IRIS
PERROTTA, Silverio
 Distribuzione geografica
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Continente #
EU - Europa 16.016
NA - Nord America 8.749
AS - Asia 6.462
SA - Sud America 1.027
AF - Africa 94
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 5
Totale 32.363
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Nazione #
RU - Federazione Russa 10.039
US - Stati Uniti d'America 8.586
SG - Singapore 2.264
IE - Irlanda 1.667
CN - Cina 1.532
IT - Italia 1.095
HK - Hong Kong 1.012
BR - Brasile 862
UA - Ucraina 734
GB - Regno Unito 729
VN - Vietnam 682
DE - Germania 630
SE - Svezia 262
FR - Francia 246
IN - India 226
FI - Finlandia 222
KR - Corea 209
JP - Giappone 151
GR - Grecia 137
TR - Turchia 112
CA - Canada 95
AR - Argentina 77
BD - Bangladesh 65
BE - Belgio 48
MX - Messico 41
PK - Pakistan 41
AT - Austria 39
NL - Olanda 35
IQ - Iraq 29
ES - Italia 25
PL - Polonia 24
ZA - Sudafrica 23
EC - Ecuador 21
ID - Indonesia 21
SA - Arabia Saudita 21
VE - Venezuela 19
UZ - Uzbekistan 16
EG - Egitto 15
CH - Svizzera 14
CO - Colombia 14
PY - Paraguay 14
CZ - Repubblica Ceca 13
DZ - Algeria 13
CL - Cile 11
EU - Europa 10
PH - Filippine 10
TN - Tunisia 10
IL - Israele 9
AE - Emirati Arabi Uniti 7
ET - Etiopia 7
MA - Marocco 7
MY - Malesia 7
BG - Bulgaria 6
DK - Danimarca 6
IR - Iran 6
DO - Repubblica Dominicana 5
HU - Ungheria 5
JO - Giordania 5
KE - Kenya 5
KZ - Kazakistan 5
PE - Perù 5
PT - Portogallo 5
RS - Serbia 5
AZ - Azerbaigian 4
CR - Costa Rica 4
LT - Lituania 4
MD - Moldavia 4
OM - Oman 4
RO - Romania 4
AU - Australia 3
BH - Bahrain 3
CI - Costa d'Avorio 3
JM - Giamaica 3
KG - Kirghizistan 3
LB - Libano 3
MK - Macedonia 3
NG - Nigeria 3
NP - Nepal 3
PA - Panama 3
SN - Senegal 3
UY - Uruguay 3
AO - Angola 2
BA - Bosnia-Erzegovina 2
CY - Cipro 2
GE - Georgia 2
HR - Croazia 2
IS - Islanda 2
MQ - Martinica 2
NI - Nicaragua 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
TT - Trinidad e Tobago 2
AL - Albania 1
AM - Armenia 1
BB - Barbados 1
BO - Bolivia 1
BS - Bahamas 1
BW - Botswana 1
EE - Estonia 1
GA - Gabon 1
Totale 32.346
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Città #
Moscow 3.607
Dublin 1.655
Jacksonville 1.136
Hong Kong 998
Singapore 975
Santa Clara 963
Chandler 898
San Jose 729
Chicago 478
Ashburn 385
Princeton 249
Beijing 242
Wilmington 237
Ho Chi Minh City 236
Caserta 219
Medford 211
Seoul 206
Hefei 205
Boardman 191
Ann Arbor 184
Bengaluru 168
Bremen 167
Hanoi 162
Falls Church 144
New York 138
San Mateo 137
Naples 130
Roxbury 127
Woodbridge 127
Dallas 112
Munich 84
The Dalles 82
São Paulo 76
Nanjing 68
Los Angeles 57
Cambridge 56
Des Moines 56
Napoli 46
Da Nang 41
Rome 37
Brussels 36
Ercolano 36
Council Bluffs 31
Nuremberg 30
Redwood City 30
Belo Horizonte 28
Elora 28
Grumo Nevano 28
Jinan 28
Düsseldorf 27
Helsinki 27
Mountain View 27
Haiphong 26
Memphis 26
Milan 25
Rio de Janeiro 25
Istanbul 24
London 24
Amsterdam 22
Houston 22
Norwalk 22
Vienna 22
Orem 21
Tianjin 21
Kunming 20
Nanchang 20
Atlanta 19
Aversa 18
Curitiba 18
Guangzhou 18
Brasília 17
Brooklyn 17
Hải Dương 17
Frankfurt am Main 16
Shenyang 16
Zhengzhou 16
Boston 15
Falkenstein 15
Tashkent 15
Turku 15
Biên Hòa 14
Montreal 14
Riyadh 14
Warsaw 14
Auburn Hills 13
Bologna 13
Johannesburg 13
Shanghai 13
Stockholm 13
Toronto 13
Baghdad 12
Campinas 12
Lahore 12
Nha Trang 12
Pozzuoli 12
Tokyo 12
Brno 11
Buenos Aires 11
Goiânia 11
Mexico City 11
Totale 17.177
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Nome #
Osteoporosis in thalassemia major: A possible role of chelation therapy. 830
Effects of germline VHL deficiency on growth, metabolism, and mitochondria 219
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry 205
A cancer-associated CDKN1B mutation induces p27 phosphorylation on a novel residue: a new mechanism for tumor suppressor loss-of-function 202
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 196
The tyrosine kinase inhibitor dasatinib induces a marked adipogenic differentiation of human multipotent mesenchymal stromal cells. 195
Iron overload enhances human mesenchymal stromal cell growth and hampers matrix calcification 187
Endocannabinoid Research Group (ERG), Italy. The endovanilloid/endocannabinoid system: a new potential target for osteoporosis therapy. 186
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura. 186
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 185
HNF-1β mutation affects PKD2 and SOCS3 expression causing renal cysts and diabetes in MODY5 kindred. 185
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 181
Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders 176
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload 174
Childhood Head and Neck Lymphadenopathy: A Report by a Single Institution (2003-2017) 174
A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity 173
Auditory cortex hypoperfusion: a metabolic hallmark in Beta Thalassemia 173
Abbreviated breast magnetic resonance imaging (FAST-MRI): A novel approach to breast cancer screening in patients with previous Hodgkin lymphoma 172
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major. 171
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation) 167
Asymptomatic intracranial aneurysms in beta-thalassemia: A three-year follow-up report 167
A phase 3 trial of luspatercept in patients with transfusion-dependent β-thalassemia 167
A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli 166
Tyrosine kinase inhibitors and mesenchymal stromal cells: effects on self-renewal, commitment and functions 165
The Italian survey on hereditary spherocytosis 164
Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: Evidence for a differentiated splenic conditioning role 164
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome 162
Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology. 160
Erythrocyte genotyping for transfusion-dependent patients at the Azienda Universitaria Policlinico of Naples 159
LEOPARD syndrome: clinical dilemmas in differential diagnosis of RASopathies. 158
Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown origin 157
Brain iron content in systemic iron overload: A beta-thalassemia quantitative MRI study 157
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity 157
Vitamin A and infancy. Biochemical, functional, and clinical aspects 156
Vitamin A and infancy. Biochemical, functional, and clinical aspects 154
4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis [3] 154
Targeted molecular therapy (modified RIST regimen) in relapsed high risk stage IV neuroblastoma: two cases report 153
A 23-month-old girl with chronic seborrhoeic' dermatitis, dehydration and failure to thrive 153
Clinical outcome of transfusions with extended red blood cell matching in β-thalassemia patients: A single-center experience 152
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function 151
Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease gene 151
A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia. 150
Genome editing and cancer therapy: handling the hypoxia-responsive pathway as a promising strategy 149
Cardiac autonomic regulation in response to a mixed meal is impaired in obese children and adolescents: the role played by insulin resistance. 149
ERITROCITOSI CONGENITA CAUSATA DA ALTERAZIONI DEL SISTEMA SENSORE DELL’OSSIGENO 149
Brain functional impairment in beta-thalassaemia: the cognitive profile in Italian neurologically asymptomatic adult patients in comparison to the reported literature 148
Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned 147
p27Kip1 serine 10 phosphorylation determines its metabolism and interaction with cyclin-dependent kinases. 146
Arg(1809) substitution in neurofibromin: further evidence of a genotype-phenotype correlation in neurofibromatosis type 1 146
Time trends of cancer incidence in childhood in Campania region: 25 years of observation 146
Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene. 145
BONE MINERAL DENSITY IMPROVEMENT IN PATIENTS WITH THALASSEMIA MAJOR ON LONG-TERM CHELATION THERAPY WITH DEFERASIROX 145
Cb2 receptor stimulation and dexamethasone restore the anti-inflammatory and immune-regulatory properties of mesenchymal stromal cells of children with immune thrombocytopenia 145
Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype-Phenotype Correlations 144
Concordanza tra visita oculistica e RM encefalo nello screening del glioma delle vie ottiche nei pazienti pediatrici con neurofibromatosi tipo 1 143
Age of first pain crisis and associated complications in the CASiRe international sickle cell disease cohort 143
Very early onset of autoimmune thyroiditis in a toddler with severe hypothyroidism presentation: A case report 141
No evidence of increased cerebrovascular involvement in adult neurologically-asymptomatic β-Thalassaemia. A multicentre multimodal magnetic resonance study 141
Iron overload causes osteoporosis in Thalassemia Major patients through interaction with TRPV1 channels. 140
Resveratrol mimics insulin activity in the adipogenic commitment of human bone marrow mesenchymal stromal cells. 139
Multiple spinal nerve enlargement and SOS1 mutation: further evidence of overlap between Neurofibromatosis type 1 and Noonan phenotype 139
Association of immune thrombocytopenia and celiac disease in children: A retrospective case control study 139
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 138
Evaluation of Browning Agents on the White Adipogenesis of Bone Marrow Mesenchymal Stromal Cells: A Contribution to Fighting Obesity 138
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 138
Transient erythroblastopenia of childhood after COVID-19 infection: a case report 137
The endovanilloid/endocannabinoid system: A new potential target for osteoporosis therapy 136
Unusual association of non-anaplastic Wilms tumor and Cornelia de Lange syndrome: Case report 136
An Educational Study Promoting the Delivery of Transcranial Doppler Ultrasound Screening in Paediatric Sickle Cell Disease: A European Multi-Centre Perspective 136
Acute kidney injury in children hospitalized for acute gastroenteritis: prevalence and risk factors 136
Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1 135
Erythropoietin receptors on cancer cells: a still open question. 134
{beta}-spectrinBari: a truncated {beta}-chain responsible for dominant hereditary spherocytosis. 134
Brain perfusion changes in beta-thalassemia 132
Von Hippel-Lindau-dependent polycythemia is endemic on the island of Ischia: identification of a novel cluster. 132
A rapid method for the detection of alpha I/65 hereditary elliptocytosis 132
National systematic approach to the management of asplenia: the set up of the Italian Network on Asplenia 131
Global geographic differences in healthcare utilization for sickle cell disease pain crises in the CASiRe cohort 131
A mutation in the acyl-coenzyme A binding domain-containing protein 5 gene (ACBD5 ) identified in autosomal dominant thrombocytopenia 130
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research 130
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations 129
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition 129
Studio retrospettivo sulle complicanze emato-oncologiche nella neurofibromatosi tipo 1 in età pediatrica 126
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 125
Long-term improvement in cardiac magnetic resonance in β-thalassemia major patients treated with deferasirox extends to patients with abnormal baseline cardiac function 125
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency 125
Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control study 125
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele 124
The endovanilloid/endocannabinoid system in human osteoclasts: Possible involvement in bone formation and resorption 124
Intermittent macrothrombocytopenia in a novel patient with Takenouchi-Kosaki syndrome and review of literature. 123
Hereditary spherocytosis (HS) due to loss of anion exchange transporter 122
Seizures in children with neurofibromatosis type 1: Is neurofibromatosis type 1 enough? 122
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis 120
Winners' cup: A national football tournament brings together Adolescent patients with cancer from all over Italy 120
Pretreatment Endocrine Disorders Due to Optic Pathway Gliomas in Pediatric Neurofibromatosis Type 1: Multicenter Study 120
Characterisation of transfusion-dependent prediabetes using continuous glucose monitoring: The Haemoglycare study 119
Genetic basis of congenital erythrocytosis: mutation update and online databases. 119
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 119
Identificazione di una mutazione del gene PAX2 in una famiglia con RVU isolato 119
Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin 118
Totale 15.567
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Categoria #
all - tutte 112.315
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 112.315
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202161 0 0 0 0 0 0 0 0 0 0 0 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
2025/202616.810 625 856 885 833 1.396 9.308 931 533 602 409 304 128
Totale 32.964