IRIS
PERROTTA, Silverio
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 15.572
NA - Nord America 7.219
AS - Asia 5.546
SA - Sud America 992
AF - Africa 85
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 4
Totale 29.428
Salva come PNG Salva come JPEG
Nazione #
RU - Federazione Russa 9.816
US - Stati Uniti d'America 7.103
SG - Singapore 2.051
IE - Irlanda 1.659
CN - Cina 1.377
IT - Italia 982
HK - Hong Kong 961
BR - Brasile 836
UA - Ucraina 732
GB - Regno Unito 706
DE - Germania 619
VN - Vietnam 261
SE - Svezia 260
FR - Francia 236
FI - Finlandia 220
IN - India 208
KR - Corea 206
JP - Giappone 144
GR - Grecia 135
TR - Turchia 109
AR - Argentina 75
CA - Canada 68
BE - Belgio 48
BD - Bangladesh 43
AT - Austria 37
PK - Pakistan 37
MX - Messico 33
IQ - Iraq 26
ZA - Sudafrica 23
EC - Ecuador 20
ID - Indonesia 20
SA - Arabia Saudita 20
NL - Olanda 18
VE - Venezuela 17
ES - Italia 16
PL - Polonia 16
UZ - Uzbekistan 15
EG - Egitto 14
PY - Paraguay 14
CH - Svizzera 13
CO - Colombia 12
CZ - Repubblica Ceca 12
DZ - Algeria 12
CL - Cile 10
EU - Europa 10
IL - Israele 9
ET - Etiopia 7
MA - Marocco 7
PH - Filippine 7
AE - Emirati Arabi Uniti 6
DK - Danimarca 6
TN - Tunisia 6
BG - Bulgaria 5
HU - Ungheria 5
IR - Iran 5
KE - Kenya 5
KZ - Kazakistan 5
RS - Serbia 5
JO - Giordania 4
MY - Malesia 4
PE - Perù 4
PT - Portogallo 4
RO - Romania 4
AZ - Azerbaigian 3
BH - Bahrain 3
DO - Repubblica Dominicana 3
KG - Kirghizistan 3
LB - Libano 3
LT - Lituania 3
MK - Macedonia 3
OM - Oman 3
PA - Panama 3
SN - Senegal 3
UY - Uruguay 3
AO - Angola 2
AU - Australia 2
BA - Bosnia-Erzegovina 2
CI - Costa d'Avorio 2
GE - Georgia 2
IS - Islanda 2
MD - Moldavia 2
NG - Nigeria 2
NI - Nicaragua 2
NO - Norvegia 2
NP - Nepal 2
NZ - Nuova Zelanda 2
AM - Armenia 1
BB - Barbados 1
BO - Bolivia 1
BS - Bahamas 1
CR - Costa Rica 1
CY - Cipro 1
EE - Estonia 1
GA - Gabon 1
GT - Guatemala 1
HN - Honduras 1
IM - Isola di Man 1
JM - Giamaica 1
KW - Kuwait 1
LK - Sri Lanka 1
Totale 29.419
Salva come PNG Salva come JPEG
Città #
Moscow 3.464
Dublin 1.649
Jacksonville 1.133
Hong Kong 957
Santa Clara 936
Chandler 898
Singapore 828
Chicago 472
Princeton 249
Wilmington 237
Beijing 222
Caserta 219
Medford 210
Seoul 206
Hefei 205
Ashburn 191
Boardman 191
Ann Arbor 184
Bengaluru 168
Bremen 167
Falls Church 144
San Mateo 137
Roxbury 127
Woodbridge 127
New York 116
Ho Chi Minh City 103
Naples 100
Dallas 96
Munich 84
The Dalles 82
São Paulo 70
Nanjing 68
Cambridge 56
Des Moines 54
Napoli 46
Hanoi 41
Brussels 36
Ercolano 36
Redwood City 30
Nuremberg 29
Rome 29
Elora 28
Grumo Nevano 28
Jinan 28
Belo Horizonte 27
Düsseldorf 27
Mountain View 27
Helsinki 25
Rio de Janeiro 25
Istanbul 24
Los Angeles 24
Norwalk 22
Milan 21
Tianjin 21
Vienna 21
Kunming 20
London 20
Nanchang 20
Houston 19
Guangzhou 18
Brasília 16
Curitiba 16
Shenyang 16
Zhengzhou 16
Aversa 15
Falkenstein 15
Turku 15
Riyadh 14
Tashkent 14
Auburn Hills 13
Johannesburg 13
Da Nang 12
Haiphong 12
Pozzuoli 12
Baghdad 11
Boston 11
Brno 11
Brooklyn 11
Campinas 11
Goiânia 11
Nocera Inferiore 11
Stockholm 11
Buenos Aires 10
Kontich 10
Lahore 10
Manaus 10
Biên Hòa 9
Columbus 9
Dhaka 9
Fairfield 9
Guayaquil 9
Porto Alegre 9
Salvador 9
San Sebastiano al Vesuvio 9
Shanghai 9
Atlanta 8
Guarulhos 8
Islamabad 8
Lappeenranta 8
Mexico City 8
Totale 15.290
Salva come PNG Salva come JPEG
Nome #
Osteoporosis in thalassemia major: A possible role of chelation therapy. 825
Effects of germline VHL deficiency on growth, metabolism, and mitochondria 202
The tyrosine kinase inhibitor dasatinib induces a marked adipogenic differentiation of human multipotent mesenchymal stromal cells. 181
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry 180
A cancer-associated CDKN1B mutation induces p27 phosphorylation on a novel residue: a new mechanism for tumor suppressor loss-of-function 175
Endocannabinoid Research Group (ERG), Italy. The endovanilloid/endocannabinoid system: a new potential target for osteoporosis therapy. 171
Blood transfusions and adverse acute events: a retrospective study from 214 transfusion-dependent pediatric patients comparing transfused blood components by apheresis or by whole blood 170
Iron overload enhances human mesenchymal stromal cell growth and hampers matrix calcification 169
HNF-1β mutation affects PKD2 and SOCS3 expression causing renal cysts and diabetes in MODY5 kindred. 168
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura. 166
Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders 166
Neuropsychiatric Manifestations, Reduced Self-Esteem and Poor Quality of Life in Children and Adolescents with Neurofibromatosis Type 1 (NF1): The Impact of Symptom Visibility and Bullying Behavior 162
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 161
Tyrosine kinase inhibitors and mesenchymal stromal cells: effects on self-renewal, commitment and functions 160
Childhood Head and Neck Lymphadenopathy: A Report by a Single Institution (2003-2017) 159
A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli 158
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload 158
The Italian survey on hereditary spherocytosis 157
Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: Evidence for a differentiated splenic conditioning role 157
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major. 156
Auditory cortex hypoperfusion: a metabolic hallmark in Beta Thalassemia 156
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation) 155
Abbreviated breast magnetic resonance imaging (FAST-MRI): A novel approach to breast cancer screening in patients with previous Hodgkin lymphoma 155
A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity 152
A phase 3 trial of luspatercept in patients with transfusion-dependent β-thalassemia 151
Asymptomatic intracranial aneurysms in beta-thalassemia: A three-year follow-up report 150
Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown origin 149
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome 149
Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology. 147
Erythrocyte genotyping for transfusion-dependent patients at the Azienda Universitaria Policlinico of Naples 147
Brain iron content in systemic iron overload: A beta-thalassemia quantitative MRI study 147
4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis [3] 146
Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease gene 144
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity 144
A 23-month-old girl with chronic seborrhoeic' dermatitis, dehydration and failure to thrive 143
A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia. 141
ERITROCITOSI CONGENITA CAUSATA DA ALTERAZIONI DEL SISTEMA SENSORE DELL’OSSIGENO 141
Cardiac autonomic regulation in response to a mixed meal is impaired in obese children and adolescents: the role played by insulin resistance. 140
Clinical outcome of transfusions with extended red blood cell matching in β-thalassemia patients: A single-center experience 139
LEOPARD syndrome: clinical dilemmas in differential diagnosis of RASopathies. 138
Targeted molecular therapy (modified RIST regimen) in relapsed high risk stage IV neuroblastoma: two cases report 138
Arg(1809) substitution in neurofibromin: further evidence of a genotype-phenotype correlation in neurofibromatosis type 1 137
Brain functional impairment in beta-thalassaemia: the cognitive profile in Italian neurologically asymptomatic adult patients in comparison to the reported literature 137
Time trends of cancer incidence in childhood in Campania region: 25 years of observation 136
Age of first pain crisis and associated complications in the CASiRe international sickle cell disease cohort 136
Genome editing and cancer therapy: handling the hypoxia-responsive pathway as a promising strategy 135
Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned 134
BONE MINERAL DENSITY IMPROVEMENT IN PATIENTS WITH THALASSEMIA MAJOR ON LONG-TERM CHELATION THERAPY WITH DEFERASIROX 133
Concordanza tra visita oculistica e RM encefalo nello screening del glioma delle vie ottiche nei pazienti pediatrici con neurofibromatosi tipo 1 133
Cb2 receptor stimulation and dexamethasone restore the anti-inflammatory and immune-regulatory properties of mesenchymal stromal cells of children with immune thrombocytopenia 132
Vitamin A and infancy. Biochemical, functional, and clinical aspects 131
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function 130
Vitamin A and infancy. Biochemical, functional, and clinical aspects 130
No evidence of increased cerebrovascular involvement in adult neurologically-asymptomatic β-Thalassaemia. A multicentre multimodal magnetic resonance study 130
Acute kidney injury in children hospitalized for acute gastroenteritis: prevalence and risk factors 130
Association of immune thrombocytopenia and celiac disease in children: A retrospective case control study 130
Very early onset of autoimmune thyroiditis in a toddler with severe hypothyroidism presentation: A case report 129
Multiple spinal nerve enlargement and SOS1 mutation: further evidence of overlap between Neurofibromatosis type 1 and Noonan phenotype 129
Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype-Phenotype Correlations 128
The endovanilloid/endocannabinoid system: A new potential target for osteoporosis therapy 126
Risk factors for endocrine complications in transfusion-dependent thalassemia patients on chelation therapy with deferasirox: a risk assessment study from a multicentre nation-wide cohort 126
p27Kip1 serine 10 phosphorylation determines its metabolism and interaction with cyclin-dependent kinases. 125
Von Hippel-Lindau-dependent polycythemia is endemic on the island of Ischia: identification of a novel cluster. 124
A rapid method for the detection of alpha I/65 hereditary elliptocytosis 124
A study of the geographic distribution and associated risk factors of leg ulcers within an international cohort of sickle cell disease patients: the CASiRe group analysis 124
Evaluation of Browning Agents on the White Adipogenesis of Bone Marrow Mesenchymal Stromal Cells: A Contribution to Fighting Obesity 124
National systematic approach to the management of asplenia: the set up of the Italian Network on Asplenia 123
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research 123
Iron overload causes osteoporosis in Thalassemia Major patients through interaction with TRPV1 channels. 122
{beta}-spectrinBari: a truncated {beta}-chain responsible for dominant hereditary spherocytosis. 122
Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene. 122
A mutation in the acyl-coenzyme A binding domain-containing protein 5 gene (ACBD5 ) identified in autosomal dominant thrombocytopenia 122
An Educational Study Promoting the Delivery of Transcranial Doppler Ultrasound Screening in Paediatric Sickle Cell Disease: A European Multi-Centre Perspective 122
Global geographic differences in healthcare utilization for sickle cell disease pain crises in the CASiRe cohort 122
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations 121
Resveratrol mimics insulin activity in the adipogenic commitment of human bone marrow mesenchymal stromal cells. 121
Unusual association of non-anaplastic Wilms tumor and Cornelia de Lange syndrome: Case report 120
Hereditary spherocytosis (HS) due to loss of anion exchange transporter 118
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele 117
Erythropoietin receptors on cancer cells: a still open question. 117
Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1 117
Seizures in children with neurofibromatosis type 1: Is neurofibromatosis type 1 enough? 117
Long-term improvement in cardiac magnetic resonance in β-thalassemia major patients treated with deferasirox extends to patients with abnormal baseline cardiac function 116
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency 116
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition 116
Intermittent macrothrombocytopenia in a novel patient with Takenouchi-Kosaki syndrome and review of literature. 115
Transient erythroblastopenia of childhood after COVID-19 infection: a case report 114
Winners' cup: A national football tournament brings together Adolescent patients with cancer from all over Italy 114
Studio retrospettivo sulle complicanze emato-oncologiche nella neurofibromatosi tipo 1 in età pediatrica 113
The endovanilloid/endocannabinoid system in human osteoclasts: Possible involvement in bone formation and resorption 113
Absence of blood donors’ anti-SARS-CoV-2 antibodies in pre-storage leukoreduced red blood cell units indicates no role of passive immunity for blood recipients 112
Neridronate improves bone mineral density and reduces back pain in β-thalassaemia patients with osteoporosis: results from a phase 2, randomized, parallel-arm, open-label study 112
Brain perfusion changes in beta-thalassemia 111
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis 111
Genetic basis of congenital erythrocytosis: mutation update and online databases. 111
Identificazione di una mutazione del gene PAX2 in una famiglia con RVU isolato 111
Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin 110
Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control study 109
Tumori renali: esperienza trentennale monoistituzionale 107
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience 107
Totale 14.270
Salva come PNG Salva come JPEG
Categoria #
all - tutte 101.288
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 101.288
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021978 0 0 0 0 0 31 257 189 26 231 183 61
2021/20221.995 175 58 63 86 543 34 105 69 78 140 179 465
2022/20233.869 389 152 336 301 375 294 12 191 1.608 35 100 76
2023/20241.270 105 40 69 137 425 120 22 56 24 10 87 175
2024/20254.059 28 41 43 122 704 454 661 440 577 438 310 241
2025/202613.860 625 856 885 836 1.396 9.262 0 0 0 0 0 0
Totale 30.014