CONTI, FRANCESCA
 Distribuzione geografica
Continente #
AS - Asia 3.615
NA - Nord America 1.914
EU - Europa 1.282
SA - Sud America 251
Continente sconosciuto - Info sul continente non disponibili 198
AF - Africa 85
OC - Oceania 3
Totale 7.348
Nazione #
US - Stati Uniti d'America 1.819
CN - Cina 1.009
SG - Singapore 973
VN - Vietnam 685
IT - Italia 571
HK - Hong Kong 258
KR - Corea 200
BD - Bangladesh 191
BR - Brasile 170
DE - Germania 116
NL - Olanda 114
FR - Francia 93
FI - Finlandia 78
IN - India 78
JP - Giappone 62
GB - Regno Unito 61
SE - Svezia 47
CA - Canada 44
RU - Federazione Russa 38
AR - Argentina 34
AT - Austria 31
IE - Irlanda 31
ID - Indonesia 30
PL - Polonia 28
MX - Messico 27
PH - Filippine 26
CI - Costa d'Avorio 23
IQ - Iraq 20
JO - Giordania 16
ZA - Sudafrica 16
BG - Bulgaria 13
UA - Ucraina 13
CL - Cile 12
ES - Italia 12
TR - Turchia 12
CH - Svizzera 11
SC - Seychelles 11
TH - Thailandia 11
PK - Pakistan 10
PY - Paraguay 8
CO - Colombia 7
EC - Ecuador 7
MA - Marocco 7
EG - Egitto 6
JM - Giamaica 6
TW - Taiwan 6
VE - Venezuela 6
GT - Guatemala 5
AE - Emirati Arabi Uniti 4
CR - Costa Rica 4
LT - Lituania 4
NG - Nigeria 4
AU - Australia 3
AZ - Azerbaigian 3
BE - Belgio 3
DZ - Algeria 3
MY - Malesia 3
PE - Perù 3
SA - Arabia Saudita 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
KZ - Kazakistan 2
LK - Sri Lanka 2
NI - Nicaragua 2
NP - Nepal 2
PR - Porto Rico 2
PT - Portogallo 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
UY - Uruguay 2
UZ - Uzbekistan 2
AL - Albania 1
CZ - Repubblica Ceca 1
ET - Etiopia 1
GM - Gambi 1
GP - Guadalupe 1
GR - Grecia 1
HN - Honduras 1
HR - Croazia 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 7.150
Città #
Singapore 689
Hefei 425
Ashburn 246
Hong Kong 240
Santa Clara 218
San Jose 202
Seoul 191
Ho Chi Minh City 183
Hanoi 168
Bologna 101
Beijing 90
Boardman 75
Los Angeles 65
Council Bluffs 63
New York 56
Helsinki 54
Tokyo 50
Lauterbourg 45
Rome 44
Milan 42
Bengaluru 35
Da Nang 35
Frankfurt am Main 32
Dublin 31
Chandler 30
Buffalo 28
Haiphong 28
São Paulo 25
Jakarta 24
Abidjan 23
Florence 22
Fairfield 20
Lappeenranta 20
Nuremberg 20
Shanghai 19
Dallas 17
Princeton 17
Turin 17
Vienna 17
Chicago 16
Houston 16
Munich 16
Southend 16
Warsaw 16
Redondo Beach 15
Rimini 15
Amman 14
Guangzhou 14
Hải Dương 13
Naples 13
Tongling 13
Sofia 12
Baghdad 11
Falkenstein 11
London 11
Mexico City 11
Montreal 11
Seattle 11
Brooklyn 10
Modena 10
Bern 9
Boydton 9
Bắc Ninh 9
Can Tho 9
Genoa 9
Jinan 8
Orem 8
Palermo 8
Santiago 8
Thái Nguyên 8
Verona 8
Woodbridge 8
Biên Hòa 7
Chennai 7
Groningen 7
Johannesburg 7
Ottawa 7
Quận Bình Thạnh 7
Rio de Janeiro 7
San Francisco 7
Shenzhen 7
Amsterdam 6
Atlanta 6
Berlin 6
Cambridge 6
Des Moines 6
Memphis 6
Qingdao 6
Tianjin 6
Toronto 6
Xi'an 6
Yubileyny 6
Brenzone 5
Charlotte 5
Düsseldorf 5
Kyiv 5
North Bergen 5
Paris 5
Parma 5
Phoenix 5
Totale 4.252
Nome #
Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children 222
Immune response against adenovirus in acute upper respiratory tract infections in immunocompetent children 201
Anti-Inflammatory and Immunomodulatory Effect of High-Dose Immunoglobulins in Children: From Approved Indications to Off-Label Use 198
Unraveling the Genetic Predisposition on Respiratory Infections: From Single Nucleotide Polymorphisms to Inborn Errors of Immunity 193
In‐Depth Immunological Typization of Children with Sickle Cell Disease: A Preliminary Insight into Its Plausible Correlation with Clinical Course and Hydroxyurea Therapy 191
Immune dysregulation associated with co-occurring germline CBL and SH2B3 variants 187
Cannabidiol in the acute phase of febrile infection-related epilepsy syndrome (FIRES) 186
Activated phosphoinositde 3-kinase (PI3Kδ) syndrome: an Italian point of view on diagnosis and new advances in treatment 169
Expanding phenotype of schimke immuno-osseous dysplasia: Congenital anomalies of the kidneys and of the urinary tract and alteration of nk cells 166
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 153
Expert insights on Hodgkin’s lymphoma development in an activated PI3K delta syndrome patient undergoing leniolisib treatment 153
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 153
Diagnosis, treatment, and follow-up of a case of Wolman disease with hemophagocytic lymphohistiocytosis 150
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 143
MicroRNA dysregulation in ataxia telangiectasia 143
Case Report: Hereditary Alpha Tryptasemia in Children: A Pediatric Case Series and a Brief Overview of Literature 142
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) 141
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) 138
Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient 134
Immune dysregulation in Kabuki syndrome: a case report of Evans syndrome and hypogammaglobulinemia 133
Immune cytopenias as a continuum in inborn errors of immunity: An in-depth clinical and immunological exploration 133
Auto-Abs neutralizing type I IFNs in patients with severe Powassan, Usutu, or Ross River virus disease 127
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunity 125
Imiquimod cream in pediatric patients: Recommendations, adverse events, and controversies 124
Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation 123
The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase 122
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 122
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet) 121
Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children 121
Early bone marrow alterations in patients with adenosine deaminase 2 deficiency across disease phenotypes and severities 121
Autoantibodies neutralizing type I IFNs underlie West Nile virus encephalitis in ∼40% of patients 120
SARS-CoV-2 infection and treatment in a cohort of patients with inborn errors of immunity 117
A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association 110
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature 103
How to: Diagnose inborn errors of intrinsic and innate immunity to viral, bacterial, mycobacterial, and fungal infections 100
Refractory immune thrombocytopenia successfully treated with bortezomib in a child with 22q11.2 deletion syndrome, complicated by Evans syndrome and hypogammaglobulinemia 97
Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity 95
Lentiviral correction of enzymatic activity restrains macrophage inflammation in adenosine deaminase 2 deficiency 95
Italian pediatric experts' consensus statement on diagnosis and management of primary atopic disorders 94
Inborn errors of immunity and cancer 92
Neuroinflammation in CTLA-4 Haploinsufficiency: Case Report of a New Variant with Remarkable Response to Targeted Therapy 89
Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up 89
Exploring Factors Influencing Changes in Incidence and Severity of Multisystem Inflammatory Syndrome in Children 87
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function 83
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function 80
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 80
MOG IgG3-Subclass Antibodies in MOG-Associated Disease: Insights From a Pediatric Case With IgG1 Deficiency and Literature Review 79
Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 78
First case of patient with two homozygous mutations in MYD88 and CARD9 genes presenting with pyogenic bacterial infections, elevated IgE, and persistent EBV viremia 76
Clinical Manifestations and Treatment Response of Patients With Syndrome of Undifferentiated Recurrent Fever (SURF) 68
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 63
NEONATAL INVASIVE HERPES INFECTIONS. INBORN ERRORS OF IMMUNITY AND PHENOCOPIES AS PREDISPOSING FACTORS 58
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 58
Immunological Aspects of Kabuki Syndrome: A Retrospective Multicenter Study of the Italian Primary Immunodeficiency Network (IPINet) 58
Spectrum of Cardiovascular Diseases in Children during High Peak Coronavirus Disease 2019 Period Infection in Northern Italy: Is There a Link? 57
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) 53
Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases 53
Inborn errors of immunity underlying a susceptibility to pyogenic infections: from innate immune system deficiency to complex phenotypes 52
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome 51
Theophylline as a precision therapy in a young girl with PIK3R1 immunodeficiency 51
Neonatal Erythroderma as an Early Sign of Primary Immunodeficiency 48
Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia 43
Gene therapy supports long-term reconstitution of patient hematopoietic stem cells in deficiency of adenosine deaminase 2 42
The impact of taci mutations: From hypogammaglobulinemia in infancy to autoimmunity in adulthood 38
Seletalisib for Activated PI3Kδ Syndromes: Open-Label Phase 1b and Extension Studies 35
Chronic granulomatous disease in Morocco: Genetic, immunological, and clinical features of 12 patients from 10 kindreds 35
Mycobacterium simiae Infection in Two Unrelated Patients with Different Forms of Inherited IFN-γR2 Deficiency 35
Cardiofaciocutaneous syndrome and immunodeficiency: data from an international multicenter cohort 31
Chilblains in a child with confirmed SARS-CoV-2 infection: a red flag for late-onset skin manifestation in previously infected individuals 28
Transient hypogammaglobulinemia of infancy 26
Thymic epithelium abnormalities in DiGeorge and Down syndrome patients contribute to dysregulation in T cell development 24
A 23-Year Follow-Up of a Patient with Gain-of-Function IkB-Alpha Mutation and Stable Full Chimerism After Hematopoietic Stem Cell Transplantation 22
Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency 20
Totale 7.348
Categoria #
all - tutte 21.499
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 21.499


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202293 0 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
2025/20264.734 413 558 364 318 396 149 407 211 764 332 326 496
2026/2027167 166 1 0 0 0 0 0 0 0 0 0 0
Totale 7.348