IRIS
GROSSO, SALVATORE
 Distribuzione geografica
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Continente #
NA - Nord America 10.578
EU - Europa 6.809
AS - Asia 1.351
AF - Africa 18
OC - Oceania 17
SA - Sud America 11
Continente sconosciuto - Info sul continente non disponibili 4
Totale 18.788
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Nazione #
US - Stati Uniti d'America 10.548
GB - Regno Unito 1.588
IE - Irlanda 1.469
CN - Cina 883
UA - Ucraina 827
IT - Italia 642
RU - Federazione Russa 567
SE - Svezia 563
FR - Francia 378
DE - Germania 328
SG - Singapore 305
FI - Finlandia 278
TR - Turchia 61
ES - Italia 46
VN - Vietnam 42
BE - Belgio 33
CZ - Repubblica Ceca 29
CA - Canada 26
NL - Olanda 26
AU - Australia 16
IN - India 16
CI - Costa d'Avorio 12
HK - Hong Kong 9
JP - Giappone 7
RO - Romania 7
IR - Iran 6
KR - Corea 5
AE - Emirati Arabi Uniti 4
CL - Cile 4
HU - Ungheria 4
AR - Argentina 3
EU - Europa 3
IL - Israele 3
LV - Lettonia 3
PL - Polonia 3
AZ - Azerbaigian 2
EC - Ecuador 2
EE - Estonia 2
GR - Grecia 2
LT - Lituania 2
LU - Lussemburgo 2
MA - Marocco 2
NO - Norvegia 2
PA - Panama 2
SI - Slovenia 2
ZA - Sudafrica 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BR - Brasile 1
BS - Bahamas 1
CH - Svizzera 1
DK - Danimarca 1
EG - Egitto 1
ID - Indonesia 1
IM - Isola di Man 1
IQ - Iraq 1
JM - Giamaica 1
LA - Repubblica Popolare Democratica del Laos 1
MN - Mongolia 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
PE - Perù 1
PH - Filippine 1
PT - Portogallo 1
RS - Serbia 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
UZ - Uzbekistan 1
Totale 18.788
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Città #
Fairfield 1.788
Dublin 1.456
Southend 1.436
Ashburn 1.011
Woodbridge 835
Chandler 831
Seattle 737
Houston 715
Wilmington 679
Jacksonville 669
Cambridge 642
Ann Arbor 507
Princeton 298
Singapore 242
Nanjing 223
Siena 165
Helsinki 146
Beijing 116
Boardman 115
San Diego 100
New York 85
Nanchang 79
Shenyang 74
San Mateo 73
Norwalk 68
Shanghai 56
Menlo Park 54
Izmir 47
Moscow 46
Málaga 44
Tianjin 42
Dong Ket 41
Milan 35
Rome 33
Hebei 32
Jiaxing 31
Zhengzhou 31
Florence 29
Changsha 28
Brno 27
Brussels 27
Jinan 25
London 25
Munich 24
San Francisco 23
Lancaster 22
Kunming 21
Ningbo 20
Hangzhou 18
Dearborn 17
Padova 16
Guangzhou 14
Santa Clara 14
Taizhou 13
Toronto 13
Abidjan 12
Los Angeles 12
Washington 12
Ottawa 11
Prescot 9
Redwood City 9
Tappahannock 9
Canberra 8
Fremont 8
Duncan 7
Kilburn 7
Naples 7
Nereto 7
Changchun 6
Dallas 6
Düsseldorf 6
Ferrara 6
Haikou 6
Hong Kong 6
Lanzhou 6
Mykolayiv 6
Perugia 6
Sesto Fiorentino 6
Waanrode 6
Bologna 5
Chiswick 5
Falls Church 5
Hounslow 5
Phoenix 5
Zanjan 5
Andover 4
Chicago 4
Columbus 4
Fort Worth 4
Lucca 4
Melbourne 4
Monte 4
Mountain View 4
Padula 4
Rimini 4
Venezia 4
Venice 4
Bergamo 3
Bolzano 3
Cagliari 3
Totale 14.229
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Nome #
MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotype 332
Chromosome 18 aberrations and epilepsy: a review 295
Drug Retention Rate and Predictive Factors of Drug Survival for Interleukin-1 Inhibitors in Systemic Juvenile Idiopathic Arthritis 266
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability. 252
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum 212
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene 200
Treatment options for periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome in children and adults: a narrative review 193
SCN1A mutation associated with atypical Panayiotopoulos syndrome 190
Massive lamotrigine poisoning. A case report 184
Chitotriosidase and soluble IL-2 receptor: comparison of two markers of sarcoidosis severity 179
Recurrent Miller Fisher syndrome in children 175
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 173
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age 169
Private inherited microdeletion/microduplications: implications in clinical practice 167
Precocious puberty with trisomy X syndrome 163
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy 161
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb 161
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features 157
Acute flaccid myelitis temporally associated with rhinovirus infection: just a coincidence? 157
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 156
De novo complete trisomy 5p clinical and neuroradiological findings 156
Hot water epilepsy and focal malformation of the parietal cortex development 155
Topiramate effects on plasma serotonin levels in children with epilepsy 150
Anticonvulsant drugs and hematological disease 149
Biological markers of oxidative stress in progressive muscular dystrophies: A preliminary study: 157 148
Oxidative stress in children affected by epileptic encephalopathies 147
Optic perineuritis: A further cause of visual loss and disc edema in children 147
2q24-q31 deletion: report of a case and review of the literature 146
Segregation analysis in typical absence epilepsy 143
Typical absence seizures associated with localization-related epilepsy: a clinical and electroencephalographic characterization 141
Refractory absence seizures: An Italian multicenter retrospective study 140
Serum levels of chitotriosidase as a marker of disease activity and clinical stage in sarcoidosis. 140
Aicardi syndrome with favorable outcome: case report and review 138
Efficacy and safety of topiramate in infants according to epilepsy syndromes 138
Transient neonatal hypothyroidism after gestational exposure to amiodarone: a follow-up of two cases 137
Thyroid function in small for gestational age newborns: A review 136
Zonisamide in children and young adults with refractory epilepsy: an open label, multicenter Italian study 133
Schinzel-Giedion syndrome: a further cause of West syndrome 133
Treating juvenile idiopathic arthritis (JIA)-related uveitis beyond TNF-α inhibition: a narrative review 133
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 132
Dexfenfluramine effective in drug-resistant temporal lobe epilepsy 131
Craniofacial dyssynostosis: case report and review 131
Long-term outcome of epilepsy in patients with Prader-Willi syndrome 131
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome 131
Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy 130
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 130
Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation 129
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 129
Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations 128
Lamotrigine in typical absence epilepsy 128
Central precocious puberty and abnormal chromosomal patterns 127
Epilepsy in neurofibromatosis 1 126
Lacosamide in children with refractory status epilepticus. A multicenter Italian experience 125
Simultaneous onset of infantile spasms in monozygotic twins 125
Valproate in adolescents with photosensitive epilepsy with generalized tonic-clonic seizures only 125
Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication 124
Linear scleroderma associated with progressive brain atrophy 124
Brain mitochondrial impairment in ethylmalonic encephalopathy 123
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review 122
Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype. 122
Chitotriosidase activity in the serum of patients with sarcoidosis and pulmonary tuberculosis 122
Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsy 121
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? 121
Late-onset childhood occipital epilepsy(Gastaut type): a family study 121
Lacosamide efficacy in epileptic syndromes with continuous spike and waves during slow sleep (CSWS) 120
Growth hormone secretion in Prader-Willi syndrome 120
Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature 120
Long-term prognosis of patients with Ehlers-Danlos syndrome and epilepsy 120
Diagnosis of Angelman syndrome: clinical and EEG criteria 120
Multiple neuroendocrine disorder in Salla disease 120
Alternating hemiplegia of childhood or Hashimoto’s encephalopathy? 120
Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalities 119
Plasmapheresis in a child affected by acute disseminated encephalomyelitis 119
Folate receptor alpha defect causes cerebral folate transport deficiency a treatable neurodegenerative disorder associated with disturbed myelin metabolism 119
null 118
Bathing epilepsy: report of two Caucasian cases 118
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy 118
Efficacy and tolerability of add-on Lacosamide in children with Lennox-Gastaut syndrome 118
Chitotriosidase activity in patients with interstitial lung disesaes 117
Childhood absence epilepsy: evolution and prognostic factors 117
Endocrine disorders in two sisters affected by MELAS syndrome 117
Levetiracetam monotherapy for children and adolescents with benign rolandic seizures 116
Epilepsy in Prader-Willi syndrome: clinical, diagnostic and treatment aspects 116
Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism 116
Inter-ictal and post-ictal circulating levels of allopregnanolone, an anticonvulsant metabolite of progesterone, in epileptic children 116
Subcortical low-intensity and restricted diffusion after first seizure in a child 115
Efficacy and tolerability of add-on lacosamide in children with Lennox-Gastaut syndrome 115
Pubertal disorders in inv dup(15) syndrome 114
A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood 114
Withdrawal of antiepileptic drugs: guidelines of the Italian League Against Epilepsy 114
Elettroencephalographic and epileptic patterns in x chromosome anomalies 113
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 113
Body mass index and serum lipid changes during treatment with valproic acid in children with epilepsy 113
Long term outcome in children affected by absence epilepsy with onset before the age of three years 111
Epilepsy in Menkes disease An electroclinical long-term study of 28 patients 110
Efficacy and safety of rufinamide in children under four years of age with drug-resistant epilepsies 110
Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy 109
Epilepsy and vaccinations: Italian guidelines 109
Photoparoxysmal responses in children with chromosomal aberrations 108
Reflex myoclonic epilepsy in infancy: a multicenter clinical study 108
Totale 13.970
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Categoria #
all - tutte 70.588
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 70.588
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.594 0 0 0 0 327 313 319 521 468 293 103 250
2020/20213.305 114 420 193 389 163 349 94 436 201 341 444 161
2021/20221.865 99 217 103 78 32 84 80 188 153 178 163 490
2022/20232.879 169 269 375 375 288 572 51 242 327 74 79 58
2023/20242.127 93 61 189 128 58 595 770 26 10 32 24 141
2024/20251.136 125 230 465 252 64 0 0 0 0 0 0 0
Totale 19.073