IRIS
GROSSO, SALVATORE
 Distribuzione geografica
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Continente #
NA - Nord America 14.510
EU - Europa 9.287
AS - Asia 4.546
SA - Sud America 950
AF - Africa 107
OC - Oceania 21
Continente sconosciuto - Info sul continente non disponibili 6
Totale 29.427
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Nazione #
US - Stati Uniti d'America 14.340
RU - Federazione Russa 2.339
CN - Cina 1.747
GB - Regno Unito 1.677
SG - Singapore 1.511
IE - Irlanda 1.477
UA - Ucraina 837
BR - Brasile 826
IT - Italia 790
SE - Svezia 589
DE - Germania 487
FR - Francia 425
HK - Hong Kong 416
FI - Finlandia 347
VN - Vietnam 236
KR - Corea 206
IN - India 94
CA - Canada 93
TR - Turchia 85
ES - Italia 69
BD - Bangladesh 50
NL - Olanda 49
ZA - Sudafrica 46
PL - Polonia 44
AR - Argentina 42
MX - Messico 39
BE - Belgio 37
CZ - Repubblica Ceca 34
JP - Giappone 27
EC - Ecuador 25
ID - Indonesia 23
IQ - Iraq 20
AU - Australia 19
CL - Cile 17
AT - Austria 16
CI - Costa d'Avorio 15
SA - Arabia Saudita 15
VE - Venezuela 14
EG - Egitto 13
PK - Pakistan 13
CO - Colombia 12
IR - Iran 11
LT - Lituania 11
MA - Marocco 11
RO - Romania 10
AE - Emirati Arabi Uniti 9
AZ - Azerbaigian 9
IL - Israele 8
JO - Giordania 8
NO - Norvegia 8
TT - Trinidad e Tobago 8
UZ - Uzbekistan 8
JM - Giamaica 7
KZ - Kazakistan 7
OM - Oman 7
NP - Nepal 6
PA - Panama 6
PE - Perù 6
PY - Paraguay 6
BG - Bulgaria 5
HU - Ungheria 5
KE - Kenya 5
BH - Bahrain 4
CR - Costa Rica 4
GR - Grecia 4
HN - Honduras 4
LB - Libano 4
LV - Lettonia 4
SN - Senegal 4
TN - Tunisia 4
AL - Albania 3
BY - Bielorussia 3
EU - Europa 3
PH - Filippine 3
PT - Portogallo 3
QA - Qatar 3
AM - Armenia 2
BB - Barbados 2
BN - Brunei Darussalam 2
CH - Svizzera 2
DK - Danimarca 2
DZ - Algeria 2
EE - Estonia 2
ET - Etiopia 2
GT - Guatemala 2
KW - Kuwait 2
LA - Repubblica Popolare Democratica del Laos 2
LU - Lussemburgo 2
MN - Mongolia 2
NI - Nicaragua 2
SI - Slovenia 2
TZ - Tanzania 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AI - Anguilla 1
BA - Bosnia-Erzegovina 1
BS - Bahamas 1
CW - ???statistics.table.value.countryCode.CW??? 1
GA - Gabon 1
GE - Georgia 1
Totale 29.413
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Città #
Dallas 1.806
Fairfield 1.796
Dublin 1.464
Southend 1.448
Ashburn 1.276
Woodbridge 840
Chandler 832
Singapore 810
Seattle 747
Houston 726
Wilmington 682
Jacksonville 671
Cambridge 642
Santa Clara 608
Moscow 572
Ann Arbor 510
Hong Kong 412
Beijing 397
Princeton 301
Nanjing 225
Seoul 202
Hefei 197
Siena 171
New York 155
Helsinki 154
Los Angeles 136
Munich 127
Boardman 116
The Dalles 111
San Diego 101
Nanchang 81
San Mateo 75
Shenyang 74
São Paulo 74
Ho Chi Minh City 72
Council Bluffs 69
Milan 68
Norwalk 68
Buffalo 62
Shanghai 60
Menlo Park 54
Turku 51
Columbus 48
Redondo Beach 48
Tianjin 48
Izmir 47
Florence 46
Málaga 44
Dong Ket 41
Rome 39
Hanoi 38
Nuremberg 37
Zhengzhou 37
Changsha 35
San Francisco 34
Jiaxing 33
London 33
Hebei 32
Warsaw 32
Brussels 31
Johannesburg 31
Montreal 30
Chicago 28
Toronto 28
Brno 27
Brooklyn 26
Jinan 26
Denver 25
Guangzhou 25
Rio de Janeiro 24
Belo Horizonte 23
Tokyo 23
Kunming 22
Lancaster 22
Poplar 22
Stockholm 22
Bengaluru 20
Chennai 20
Hangzhou 20
Ningbo 20
Atlanta 19
Dearborn 17
Phoenix 17
Ottawa 16
Padova 16
Abidjan 15
Brasília 15
Ankara 14
Mexico City 14
Orem 14
Taizhou 14
Washington 14
Amsterdam 13
Boston 13
Lucca 12
Porto Alegre 12
Düsseldorf 11
Naples 11
Bologna 10
Baku 9
Totale 20.506
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Nome #
MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotype 435
Chromosome 18 aberrations and epilepsy: a review 361
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability. 333
Drug Retention Rate and Predictive Factors of Drug Survival for Interleukin-1 Inhibitors in Systemic Juvenile Idiopathic Arthritis 313
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age 296
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features 291
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum 290
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb 278
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 275
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene 267
Chitotriosidase and soluble IL-2 receptor: comparison of two markers of sarcoidosis severity 266
2q24-q31 deletion: report of a case and review of the literature 266
Massive lamotrigine poisoning. A case report 253
Aicardi syndrome with favorable outcome: case report and review 252
Private inherited microdeletion/microduplications: implications in clinical practice 251
De novo complete trisomy 5p clinical and neuroradiological findings 237
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 235
Acute flaccid myelitis temporally associated with rhinovirus infection: just a coincidence? 235
Recurrent Miller Fisher syndrome in children 233
Efficacy and safety of topiramate in infants according to epilepsy syndromes 229
SCN1A mutation associated with atypical Panayiotopoulos syndrome 227
Hot water epilepsy and focal malformation of the parietal cortex development 226
Treatment options for periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome in children and adults: a narrative review 223
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy 222
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 218
Biological markers of oxidative stress in progressive muscular dystrophies: A preliminary study: 157 218
A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood 217
Oxidative stress in children affected by epileptic encephalopathies 216
Anticonvulsant drugs and hematological disease 216
Central precocious puberty and abnormal chromosomal patterns 215
Precocious puberty with trisomy X syndrome 213
Elettroencephalographic and epileptic patterns in x chromosome anomalies 212
Transient neonatal hypothyroidism after gestational exposure to amiodarone: a follow-up of two cases 210
Segregation analysis in typical absence epilepsy 208
Chitotriosidase activity in patients with interstitial lung disesaes 207
Typical absence seizures associated with localization-related epilepsy: a clinical and electroencephalographic characterization 206
Serum levels of chitotriosidase as a marker of disease activity and clinical stage in sarcoidosis. 206
Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation 205
Optic perineuritis: A further cause of visual loss and disc edema in children 205
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 203
Schinzel-Giedion syndrome: a further cause of West syndrome 201
Childhood absence epilepsy: evolution and prognostic factors 200
Bathing epilepsy: report of two Caucasian cases 199
Thyroid function in small for gestational age newborns: A review 199
Craniofacial dyssynostosis: case report and review 198
Antiepileptic drugs: role in paediatric poisoning 197
Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy 196
Dexfenfluramine effective in drug-resistant temporal lobe epilepsy 196
Association of celiac disease in patients with multiple sclerosis in Tuscany 196
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? 191
Lamotrigine in typical absence epilepsy 190
Association of Chiari I malformation, mental retardation, speech delay and epilepsy: a specific desorder ? 189
Brain mitochondrial impairment in ethylmalonic encephalopathy 188
Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature 186
Growth hormone secretion in Prader-Willi syndrome 184
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 183
Epilepsy and elettroencephalographic finding in pericentric inversion of chromosome 12 183
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome 182
Anakinra drug retention rate and predictive factors of long-term response in systemic juvenile idiopathic arthritis and adult onset still disease 182
Multiple neuroendocrine disorder in Salla disease 182
Lacosamide in children with refractory status epilepticus. A multicenter Italian experience 181
Epilepsy in neurofibromatosis 1 181
Chitotriosidase activity in the serum of patients with sarcoidosis and pulmonary tuberculosis 180
Late-onset childhood occipital epilepsy(Gastaut type): a family study 180
Lacosamide efficacy in epileptic syndromes with continuous spike and waves during slow sleep (CSWS) 179
Topiramate effects on plasma serotonin levels in children with epilepsy 179
17p13.3 microdeletion including YWHAE and CRK genes: towards a clinical characterization 177
Body mass index and serum lipid changes during treatment with valproic acid in children with epilepsy 176
Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype. 174
Diagnosis of Angelman syndrome: clinical and EEG criteria 173
Refractory absence seizures: An Italian multicenter retrospective study 172
Plasmapheresis in a child affected by acute disseminated encephalomyelitis 172
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 170
Subcortical low-intensity and restricted diffusion after first seizure in a child 169
Acute ataxia in paediatric emergency departments: A multicentre Italian study 168
Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy 167
Zonisamide in children and young adults with refractory epilepsy: an open label, multicenter Italian study 167
Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations 166
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review 166
CKAP2L mutation confirms the diagnosis of Filippi syndrome 166
Valproate in adolescents with photosensitive epilepsy with generalized tonic-clonic seizures only 164
Treating juvenile idiopathic arthritis (JIA)-related uveitis beyond TNF-α inhibition: a narrative review 164
Alternating hemiplegia of childhood or Hashimoto’s encephalopathy? 164
24-h continuous non-invasive multiparameter home monitoring of vitals in patients with Rett syndrome by an innovative wearable technology: evidence of an overlooked chronic fatigue status 163
Simultaneous onset of infantile spasms in monozygotic twins 163
Photoparoxysmal responses in children with chromosomal aberrations 162
Endocrine disorders in two sisters affected by MELAS syndrome 160
Long-term outcome of epilepsy in patients with Prader-Willi syndrome 160
Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalities 159
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy 159
Long-term prognosis of patients with Ehlers-Danlos syndrome and epilepsy 157
Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsy 156
Next-generation sequencing approach to hyperCKemia: A 2-year cohort study 156
Oxidative stress in epilepsy 156
Linear scleroderma associated with progressive brain atrophy 156
Ethylmalonic encephalopathy: further clinical and neuroradiological characterization 155
Seizures and electroencephalographic findings in CDKL5 mutations: case report and review 154
L-2 Hydroxyglutaric Aciduria Magnetization Transfer Contrast and Diffusion Weighted Magnetic Resonance Imaging Findings. A case Report 153
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy 152
Pubertal disorders in inv dup(15) syndrome 151
Totale 20.318
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Categoria #
all - tutte 100.754
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 100.754
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.068 0 0 0 0 0 365 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
2024/20254.321 125 232 470 254 514 232 99 254 432 180 465 1.064
2025/20267.400 758 1.551 1.383 1.437 2.168 103 0 0 0 0 0 0
Totale 29.748