CIRILLO, EMILIA
 Distribuzione geografica
Continente #
NA - Nord America 1.647
AS - Asia 621
EU - Europa 619
AF - Africa 31
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 4
SA - Sud America 1
Totale 2.927
Nazione #
US - Stati Uniti d'America 1.624
IT - Italia 283
SG - Singapore 266
CN - Cina 220
VN - Vietnam 80
IE - Irlanda 60
FI - Finlandia 59
DE - Germania 47
NL - Olanda 40
SE - Svezia 40
UA - Ucraina 37
CI - Costa d'Avorio 24
CA - Canada 22
TR - Turchia 21
FR - Francia 18
IN - India 17
GB - Regno Unito 13
HK - Hong Kong 8
RU - Federazione Russa 8
EG - Egitto 7
AU - Australia 4
BE - Belgio 4
EU - Europa 4
CH - Svizzera 2
ES - Italia 2
GR - Grecia 2
IL - Israele 2
JP - Giappone 2
SA - Arabia Saudita 2
SI - Slovenia 2
AE - Emirati Arabi Uniti 1
BR - Brasile 1
MT - Malta 1
MX - Messico 1
PH - Filippine 1
PL - Polonia 1
TW - Taiwan 1
Totale 2.927
Città #
Chandler 363
Singapore 229
Santa Clara 214
Dong Ket 80
Millbury 72
Ashburn 61
Beijing 59
Napoli 53
Nanjing 51
Princeton 50
Jacksonville 40
Wilmington 40
Des Moines 35
Boston 30
Amsterdam 28
Naples 27
Lawrence 19
Houston 18
Ottawa 18
Seattle 18
Milan 16
Nanchang 15
Boardman 14
Dallas 14
Pune 14
Woodbridge 14
Helsinki 13
Falls Church 12
Hebei 10
Rome 10
Castellana Grotte 8
Hong Kong 8
Dublin 7
Falkenstein 7
Neenah 7
Tianjin 7
Fairfield 6
Los Angeles 6
Shenyang 6
Xi'an 5
Ann Arbor 4
Cairo 4
Changsha 4
Kronberg 4
Kunming 4
Mcallen 4
San Mateo 4
Brescia 3
Guangzhou 3
Hanover 3
Indiana 3
Jiaxing 3
Lappeenranta 3
Norwalk 3
Orange 3
Palermo 3
Redwood City 3
Sydney 3
Waanrode 3
Wuhan 3
Altopascio 2
Athens 2
Barakaldo 2
Bari 2
Benevento 2
Bologna 2
Boscotrecase 2
Casapulla 2
Corsano 2
Dearborn 2
Frankfurt Am Main 2
Frankfurt am Main 2
Fremont 2
Genova 2
Limbiate 2
Livorno 2
London 2
Montemarciano 2
Montréal 2
Nocera Inferiore 2
Perugia 2
Redmond 2
Riyadh 2
San Giorgio a Cremano 2
Stockholm 2
Tappahannock 2
Turin 2
Villaricca 2
Washington 2
Afragola 1
Ascoli Piceno 1
Augusta 1
Birzebbuga 1
Brisbane 1
Brussels 1
Cambridge 1
Casoria 1
Cesena 1
Changchun 1
Chengdu 1
Totale 1.840
Nome #
DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother 113
TLR9 signaling in patients with ectodermal dysplasia and immunodeficiency associated with Nuclear Factor Essential Modulator (NEMO) mutations 76
Intrathecal amphotericin B therapy in a patient with X-linked chronic granulomatous disease and refractory cerebral invasive aspergillosis 74
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 70
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. 70
Gastrointestinal involvement in patients affected with 22q11.2 deletion syndrome 68
Clinical, Immunological, and Functional Characterization of Six Patients with Very High IgM Levels 66
DiGeorge-like Syndrome in a Child with a 3p12.3 Deletion Involving MIR4273 Gene Born to a Mother with Gestational Diabetes Mellitus 63
Novel STAT1 gain of function mutation and suppurative infections 62
Altered signaling through IL-12 receptor in children with very high serum IgE levels 61
Unraveling the link between ectodermal disorders and primary immunodeficiencies 57
Otolarylogical features in a cohort of patients affected with 22q11.2 deletion syndrome: a monocentric survey 56
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects 54
Diagnostics of Primary immunodeficiencies through next-generation sequencing 54
Unbalanced Immune System: Immunodeficiencies and Autoimmunity 53
Severe combined immunodeficiency-an update 49
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network 48
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 48
CD4+ T Cell Defects in a Mulibrey Patient With Specific TRIM37 Mutations 48
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasia 47
FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches 47
Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study 47
Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause. 46
DiGeorge Syndrome 45
Steroid treatment in Ataxia-Telangiectasia induces alterations of functional magnetic resonance imaging during prono-supination task. 44
X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management, and outcome of the disease. 43
Immunodeficienze primitive: cosa c’è di nuovo 43
Cutaneous vasculitis in patients with autoimmune polyendocrine syndrome type 1: report of a case and brief review of the literature 43
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children 43
Complement system network in cell physiology and in human diseases 43
B cells from nuclear factor kB essential modulator deficient patients fail to differentiate to antibody secreting cells in response to TLR9 ligand 42
Minimum effective betamethasone dosage on the neurological phenotype in patients with Ataxia-Telangiectasia: a multicenter observer-blind study 41
Novel Findings into AIRE Genetics and Functioning: Clinical Implications 40
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) 40
A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome 39
Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 39
Clinical Manifestations of 22q11.2 Deletion Syndrome 39
A novel form of hyper-IgM syndrome 38
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet) 37
Intergenerational familial phenotipic variability in 22Q11.2 subjects: a multicenter study within the italian primary immunodeficiencies network (IPINET) 37
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 37
Genetic basis of altered central tolerance and autoimmune diseases: a lesson from AIRE mutations 36
NADPH Oxidase Deficiency: A Multisystem Approach 36
Evaluation of executive functions in subjects affected with 22Q11.2 deletion syndrome: a neuroanatomical hypothesis 35
Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 34
Case Report: Severe Rhabdomyolysis and Multiorgan Failure After ChAdOx1 nCoV-19 Vaccination 33
Elevated IgM levels in a patient with a de novo 13Q12.3Q14.11 deletion, mimicking an A-T like phenotype 32
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 32
Gamma chain transducing element: a shared pathway between endocrine and immune system 31
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome 30
SCID-like phenotype associated with an inhibitory autoreactive immunoglobulin 29
Chronic granulomatous disease with gastrointestinal presentation: diagnostic pitfalls and novel ultrastructural findings 29
Different Degrees of NADPH Oxidase 2 Regulation and In Vivo Platelet Activation: Lesson From Chronic Granulomatous Disease 29
Two Brothers with Atypical UNC13D-Related Hemophagocytic Lymphohistiocytosis Characterized by Massive Lung and Brain Involvement 29
Estimate the minimum therpeutically effective dosage of short-term therapy with Betamethasone on neurologicaal symptoms in patients affected with Ataxia-Telangectasia 28
Intergenerational anticipation of disease onset in people with multiple autoimmune syndrome. 27
A case of Incontinentia Pigmenti associated with congenital absence of portal vein system and nodular regenerative hyperplasia 27
T-Cell Immunodeficiencies With Congenital Alterations of Thymic Development: Genes Implicated and Differential Immunological and Clinical Features 27
Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 Deletion 27
In ataxia-Telangiectasia betamethasone response correlates inversely to cerebellar atrophy and directly to antioxidative capacity 26
Respiratory Manifestations in Primary Immunodeficiencies: Findings From a Pediatric and Adult Cohort 26
Epigenetic Alterations in Inborn Errors of Immunity 26
SARS-CoV-2 Infection in the Immunodeficient Host: Necessary and Dispensable Immune Pathways 24
In ataxia-teleangiectasia betamethasone response is inversely correlated to cerebellar atrophy and directly to antioxidative capacity. 23
In Ataxia-Teleangectasia betamethasone response correlates inversely to cerebellar atrophy and directly to antioxidative capacity. 22
Severe combined immunodeficiences: new and old scenarios 22
Retrospective analysis of 21 pediatric patients affected with hemophagocytic syndrome of unknown genetic cause: clinical features and outcome 22
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations 20
The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase 19
Rare solid tumors in a patient with Wiskott–Aldrich syndrome after hematopoietic stem cell transplantation: case report and review of literature 19
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors 17
Estimate the minimum therapeutically effective dosage of short term therapy with betamethasone on neurological symptoms in patients affected with Ataxia- Teleangectasia 17
Reduced atherosclerotic burden in subjects with genetically determined low oxidative stress 16
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 15
Mechanisms of immune tolerance breakdown in inborn errors of immunity 14
The effects of betamethasone therapy on neurological functions in A-T patients 13
Recurrent cold suppurative granulomatous lymphadenitis 13
In adult X-CGD patients, regulatory T cells are expanded while activated T cells display a NOX2-independent ROS increase 13
A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association 12
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 11
Case report: EBV-related eye orbits and sinuses lymphohistiocytic infiltration responsive to rituximab in a patient with X lymphoproliferative syndrome type 1 10
Neonatal alloimmune neutropenia: diagnosis and management of 31 Italian patients 10
Immunological Aspects of Kabuki Syndrome: A Retrospective Multicenter Study of the Italian Primary Immunodeficiency Network (IPINet) 10
Oral thrush and onychomycosis 9
Development of cancer surveillance guidelines in ataxia telangiectasia: A Delphi‐based consensus survey of international experts 7
MicroRNA dysregulation in ataxia telangiectasia 3
Totale 3.100
Categoria #
all - tutte 14.387
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 14.387


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020111 0 0 0 0 0 0 0 3 2 34 52 20
2020/2021243 10 8 21 18 24 21 9 7 15 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
2024/2025651 119 134 20 23 109 240 6 0 0 0 0 0
Totale 3.100