CONTI, FRANCESCA
 Distribuzione geografica
Continente #
AS - Asia 3.404
NA - Nord America 1.432
EU - Europa 1.101
SA - Sud America 238
AF - Africa 85
OC - Oceania 3
Totale 6.263
Nazione #
US - Stati Uniti d'America 1.371
CN - Cina 1.002
SG - Singapore 954
VN - Vietnam 681
IT - Italia 409
HK - Hong Kong 252
KR - Corea 200
BR - Brasile 157
DE - Germania 115
NL - Olanda 107
FR - Francia 90
FI - Finlandia 78
IN - India 77
JP - Giappone 62
GB - Regno Unito 60
SE - Svezia 45
RU - Federazione Russa 38
AR - Argentina 34
AT - Austria 31
IE - Irlanda 31
ID - Indonesia 30
PL - Polonia 28
PH - Filippine 26
CA - Canada 25
MX - Messico 25
CI - Costa d'Avorio 23
BD - Bangladesh 20
IQ - Iraq 20
JO - Giordania 16
ZA - Sudafrica 16
UA - Ucraina 13
BG - Bulgaria 12
CL - Cile 12
SC - Seychelles 11
TH - Thailandia 11
TR - Turchia 11
CH - Svizzera 10
PK - Pakistan 10
ES - Italia 9
PY - Paraguay 8
CO - Colombia 7
EC - Ecuador 7
MA - Marocco 7
EG - Egitto 6
TW - Taiwan 6
VE - Venezuela 6
AE - Emirati Arabi Uniti 4
JM - Giamaica 4
LT - Lituania 4
NG - Nigeria 4
AU - Australia 3
AZ - Azerbaigian 3
BE - Belgio 3
DZ - Algeria 3
GT - Guatemala 3
MY - Malesia 3
PE - Perù 3
TG - Togo 3
TN - Tunisia 3
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
BY - Bielorussia 2
GH - Ghana 2
IR - Iran 2
IS - Islanda 2
KE - Kenya 2
LK - Sri Lanka 2
NP - Nepal 2
PT - Portogallo 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
UY - Uruguay 2
UZ - Uzbekistan 2
AL - Albania 1
CR - Costa Rica 1
CZ - Repubblica Ceca 1
ET - Etiopia 1
GM - Gambi 1
GR - Grecia 1
HR - Croazia 1
KZ - Kazakistan 1
LB - Libano 1
LI - Liechtenstein 1
LU - Lussemburgo 1
MM - Myanmar 1
MN - Mongolia 1
MR - Mauritania 1
NO - Norvegia 1
PA - Panama 1
PS - Palestinian Territory 1
RO - Romania 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
TT - Trinidad e Tobago 1
Totale 6.263
Città #
Singapore 673
Hefei 425
Hong Kong 234
Ashburn 212
Santa Clara 210
Seoul 191
San Jose 184
Ho Chi Minh City 181
Hanoi 166
Bologna 95
Beijing 86
Boardman 60
Helsinki 54
Tokyo 50
Los Angeles 47
Lauterbourg 45
Council Bluffs 43
New York 43
Bengaluru 35
Da Nang 35
Frankfurt am Main 32
Dublin 31
Chandler 30
Milan 30
Haiphong 28
Jakarta 24
Abidjan 23
Rome 22
Fairfield 20
Lappeenranta 20
Nuremberg 20
Buffalo 19
Shanghai 18
Vienna 17
Munich 16
Princeton 16
Southend 16
Warsaw 16
Florence 15
Houston 15
Redondo Beach 15
Amman 14
Dallas 14
Guangzhou 14
Hải Dương 13
São Paulo 13
Tongling 13
Turin 13
Chicago 12
Sofia 12
Baghdad 11
Falkenstein 11
London 11
Rimini 11
Montreal 10
Bern 9
Boydton 9
Brooklyn 9
Bắc Ninh 9
Can Tho 9
Mexico City 9
Modena 9
Seattle 9
Jinan 8
Santiago 8
Thái Nguyên 8
Woodbridge 8
Biên Hòa 7
Chennai 7
Genoa 7
Groningen 7
Johannesburg 7
Orem 7
Quận Bình Thạnh 7
Rio de Janeiro 7
Shenzhen 7
Amsterdam 6
Berlin 6
Cambridge 6
Des Moines 6
Naples 6
Ottawa 6
Qingdao 6
Tianjin 6
Xi'an 6
Yubileyny 6
Düsseldorf 5
Kyiv 5
North Bergen 5
Paris 5
Parma 5
Phoenix 5
Phủ Lý 5
Portsmouth 5
Quận Ba 5
Roubaix 5
Shenyang 5
Thái Bình 5
Verona 5
Zhengzhou 5
Totale 3.981
Nome #
Immune response against adenovirus in acute upper respiratory tract infections in immunocompetent children 199
Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children 196
In‐Depth Immunological Typization of Children with Sickle Cell Disease: A Preliminary Insight into Its Plausible Correlation with Clinical Course and Hydroxyurea Therapy 184
Cannabidiol in the acute phase of febrile infection-related epilepsy syndrome (FIRES) 181
Immune dysregulation associated with co-occurring germline CBL and SH2B3 variants 178
Anti-Inflammatory and Immunomodulatory Effect of High-Dose Immunoglobulins in Children: From Approved Indications to Off-Label Use 177
Expanding phenotype of schimke immuno-osseous dysplasia: Congenital anomalies of the kidneys and of the urinary tract and alteration of nk cells 163
Activated phosphoinositde 3-kinase (PI3Kδ) syndrome: an Italian point of view on diagnosis and new advances in treatment 158
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 150
Diagnosis, treatment, and follow-up of a case of Wolman disease with hemophagocytic lymphohistiocytosis 147
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 142
Expert insights on Hodgkin’s lymphoma development in an activated PI3K delta syndrome patient undergoing leniolisib treatment 142
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 141
MicroRNA dysregulation in ataxia telangiectasia 138
Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient (Frontiers in Pediatrics, (2021), 9, (702546), 10.3389/fped.2021.702546) 133
Case Report: Hereditary Alpha Tryptasemia in Children: A Pediatric Case Series and a Brief Overview of Literature 132
Immune cytopenias as a continuum in inborn errors of immunity: An in-depth clinical and immunological exploration 131
Immune dysregulation in Kabuki syndrome: a case report of Evans syndrome and hypogammaglobulinemia 123
Imiquimod cream in pediatric patients: Recommendations, adverse events, and controversies 123
The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase 121
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunity 120
Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient 120
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet) 118
Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children 118
Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation 116
Auto-Abs neutralizing type I IFNs in patients with severe Powassan, Usutu, or Ross River virus disease 115
Autoantibodies neutralizing type I IFNs underlie West Nile virus encephalitis in ∼40% of patients 115
Early bone marrow alterations in patients with adenosine deaminase 2 deficiency across disease phenotypes and severities 112
A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association 108
Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity 93
Lentiviral correction of enzymatic activity restrains macrophage inflammation in adenosine deaminase 2 deficiency 91
How to: Diagnose inborn errors of intrinsic and innate immunity to viral, bacterial, mycobacterial, and fungal infections 89
Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up 87
SARS-CoV-2 infection and treatment in a cohort of patients with inborn errors of immunity 86
Exploring Factors Influencing Changes in Incidence and Severity of Multisystem Inflammatory Syndrome in Children 83
Refractory immune thrombocytopenia successfully treated with bortezomib in a child with 22q11.2 deletion syndrome, complicated by Evans syndrome and hypogammaglobulinemia 81
Transplantation to save the life, TSH screening to save the brain: A report and brief literature review of autoimmune thyroid disease after HSCT for severe combined immunodeficiency 79
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature 75
Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 74
Granulomatous lymphocytic interstitial lung disease in common variable immune deficiency: an in-depth clinical, immunological, functional and radiological exploration with a focus on its management, challenged by chronic CMV infection 72
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function 71
First case of patient with two homozygous mutations in MYD88 and CARD9 genes presenting with pyogenic bacterial infections, elevated IgE, and persistent EBV viremia 71
Inborn errors of immunity and cancer 63
Neuroinflammation in CTLA-4 Haploinsufficiency: Case Report of a New Variant with Remarkable Response to Targeted Therapy 61
Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase δ syndrome: The European society for immunodeficiencies-activated phosphoinositide 3-kinase δ syndrome registry 60
Long-term outcome in Wiskott-Aldrich syndrome and X-linked thrombocytopenia patients: an observational -prospective multi-center study of the Italian Primary Immune Deficiency Network (IPINET) 58
Immunological Aspects of Kabuki Syndrome: A Retrospective Multicenter Study of the Italian Primary Immunodeficiency Network (IPINet) 57
Unraveling the Genetic Predisposition on Respiratory Infections: From Single Nucleotide Polymorphisms to Inborn Errors of Immunity 55
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 54
MOG IgG3-Subclass Antibodies in MOG-Associated Disease: Insights From a Pediatric Case With IgG1 Deficiency and Literature Review 54
Spectrum of Cardiovascular Diseases in Children during High Peak Coronavirus Disease 2019 Period Infection in Northern Italy: Is There a Link? 53
Inborn errors of immunity underlying a susceptibility to pyogenic infections: from innate immune system deficiency to complex phenotypes 51
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome 51
Corrigendum : Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies (Frontiers in Immunology (2019) 10 (316) DOI: 10.3389/fimmu.2019.00316) 50
Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases 49
Theophylline as a precision therapy in a young girl with PIK3R1 immunodeficiency 48
Neonatal Erythroderma as an Early Sign of Primary Immunodeficiency 44
Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia 41
Italian pediatric experts' consensus statement on diagnosis and management of primary atopic disorders 41
NEONATAL INVASIVE HERPES INFECTIONS. INBORN ERRORS OF IMMUNITY AND PHENOCOPIES AS PREDISPOSING FACTORS 40
The impact of taci mutations: From hypogammaglobulinemia in infancy to autoimmunity in adulthood 37
Clinical Manifestations and Treatment Response of Patients With Syndrome of Undifferentiated Recurrent Fever (SURF) 37
Seletalisib for Activated PI3Kδ Syndromes: Open-Label Phase 1b and Extension Studies 34
Mycobacterium simiae Infection in Two Unrelated Patients with Different Forms of Inherited IFN-γR2 Deficiency 34
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function 33
Chronic granulomatous disease in Morocco: Genetic, immunological, and clinical features of 12 patients from 10 kindreds 33
Gene therapy supports long-term reconstitution of patient hematopoietic stem cells in deficiency of adenosine deaminase 2 29
Cardiofaciocutaneous syndrome and immunodeficiency: data from an international multicenter cohort 27
Chilblains in a child with confirmed SARS-CoV-2 infection: a red flag for late-onset skin manifestation in previously infected individuals 27
Transient hypogammaglobulinemia of infancy 25
A 23-Year Follow-Up of a Patient with Gain-of-Function IkB-Alpha Mutation and Stable Full Chimerism After Hematopoietic Stem Cell Transplantation 21
Thymic epithelium abnormalities in DiGeorge and Down syndrome patients contribute to dysregulation in T cell development 21
Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency 20
Totale 6.461
Categoria #
all - tutte 18.614
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 18.614


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202113 0 0 0 0 0 0 0 0 0 0 0 13
2021/202295 2 0 4 5 7 5 0 14 11 4 27 16
2022/2023269 16 19 10 17 30 18 7 20 60 8 27 37
2023/2024234 0 14 4 15 12 87 24 28 8 27 5 10
2024/20251.775 46 197 119 102 274 83 123 59 33 175 172 392
2025/20264.014 413 558 364 318 396 149 407 211 764 332 102 0
Totale 6.461