IRIS
GROSSO, SALVATORE
 Distribuzione geografica
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Continente #
NA - Nord America 11.395
EU - Europa 7.062
AS - Asia 1.759
SA - Sud America 339
AF - Africa 29
OC - Oceania 18
Continente sconosciuto - Info sul continente non disponibili 4
Totale 20.606
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Nazione #
US - Stati Uniti d'America 11.344
GB - Regno Unito 1.614
IE - Irlanda 1.476
CN - Cina 908
UA - Ucraina 828
IT - Italia 710
SG - Singapore 606
RU - Federazione Russa 581
SE - Svezia 569
FR - Francia 395
DE - Germania 380
BR - Brasile 303
FI - Finlandia 295
TR - Turchia 63
ES - Italia 48
HK - Hong Kong 43
VN - Vietnam 42
BE - Belgio 37
CA - Canada 37
NL - Olanda 33
CZ - Repubblica Ceca 32
AU - Australia 17
IN - India 16
AT - Austria 13
CI - Costa d'Avorio 12
AR - Argentina 10
RO - Romania 8
CL - Cile 7
JP - Giappone 7
MA - Marocco 7
NO - Norvegia 7
AE - Emirati Arabi Uniti 6
EC - Ecuador 6
IR - Iran 6
AZ - Azerbaigian 5
BD - Bangladesh 5
HU - Ungheria 5
IL - Israele 5
KR - Corea 5
PK - Pakistan 5
VE - Venezuela 5
CO - Colombia 4
EG - Egitto 4
IQ - Iraq 4
KZ - Kazakistan 4
PA - Panama 4
PL - Polonia 4
BY - Bielorussia 3
EU - Europa 3
HN - Honduras 3
JM - Giamaica 3
LT - Lituania 3
LV - Lettonia 3
OM - Oman 3
QA - Qatar 3
UZ - Uzbekistan 3
ZA - Sudafrica 3
AM - Armenia 2
BN - Brunei Darussalam 2
CH - Svizzera 2
CR - Costa Rica 2
DK - Danimarca 2
EE - Estonia 2
GR - Grecia 2
JO - Giordania 2
LA - Repubblica Popolare Democratica del Laos 2
LU - Lussemburgo 2
MN - Mongolia 2
NP - Nepal 2
PE - Perù 2
PH - Filippine 2
SI - Slovenia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
BA - Bosnia-Erzegovina 1
BS - Bahamas 1
DZ - Algeria 1
GE - Georgia 1
ID - Indonesia 1
IM - Isola di Man 1
KE - Kenya 1
KG - Kirghizistan 1
MX - Messico 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
PY - Paraguay 1
RS - Serbia 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
UY - Uruguay 1
Totale 20.606
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Città #
Fairfield 1.796
Dublin 1.463
Southend 1.448
Ashburn 1.017
Woodbridge 839
Chandler 832
Seattle 741
Houston 722
Wilmington 682
Jacksonville 669
Cambridge 642
Santa Clara 583
Ann Arbor 510
Princeton 301
Singapore 249
Nanjing 224
Siena 171
Helsinki 153
Beijing 118
Boardman 116
San Diego 101
New York 89
Nanchang 79
San Mateo 75
Shenyang 74
Norwalk 68
Shanghai 57
Menlo Park 54
Milan 54
Council Bluffs 51
Moscow 48
Izmir 47
Málaga 44
Tianjin 42
Dong Ket 41
Hong Kong 40
Florence 35
The Dalles 35
Rome 33
Hebei 32
Jiaxing 32
Nuremberg 32
Brussels 31
Munich 31
Zhengzhou 31
Changsha 28
Brno 27
London 27
Jinan 26
San Francisco 23
Kunming 22
Lancaster 22
Los Angeles 22
Ningbo 20
Guangzhou 19
Toronto 19
Hangzhou 18
São Paulo 18
Dearborn 17
Ottawa 16
Padova 16
Taizhou 13
Abidjan 12
Washington 12
Düsseldorf 11
Naples 11
Belo Horizonte 10
Duncan 9
Lauterbourg 9
Prescot 9
Redwood City 9
Rio de Janeiro 9
Tappahannock 9
Canberra 8
Fremont 8
Lucca 8
Brasília 7
Kilburn 7
Nereto 7
Portsmouth 7
São Bernardo do Campo 7
Turku 7
Changchun 6
Dallas 6
Falkenstein 6
Ferrara 6
Haikou 6
Lanzhou 6
Mykolayiv 6
Newark 6
Perugia 6
Sesto Fiorentino 6
Vienna 6
Waanrode 6
Baku 5
Bologna 5
Chiswick 5
Falls Church 5
Hounslow 5
North Bergen 5
Totale 15.163
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Nome #
MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotype 364
Chromosome 18 aberrations and epilepsy: a review 307
Drug Retention Rate and Predictive Factors of Drug Survival for Interleukin-1 Inhibitors in Systemic Juvenile Idiopathic Arthritis 282
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability. 269
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum 225
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene 215
SCN1A mutation associated with atypical Panayiotopoulos syndrome 201
Treatment options for periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome in children and adults: a narrative review 200
Chitotriosidase and soluble IL-2 receptor: comparison of two markers of sarcoidosis severity 193
Massive lamotrigine poisoning. A case report 193
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 189
Recurrent Miller Fisher syndrome in children 188
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age 178
Private inherited microdeletion/microduplications: implications in clinical practice 176
Precocious puberty with trisomy X syndrome 176
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb 173
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy 169
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features 168
De novo complete trisomy 5p clinical and neuroradiological findings 167
Acute flaccid myelitis temporally associated with rhinovirus infection: just a coincidence? 166
Hot water epilepsy and focal malformation of the parietal cortex development 166
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 164
Anticonvulsant drugs and hematological disease 161
Biological markers of oxidative stress in progressive muscular dystrophies: A preliminary study: 157 161
Oxidative stress in children affected by epileptic encephalopathies 159
Topiramate effects on plasma serotonin levels in children with epilepsy 158
Optic perineuritis: A further cause of visual loss and disc edema in children 157
2q24-q31 deletion: report of a case and review of the literature 155
Typical absence seizures associated with localization-related epilepsy: a clinical and electroencephalographic characterization 155
Efficacy and safety of topiramate in infants according to epilepsy syndromes 154
Serum levels of chitotriosidase as a marker of disease activity and clinical stage in sarcoidosis. 154
Segregation analysis in typical absence epilepsy 153
Aicardi syndrome with favorable outcome: case report and review 151
Refractory absence seizures: An Italian multicenter retrospective study 147
Transient neonatal hypothyroidism after gestational exposure to amiodarone: a follow-up of two cases 145
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 145
Dexfenfluramine effective in drug-resistant temporal lobe epilepsy 144
Thyroid function in small for gestational age newborns: A review 144
Schinzel-Giedion syndrome: a further cause of West syndrome 143
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome 142
Treating juvenile idiopathic arthritis (JIA)-related uveitis beyond TNF-α inhibition: a narrative review 142
Central precocious puberty and abnormal chromosomal patterns 142
Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy 141
Craniofacial dyssynostosis: case report and review 141
Zonisamide in children and young adults with refractory epilepsy: an open label, multicenter Italian study 139
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 139
Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation 139
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 139
Long-term outcome of epilepsy in patients with Prader-Willi syndrome 137
Epilepsy in neurofibromatosis 1 137
Lamotrigine in typical absence epilepsy 137
Linear scleroderma associated with progressive brain atrophy 137
Late-onset childhood occipital epilepsy(Gastaut type): a family study 136
Chitotriosidase activity in patients with interstitial lung disesaes 135
Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations 135
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? 135
Chitotriosidase activity in the serum of patients with sarcoidosis and pulmonary tuberculosis 135
Elettroencephalographic and epileptic patterns in x chromosome anomalies 133
Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature 132
Lacosamide in children with refractory status epilepticus. A multicenter Italian experience 131
Plasmapheresis in a child affected by acute disseminated encephalomyelitis 131
Pubertal disorders in inv dup(15) syndrome 131
Simultaneous onset of infantile spasms in monozygotic twins 130
Valproate in adolescents with photosensitive epilepsy with generalized tonic-clonic seizures only 130
Brain mitochondrial impairment in ethylmalonic encephalopathy 130
Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication 130
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review 130
A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood 130
Alternating hemiplegia of childhood or Hashimoto’s encephalopathy? 130
Childhood absence epilepsy: evolution and prognostic factors 129
Lacosamide efficacy in epileptic syndromes with continuous spike and waves during slow sleep (CSWS) 129
Growth hormone secretion in Prader-Willi syndrome 129
Bathing epilepsy: report of two Caucasian cases 129
Endocrine disorders in two sisters affected by MELAS syndrome 129
Efficacy and tolerability of add-on Lacosamide in children with Lennox-Gastaut syndrome 129
Multiple neuroendocrine disorder in Salla disease 128
Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsy 127
Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype. 127
Diagnosis of Angelman syndrome: clinical and EEG criteria 127
Long-term prognosis of patients with Ehlers-Danlos syndrome and epilepsy 126
Subcortical low-intensity and restricted diffusion after first seizure in a child 125
Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalities 125
Folate receptor alpha defect causes cerebral folate transport deficiency a treatable neurodegenerative disorder associated with disturbed myelin metabolism 125
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy 124
Levetiracetam monotherapy for children and adolescents with benign rolandic seizures 124
Epilepsy in Prader-Willi syndrome: clinical, diagnostic and treatment aspects 124
Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism 124
Inter-ictal and post-ictal circulating levels of allopregnanolone, an anticonvulsant metabolite of progesterone, in epileptic children 124
Body mass index and serum lipid changes during treatment with valproic acid in children with epilepsy 124
Efficacy and tolerability of add-on lacosamide in children with Lennox-Gastaut syndrome 123
Seizures and electroencephalographic findings in CDKL5 mutations: case report and review 121
Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy 120
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 120
Antiepileptic drugs: role in paediatric poisoning 119
Withdrawal of antiepileptic drugs: guidelines of the Italian League Against Epilepsy 119
null 118
Long term outcome in children affected by absence epilepsy with onset before the age of three years 118
Management of status dystonicus in children. Cases reportand review 117
Efficacy and safety of rufinamide in children under four years of age with drug-resistant epilepsies 117
Epilepsy in Menkes disease An electroclinical long-term study of 28 patients 116
Totale 15.007
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Categoria #
all - tutte 81.089
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 81.089
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020353 0 0 0 0 0 0 0 0 0 0 103 250
2020/20213.350 114 420 193 389 166 365 97 445 207 344 446 164
2021/20221.888 99 218 105 79 32 85 81 193 156 180 166 494
2022/20232.892 171 270 379 377 288 574 51 242 329 74 79 58
2023/20242.136 93 61 190 128 59 599 770 27 10 32 24 143
2024/20252.894 125 232 470 254 514 232 99 254 432 180 102 0
Totale 20.921