IRIS
STRIANO, PASQUALE
 Distribuzione geografica
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Continente #
NA - Nord America 1.539
AS - Asia 696
EU - Europa 691
AF - Africa 13
SA - Sud America 11
OC - Oceania 1
Totale 2.951
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Nazione #
US - Stati Uniti d'America 1.476
SG - Singapore 308
IT - Italia 229
CN - Cina 181
SE - Svezia 172
HK - Hong Kong 170
NL - Olanda 66
FI - Finlandia 65
CA - Canada 59
DE - Germania 57
IE - Irlanda 54
VN - Vietnam 17
GB - Regno Unito 13
CI - Costa d'Avorio 12
IN - India 11
RU - Federazione Russa 11
BR - Brasile 10
FR - Francia 7
UA - Ucraina 7
JP - Giappone 5
MX - Messico 4
BE - Belgio 3
RS - Serbia 2
AR - Argentina 1
AU - Australia 1
BY - Bielorussia 1
ES - Italia 1
IR - Iran 1
JO - Giordania 1
KR - Corea 1
LV - Lettonia 1
MA - Marocco 1
MK - Macedonia 1
SM - San Marino 1
TR - Turchia 1
Totale 2.951
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Città #
Chandler 313
Singapore 256
Hong Kong 170
Santa Clara 126
Amsterdam 63
Boston 59
Ottawa 58
Millbury 57
Princeton 57
Nanjing 55
Ashburn 50
Jacksonville 42
Kronberg 38
Boardman 37
Naples 35
Wilmington 35
Des Moines 24
Nanchang 23
Milan 21
Ann Arbor 20
Beijing 20
Lawrence 20
Falls Church 19
Norwalk 19
Woodbridge 18
Napoli 17
Dong Ket 16
Jiaxing 16
Houston 15
Rome 15
Seattle 12
Fairfield 10
Kunming 9
Shenyang 9
Helsinki 8
Tianjin 8
Hebei 7
Bologna 6
Borgosatollo 5
Changsha 5
Los Angeles 5
Redmond 5
Redwood City 5
Caserta 4
Catania 4
Hangzhou 4
Kagoya 4
Lappeenranta 4
Munich 4
Rimini 4
Shanghai 4
Tappahannock 4
West Jordan 4
Cambridge 3
Castellarano 3
Coyoacán 3
Falkenstein 3
Nancy 3
New York 3
Belgrade 2
Bronte 2
Chengdu 2
Cologne 2
Dublin 2
Formia 2
Fort Worth 2
Lanzhou 2
London 2
Monterotondo 2
Montesilvano Marina 2
Moscow 2
Nuremberg 2
Pomezia 2
Ravenna 2
San Mateo 2
Sassari 2
Selargius 2
Siracusa 2
Verona 2
Waanrode 2
Wuhan 2
Zhengzhou 2
Acerra 1
Afragola 1
Akron 1
Amman 1
Asti 1
Atlanta 1
Avigliano 1
Bedizzole 1
Brussels 1
Capodrise 1
Castelnuovo Rangone 1
Cesa 1
Changchun 1
Concordia 1
Crown Point 1
Edinburgh 1
Frankfurt am Main 1
Fremont 1
Totale 1.930
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Nome #
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome). 73
22-year-old girl with status epilepticus and progressive neurological symptoms. 65
Diagnostic implications of genetic copy number variation in epilepsy plus 56
A pilot open-label trial of zonisamide in Unverricht-Lundborg disease. 53
Limited place for plasma monitoring of new antiepileptic drugs in clinical practice. 51
Children grow-up... 50
Comment to: Diabetic hyperglycemia is associated with the severity of epileptic seizures in adults. 50
Diagnosis and management of type 1 sialidosis: Clinical insights from long-term care of four unrelated patients 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
Insulinoma presenting as refractory late-onset epilepsy. 49
Severe pulmonary congestion in a near miss at the first seizure: Further evidence for respiratory dysfunction in sudden unexpected death in epilepsy 48
Epileptic seizures in multiple sclerosis: clinical and EEG correlations. 47
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. 46
KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum. 46
Sudden death in Unverricht-Lundborg patients: is serotonin the key? 45
Hyperhomocysteinemia and retinal vascular changes in patients with epilepsy. 45
Genotype-phenotype spectrum and correlations in Xia-Gibbs syndrome: Report of five novel cases and literature review 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
Comment to: Status epilepticus induced by star fruit intoxication in patients with chronic renal disease. 43
Response to: 'Cortical tremor or cortical pseudotremor?'. 43
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 43
Familial cortical tremor and epilepsy: A well-defined syndrome with genetic heterogeneity waiting for nosological placement in the ILAE classification. 42
Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants 42
Posterior reversible encephalopathy syndrome in intensive care medicine. 41
Refractory, life-threatening status epilepticus in a 3-year-old girl. 41
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox-Gastaut Syndrome. 41
Is epilepsy a real problem in multiple sclerosis patients? 40
Small hypothalamic hamartomas and gelastic seizures. 40
Abnormal sensorimotor cortex and thalamo-cortical networks in familial adult myoclonic epilepsy type 2: pathophysiology and diagnostic implications 40
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
Re: Fame 3: a novel form of progressive myoclonus and epilepsy. 38
The spectrum of intermediate SCN8A-related epilepsy 38
The syndrome gelastic seizures-hypothalamic hamartoma: severe, potentially reversible encephalopathy. 37
Cortical tremor: a tantalizing conundrum between cortex and cerebellum 37
Chitosan may decrease serum valproate and increase the risk of seizure reappearance. 36
Efficacy of levetiracetam in the treatment of drug-resistant Rett syndrome. 35
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 35
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
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
Temporal-parietal-occipital epilepsy in GEFS+ associated with SCN1A mutation 33
Lesional reflex epilepsy associated with the thought of food. 31
Comment on "Factors influencing clinical features of absence seizures". 31
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 31
Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME. 30
Epileptogenesis due to peripheral injury as a cause of focal epilepsy. 30
Cyclic Vomiting Syndrome in Children 30
Eyelid fluttering, typical EEG pattern, and impaired intellectual function: a homogeneous epileptic condition among the patients presenting with eyelid myoclonia. 29
Neurological features and long-term follow-up in 15q11.2-13.1 duplication. 29
Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations 29
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 29
Is retinal assessment useful in epileptic patients with hyperhomocysteinemia? 27
Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors 27
Gabapentin: a Ca2+ channel alpha 2-delta ligand far beyond epilepsy therapy. 26
Clinical spectrum and critical care management of posterior reversible encephalopathy syndrome (PRES) 26
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies. 26
Cannabidiol in Pharmacoresistant Epilepsy: Clinical Pharmacokinetic Data From an Expanded Access Program 25
Effects of three-months folate supplementation on early vascular abnormalities in hyperhomocysteinemic patients with epilepsy 24
Novel biallelic variants expand the phenotype of NAA20-related syndrome 24
Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences 24
Transient epileptic amnesia: a new epileptic syndrome in development? 23
Psychiatric features in gelastic epilepsy and hypothalamic hamartoma: long-term psychodiagnostic observations. 22
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients 21
Myoclonus: Differential diagnosis and current management 20
Typical progression of myoclonic epilepsy of the Lafora type: a case report. 20
Reflex myoclonic epilepsy in infancy: A multicenter clinical study. 20
Epilepsy and multiple sclerosis: Review of literature and our epilepsy center's experience 19
Topiramate-associated worsening symptoms in a patient with familial hemiplegic migraine 18
LGI1 microdeletion in autosomal dominant lateral temporal epilepsy. 18
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus 17
Spectrum of epilepsy with eyelid myoclonia: Delineation of disease subtypes from a large multicenter study 16
Epilepsy Course and Developmental Trajectories in STXBP1 -DEE 16
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis 16
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy 15
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing 15
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine 15
Epileptic myoclonus as ciprofloxacin-associated adverse effect [8] 14
Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death. 14
An Italian consensus on the management of Lennox-Gastaut syndrome 13
Reply to "Epilepsies in children--the power of making a syndrome diagnosis". 13
West syndrome associated with 14q12 duplications harboring FOXG1 13
Erratum: Posterior reversible encephalopathy syndrome and spinal epidural haematoma in a hypertensive patient (European Journal of Anaesthesiology (2007) 21 (1065-1067)) 13
Clinical features and genotype–phenotype correlations in epilepsy patients with de novo DYNC1H1 variants 12
Posterior reversible encephalopathy syndrome (PRES) in the parturient with preeclampsia after inadvertent dural puncture 12
Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbidities 11
Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia 11
Electroencephalographic features in dravet syndrome: five-year follow-up study in 22 patients 11
Perampanel as precision therapy in rare genetic epilepsies 11
Space-borne DInSAR measurements exploitation for risk classification of bridge networks 10
Epidemiology and familial clustering of pediatric epilepsy in the geographic isolate of Ischia 10
National scale full-resolution P-SBAS processing for the investigation of critical infrastructure deformations related to the built-up environment  8
Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical Development 8
First and Second Generation Cosmo-Skymed Advanced Dinsar Processing for Investigating Deformations Affecting The Built-up Environment 8
Epilepsy, EEG and chromosomal rearrangements 7
Totale 3.061
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Categoria #
all - tutte 14.962
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 14.962
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202045 0 0 0 0 0 0 3 0 0 10 27 5
2020/2021309 19 19 64 36 25 51 4 0 26 21 24 20
2021/2022528 62 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
2024/2025775 151 150 11 26 77 169 191 0 0 0 0 0
Totale 3.081