IRIS
PERROTTA, Silverio
 Distribuzione geografica
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Continente #
EU - Europa 8.800
NA - Nord America 7.187
AS - Asia 5.457
SA - Sud America 974
AF - Africa 74
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 4
Totale 22.506
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Nazione #
US - Stati Uniti d'America 7.072
RU - Federazione Russa 3.057
SG - Singapore 2.017
IE - Irlanda 1.659
CN - Cina 1.371
IT - Italia 975
HK - Hong Kong 960
BR - Brasile 823
UA - Ucraina 732
GB - Regno Unito 704
DE - Germania 618
SE - Svezia 260
FR - Francia 236
VN - Vietnam 232
FI - Finlandia 220
IN - India 207
KR - Corea 206
JP - Giappone 144
GR - Grecia 135
TR - Turchia 108
AR - Argentina 73
CA - Canada 67
BE - Belgio 48
BD - Bangladesh 39
AT - Austria 35
PK - Pakistan 35
MX - Messico 33
IQ - Iraq 21
EC - Ecuador 20
ID - Indonesia 20
SA - Arabia Saudita 20
ZA - Sudafrica 20
NL - Olanda 18
ES - Italia 16
PL - Polonia 15
VE - Venezuela 15
EG - Egitto 14
PY - Paraguay 14
CH - Svizzera 13
UZ - Uzbekistan 13
CO - Colombia 12
CZ - Repubblica Ceca 12
DZ - Algeria 10
EU - Europa 10
CL - Cile 9
IL - Israele 7
PH - Filippine 7
AE - Emirati Arabi Uniti 6
DK - Danimarca 6
ET - Etiopia 6
MA - Marocco 6
TN - Tunisia 6
BG - Bulgaria 5
HU - Ungheria 5
IR - Iran 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
KE - Kenya 3
LB - Libano 3
LT - Lituania 3
MK - Macedonia 3
OM - Oman 3
PA - Panama 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
KG - Kirghizistan 2
MD - Moldavia 2
NG - Nigeria 2
NI - Nicaragua 2
NO - Norvegia 2
NP - Nepal 2
NZ - Nuova Zelanda 2
SN - Senegal 2
AM - Armenia 1
BB - Barbados 1
BO - Bolivia 1
BS - Bahamas 1
CR - Costa Rica 1
CY - Cipro 1
EE - Estonia 1
GT - Guatemala 1
HN - Honduras 1
IM - Isola di Man 1
JM - Giamaica 1
LK - Sri Lanka 1
LU - Lussemburgo 1
LV - Lettonia 1
Totale 22.499
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Città #
Dublin 1.649
Jacksonville 1.133
Moscow 999
Hong Kong 956
Santa Clara 935
Chandler 898
Singapore 794
Chicago 472
Princeton 249
Wilmington 237
Beijing 222
Caserta 219
Medford 210
Seoul 206
Hefei 205
Boardman 191
Ann Arbor 184
Ashburn 171
Bengaluru 168
Bremen 167
Falls Church 144
San Mateo 137
Roxbury 127
Woodbridge 127
New York 115
Dallas 95
Naples 95
Ho Chi Minh City 93
Munich 84
The Dalles 82
Nanjing 68
São Paulo 68
Cambridge 56
Des Moines 54
Napoli 46
Hanoi 38
Brussels 36
Ercolano 36
Redwood City 30
Rome 29
Elora 28
Grumo Nevano 28
Jinan 28
Nuremberg 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
Kunming 20
London 20
Nanchang 20
Houston 19
Vienna 19
Guangzhou 18
Brasília 16
Curitiba 16
Shenyang 16
Zhengzhou 16
Aversa 15
Falkenstein 15
Turku 15
Riyadh 14
Auburn Hills 13
Pozzuoli 12
Tashkent 12
Boston 11
Brno 11
Brooklyn 11
Goiânia 11
Haiphong 11
Nocera Inferiore 11
Stockholm 11
Buenos Aires 10
Campinas 10
Johannesburg 10
Kontich 10
Manaus 10
Baghdad 9
Columbus 9
Da Nang 9
Fairfield 9
Guayaquil 9
Lahore 9
Porto Alegre 9
Salvador 9
San Sebastiano al Vesuvio 9
Shanghai 9
Atlanta 8
Biên Hòa 8
Dhaka 8
Guarulhos 8
Lappeenranta 8
Mexico City 8
Ningbo 8
Totale 12.729
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Nome #
Osteoporosis in thalassemia major: A possible role of chelation therapy. 795
Effects of germline VHL deficiency on growth, metabolism, and mitochondria 162
The tyrosine kinase inhibitor dasatinib induces a marked adipogenic differentiation of human multipotent mesenchymal stromal cells. 153
HNF-1β mutation affects PKD2 and SOCS3 expression causing renal cysts and diabetes in MODY5 kindred. 142
Endocannabinoid Research Group (ERG), Italy. The endovanilloid/endocannabinoid system: a new potential target for osteoporosis therapy. 136
Iron overload enhances human mesenchymal stromal cell growth and hampers matrix calcification 136
Tyrosine kinase inhibitors and mesenchymal stromal cells: effects on self-renewal, commitment and functions 136
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry 135
The Italian survey on hereditary spherocytosis 134
A cancer-associated CDKN1B mutation induces p27 phosphorylation on a novel residue: a new mechanism for tumor suppressor loss-of-function 134
Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders 129
Endocrine function and bone disease during long-term chelation therapy with deferasirox in patients with β-thalassemia major. 126
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura. 126
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload 126
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 126
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 121
Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology. 121
A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli 121
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range. 120
Childhood Head and Neck Lymphadenopathy: A Report by a Single Institution (2003-2017) 120
A phase 3 trial of luspatercept in patients with transfusion-dependent β-thalassemia 120
Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: Evidence for a differentiated splenic conditioning role 118
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation) 117
A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity 116
Erythrocyte genotyping for transfusion-dependent patients at the Azienda Universitaria Policlinico of Naples 116
Auditory cortex hypoperfusion: a metabolic hallmark in Beta Thalassemia 116
ERITROCITOSI CONGENITA CAUSATA DA ALTERAZIONI DEL SISTEMA SENSORE DELL’OSSIGENO 114
Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown origin 113
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome 112
A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia. 111
LEOPARD syndrome: clinical dilemmas in differential diagnosis of RASopathies. 111
Abbreviated breast magnetic resonance imaging (FAST-MRI): A novel approach to breast cancer screening in patients with previous Hodgkin lymphoma 111
Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease gene 110
Asymptomatic intracranial aneurysms in beta-thalassemia: A three-year follow-up report 109
Time trends of cancer incidence in childhood in Campania region: 25 years of observation 108
Cardiac autonomic regulation in response to a mixed meal is impaired in obese children and adolescents: the role played by insulin resistance. 107
Very early onset of autoimmune thyroiditis in a toddler with severe hypothyroidism presentation: A case report 107
Targeted molecular therapy (modified RIST regimen) in relapsed high risk stage IV neuroblastoma: two cases report 107
A 23-month-old girl with chronic seborrhoeic' dermatitis, dehydration and failure to thrive 107
4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis [3] 106
p27Kip1 serine 10 phosphorylation determines its metabolism and interaction with cyclin-dependent kinases. 105
Brain iron content in systemic iron overload: A beta-thalassemia quantitative MRI study 105
Arg(1809) substitution in neurofibromin: further evidence of a genotype-phenotype correlation in neurofibromatosis type 1 105
Concordanza tra visita oculistica e RM encefalo nello screening del glioma delle vie ottiche nei pazienti pediatrici con neurofibromatosi tipo 1 104
Vitamin A and infancy. Biochemical, functional, and clinical aspects 103
Multiple spinal nerve enlargement and SOS1 mutation: further evidence of overlap between Neurofibromatosis type 1 and Noonan phenotype 103
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function 102
The endovanilloid/endocannabinoid system: A new potential target for osteoporosis therapy 102
Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene. 102
Vitamin A and infancy. Biochemical, functional, and clinical aspects 102
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity 102
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations 99
Clinical outcome of transfusions with extended red blood cell matching in β-thalassemia patients: A single-center experience 99
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 99
Von Hippel-Lindau-dependent polycythemia is endemic on the island of Ischia: identification of a novel cluster. 98
Age of first pain crisis and associated complications in the CASiRe international sickle cell disease cohort 98
BONE MINERAL DENSITY IMPROVEMENT IN PATIENTS WITH THALASSEMIA MAJOR ON LONG-TERM CHELATION THERAPY WITH DEFERASIROX 97
National systematic approach to the management of asplenia: the set up of the Italian Network on Asplenia 97
Genome editing and cancer therapy: handling the hypoxia-responsive pathway as a promising strategy 96
Resveratrol mimics insulin activity in the adipogenic commitment of human bone marrow mesenchymal stromal cells. 96
Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1 96
Seizures in children with neurofibromatosis type 1: Is neurofibromatosis type 1 enough? 96
Brain functional impairment in beta-thalassaemia: the cognitive profile in Italian neurologically asymptomatic adult patients in comparison to the reported literature 96
Association of immune thrombocytopenia and celiac disease in children: A retrospective case control study 96
Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned 96
Iron overload causes osteoporosis in Thalassemia Major patients through interaction with TRPV1 channels. 95
Unusual association of non-anaplastic Wilms tumor and Cornelia de Lange syndrome: Case report 95
Acute kidney injury in children hospitalized for acute gastroenteritis: prevalence and risk factors 95
An Analysis of Racial and Ethnic Backgrounds Within the CASiRe International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research 94
Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype-Phenotype Correlations 93
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency 93
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition 93
Erythropoietin receptors on cancer cells: a still open question. 93
Hereditary spherocytosis (HS) due to loss of anion exchange transporter 93
{beta}-spectrinBari: a truncated {beta}-chain responsible for dominant hereditary spherocytosis. 93
Cb2 receptor stimulation and dexamethasone restore the anti-inflammatory and immune-regulatory properties of mesenchymal stromal cells of children with immune thrombocytopenia 93
No evidence of increased cerebrovascular involvement in adult neurologically-asymptomatic β-Thalassaemia. A multicentre multimodal magnetic resonance study 93
Long-term improvement in cardiac magnetic resonance in β-thalassemia major patients treated with deferasirox extends to patients with abnormal baseline cardiac function 92
Identificazione di una mutazione del gene PAX2 in una famiglia con RVU isolato 92
A rapid method for the detection of alpha I/65 hereditary elliptocytosis 91
Genetic basis of congenital erythrocytosis: mutation update and online databases. 90
Studio retrospettivo sulle complicanze emato-oncologiche nella neurofibromatosi tipo 1 in età pediatrica 90
Global geographic differences in healthcare utilization for sickle cell disease pain crises in the CASiRe cohort 90
Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin 89
A mutation in the acyl-coenzyme A binding domain-containing protein 5 gene (ACBD5 ) identified in autosomal dominant thrombocytopenia 89
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 89
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis 88
An Educational Study Promoting the Delivery of Transcranial Doppler Ultrasound Screening in Paediatric Sickle Cell Disease: A European Multi-Centre Perspective 88
Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis 87
Tumori renali: esperienza trentennale monoistituzionale 87
Intermittent macrothrombocytopenia in a novel patient with Takenouchi-Kosaki syndrome and review of literature. 87
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 86
Treatment with short-term, high-dose cyclosporin A in children with refractory chronic idiopathic thrombocytopenic purpura 86
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele 86
Analysis of N-ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissues 85
The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum 85
Increased Membrane‐Protein Methylation in Hereditary Spherocytosis: A Marker of Cytoskeletal Disarray 85
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience 85
Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and Anzio 84
The endovanilloid/endocannabinoid system in human osteoclasts: Possible involvement in bone formation and resorption 84
Totale 11.167
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Categoria #
all - tutte 91.692
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 91.692
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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
2025/20266.938 625 856 885 836 1.396 2.340 0 0 0 0 0 0
Totale 23.092