IRIS
GROSSO, SALVATORE
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 16.648
EU - Europa 10.509
AS - Asia 5.850
SA - Sud America 1.089
Continente sconosciuto - Info sul continente non disponibili 332
AF - Africa 279
OC - Oceania 33
Totale 34.740
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 16.402
RU - Federazione Russa 2.343
CN - Cina 1.969
SG - Singapore 1.765
GB - Regno Unito 1.725
IT - Italia 1.658
IE - Irlanda 1.482
BR - Brasile 905
UA - Ucraina 842
VN - Vietnam 653
FR - Francia 606
SE - Svezia 593
DE - Germania 509
HK - Hong Kong 481
FI - Finlandia 373
BD - Bangladesh 219
KR - Corea 209
IN - India 141
ZA - Sudafrica 137
CA - Canada 131
TR - Turchia 92
ES - Italia 80
AR - Argentina 62
NL - Olanda 57
PL - Polonia 56
IQ - Iraq 50
MX - Messico 49
NG - Nigeria 48
BE - Belgio 37
JP - Giappone 37
CZ - Repubblica Ceca 34
EC - Ecuador 32
AU - Australia 31
CL - Cile 25
ID - Indonesia 25
SA - Arabia Saudita 23
PK - Pakistan 21
VE - Venezuela 21
CO - Colombia 20
EG - Egitto 20
MA - Marocco 19
AT - Austria 17
CI - Costa d'Avorio 16
UZ - Uzbekistan 15
AE - Emirati Arabi Uniti 14
JO - Giordania 14
KZ - Kazakistan 14
LT - Lituania 14
RO - Romania 14
JM - Giamaica 13
KE - Kenya 13
NP - Nepal 13
IR - Iran 12
PH - Filippine 11
TT - Trinidad e Tobago 11
AZ - Azerbaigian 10
PY - Paraguay 10
IL - Israele 9
NO - Norvegia 9
OM - Oman 9
AL - Albania 8
CR - Costa Rica 7
PA - Panama 7
PE - Perù 7
HU - Ungheria 6
NI - Nicaragua 6
SN - Senegal 6
BG - Bulgaria 5
CH - Svizzera 5
DK - Danimarca 5
GT - Guatemala 5
PT - Portogallo 5
SV - El Salvador 5
TN - Tunisia 5
BH - Bahrain 4
ET - Etiopia 4
GR - Grecia 4
HN - Honduras 4
LB - Libano 4
LV - Lettonia 4
MY - Malesia 4
PS - Palestinian Territory 4
BB - Barbados 3
BO - Bolivia 3
BY - Bielorussia 3
EU - Europa 3
LA - Repubblica Popolare Democratica del Laos 3
MN - Mongolia 3
QA - Qatar 3
SC - Seychelles 3
SY - Repubblica araba siriana 3
TH - Thailandia 3
UY - Uruguay 3
AM - Armenia 2
BN - Brunei Darussalam 2
BS - Bahamas 2
CM - Camerun 2
DZ - Algeria 2
EE - Estonia 2
GE - Georgia 2
Totale 34.381
Salva come PNG Salva come JPEG
Città #
Dallas 1.826
Fairfield 1.796
Ashburn 1.607
Dublin 1.466
Southend 1.448
Singapore 916
Woodbridge 840
Chandler 832
Seattle 751
Houston 736
Santa Clara 685
Wilmington 683
Jacksonville 672
Cambridge 642
Moscow 573
Ann Arbor 510
San Jose 490
Milan 466
Hong Kong 456
Beijing 412
Council Bluffs 372
Princeton 301
The Dalles 229
Hefei 228
Nanjing 225
Seoul 204
Ho Chi Minh City 200
New York 195
Los Angeles 189
Siena 176
Helsinki 175
Rome 169
Lauterbourg 166
Hanoi 144
Munich 127
Johannesburg 118
Boardman 117
San Diego 106
São Paulo 83
Nanchang 81
Columbus 78
Buffalo 75
San Mateo 75
Shenyang 74
Norwalk 68
Shanghai 64
Orem 55
Menlo Park 54
Figino 52
Turku 51
Tianjin 50
Florence 49
Abuja 48
Redondo Beach 48
Izmir 47
San Francisco 46
Chicago 44
Málaga 44
Montreal 43
Warsaw 43
Dong Ket 41
Nuremberg 38
Zhengzhou 38
London 37
Turin 37
Changsha 35
Toronto 34
Chennai 33
Jiaxing 33
Brooklyn 32
Da Nang 32
Denver 32
Hebei 32
Brussels 31
Tokyo 30
Rio de Janeiro 29
Haiphong 28
Brno 27
Phoenix 27
Atlanta 26
Guangzhou 26
Jinan 26
Lancaster 25
Belo Horizonte 24
Naples 24
Stockholm 24
Frankfurt am Main 23
Hangzhou 23
Poplar 23
Kunming 22
Bengaluru 21
Ningbo 20
Washington 20
Mexico City 19
Boston 18
Baghdad 17
Dearborn 17
Abidjan 16
Amsterdam 16
Bologna 16
Totale 23.592
Salva come PNG Salva come JPEG
Nome #
MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotype 473
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability. 393
Chromosome 18 aberrations and epilepsy: a review 391
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age 355
Drug Retention Rate and Predictive Factors of Drug Survival for Interleukin-1 Inhibitors in Systemic Juvenile Idiopathic Arthritis 340
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features 336
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum 325
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 322
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb 320
2q24-q31 deletion: report of a case and review of the literature 315
Massive lamotrigine poisoning. A case report 315
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene 294
Chitotriosidase and soluble IL-2 receptor: comparison of two markers of sarcoidosis severity 293
Private inherited microdeletion/microduplications: implications in clinical practice 279
Aicardi syndrome with favorable outcome: case report and review 278
Biological markers of oxidative stress in progressive muscular dystrophies: A preliminary study: 157 258
Recurrent Miller Fisher syndrome in children 257
Efficacy and safety of topiramate in infants according to epilepsy syndromes 256
Acute flaccid myelitis temporally associated with rhinovirus infection: just a coincidence? 256
De novo complete trisomy 5p clinical and neuroradiological findings 253
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 252
A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood 252
Hot water epilepsy and focal malformation of the parietal cortex development 250
Treatment options for periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome in children and adults: a narrative review 249
Anticonvulsant drugs and hematological disease 248
SCN1A mutation associated with atypical Panayiotopoulos syndrome 247
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy 244
Thyroid function in small for gestational age newborns: A review 243
Oxidative stress in children affected by epileptic encephalopathies 242
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 242
Serum levels of chitotriosidase as a marker of disease activity and clinical stage in sarcoidosis 241
Optic perineuritis: A further cause of visual loss and disc edema in children 240
Precocious puberty with trisomy X syndrome 239
Central precocious puberty and abnormal chromosomal patterns 237
Chitotriosidase activity in patients with interstitial lung disesaes 236
Elettroencephalographic and epileptic patterns in x chromosome anomalies 236
Segregation analysis in typical absence epilepsy 235
Typical absence seizures associated with localization-related epilepsy: a clinical and electroencephalographic characterization 233
Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype. 231
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 228
Schinzel-Giedion syndrome: a further cause of West syndrome 228
Antiepileptic drugs: role in paediatric poisoning 228
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 226
Bathing epilepsy: report of two Caucasian cases 225
Association of celiac disease in patients with multiple sclerosis in Tuscany 225
Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation 223
Childhood absence epilepsy: evolution and prognostic factors 222
Craniofacial dyssynostosis: case report and review 222
Lamotrigine in typical absence epilepsy 222
AUTS2-related syndrome: Insights from a large European cohort 221
Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy 220
Transient neonatal hypothyroidism after gestational exposure to amiodarone: a follow-up of two cases 220
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy 219
Dexfenfluramine effective in drug-resistant temporal lobe epilepsy 218
17p13.3 microdeletion including YWHAE and CRK genes: towards a clinical characterization 218
Association of Chiari I malformation, mental retardation, speech delay and epilepsy: a specific desorder ? 218
Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature 215
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome 214
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? 214
Anakinra drug retention rate and predictive factors of long-term response in systemic juvenile idiopathic arthritis and adult onset still disease 214
Epilepsy in neurofibromatosis 1 212
Subcortical low-intensity and restricted diffusion after first seizure in a child 209
Lacosamide efficacy in epileptic syndromes with continuous spike and waves during slow sleep (CSWS) 209
Epilepsy and elettroencephalographic finding in pericentric inversion of chromosome 12 208
Treating juvenile idiopathic arthritis (JIA)-related uveitis beyond TNF-α inhibition: a narrative review 208
Acute ataxia in paediatric emergency departments: A multicentre Italian study 207
Lacosamide in children with refractory status epilepticus. A multicenter Italian experience 206
Growth hormone secretion in Prader-Willi syndrome 205
Brain mitochondrial impairment in ethylmalonic encephalopathy 205
Topiramate effects on plasma serotonin levels in children with epilepsy 204
Multiple neuroendocrine disorder in Salla disease 203
Chitotriosidase activity in the serum of patients with sarcoidosis and pulmonary tuberculosis 202
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 201
Late-onset childhood occipital epilepsy(Gastaut type): a family study 200
Diagnosis of Angelman syndrome: clinical and EEG criteria 199
Refractory absence seizures: An Italian multicenter retrospective study 195
CKAP2L mutation confirms the diagnosis of Filippi syndrome 195
Body mass index and serum lipid changes during treatment with valproic acid in children with epilepsy 195
Hints for Genetic and Clinical Differentiation of Adult-Onset Monogenic Autoinflammatory Diseases 194
Ethylmalonic encephalopathy: further clinical and neuroradiological characterization 193
Epilepsy in Menkes disease An electroclinical long-term study of 28 patients 192
Comparison of Early vs. Delayed Anakinra Treatment in Patients With Adult Onset Still's Disease and Effect on Clinical and Laboratory Outcomes 192
Natural history of KBG syndrome in a large European cohort 192
Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy 191
Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsy 191
Plasmapheresis in a child affected by acute disseminated encephalomyelitis 191
Alternating hemiplegia of childhood or Hashimoto’s encephalopathy? 191
Valproate in adolescents with photosensitive epilepsy with generalized tonic-clonic seizures only 189
Next-generation sequencing approach to hyperCKemia: A 2-year cohort study 188
Oxidative stress in epilepsy 187
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review 186
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 185
Efficacy and safety of topiramate in refractory epilepsy of childhood: long-term follow-up study 183
Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations 183
Linear scleroderma associated with progressive brain atrophy 182
Photoparoxysmal responses in children with chromosomal aberrations 180
Zonisamide in children and young adults with refractory epilepsy: an open label, multicenter Italian study 180
Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalities 180
Intractable reflex audiogenic seizures in Aicardi syndrome 180
Anakinra and canakinumab for patients with R92Q-associated autoinflammatory syndrome: a multicenter observational study from the AIDA Network 177
Totale 23.316
Salva come PNG Salva come JPEG
Categoria #
all - tutte 115.899
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 115.899
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.789 0 218 105 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
2025/202611.569 758 1.551 1.383 1.437 2.168 434 1.226 332 342 538 469 931
2026/2027823 472 351 0 0 0 0 0 0 0 0 0 0
Totale 34.740