome in intensive care medicine. 32
Re: Fame 3: a novel form of progressive myoclonus and epilepsy. 32
Hyperhomocysteinemia in epileptic patients on new antiepileptic drugs. 32
Small hypothalamic hamartomas and gelastic seizures. 32
Aspetti clinico-neuroradiologici e terapeutici dell’encefalopatia posteriore reversibile (PRES) 32
A t(4;9)(q34;p22) translocation associated with partial epilepsy, mental retardation, and dysmorphism. 31
The syndrome gelastic seizures-hypothalamic hamartoma: severe, potentially reversible encephalopathy. 31
A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy. 31
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 31
Electroclinical and genetic findings in a family with cortical tremor, myoclonus, and epilepsy. 30
The clinical spectrum and natural history of gelastic epilepsy-hypothalamic hamartoma syndrome 30
Chitosan may decrease serum valproate and increase the risk of seizure reappearance. 30
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations. 30
Gelastic seizures-hypothalamic hamartoma syndrome: study on five patients | [Sindrome crisi gelastiche-amartoma ipotalamico: studio di cinque casi]. 30
Clinical and genetic findings in 26 Italian patients with Lafora disease. 29
Epileptic seizures can follow high doses of oral vardenafil. 29
Unfavourable outcome of Hashimoto encephalopathy due to status epilepticus. One autopsy case. 29
Frontotemporal dementia presenting as Gescwind's syndrome 29
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 29
Spinal muscular atrophy and progressive myoclonic epilepsy: one case report and characteristics of the epileptic syndrome. Seizure. 28
Posterior reversible encephalopathy syndrome (PRES) in critically ill obstetric patients. 28
Autoantibodies to glutamic acid decarboxylase (GAD) in focal and generalized epilepsy: A study on 233 patients. 28
PRES: a dramatic but potentially reversible syndrome needing a prompt diagnosis. 28
Eyelid fluttering, typical EEG pattern, and impaired intellectual function: a homogeneous epileptic condition among the patients presenting with eyelid myoclonia. 28
Comment on "Factors influencing clinical features of absence seizures". 28
A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2. 28
A proof-of-concept trial of the whey protein alfa-lactalbumin in chronic cortical myoclonus. 28
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 28
Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy. 28
Clinical spectrum and critical care management of Posterior Reversible Encephalopathy Syndrome (PRES) 28
Levetiracetam for cerebellar tremor in multiple sclerosis: an open-label pilot tolerability and efficacy study. 27
Efficacy of levetiracetam in the treatment of drug-resistant Rett syndrome. 27
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases. 27
Epileptogenesis due to peripheral injury as a cause of focal epilepsy. 26
A pilot open-label trial of zonisamide inUnverricht-Lundborg disease. 26
Conventional EEG in the differential diagnosis of dementia syndromes. 26
Benign intracranial hypertension of obese women. A twenty cases report. 26
Adult onset Rasmussen’s Encephalitis: a case report. 26
Typical progression of myoclonic epilepsy of the Lafora type: a case report 25
Is epilepsy a real problem in multiple sclerosis patients? 25
Cerebellar ataxia and hypogonadism. A clinicopathological report. 25
Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion. 25
Lesional reflex epilepsy associated with the thought of food. 24
Epilepsy Syndromes in Development. Introduction. 24
Suppression of myoclonus in SCA2 by piracetam. 24
An Unusual Case of Kleine-levin Syndrome Associated With Sleep Terrors 24
Vigabatrin in add-on therapy in partial, drug-resistant epilepsies. Are there any predictive criteria for its efficacy? 24
ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy. 24
Totale 3.484
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Categoria #
all - tutte 23.790
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 23.790
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201913 0 0 0 0 0 0 0 0 0 0 3 10
2019/2020633 319 33 42 2 39 3 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
2023/2024552 41 145 112 44 40 31 32 82 6 19 0 0
Totale 5.468