IRIS
STRIANO, PASQUALE
 Distribuzione geografica
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Continente #
NA - Nord America 1.474
EU - Europa 659
AS - Asia 475
AF - Africa 13
SA - Sud America 11
OC - Oceania 1
Totale 2.633
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Nazione #
US - Stati Uniti d'America 1.412
SG - Singapore 267
IT - Italia 223
SE - Svezia 172
CN - Cina 169
NL - Olanda 64
CA - Canada 59
FI - Finlandia 57
IE - Irlanda 54
DE - Germania 52
VN - Vietnam 17
GB - Regno Unito 13
CI - Costa d'Avorio 12
IN - India 11
BR - Brasile 10
FR - Francia 7
UA - Ucraina 7
JP - Giappone 5
MX - Messico 3
BE - Belgio 2
HK - Hong Kong 2
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
RU - Federazione Russa 1
SM - San Marino 1
TR - Turchia 1
Totale 2.633
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Città #
Chandler 313
Singapore 215
Santa Clara 102
Amsterdam 62
Boston 59
Ottawa 58
Millbury 57
Princeton 57
Nanjing 55
Ashburn 49
Jacksonville 42
Kronberg 38
Boardman 37
Wilmington 35
Naples 34
Des Moines 24
Nanchang 23
Ann Arbor 20
Lawrence 20
Milan 20
Falls Church 19
Norwalk 19
Beijing 18
Woodbridge 18
Napoli 17
Dong Ket 16
Jiaxing 16
Houston 15
Rome 12
Fairfield 10
Kunming 9
Shenyang 9
Tianjin 8
Hebei 7
Bologna 6
Borgosatollo 5
Changsha 5
Los Angeles 5
Redmond 5
Redwood City 5
Seattle 5
Caserta 4
Catania 4
Kagoya 4
Lappeenranta 4
Munich 4
Rimini 4
Tappahannock 4
West Jordan 4
Cambridge 3
Castellarano 3
Coyoacán 3
Hangzhou 3
Nancy 3
New York 3
Belgrade 2
Bronte 2
Chengdu 2
Cologne 2
Dublin 2
Formia 2
Fort Worth 2
Hong Kong 2
Lanzhou 2
London 2
Monterotondo 2
Montesilvano Marina 2
Pomezia 2
Ravenna 2
San Mateo 2
Sassari 2
Selargius 2
Shanghai 2
Siracusa 2
Verona 2
Waanrode 2
Wuhan 2
Acerra 1
Afragola 1
Akron 1
Amman 1
Asti 1
Atlanta 1
Avigliano 1
Bedizzole 1
Capodrise 1
Castelnuovo Rangone 1
Cesa 1
Changchun 1
Concordia 1
Crown Point 1
Edinburgh 1
Frankfurt am Main 1
Fremont 1
Giulianova 1
Gloucester 1
Grosseto 1
Hanoi 1
Islington 1
Istanbul 1
Totale 1.666
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Nome #
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome). 69
22-year-old girl with status epilepticus and progressive neurological symptoms. 62
Diagnostic implications of genetic copy number variation in epilepsy plus 52
A pilot open-label trial of zonisamide in Unverricht-Lundborg disease. 50
Limited place for plasma monitoring of new antiepileptic drugs in clinical practice. 48
Children grow-up... 47
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. 46
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families. 46
Insulinoma presenting as refractory late-onset epilepsy. 46
Severe pulmonary congestion in a near miss at the first seizure: Further evidence for respiratory dysfunction in sudden unexpected death in epilepsy 45
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. 45
Comment to: Diabetic hyperglycemia is associated with the severity of epileptic seizures in adults. 45
Epileptic seizures in multiple sclerosis: clinical and EEG correlations. 43
Sudden death in Unverricht-Lundborg patients: is serotonin the key? 43
Hyperhomocysteinemia and retinal vascular changes in patients with epilepsy. 43
Comment to: Status epilepticus induced by star fruit intoxication in patients with chronic renal disease. 43
Diagnosis and management of type 1 sialidosis: Clinical insights from long-term care of four unrelated patients 43
KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum. 42
Genotype-phenotype spectrum and correlations in Xia-Gibbs syndrome: Report of five novel cases and literature review 41
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins. 41
Response to: 'Cortical tremor or cortical pseudotremor?'. 41
Lateralizing value of the auditory aura in partial seizures. 39
Familial cortical tremor and epilepsy: A well-defined syndrome with genetic heterogeneity waiting for nosological placement in the ILAE classification. 39
Eyelid myoclonia with absences: an overlooked epileptic syndrome? 39
Refractory, life-threatening status epilepticus in a 3-year-old girl. 38
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 38
New and investigational antiepileptic drugs. 37
Is epilepsy a real problem in multiple sclerosis patients? 37
A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy. 37
Small hypothalamic hamartomas and gelastic seizures. 37
Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants 37
Abnormal sensorimotor cortex and thalamo-cortical networks in familial adult myoclonic epilepsy type 2: pathophysiology and diagnostic implications 37
Posterior reversible encephalopathy syndrome in intensive care medicine. 36
Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases. 36
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox-Gastaut Syndrome. 36
Re: Fame 3: a novel form of progressive myoclonus and epilepsy. 35
The syndrome gelastic seizures-hypothalamic hamartoma: severe, potentially reversible encephalopathy. 35
The spectrum of intermediate SCN8A-related epilepsy 34
Cortical tremor: a tantalizing conundrum between cortex and cerebellum 34
Efficacy of levetiracetam in the treatment of drug-resistant Rett syndrome. 32
Chitosan may decrease serum valproate and increase the risk of seizure reappearance. 32
Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy. 32
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 31
Comment on "Factors influencing clinical features of absence seizures". 30
Epileptogenesis due to peripheral injury as a cause of focal epilepsy. 30
Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion. 30
Eyelid fluttering, typical EEG pattern, and impaired intellectual function: a homogeneous epileptic condition among the patients presenting with eyelid myoclonia. 29
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing 28
Lesional reflex epilepsy associated with the thought of food. 28
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 28
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 28
Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME. 27
Is retinal assessment useful in epileptic patients with hyperhomocysteinemia? 27
Gabapentin: a Ca2+ channel alpha 2-delta ligand far beyond epilepsy therapy. 26
Neurological features and long-term follow-up in 15q11.2-13.1 duplication. 25
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations. 25
Temporal-parietal-occipital epilepsy in GEFS+ associated with SCN1A mutation 25
Cyclic Vomiting Syndrome in Children 25
Clinical spectrum and critical care management of posterior reversible encephalopathy syndrome (PRES) 23
Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors 23
Cannabidiol in Pharmacoresistant Epilepsy: Clinical Pharmacokinetic Data From an Expanded Access Program 23
Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations 22
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies. 22
Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences 22
Transient epileptic amnesia: a new epileptic syndrome in development? 21
Effects of three-months folate supplementation on early vascular abnormalities in hyperhomocysteinemic patients with epilepsy 20
Psychiatric features in gelastic epilepsy and hypothalamic hamartoma: long-term psychodiagnostic observations. 20
Novel biallelic variants expand the phenotype of NAA20-related syndrome 19
Reflex myoclonic epilepsy in infancy: A multicenter clinical study. 18
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients 18
Topiramate-associated worsening symptoms in a patient with familial hemiplegic migraine 17
Typical progression of myoclonic epilepsy of the Lafora type: a case report. 17
LGI1 microdeletion in autosomal dominant lateral temporal epilepsy. 17
Epilepsy and multiple sclerosis: Review of literature and our epilepsy center's experience 17
Myoclonus: Differential diagnosis and current management 16
Spectrum of epilepsy with eyelid myoclonia: Delineation of disease subtypes from a large multicenter study 13
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine 13
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing 12
Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death. 12
West syndrome associated with 14q12 duplications harboring FOXG1 12
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis 12
Erratum: Posterior reversible encephalopathy syndrome and spinal epidural haematoma in a hypertensive patient (European Journal of Anaesthesiology (2007) 21 (1065-1067)) 12
Epileptic myoclonus as ciprofloxacin-associated adverse effect [8] 11
Posterior reversible encephalopathy syndrome (PRES) in the parturient with preeclampsia after inadvertent dural puncture 11
Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbidities 10
Electroencephalographic features in dravet syndrome: five-year follow-up study in 22 patients 10
An Italian consensus on the management of Lennox-Gastaut syndrome 10
Epilepsy Course and Developmental Trajectories in STXBP1 -DEE 10
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus 10
Reply to "Epilepsies in children--the power of making a syndrome diagnosis". 10
Epidemiology and familial clustering of pediatric epilepsy in the geographic isolate of Ischia 10
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy 9
Clinical features and genotype–phenotype correlations in epilepsy patients with de novo DYNC1H1 variants 8
Space-borne DInSAR measurements exploitation for risk classification of bridge networks 7
Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia 7
A solved puzzle: Familial adult myoclonus epilepsy is a new expansion repeats disorder 7
Perampanel as precision therapy in rare genetic epilepsies 7
First and Second Generation Cosmo-Skymed Advanced Dinsar Processing for Investigating Deformations Affecting The Built-up Environment 5
National scale full-resolution P-SBAS processing for the investigation of critical infrastructure deformations related to the built-up environment  4
Epilepsy, EEG and chromosomal rearrangements 4
Totale 2.751
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Categoria #
all - tutte 13.730
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 13.730
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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
2024/2025454 151 150 11 26 77 39 0 0 0 0 0 0
Totale 2.760