IRIS
CIRILLO, EMILIA
 Distribuzione geografica
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Continente #
AS - Asia 4.212
NA - Nord America 4.181
EU - Europa 2.748
SA - Sud America 484
Continente sconosciuto - Info sul continente non disponibili 187
AF - Africa 104
OC - Oceania 8
Totale 11.924
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Nazione #
US - Stati Uniti d'America 4.011
SG - Singapore 1.775
RU - Federazione Russa 1.391
VN - Vietnam 882
CN - Cina 827
IT - Italia 479
BR - Brasile 363
HK - Hong Kong 270
DE - Germania 180
FR - Francia 159
CA - Canada 99
BD - Bangladesh 93
FI - Finlandia 92
GB - Regno Unito 88
IN - India 76
NL - Olanda 71
IE - Irlanda 69
JP - Giappone 64
UA - Ucraina 52
SE - Svezia 49
MX - Messico 46
AR - Argentina 44
KR - Corea 34
TR - Turchia 34
ZA - Sudafrica 29
EC - Ecuador 25
IQ - Iraq 25
CI - Costa d'Avorio 24
AT - Austria 23
PL - Polonia 23
ES - Italia 22
PH - Filippine 21
CO - Colombia 19
ID - Indonesia 16
TH - Thailandia 16
EG - Egitto 13
UZ - Uzbekistan 11
MA - Marocco 9
TW - Taiwan 9
AE - Emirati Arabi Uniti 8
BE - Belgio 8
AU - Australia 7
KE - Kenya 7
PK - Pakistan 7
VE - Venezuela 7
CL - Cile 6
IL - Israele 6
LT - Lituania 6
PY - Paraguay 6
CR - Costa Rica 5
JM - Giamaica 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
TT - Trinidad e Tobago 4
ET - Etiopia 3
HU - Ungheria 3
MT - Malta 3
MY - Malesia 3
PS - Palestinian Territory 3
PT - Portogallo 3
SA - Arabia Saudita 3
AZ - Azerbaigian 2
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
CY - Cipro 2
CZ - Repubblica Ceca 2
DO - Repubblica Dominicana 2
GR - Grecia 2
GT - Guatemala 2
HN - Honduras 2
KG - Kirghizistan 2
LA - Repubblica Popolare Democratica del Laos 2
MM - Myanmar 2
NP - Nepal 2
RO - Romania 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
AD - Andorra 1
AL - Albania 1
AO - Angola 1
AW - Aruba 1
BB - Barbados 1
BF - Burkina Faso 1
BG - Bulgaria 1
BW - Botswana 1
CD - Congo 1
CW - ???statistics.table.value.countryCode.CW??? 1
GE - Georgia 1
GF - Guiana Francese 1
GY - Guiana 1
HR - Croazia 1
LB - Libano 1
Totale 11.727
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Città #
Singapore 871
San Jose 629
Ashburn 369
Chandler 363
Moscow 329
Beijing 280
Santa Clara 264
Hong Kong 244
Ho Chi Minh City 230
Hanoi 171
Hefei 140
Los Angeles 131
The Dalles 119
Council Bluffs 114
New York 88
Buffalo 81
Dong Ket 80
Lauterbourg 80
Millbury 72
Tokyo 58
Nanjing 53
Napoli 53
Princeton 50
Dallas 49
Boston 48
Naples 48
Wilmington 43
Amsterdam 42
Jacksonville 42
Des Moines 38
Frankfurt am Main 37
Munich 37
São Paulo 37
Haiphong 36
Milan 35
Redondo Beach 33
Seattle 32
Da Nang 30
Houston 30
Chicago 29
Phoenix 28
London 27
Orem 27
Brooklyn 25
Helsinki 25
Toronto 25
Seoul 23
Atlanta 22
Montreal 21
Ottawa 21
Rome 21
Mexico City 20
Lawrence 19
Nuremberg 19
Warsaw 19
Chennai 17
Falkenstein 17
Turku 17
Düsseldorf 15
Nanchang 15
Poplar 15
Pune 15
Boardman 14
Dublin 14
Woodbridge 14
Biên Hòa 13
Falls Church 13
Quito 13
Rio de Janeiro 13
Tianjin 12
Charlotte 11
Manchester 11
Stockholm 11
Vienna 11
Hebei 10
Denver 9
Hải Dương 9
Johannesburg 9
Kochi 9
Quận Bình Thạnh 9
Tashkent 9
Thái Bình 9
Baghdad 8
Belo Horizonte 8
Cairo 8
Castellana Grotte 8
Medellín 8
Pasadena 8
Querétaro 8
Roubaix 8
Bangkok 7
Bắc Giang 7
Changsha 7
City of London 7
Lappeenranta 7
Nairobi 7
Neenah 7
Ninh Bình 7
Thái Nguyên 7
Turin 7
Totale 6.325
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Nome #
Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study 296
DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother 248
Case report: EBV-related eye orbits and sinuses lymphohistiocytic infiltration responsive to rituximab in a patient with X lymphoproliferative syndrome type 1 200
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 192
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. 188
Clinical, Immunological, and Functional Characterization of Six Patients with Very High IgM Levels 182
Intrathecal amphotericin B therapy in a patient with X-linked chronic granulomatous disease and refractory cerebral invasive aspergillosis 172
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet) 171
CD4+ T Cell Defects in a Mulibrey Patient With Specific TRIM37 Mutations 169
Immunodeficienze primitive: cosa c’è di nuovo 168
Gastrointestinal involvement in patients affected with 22q11.2 deletion syndrome 167
TLR9 signaling in patients with ectodermal dysplasia and immunodeficiency associated with Nuclear Factor Essential Modulator (NEMO) mutations 167
DiGeorge-like Syndrome in a Child with a 3p12.3 Deletion Involving MIR4273 Gene Born to a Mother with Gestational Diabetes Mellitus 167
A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association 164
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 161
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network 161
Severe combined immunodeficiency-an update 160
The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase 156
Novel STAT1 gain of function mutation and suppurative infections 156
Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 156
Steroid treatment in Ataxia-Telangiectasia induces alterations of functional magnetic resonance imaging during prono-supination task. 155
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 154
DiGeorge Syndrome 153
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 152
X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management, and outcome of the disease. 150
Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause. 150
Diagnostics of Primary immunodeficiencies through next-generation sequencing 148
Rare solid tumors in a patient with Wiskott–Aldrich syndrome after hematopoietic stem cell transplantation: case report and review of literature 146
Elevated IgM levels in a patient with a de novo 13Q12.3Q14.11 deletion, mimicking an A-T like phenotype 145
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) 145
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors 142
Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 141
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunity 139
Unbalanced Immune System: Immunodeficiencies and Autoimmunity 138
Otolarylogical features in a cohort of patients affected with 22q11.2 deletion syndrome: a monocentric survey 138
Unraveling the link between ectodermal disorders and primary immunodeficiencies 137
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 137
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 137
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasia 135
Altered signaling through IL-12 receptor in children with very high serum IgE levels 134
Novel Findings into AIRE Genetics and Functioning: Clinical Implications 133
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects 131
Severe combined immunodeficiences: new and old scenarios 129
Intergenerational familial phenotipic variability in 22Q11.2 subjects: a multicenter study within the italian primary immunodeficiencies network (IPINET) 129
Complement system network in cell physiology and in human diseases 126
Minimum effective betamethasone dosage on the neurological phenotype in patients with Ataxia-Telangiectasia: a multicenter observer-blind study 125
A novel form of hyper-IgM syndrome 123
Retrospective analysis of 21 pediatric patients affected with hemophagocytic syndrome of unknown genetic cause: clinical features and outcome 123
Three Unrelated Patients of Roma Ethnicity from a Single Center Carrying the Same Deletion in MYD88 Gene: A Founder Effect? 122
SCID-like phenotype associated with an inhibitory autoreactive immunoglobulin 122
Evaluation of executive functions in subjects affected with 22Q11.2 deletion syndrome: a neuroanatomical hypothesis 122
FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches 122
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children 122
Epigenetic Alterations in Inborn Errors of Immunity 121
Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 Deletion 121
Neonatal alloimmune neutropenia: diagnosis and management of 31 Italian patients 120
Characterization of a WAS splice-site variant in a patient with Wiskott-Aldrich syndrome 120
Genetic basis of altered central tolerance and autoimmune diseases: a lesson from AIRE mutations 120
Respiratory Manifestations in Primary Immunodeficiencies: Findings From a Pediatric and Adult Cohort 120
Clinical Manifestations of 22q11.2 Deletion Syndrome 120
SARS-CoV-2 Infection in the Immunodeficient Host: Necessary and Dispensable Immune Pathways 118
Chronic granulomatous disease with gastrointestinal presentation: diagnostic pitfalls and novel ultrastructural findings 117
NADPH Oxidase Deficiency: A Multisystem Approach 117
A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome 116
Mechanisms of immune tolerance breakdown in inborn errors of immunity 114
In adult X-CGD patients, regulatory T cells are expanded while activated T cells display a NOX2-independent ROS increase 113
In ataxia-Telangiectasia betamethasone response correlates inversely to cerebellar atrophy and directly to antioxidative capacity 111
Estimate the minimum therpeutically effective dosage of short-term therapy with Betamethasone on neurologicaal symptoms in patients affected with Ataxia-Telangectasia 108
A case of Incontinentia Pigmenti associated with congenital absence of portal vein system and nodular regenerative hyperplasia 108
T-Cell Immunodeficiencies With Congenital Alterations of Thymic Development: Genes Implicated and Differential Immunological and Clinical Features 107
Cutaneous vasculitis in patients with autoimmune polyendocrine syndrome type 1: report of a case and brief review of the literature 106
MicroRNA dysregulation in ataxia telangiectasia 100
Case Report: Severe Rhabdomyolysis and Multiorgan Failure After ChAdOx1 nCoV-19 Vaccination 99
Immunological Aspects of Kabuki Syndrome: A Retrospective Multicenter Study of the Italian Primary Immunodeficiency Network (IPINet) 99
A novel pathogenic variant causing POU3F3-related neurodevelopmental disorder in a child presenting with infantile epileptic spasms syndrome: Expanding the epileptic phenotype 96
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome 96
Reduced atherosclerotic burden in subjects with genetically determined low oxidative stress 94
Gamma chain transducing element: a shared pathway between endocrine and immune system 93
Intergenerational anticipation of disease onset in people with multiple autoimmune syndrome. 93
Oral thrush and onychomycosis 92
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations 92
In Ataxia-Teleangectasia betamethasone response correlates inversely to cerebellar atrophy and directly to antioxidative capacity. 91
The effects of betamethasone therapy on neurological functions in A-T patients 91
Allergic Manifestations of Inborn Errors of Immunity 90
B cells from nuclear factor kB essential modulator deficient patients fail to differentiate to antibody secreting cells in response to TLR9 ligand 90
Two Brothers with Atypical UNC13D-Related Hemophagocytic Lymphohistiocytosis Characterized by Massive Lung and Brain Involvement 90
Estimate the minimum therapeutically effective dosage of short term therapy with betamethasone on neurological symptoms in patients affected with Ataxia- Teleangectasia 84
Different Degrees of NADPH Oxidase 2 Regulation and In Vivo Platelet Activation: Lesson From Chronic Granulomatous Disease 79
Development of cancer surveillance guidelines in ataxia telangiectasia: A Delphi‐based consensus survey of international experts 61
In ataxia-teleangiectasia betamethasone response is inversely correlated to cerebellar atrophy and directly to antioxidative capacity. 59
Recurrent cold suppurative granulomatous lymphadenitis 52
Totale 11.924
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Categoria #
all - tutte 37.993
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 37.993
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022438 0 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
2025/20265.945 574 436 586 543 1.051 215 686 265 711 359 151 368
2026/2027532 149 223 160 0 0 0 0 0 0 0 0 0
Totale 11.924