IRIS
GROSSO, SALVATORE
 Distribuzione geografica
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Continente #
NA - Nord America 10.476
EU - Europa 6.355
AS - Asia 1.132
OC - Oceania 17
SA - Sud America 7
Continente sconosciuto - Info sul continente non disponibili 4
AF - Africa 2
Totale 17.993
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Nazione #
US - Stati Uniti d'America 10.452
GB - Regno Unito 1.585
IE - Irlanda 1.468
CN - Cina 862
UA - Ucraina 826
IT - Italia 598
SE - Svezia 563
FR - Francia 378
DE - Germania 314
FI - Finlandia 274
RU - Federazione Russa 192
SG - Singapore 115
TR - Turchia 61
ES - Italia 46
VN - Vietnam 41
BE - Belgio 33
CZ - Repubblica Ceca 29
NL - Olanda 23
CA - Canada 20
AU - Australia 16
IN - India 15
HK - Hong Kong 9
IR - Iran 6
RO - Romania 6
KR - Corea 5
JP - Giappone 4
AE - Emirati Arabi Uniti 3
EU - Europa 3
AZ - Azerbaigian 2
CL - Cile 2
EC - Ecuador 2
EE - Estonia 2
GR - Grecia 2
HU - Ungheria 2
IL - Israele 2
LT - Lituania 2
PA - Panama 2
PL - Polonia 2
SI - Slovenia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AR - Argentina 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
LU - Lussemburgo 1
LV - Lettonia 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
Totale 17.993
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Città #
Fairfield 1.788
Dublin 1.455
Southend 1.436
Ashburn 1.009
Woodbridge 835
Chandler 831
Seattle 737
Houston 715
Wilmington 679
Jacksonville 669
Cambridge 642
Ann Arbor 507
Princeton 298
Nanjing 223
Siena 153
Helsinki 142
Beijing 116
Boardman 115
San Diego 100
New York 84
Nanchang 79
Shenyang 74
San Mateo 73
Singapore 73
Norwalk 68
Menlo Park 54
Shanghai 53
Izmir 47
Moscow 46
Málaga 44
Tianjin 42
Dong Ket 41
Hebei 32
Jiaxing 31
Zhengzhou 31
Florence 29
Milan 29
Changsha 28
Brno 27
Brussels 27
Jinan 25
Rome 24
London 23
San Francisco 23
Lancaster 22
Kunming 21
Ningbo 20
Hangzhou 18
Dearborn 17
Padova 16
Taizhou 13
Guangzhou 12
Washington 12
Munich 10
Ottawa 9
Prescot 9
Redwood City 9
Tappahannock 9
Toronto 9
Canberra 8
Fremont 8
Duncan 7
Kilburn 7
Nereto 7
Changchun 6
Dallas 6
Düsseldorf 6
Haikou 6
Hong Kong 6
Lanzhou 6
Los Angeles 6
Mykolayiv 6
Perugia 6
Sesto Fiorentino 6
Waanrode 6
Chiswick 5
Falls Church 5
Hounslow 5
Naples 5
Phoenix 5
Zanjan 5
Andover 4
Bologna 4
Chicago 4
Ferrara 4
Lucca 4
Melbourne 4
Monte 4
Mountain View 4
Padula 4
Venezia 4
Venice 4
Bergamo 3
Bolzano 3
Cagliari 3
Cassino 3
Città di Castello 3
Cossato 3
Elk Grove 3
Falkenstein 3
Totale 13.964
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Nome #
MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotype 304
Chromosome 18 aberrations and epilepsy: a review 288
Drug Retention Rate and Predictive Factors of Drug Survival for Interleukin-1 Inhibitors in Systemic Juvenile Idiopathic Arthritis 261
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability. 245
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum 206
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene 193
Treatment options for periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome in children and adults: a narrative review 191
SCN1A mutation associated with atypical Panayiotopoulos syndrome 188
Massive lamotrigine poisoning. A case report 181
Recurrent Miller Fisher syndrome in children 170
Chitotriosidase and soluble IL-2 receptor: comparison of two markers of sarcoidosis severity 169
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 167
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age 162
Private inherited microdeletion/microduplications: implications in clinical practice 161
Precocious puberty with trisomy X syndrome 158
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy 157
Acute flaccid myelitis temporally associated with rhinovirus infection: just a coincidence? 152
De novo complete trisomy 5p clinical and neuroradiological findings 150
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features 150
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb 150
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 149
Hot water epilepsy and focal malformation of the parietal cortex development 149
Topiramate effects on plasma serotonin levels in children with epilepsy 148
Anticonvulsant drugs and hematological disease 146
Optic perineuritis: A further cause of visual loss and disc edema in children 144
Biological markers of oxidative stress in progressive muscular dystrophies: A preliminary study: 157 144
Oxidative stress in children affected by epileptic encephalopathies 142
2q24-q31 deletion: report of a case and review of the literature 141
Segregation analysis in typical absence epilepsy 137
Refractory absence seizures: An Italian multicenter retrospective study 136
Typical absence seizures associated with localization-related epilepsy: a clinical and electroencephalographic characterization 136
Serum levels of chitotriosidase as a marker of disease activity and clinical stage in sarcoidosis. 134
Transient neonatal hypothyroidism after gestational exposure to amiodarone: a follow-up of two cases 132
Aicardi syndrome with favorable outcome: case report and review 132
Efficacy and safety of topiramate in infants according to epilepsy syndromes 132
Zonisamide in children and young adults with refractory epilepsy: an open label, multicenter Italian study 131
Treating juvenile idiopathic arthritis (JIA)-related uveitis beyond TNF-α inhibition: a narrative review 130
Thyroid function in small for gestational age newborns: A review 129
Long-term outcome of epilepsy in patients with Prader-Willi syndrome 128
Dexfenfluramine effective in drug-resistant temporal lobe epilepsy 127
Craniofacial dyssynostosis: case report and review 127
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 127
Schinzel-Giedion syndrome: a further cause of West syndrome 126
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 124
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome 124
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 124
Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations 123
Lacosamide in children with refractory status epilepticus. A multicenter Italian experience 122
Simultaneous onset of infantile spasms in monozygotic twins 122
Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation 122
Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication 122
Linear scleroderma associated with progressive brain atrophy 122
Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy 121
Valproate in adolescents with photosensitive epilepsy with generalized tonic-clonic seizures only 121
Lamotrigine in typical absence epilepsy 121
Central precocious puberty and abnormal chromosomal patterns 121
null 118
Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsy 118
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review 118
Long-term prognosis of patients with Ehlers-Danlos syndrome and epilepsy 118
Lacosamide efficacy in epileptic syndromes with continuous spike and waves during slow sleep (CSWS) 117
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy 117
Brain mitochondrial impairment in ethylmalonic encephalopathy 117
Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype. 117
Epilepsy in neurofibromatosis 1 117
Folate receptor alpha defect causes cerebral folate transport deficiency a treatable neurodegenerative disorder associated with disturbed myelin metabolism 117
Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalities 116
Endocrine disorders in two sisters affected by MELAS syndrome 116
Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature 116
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? 116
Chitotriosidase activity in the serum of patients with sarcoidosis and pulmonary tuberculosis 116
Efficacy and tolerability of add-on Lacosamide in children with Lennox-Gastaut syndrome 115
Plasmapheresis in a child affected by acute disseminated encephalomyelitis 115
Late-onset childhood occipital epilepsy(Gastaut type): a family study 115
Multiple neuroendocrine disorder in Salla disease 115
Alternating hemiplegia of childhood or Hashimoto’s encephalopathy? 115
Growth hormone secretion in Prader-Willi syndrome 114
Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism 114
Childhood absence epilepsy: evolution and prognostic factors 113
Levetiracetam monotherapy for children and adolescents with benign rolandic seizures 113
Epilepsy in Prader-Willi syndrome: clinical, diagnostic and treatment aspects 113
Inter-ictal and post-ictal circulating levels of allopregnanolone, an anticonvulsant metabolite of progesterone, in epileptic children 113
Diagnosis of Angelman syndrome: clinical and EEG criteria 113
Efficacy and tolerability of add-on lacosamide in children with Lennox-Gastaut syndrome 113
Chitotriosidase activity in patients with interstitial lung disesaes 112
Bathing epilepsy: report of two Caucasian cases 112
Pubertal disorders in inv dup(15) syndrome 112
Subcortical low-intensity and restricted diffusion after first seizure in a child 111
Withdrawal of antiepileptic drugs: guidelines of the Italian League Against Epilepsy 111
Elettroencephalographic and epileptic patterns in x chromosome anomalies 109
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 109
Long term outcome in children affected by absence epilepsy with onset before the age of three years 108
A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood 108
Epilepsy and vaccinations: Italian guidelines 107
Efficacy and safety of rufinamide in children under four years of age with drug-resistant epilepsies 107
Epilepsy in Menkes disease An electroclinical long-term study of 28 patients 106
Body mass index and serum lipid changes during treatment with valproic acid in children with epilepsy 106
Reflex myoclonic epilepsy in infancy: a multicenter clinical study 105
Lacosamide in pediatric and adult patients: comparison of efficacy and safety 105
Levetiracetam monotherapy for childhood occipital epilepsy of gastaut 105
Totale 13.487
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Categoria #
all - tutte 64.852
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 64.852
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.748 0 163 301 690 327 313 319 521 468 293 103 250
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
2024/2025323 125 198 0 0 0 0 0 0 0 0 0 0
Totale 18.260