IRIS
GROSSO, SALVATORE
 Distribuzione geografica
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Continente #
NA - Nord America 15.903
EU - Europa 9.793
AS - Asia 5.783
SA - Sud America 1.078
AF - Africa 276
OC - Oceania 33
Continente sconosciuto - Info sul continente non disponibili 6
Totale 32.872
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Nazione #
US - Stati Uniti d'America 15.686
RU - Federazione Russa 2.343
CN - Cina 1.946
SG - Singapore 1.753
GB - Regno Unito 1.723
IE - Irlanda 1.481
IT - Italia 955
BR - Brasile 899
UA - Ucraina 841
VN - Vietnam 652
FR - Francia 606
SE - Svezia 592
DE - Germania 508
HK - Hong Kong 476
FI - Finlandia 373
KR - Corea 208
BD - Bangladesh 203
IN - India 139
ZA - Sudafrica 137
CA - Canada 121
TR - Turchia 92
ES - Italia 78
AR - Argentina 61
NL - Olanda 56
PL - Polonia 56
IQ - Iraq 50
NG - Nigeria 48
MX - Messico 47
BE - Belgio 37
JP - Giappone 35
CZ - Repubblica Ceca 34
AU - Australia 31
EC - Ecuador 31
CL - Cile 25
ID - Indonesia 25
SA - Arabia Saudita 23
PK - Pakistan 21
EG - Egitto 20
CO - Colombia 19
MA - Marocco 19
VE - Venezuela 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
KE - Kenya 13
NP - Nepal 13
RO - Romania 13
IR - Iran 12
AZ - Azerbaigian 10
JM - Giamaica 10
PH - Filippine 10
PY - Paraguay 10
TT - Trinidad e Tobago 10
IL - Israele 9
NO - Norvegia 9
OM - Oman 9
AL - Albania 7
PE - Perù 7
HU - Ungheria 6
PA - Panama 6
SN - Senegal 6
BG - Bulgaria 5
CH - Svizzera 5
PT - Portogallo 5
TN - Tunisia 5
BH - Bahrain 4
CR - Costa Rica 4
DK - Danimarca 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
GT - Guatemala 3
MN - Mongolia 3
NI - Nicaragua 3
QA - Qatar 3
SY - Repubblica araba siriana 3
UY - Uruguay 3
AM - Armenia 2
BN - Brunei Darussalam 2
CM - Camerun 2
DZ - Algeria 2
EE - Estonia 2
GE - Georgia 2
KG - Kirghizistan 2
KW - Kuwait 2
LA - Repubblica Popolare Democratica del Laos 2
LU - Lussemburgo 2
RS - Serbia 2
Totale 32.845
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Città #
Dallas 1.820
Fairfield 1.796
Ashburn 1.476
Dublin 1.466
Southend 1.448
Singapore 909
Woodbridge 840
Chandler 832
Seattle 748
Houston 733
Wilmington 683
Jacksonville 672
Cambridge 642
Santa Clara 630
Moscow 573
Ann Arbor 510
San Jose 476
Hong Kong 453
Beijing 404
Princeton 301
The Dalles 229
Hefei 228
Nanjing 225
Seoul 203
Ho Chi Minh City 200
New York 188
Los Angeles 180
Helsinki 175
Siena 172
Lauterbourg 166
Hanoi 144
Munich 127
Johannesburg 118
Boardman 117
Council Bluffs 115
San Diego 106
Milan 88
São Paulo 83
Nanchang 81
San Mateo 75
Shenyang 74
Buffalo 73
Norwalk 68
Shanghai 62
Orem 55
Menlo Park 54
Rome 51
Turku 51
Columbus 50
Tianjin 49
Abuja 48
Florence 48
Redondo Beach 48
Izmir 47
Málaga 44
San Francisco 43
Warsaw 43
Dong Ket 41
Montreal 41
Nuremberg 38
Zhengzhou 38
Chicago 37
London 37
Changsha 35
Toronto 34
Chennai 33
Jiaxing 33
Da Nang 32
Hebei 32
Brussels 31
Denver 31
Brooklyn 30
Tokyo 30
Rio de Janeiro 29
Haiphong 28
Brno 27
Guangzhou 26
Jinan 26
Phoenix 25
Belo Horizonte 24
Lancaster 24
Stockholm 24
Atlanta 23
Frankfurt am Main 23
Hangzhou 23
Poplar 23
Kunming 22
Bengaluru 21
Ningbo 20
Mexico City 18
Baghdad 17
Dearborn 17
Abidjan 16
Amsterdam 16
Ottawa 16
Padova 16
Washington 16
Ankara 15
Biên Hòa 15
Boston 15
Totale 22.458
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Nome #
MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotype 460
Chromosome 18 aberrations and epilepsy: a review 385
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability. 381
Drug Retention Rate and Predictive Factors of Drug Survival for Interleukin-1 Inhibitors in Systemic Juvenile Idiopathic Arthritis 333
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age 331
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features 325
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb 313
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 311
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum 308
Massive lamotrigine poisoning. A case report 307
2q24-q31 deletion: report of a case and review of the literature 306
Chitotriosidase and soluble IL-2 receptor: comparison of two markers of sarcoidosis severity 288
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene 285
Private inherited microdeletion/microduplications: implications in clinical practice 273
Aicardi syndrome with favorable outcome: case report and review 271
Efficacy and safety of topiramate in infants according to epilepsy syndromes 253
De novo complete trisomy 5p clinical and neuroradiological findings 250
Acute flaccid myelitis temporally associated with rhinovirus infection: just a coincidence? 249
Recurrent Miller Fisher syndrome in children 247
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 246
A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood 244
Biological markers of oxidative stress in progressive muscular dystrophies: A preliminary study: 157 243
SCN1A mutation associated with atypical Panayiotopoulos syndrome 240
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy 240
Oxidative stress in children affected by epileptic encephalopathies 239
Hot water epilepsy and focal malformation of the parietal cortex development 238
Treatment options for periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome in children and adults: a narrative review 236
Anticonvulsant drugs and hematological disease 235
Thyroid function in small for gestational age newborns: A review 232
Central precocious puberty and abnormal chromosomal patterns 232
Chitotriosidase activity in patients with interstitial lung disesaes 231
Elettroencephalographic and epileptic patterns in x chromosome anomalies 230
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 229
Optic perineuritis: A further cause of visual loss and disc edema in children 229
Precocious puberty with trisomy X syndrome 228
Segregation analysis in typical absence epilepsy 227
Serum levels of chitotriosidase as a marker of disease activity and clinical stage in sarcoidosis. 225
Typical absence seizures associated with localization-related epilepsy: a clinical and electroencephalographic characterization 223
Association of celiac disease in patients with multiple sclerosis in Tuscany 223
Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation 221
Antiepileptic drugs: role in paediatric poisoning 221
Childhood absence epilepsy: evolution and prognostic factors 220
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 220
Craniofacial dyssynostosis: case report and review 218
Schinzel-Giedion syndrome: a further cause of West syndrome 217
Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy 216
Transient neonatal hypothyroidism after gestational exposure to amiodarone: a follow-up of two cases 215
17p13.3 microdeletion including YWHAE and CRK genes: towards a clinical characterization 214
AUTS2-related syndrome: Insights from a large European cohort 211
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 211
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? 211
Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype. 210
Epilepsy in neurofibromatosis 1 210
Bathing epilepsy: report of two Caucasian cases 209
Lamotrigine in typical absence epilepsy 209
Association of Chiari I malformation, mental retardation, speech delay and epilepsy: a specific desorder ? 209
Dexfenfluramine effective in drug-resistant temporal lobe epilepsy 208
Lacosamide efficacy in epileptic syndromes with continuous spike and waves during slow sleep (CSWS) 205
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome 204
Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature 203
Anakinra drug retention rate and predictive factors of long-term response in systemic juvenile idiopathic arthritis and adult onset still disease 203
Lacosamide in children with refractory status epilepticus. A multicenter Italian experience 202
Brain mitochondrial impairment in ethylmalonic encephalopathy 202
Growth hormone secretion in Prader-Willi syndrome 200
Epilepsy and elettroencephalographic finding in pericentric inversion of chromosome 12 200
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 196
Topiramate effects on plasma serotonin levels in children with epilepsy 195
Acute ataxia in paediatric emergency departments: A multicentre Italian study 195
Treating juvenile idiopathic arthritis (JIA)-related uveitis beyond TNF-α inhibition: a narrative review 194
Multiple neuroendocrine disorder in Salla disease 194
Chitotriosidase activity in the serum of patients with sarcoidosis and pulmonary tuberculosis 193
Late-onset childhood occipital epilepsy(Gastaut type): a family study 192
Body mass index and serum lipid changes during treatment with valproic acid in children with epilepsy 192
Diagnosis of Angelman syndrome: clinical and EEG criteria 192
Subcortical low-intensity and restricted diffusion after first seizure in a child 191
CKAP2L mutation confirms the diagnosis of Filippi syndrome 191
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy 190
Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsy 184
Refractory absence seizures: An Italian multicenter retrospective study 184
Valproate in adolescents with photosensitive epilepsy with generalized tonic-clonic seizures only 184
Plasmapheresis in a child affected by acute disseminated encephalomyelitis 184
Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy 183
Ethylmalonic encephalopathy: further clinical and neuroradiological characterization 180
Epilepsy in Menkes disease An electroclinical long-term study of 28 patients 179
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 179
Next-generation sequencing approach to hyperCKemia: A 2-year cohort study 179
Alternating hemiplegia of childhood or Hashimoto’s encephalopathy? 179
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review 178
Hints for Genetic and Clinical Differentiation of Adult-Onset Monogenic Autoinflammatory Diseases 178
Comparison of Early vs. Delayed Anakinra Treatment in Patients With Adult Onset Still's Disease and Effect on Clinical and Laboratory Outcomes 177
Natural history of KBG syndrome in a large European cohort 176
Efficacy and safety of topiramate in refractory epilepsy of childhood: long-term follow-up study 175
Zonisamide in children and young adults with refractory epilepsy: an open label, multicenter Italian study 175
Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalities 175
Variant late infantile neuronal ceroid lipofuscinosis because of CLN1 mutations 173
Oxidative stress in epilepsy 173
Chitotriosidase analysis in bronchoalveolar lavage of patients with sarcoidosis. 170
Intractable reflex audiogenic seizures in Aicardi syndrome 169
Photoparoxysmal responses in children with chromosomal aberrations 168
Malformation of the cortical development in Neurofibromatosis type 1 168
Totale 22.400
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Categoria #
all - tutte 110.781
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 110.781
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021164 0 0 0 0 0 0 0 0 0 0 0 164
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
2025/202610.850 758 1.551 1.383 1.437 2.168 434 1.226 332 342 538 469 212
Totale 33.198