IRIS
CIRILLO, EMILIA
 Distribuzione geografica
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Continente #
AS - Asia 4.104
NA - Nord America 3.337
EU - Europa 2.663
SA - Sud America 468
AF - Africa 103
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 5
Totale 10.687
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Nazione #
US - Stati Uniti d'America 3.219
SG - Singapore 1.771
RU - Federazione Russa 1.391
VN - Vietnam 879
CN - Cina 805
IT - Italia 407
BR - Brasile 357
HK - Hong Kong 269
DE - Germania 180
FR - Francia 158
FI - Finlandia 92
GB - Regno Unito 84
IN - India 76
NL - Olanda 70
IE - Irlanda 69
JP - Giappone 64
CA - Canada 62
UA - Ucraina 51
SE - Svezia 47
MX - Messico 43
AR - Argentina 42
KR - Corea 34
TR - Turchia 32
ZA - Sudafrica 29
IQ - Iraq 25
BD - Bangladesh 24
CI - Costa d'Avorio 24
AT - Austria 23
EC - Ecuador 23
PL - Polonia 23
PH - Filippine 21
ES - Italia 20
CO - Colombia 15
ID - Indonesia 15
TH - Thailandia 14
EG - Egitto 13
UZ - Uzbekistan 11
MA - Marocco 9
TW - Taiwan 9
BE - Belgio 8
KE - Kenya 7
PK - Pakistan 7
AE - Emirati Arabi Uniti 6
AU - Australia 6
IL - Israele 6
LT - Lituania 6
PY - Paraguay 6
VE - Venezuela 6
CL - Cile 5
KZ - Kazakistan 5
PE - Perù 5
TN - Tunisia 5
UY - Uruguay 5
CH - Svizzera 4
DK - Danimarca 4
DZ - Algeria 4
EU - Europa 4
JO - Giordania 4
OM - Oman 4
CR - Costa Rica 3
ET - Etiopia 3
HU - Ungheria 3
MT - Malta 3
PS - Palestinian Territory 3
PT - Portogallo 3
SA - Arabia Saudita 3
TT - Trinidad e Tobago 3
AZ - Azerbaigian 2
BO - Bolivia 2
CY - Cipro 2
CZ - Repubblica Ceca 2
GR - Grecia 2
JM - Giamaica 2
KG - Kirghizistan 2
LA - Repubblica Popolare Democratica del Laos 2
MY - Malesia 2
NP - Nepal 2
RO - Romania 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
AD - Andorra 1
AL - Albania 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BF - Burkina Faso 1
BG - Bulgaria 1
BW - Botswana 1
CD - Congo 1
CW - ???statistics.table.value.countryCode.CW??? 1
DO - Repubblica Dominicana 1
GE - Georgia 1
GF - Guiana Francese 1
GY - Guiana 1
HR - Croazia 1
LB - Libano 1
LC - Santa Lucia 1
LV - Lettonia 1
MM - Myanmar 1
MW - Malawi 1
Totale 10.677
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Città #
Singapore 870
San Jose 493
Chandler 363
Moscow 329
Ashburn 279
Beijing 274
Hong Kong 244
Santa Clara 233
Ho Chi Minh City 228
Hanoi 171
Hefei 140
The Dalles 119
Los Angeles 89
Dong Ket 80
Lauterbourg 80
Millbury 72
Tokyo 58
Nanjing 53
Napoli 53
Princeton 50
Boston 47
Amsterdam 42
Naples 41
Wilmington 41
Jacksonville 40
New York 38
Buffalo 37
Des Moines 37
Frankfurt am Main 37
Munich 37
Haiphong 36
São Paulo 35
Dallas 34
Redondo Beach 33
Da Nang 30
Houston 28
London 27
Seattle 27
Orem 26
Helsinki 25
Milan 23
Seoul 23
Brooklyn 22
Ottawa 20
Lawrence 19
Nuremberg 19
Atlanta 18
Mexico City 18
Warsaw 18
Chennai 17
Chicago 17
Falkenstein 17
Montreal 17
Rome 17
Turku 17
Council Bluffs 16
Düsseldorf 15
Nanchang 15
Poplar 15
Pune 15
Boardman 14
Dublin 14
Phoenix 14
Woodbridge 14
Biên Hòa 13
Rio de Janeiro 13
Falls Church 12
Quito 12
Tianjin 12
Vienna 11
Hebei 10
Manchester 10
Denver 9
Hải Dương 9
Johannesburg 9
Kochi 9
Quận Bình Thạnh 9
Stockholm 9
Tashkent 9
Thái Bình 9
Toronto 9
Baghdad 8
Belo Horizonte 8
Cairo 8
Castellana Grotte 8
Querétaro 8
Roubaix 8
Bangkok 7
Bắc Giang 7
Lappeenranta 7
Nairobi 7
Neenah 7
Ninh Bình 7
Thái Nguyên 7
Brasília 6
Changsha 6
City of London 6
Curitiba 6
Fairfield 6
Long Xuyen 6
Totale 5.697
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Nome #
DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother 238
Case report: EBV-related eye orbits and sinuses lymphohistiocytic infiltration responsive to rituximab in a patient with X lymphoproliferative syndrome type 1 194
De novo 13q12.3q14.11 deletion involving BRCA2 gene in a patient with developmental delay, elevated IgM levels, transient ataxia and cerebellar hypoplasia, mimicking an A-T like phenotype. 183
Chronic mucocutaneous candidiasis, recurrent herpetic infections and suppurative eyelid infections in a patient carrying a novel gain-of-function mutation in the STAT1 DNA-binding domain 180
Clinical, Immunological, and Functional Characterization of Six Patients with Very High IgM Levels 174
Intrathecal amphotericin B therapy in a patient with X-linked chronic granulomatous disease and refractory cerebral invasive aspergillosis 165
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet) 162
TLR9 signaling in patients with ectodermal dysplasia and immunodeficiency associated with Nuclear Factor Essential Modulator (NEMO) mutations 161
DiGeorge-like Syndrome in a Child with a 3p12.3 Deletion Involving MIR4273 Gene Born to a Mother with Gestational Diabetes Mellitus 159
Gastrointestinal involvement in patients affected with 22q11.2 deletion syndrome 157
CD4+ T Cell Defects in a Mulibrey Patient With Specific TRIM37 Mutations 155
Steroid treatment in Ataxia-Telangiectasia induces alterations of functional magnetic resonance imaging during prono-supination task. 154
Severe combined immunodeficiency-an update 151
Novel STAT1 gain of function mutation and suppurative infections 151
Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 149
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 148
The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase 147
Immunodeficienze primitive: cosa c’è di nuovo 147
Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause. 146
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 146
X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management, and outcome of the disease. 141
Elevated IgM levels in a patient with a de novo 13Q12.3Q14.11 deletion, mimicking an A-T like phenotype 141
Diagnostics of Primary immunodeficiencies through next-generation sequencing 141
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network 140
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors 137
Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 134
A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association 133
Unraveling the link between ectodermal disorders and primary immunodeficiencies 132
Health-Related Quality of Life and Emotional Difficulties in Chronic Granulomatous Disease: Data on Adult and Pediatric Patients from Italian Network for Primary Immunodeficiency (IPINet) 132
Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity 131
Unbalanced Immune System: Immunodeficiencies and Autoimmunity 130
Otolarylogical features in a cohort of patients affected with 22q11.2 deletion syndrome: a monocentric survey 130
DiGeorge Syndrome 129
In Ataxia-Telangiectasia, Oral Betamethasone Administration Ameliorates Lymphocytes Functionality through Modulation of the IL-7/IL-7Rα Axis Paralleling the Neurological Behavior: A Comparative Report of Two Cases 129
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects 126
Novel Findings into AIRE Genetics and Functioning: Clinical Implications 125
Altered signaling through IL-12 receptor in children with very high serum IgE levels 124
Intergenerational familial phenotipic variability in 22Q11.2 subjects: a multicenter study within the italian primary immunodeficiencies network (IPINET) 123
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasia 121
Severe combined immunodeficiences: new and old scenarios 120
Complement system network in cell physiology and in human diseases 120
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunity 118
Rare solid tumors in a patient with Wiskott–Aldrich syndrome after hematopoietic stem cell transplantation: case report and review of literature 118
A novel form of hyper-IgM syndrome 118
Evaluation of executive functions in subjects affected with 22Q11.2 deletion syndrome: a neuroanatomical hypothesis 118
Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job’s syndrome 117
SCID-like phenotype associated with an inhibitory autoreactive immunoglobulin 117
Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 Deletion 117
Retrospective analysis of 21 pediatric patients affected with hemophagocytic syndrome of unknown genetic cause: clinical features and outcome 116
Minimum effective betamethasone dosage on the neurological phenotype in patients with Ataxia-Telangiectasia: a multicenter observer-blind study 116
FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches 115
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children 115
Epigenetic Alterations in Inborn Errors of Immunity 114
Chronic granulomatous disease with gastrointestinal presentation: diagnostic pitfalls and novel ultrastructural findings 112
NADPH Oxidase Deficiency: A Multisystem Approach 112
Respiratory Manifestations in Primary Immunodeficiencies: Findings From a Pediatric and Adult Cohort 112
SARS-CoV-2 Infection in the Immunodeficient Host: Necessary and Dispensable Immune Pathways 111
Three Unrelated Patients of Roma Ethnicity from a Single Center Carrying the Same Deletion in MYD88 Gene: A Founder Effect? 110
Genetic basis of altered central tolerance and autoimmune diseases: a lesson from AIRE mutations 109
A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome 109
Mechanisms of immune tolerance breakdown in inborn errors of immunity 107
In ataxia-Telangiectasia betamethasone response correlates inversely to cerebellar atrophy and directly to antioxidative capacity 107
Characterization of a WAS splice-site variant in a patient with Wiskott-Aldrich syndrome 106
Neonatal alloimmune neutropenia: diagnosis and management of 31 Italian patients 104
Clinical Manifestations of 22q11.2 Deletion Syndrome 104
Estimate the minimum therpeutically effective dosage of short-term therapy with Betamethasone on neurologicaal symptoms in patients affected with Ataxia-Telangectasia 103
T-Cell Immunodeficiencies With Congenital Alterations of Thymic Development: Genes Implicated and Differential Immunological and Clinical Features 102
In adult X-CGD patients, regulatory T cells are expanded while activated T cells display a NOX2-independent ROS increase 102
Cutaneous vasculitis in patients with autoimmune polyendocrine syndrome type 1: report of a case and brief review of the literature 100
A case of Incontinentia Pigmenti associated with congenital absence of portal vein system and nodular regenerative hyperplasia 99
MicroRNA dysregulation in ataxia telangiectasia 95
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome 93
Case Report: Severe Rhabdomyolysis and Multiorgan Failure After ChAdOx1 nCoV-19 Vaccination 92
Reduced atherosclerotic burden in subjects with genetically determined low oxidative stress 89
Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study 89
Two Brothers with Atypical UNC13D-Related Hemophagocytic Lymphohistiocytosis Characterized by Massive Lung and Brain Involvement 88
Immunological Aspects of Kabuki Syndrome: A Retrospective Multicenter Study of the Italian Primary Immunodeficiency Network (IPINet) 88
In Ataxia-Teleangectasia betamethasone response correlates inversely to cerebellar atrophy and directly to antioxidative capacity. 87
Intergenerational anticipation of disease onset in people with multiple autoimmune syndrome. 87
B cells from nuclear factor kB essential modulator deficient patients fail to differentiate to antibody secreting cells in response to TLR9 ligand 85
The effects of betamethasone therapy on neurological functions in A-T patients 84
Gamma chain transducing element: a shared pathway between endocrine and immune system 83
A novel pathogenic variant causing POU3F3-related neurodevelopmental disorder in a child presenting with infantile epileptic spasms syndrome: Expanding the epileptic phenotype 82
Allergic Manifestations of Inborn Errors of Immunity 82
Estimate the minimum therapeutically effective dosage of short term therapy with betamethasone on neurological symptoms in patients affected with Ataxia- Teleangectasia 78
Different Degrees of NADPH Oxidase 2 Regulation and In Vivo Platelet Activation: Lesson From Chronic Granulomatous Disease 71
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations 68
Oral thrush and onychomycosis 60
In ataxia-teleangiectasia betamethasone response is inversely correlated to cerebellar atrophy and directly to antioxidative capacity. 53
Development of cancer surveillance guidelines in ataxia telangiectasia: A Delphi‐based consensus survey of international experts 53
Recurrent cold suppurative granulomatous lymphadenitis 47
Totale 10.868
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Categoria #
all - tutte 31.579
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 31.579
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021110 0 0 0 0 0 0 0 0 0 5 23 82
2021/2022448 10 0 1 7 4 15 1 17 75 49 110 159
2022/2023696 79 86 15 79 100 81 1 58 118 31 35 13
2023/2024404 12 63 34 26 26 38 8 46 31 10 81 29
2024/20252.998 119 134 20 23 109 240 227 207 190 314 1.156 259
2025/20265.421 574 436 586 543 1.051 215 686 265 711 354 0 0
Totale 10.868