IRIS
CIRILLO, EMILIA
 Distribuzione geografica
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Continente #
NA - Nord America 1.312
EU - Europa 516
AS - Asia 299
AF - Africa 30
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 4
SA - Sud America 1
Totale 2.166
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Nazione #
US - Stati Uniti d'America 1.290
IT - Italia 220
CN - Cina 165
VN - Vietnam 80
IE - Irlanda 60
FI - Finlandia 45
SE - Svezia 39
DE - Germania 37
UA - Ucraina 37
NL - Olanda 34
CI - Costa d'Avorio 24
CA - Canada 21
TR - Turchia 21
FR - Francia 18
IN - India 17
GB - Regno Unito 12
EG - Egitto 6
HK - Hong Kong 6
AU - Australia 4
EU - Europa 4
BE - Belgio 3
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
RU - Federazione Russa 1
SG - Singapore 1
TW - Taiwan 1
Totale 2.166
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Città #
Chandler 363
Dong Ket 80
Millbury 72
Ashburn 58
Beijing 58
Napoli 53
Nanjing 51
Princeton 50
Jacksonville 40
Wilmington 40
Des Moines 35
Boston 30
Amsterdam 28
Naples 21
Lawrence 19
Houston 18
Ottawa 18
Nanchang 15
Pune 14
Woodbridge 14
Falls Church 12
Seattle 12
Boardman 11
Hebei 10
Castellana Grotte 8
Dublin 7
Milan 7
Neenah 7
Fairfield 6
Hong Kong 6
Shenyang 6
Tianjin 6
Ann Arbor 4
Changsha 4
Kronberg 4
Kunming 4
Mcallen 4
San Mateo 4
Brescia 3
Cairo 3
Hanover 3
Indiana 3
Jiaxing 3
Norwalk 3
Orange 3
Redwood City 3
Sydney 3
Waanrode 3
Athens 2
Barakaldo 2
Bologna 2
Boscotrecase 2
Casapulla 2
Corsano 2
Dearborn 2
Frankfurt Am Main 2
Fremont 2
Genova 2
Limbiate 2
Livorno 2
London 2
Montemarciano 2
Montréal 2
Nocera Inferiore 2
Redmond 2
Riyadh 2
Rome 2
San Giorgio a Cremano 2
Tappahannock 2
Turin 2
Washington 2
Ascoli Piceno 1
Augusta 1
Benevento 1
Birzebbuga 1
Brisbane 1
Cambridge 1
Casoria 1
Changchun 1
Cologne 1
Coquitlam 1
Cormeilles-en-Parisis 1
Council Bluffs 1
Duino-Aurisina 1
Edinburgh 1
Fisciano 1
Forlì 1
Gesualdo 1
Ghedi 1
Guangzhou 1
Guarulhos 1
Gulf Breeze 1
Gustavo Adolfo Madero 1
Helsinki 1
Jinan 1
Jupiter 1
Kaohsiung 1
Kingwood 1
Lanzhou 1
Lappeenranta 1
Totale 1.304
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Nome #
DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother 101
Intrathecal amphotericin B therapy in a patient with X-linked chronic granulomatous disease and refractory cerebral invasive aspergillosis 70
TLR9 signaling in patients with ectodermal dysplasia and immunodeficiency associated with Nuclear Factor Essential Modulator (NEMO) mutations 68
Gastrointestinal involvement in patients affected with 22q11.2 deletion syndrome 60
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 58
Novel STAT1 gain of function mutation and suppurative infections 54
Clinical, Immunological, and Functional Characterization of Six Patients with Very High IgM Levels 54
Altered signaling through IL-12 receptor in children with very high serum IgE levels 53
Unraveling the link between ectodermal disorders and primary immunodeficiencies 51
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. 51
DiGeorge-like Syndrome in a Child with a 3p12.3 Deletion Involving MIR4273 Gene Born to a Mother with Gestational Diabetes Mellitus 50
Otolarylogical features in a cohort of patients affected with 22q11.2 deletion syndrome: a monocentric survey 50
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects 49
Diagnostics of Primary immunodeficiencies through next-generation sequencing 45
Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study 43
Unbalanced Immune System: Immunodeficiencies and Autoimmunity 42
Severe combined immunodeficiency-an update 41
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasia 40
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children 40
FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches 38
CD4+ T Cell Defects in a Mulibrey Patient With Specific TRIM37 Mutations 38
B cells from nuclear factor kB essential modulator deficient patients fail to differentiate to antibody secreting cells in response to TLR9 ligand 37
Complement system network in cell physiology and in human diseases 37
Steroid treatment in Ataxia-Telangiectasia induces alterations of functional magnetic resonance imaging during prono-supination task. 36
Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause. 36
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network 36
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 36
Novel Findings into AIRE Genetics and Functioning: Clinical Implications 35
DiGeorge Syndrome 35
Immunodeficienze primitive: cosa c’è di nuovo 34
Cutaneous vasculitis in patients with autoimmune polyendocrine syndrome type 1: report of a case and brief review of the literature 34
NADPH Oxidase Deficiency: A Multisystem Approach 33
X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management, and outcome of the disease. 32
A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome 32
Minimum effective betamethasone dosage on the neurological phenotype in patients with Ataxia-Telangiectasia: a multicenter observer-blind study 32
A novel form of hyper-IgM syndrome 31
Clinical Manifestations of 22q11.2 Deletion Syndrome 30
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 29
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) 28
Case Report: Severe Rhabdomyolysis and Multiorgan Failure After ChAdOx1 nCoV-19 Vaccination 28
Evaluation of executive functions in subjects affected with 22Q11.2 deletion syndrome: a neuroanatomical hypothesis 27
Intergenerational familial phenotipic variability in 22Q11.2 subjects: a multicenter study within the italian primary immunodeficiencies network (IPINET) 27
Genetic basis of altered central tolerance and autoimmune diseases: a lesson from AIRE mutations 26
Elevated IgM levels in a patient with a de novo 13Q12.3Q14.11 deletion, mimicking an A-T like phenotype 25
Chronic granulomatous disease with gastrointestinal presentation: diagnostic pitfalls and novel ultrastructural findings 24
Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency 23
Gamma chain transducing element: a shared pathway between endocrine and immune system 23
A case of Incontinentia Pigmenti associated with congenital absence of portal vein system and nodular regenerative hyperplasia 23
Different Degrees of NADPH Oxidase 2 Regulation and In Vivo Platelet Activation: Lesson From Chronic Granulomatous Disease 22
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome 22
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 22
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet) 21
SCID-like phenotype associated with an inhibitory autoreactive immunoglobulin 21
Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 21
Estimate the minimum therpeutically effective dosage of short-term therapy with Betamethasone on neurologicaal symptoms in patients affected with Ataxia-Telangectasia 20
Two Brothers with Atypical UNC13D-Related Hemophagocytic Lymphohistiocytosis Characterized by Massive Lung and Brain Involvement 20
T-Cell Immunodeficiencies With Congenital Alterations of Thymic Development: Genes Implicated and Differential Immunological and Clinical Features 20
Intergenerational anticipation of disease onset in people with multiple autoimmune syndrome. 19
In ataxia-Telangiectasia betamethasone response correlates inversely to cerebellar atrophy and directly to antioxidative capacity 18
Respiratory Manifestations in Primary Immunodeficiencies: Findings From a Pediatric and Adult Cohort 18
SARS-CoV-2 Infection in the Immunodeficient Host: Necessary and Dispensable Immune Pathways 16
Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 Deletion 16
In Ataxia-Teleangectasia betamethasone response correlates inversely to cerebellar atrophy and directly to antioxidative capacity. 15
Retrospective analysis of 21 pediatric patients affected with hemophagocytic syndrome of unknown genetic cause: clinical features and outcome 14
In ataxia-teleangiectasia betamethasone response is inversely correlated to cerebellar atrophy and directly to antioxidative capacity. 13
Severe combined immunodeficiences: new and old scenarios 13
Epigenetic Alterations in Inborn Errors of Immunity 13
Estimate the minimum therapeutically effective dosage of short term therapy with betamethasone on neurological symptoms in patients affected with Ataxia- Teleangectasia 10
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations 10
Reduced atherosclerotic burden in subjects with genetically determined low oxidative stress 9
The effects of betamethasone therapy on neurological functions in A-T patients 7
Recurrent cold suppurative granulomatous lymphadenitis 5
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 4
Mechanisms of immune tolerance breakdown in inborn errors of immunity 4
The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase 3
A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association 3
In adult X-CGD patients, regulatory T cells are expanded while activated T cells display a NOX2-independent ROS increase 3
Oral thrush and onychomycosis 2
Neonatal alloimmune neutropenia: diagnosis and management of 31 Italian patients 2
Rare solid tumors in a patient with Wiskott–Aldrich syndrome after hematopoietic stem cell transplantation: case report and review of literature 1
Development of cancer surveillance guidelines in ataxia telangiectasia: A Delphi‐based consensus survey of international experts 1
Totale 2.333
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Categoria #
all - tutte 8.453
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 8.453
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201918 0 0 0 0 0 0 0 0 0 10 4 4
2019/2020244 91 2 12 5 12 11 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
2023/2024288 12 63 34 26 26 38 8 46 30 5 0 0
Totale 2.333