IRIS
PERROTTA, Silverio
 Distribuzione geografica
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Continente #
EU - Europa 16.063
NA - Nord America 9.251
AS - Asia 6.558
SA - Sud America 1.039
Continente sconosciuto - Info sul continente non disponibili 612
AF - Africa 94
OC - Oceania 5
Totale 33.622
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Nazione #
RU - Federazione Russa 10.039
US - Stati Uniti d'America 9.058
SG - Singapore 2.337
IE - Irlanda 1.667
CN - Cina 1.543
IT - Italia 1.124
HK - Hong Kong 1.019
BR - Brasile 866
UA - Ucraina 735
GB - Regno Unito 730
VN - Vietnam 682
DE - Germania 634
SE - Svezia 262
FR - Francia 250
IN - India 227
FI - Finlandia 223
KR - Corea 210
JP - Giappone 153
GR - Grecia 138
TR - Turchia 112
CA - Canada 106
AR - Argentina 78
BD - Bangladesh 65
BE - Belgio 48
MX - Messico 43
PK - Pakistan 41
AT - Austria 39
NL - Olanda 35
IQ - Iraq 29
ES - Italia 27
PL - Polonia 25
EC - Ecuador 23
ZA - Sudafrica 23
ID - Indonesia 21
SA - Arabia Saudita 21
VE - Venezuela 20
CO - Colombia 16
UZ - Uzbekistan 16
EG - Egitto 15
CH - Svizzera 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
CR - Costa Rica 7
ET - Etiopia 7
MA - Marocco 7
MY - Malesia 7
PT - Portogallo 7
BG - Bulgaria 6
DK - Danimarca 6
HU - Ungheria 6
IR - Iran 6
PE - Perù 6
DO - Repubblica Dominicana 5
JO - Giordania 5
KE - Kenya 5
KZ - Kazakistan 5
RS - Serbia 5
AZ - Azerbaigian 4
GT - Guatemala 4
JM - Giamaica 4
LT - Lituania 4
MD - Moldavia 4
OM - Oman 4
RO - Romania 4
TT - Trinidad e Tobago 4
UY - Uruguay 4
AU - Australia 3
BH - Bahrain 3
CI - Costa d'Avorio 3
KG - Kirghizistan 3
LB - Libano 3
MK - Macedonia 3
NG - Nigeria 3
NI - Nicaragua 3
NP - Nepal 3
PA - Panama 3
SN - Senegal 3
SV - El Salvador 3
AM - Armenia 2
AO - Angola 2
BA - Bosnia-Erzegovina 2
CY - Cipro 2
GD - Grenada 2
GE - Georgia 2
HN - Honduras 2
HR - Croazia 2
IS - Islanda 2
MQ - Martinica 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
PR - Porto Rico 2
AL - Albania 1
BB - Barbados 1
Totale 33.001
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Città #
Moscow 3.607
Dublin 1.655
Jacksonville 1.136
Hong Kong 1.004
Santa Clara 995
Singapore 993
Chandler 898
San Jose 735
Chicago 481
Ashburn 460
Beijing 249
Princeton 249
Wilmington 237
Ho Chi Minh City 236
Caserta 219
Medford 211
Seoul 207
Hefei 205
Boardman 192
Ann Arbor 184
Bengaluru 169
Bremen 167
Hanoi 162
Falls Church 144
New York 139
Naples 137
San Mateo 137
Roxbury 127
Woodbridge 127
Dallas 115
Council Bluffs 96
Munich 84
The Dalles 82
São Paulo 76
Nanjing 68
Los Angeles 64
Cambridge 56
Des Moines 56
Napoli 46
Da Nang 41
Rome 38
Brussels 36
Ercolano 36
Nuremberg 30
Redwood City 30
Belo Horizonte 28
Elora 28
Grumo Nevano 28
Jinan 28
Memphis 28
Düsseldorf 27
Helsinki 27
Milan 27
Mountain View 27
Haiphong 26
London 25
Rio de Janeiro 25
Houston 24
Istanbul 24
Amsterdam 22
Atlanta 22
Norwalk 22
Vienna 22
Orem 21
Tianjin 21
Frankfurt am Main 20
Kunming 20
Nanchang 20
Brooklyn 19
Aversa 18
Curitiba 18
Guangzhou 18
Montreal 18
Brasília 17
Hải Dương 17
Shenyang 16
Zhengzhou 16
Boston 15
Falkenstein 15
Tashkent 15
Toronto 15
Turku 15
Biên Hòa 14
Riyadh 14
Shanghai 14
Tokyo 14
Warsaw 14
Auburn Hills 13
Bologna 13
Johannesburg 13
Mexico City 13
Stockholm 13
Baghdad 12
Campinas 12
Florence 12
Lahore 12
Nha Trang 12
Pozzuoli 12
San Francisco 12
Brno 11
Totale 17.440
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Nome #
Osteoporosis in thalassemia major: A possible role of chelation therapy. 831
Effects of germline VHL deficiency on growth, metabolism, and mitochondria 225
Juvenile erythrocytosis in children after liver transplantation: prevalence, risk factors and outcome 209
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry 206
A cancer-associated CDKN1B mutation induces p27 phosphorylation on a novel residue: a new mechanism for tumor suppressor loss-of-function 203
The tyrosine kinase inhibitor dasatinib induces a marked adipogenic differentiation of human multipotent mesenchymal stromal cells. 198
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 198
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 188
Iron overload enhances human mesenchymal stromal cell growth and hampers matrix calcification 188
Endocannabinoid Research Group (ERG), Italy. The endovanilloid/endocannabinoid system: a new potential target for osteoporosis therapy. 187
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura. 187
HNF-1β mutation affects PKD2 and SOCS3 expression causing renal cysts and diabetes in MODY5 kindred. 186
Screening for sickle cell disease by point-of-care tests in Italy: pilot study on 1000 at risk children 185
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 184
Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders 177
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload 177
Auditory cortex hypoperfusion: a metabolic hallmark in Beta Thalassemia 176
Childhood Head and Neck Lymphadenopathy: A Report by a Single Institution (2003-2017) 175
A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity 174
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major. 173
Abbreviated breast magnetic resonance imaging (FAST-MRI): A novel approach to breast cancer screening in patients with previous Hodgkin lymphoma 172
A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli 169
Tyrosine kinase inhibitors and mesenchymal stromal cells: effects on self-renewal, commitment and functions 169
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
Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: Evidence for a differentiated splenic conditioning role 166
The Italian survey on hereditary spherocytosis 165
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome 163
Brain iron content in systemic iron overload: A beta-thalassemia quantitative MRI study 161
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 160
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity 160
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
Vitamin A and infancy. Biochemical, functional, and clinical aspects 156
4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis [3] 156
Vitamin A and infancy. Biochemical, functional, and clinical aspects 156
A 23-month-old girl with chronic seborrhoeic' dermatitis, dehydration and failure to thrive 155
Targeted molecular therapy (modified RIST regimen) in relapsed high risk stage IV neuroblastoma: two cases report 154
Clinical outcome of transfusions with extended red blood cell matching in β-thalassemia patients: A single-center experience 153
Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease gene 152
Genome editing and cancer therapy: handling the hypoxia-responsive pathway as a promising strategy 151
A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia. 151
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
Cardiac autonomic regulation in response to a mixed meal is impaired in obese children and adolescents: the role played by insulin resistance. 151
ERITROCITOSI CONGENITA CAUSATA DA ALTERAZIONI DEL SISTEMA SENSORE DELL’OSSIGENO 150
Brain functional impairment in beta-thalassaemia: the cognitive profile in Italian neurologically asymptomatic adult patients in comparison to the reported literature 149
p27Kip1 serine 10 phosphorylation determines its metabolism and interaction with cyclin-dependent kinases. 148
Time trends of cancer incidence in childhood in Campania region: 25 years of observation 148
Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned 148
Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype-Phenotype Correlations 146
BONE MINERAL DENSITY IMPROVEMENT IN PATIENTS WITH THALASSEMIA MAJOR ON LONG-TERM CHELATION THERAPY WITH DEFERASIROX 146
Arg(1809) substitution in neurofibromin: further evidence of a genotype-phenotype correlation in neurofibromatosis type 1 146
Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene. 145
Very early onset of autoimmune thyroiditis in a toddler with severe hypothyroidism presentation: A case report 145
Cb2 receptor stimulation and dexamethasone restore the anti-inflammatory and immune-regulatory properties of mesenchymal stromal cells of children with immune thrombocytopenia 145
Age of first pain crisis and associated complications in the CASiRe international sickle cell disease cohort 144
Concordanza tra visita oculistica e RM encefalo nello screening del glioma delle vie ottiche nei pazienti pediatrici con neurofibromatosi tipo 1 143
No evidence of increased cerebrovascular involvement in adult neurologically-asymptomatic β-Thalassaemia. A multicentre multimodal magnetic resonance study 142
Iron overload causes osteoporosis in Thalassemia Major patients through interaction with TRPV1 channels. 141
Evaluation of Browning Agents on the White Adipogenesis of Bone Marrow Mesenchymal Stromal Cells: A Contribution to Fighting Obesity 141
Resveratrol mimics insulin activity in the adipogenic commitment of human bone marrow mesenchymal stromal cells. 140
Multiple spinal nerve enlargement and SOS1 mutation: further evidence of overlap between Neurofibromatosis type 1 and Noonan phenotype 140
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 139
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 139
Association of immune thrombocytopenia and celiac disease in children: A retrospective case control study 139
Transient erythroblastopenia of childhood after COVID-19 infection: a case report 138
Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1 137
An Educational Study Promoting the Delivery of Transcranial Doppler Ultrasound Screening in Paediatric Sickle Cell Disease: A European Multi-Centre Perspective 137
Acute kidney injury in children hospitalized for acute gastroenteritis: prevalence and risk factors 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
Erythropoietin receptors on cancer cells: a still open question. 135
{beta}-spectrinBari: a truncated {beta}-chain responsible for dominant hereditary spherocytosis. 135
A rapid method for the detection of alpha I/65 hereditary elliptocytosis 134
Brain perfusion changes in beta-thalassemia 133
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition 133
Von Hippel-Lindau-dependent polycythemia is endemic on the island of Ischia: identification of a novel cluster. 133
Global geographic differences in healthcare utilization for sickle cell disease pain crises in the CASiRe cohort 132
A mutation in the acyl-coenzyme A binding domain-containing protein 5 gene (ACBD5 ) identified in autosomal dominant thrombocytopenia 131
National systematic approach to the management of asplenia: the set up of the Italian Network on Asplenia 131
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research 131
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations 130
Long-term improvement in cardiac magnetic resonance in β-thalassemia major patients treated with deferasirox extends to patients with abnormal baseline cardiac function 129
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency 128
Studio retrospettivo sulle complicanze emato-oncologiche nella neurofibromatosi tipo 1 in età pediatrica 128
Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control study 127
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 126
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele 126
Seizures in children with neurofibromatosis type 1: Is neurofibromatosis type 1 enough? 126
Hereditary spherocytosis (HS) due to loss of anion exchange transporter 125
The endovanilloid/endocannabinoid system in human osteoclasts: Possible involvement in bone formation and resorption 125
Intermittent macrothrombocytopenia in a novel patient with Takenouchi-Kosaki syndrome and review of literature. 125
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis 123
Characterisation of transfusion-dependent prediabetes using continuous glucose monitoring: The Haemoglycare study 121
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 121
Identificazione di una mutazione del gene PAX2 in una famiglia con RVU isolato 121
Winners' cup: A national football tournament brings together Adolescent patients with cancer from all over Italy 121
Pretreatment Endocrine Disorders Due to Optic Pathway Gliomas in Pediatric Neurofibromatosis Type 1: Multicenter Study 121
Totale 15.870
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Categoria #
all - tutte 117.645
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 117.645
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.820 0 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
2025/202616.826 625 856 885 833 1.396 9.308 931 533 602 409 304 144
2026/2027642 246 396 0 0 0 0 0 0 0 0 0 0
Totale 33.622