CRIS Current Research Information System

CONTI, FRANCESCA
 Distribuzione geografica
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Continente #
AS - Asia 3.660
NA - Nord America 2.454
EU - Europa 1.361
SA - Sud America 263
Continente sconosciuto - Info sul continente non disponibili 198
AF - Africa 86
OC - Oceania 3
Totale 8.025
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Nazione #
US - Stati Uniti d'America 2.320
CN - Cina 1.011
SG - Singapore 980
VN - Vietnam 686
IT - Italia 632
HK - Hong Kong 260
BD - Bangladesh 205
KR - Corea 200
BR - Brasile 174
NL - Olanda 117
DE - Germania 116
FR - Francia 93
IN - India 81
FI - Finlandia 78
GB - Regno Unito 69
JP - Giappone 63
CA - Canada 60
SE - Svezia 47
RU - Federazione Russa 38
AR - Argentina 34
ID - Indonesia 33
AT - Austria 32
IE - Irlanda 31
MX - Messico 28
PL - Polonia 28
PH - Filippine 26
CI - Costa d'Avorio 23
IQ - Iraq 20
JO - Giordania 16
TR - Turchia 16
ZA - Sudafrica 16
UA - Ucraina 14
BG - Bulgaria 13
CL - Cile 13
TH - Thailandia 13
CH - Svizzera 12
ES - Italia 12
SC - Seychelles 11
CR - Costa Rica 10
PK - Pakistan 10
VE - Venezuela 10
CO - Colombia 9
JM - Giamaica 9
EC - Ecuador 8
PY - Paraguay 8
GT - Guatemala 7
MA - Marocco 7
NI - Nicaragua 7
TW - Taiwan 7
EG - Egitto 6
SA - Arabia Saudita 6
AE - Emirati Arabi Uniti 5
BE - Belgio 5
LT - Lituania 4
NG - Nigeria 4
AU - Australia 3
AZ - Azerbaigian 3
DZ - Algeria 3
KE - Kenya 3
KZ - Kazakistan 3
MY - Malesia 3
PE - Perù 3
PR - Porto Rico 3
TG - Togo 3
TN - Tunisia 3
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
BY - Bielorussia 2
GH - Ghana 2
HN - Honduras 2
IR - Iran 2
IS - Islanda 2
LK - Sri Lanka 2
NP - Nepal 2
PT - Portogallo 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
SV - El Salvador 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
UZ - Uzbekistan 2
AL - Albania 1
CZ - Repubblica Ceca 1
EE - Estonia 1
ET - Etiopia 1
GD - Grenada 1
GM - Gambi 1
GP - Guadalupe 1
GR - Grecia 1
HR - Croazia 1
HT - Haiti 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
Totale 7.825
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Città #
Singapore 696
Hefei 425
Ashburn 272
Hong Kong 242
Santa Clara 227
San Jose 223
Seoul 191
Ho Chi Minh City 184
Hanoi 168
Council Bluffs 134
Bologna 101
Beijing 91
Boardman 76
Los Angeles 75
New York 67
Rome 56
Helsinki 54
Milan 52
Tokyo 51
Lauterbourg 45
Bengaluru 35
Da Nang 35
Frankfurt am Main 32
Chandler 31
Chicago 31
Dublin 31
Buffalo 29
Haiphong 28
São Paulo 25
Fairfield 24
Florence 24
Jakarta 24
Abidjan 23
Dallas 22
Lappeenranta 20
Nuremberg 20
Shanghai 20
Turin 19
Princeton 18
Vienna 17
Houston 16
Munich 16
Southend 16
Warsaw 16
Redondo Beach 15
Rimini 15
Amman 14
Guangzhou 14
Brooklyn 13
Hải Dương 13
Montreal 13
Naples 13
Seattle 13
Tongling 13
Cambridge 12
London 12
Sofia 12
Baghdad 11
Falkenstein 11
Mexico City 11
Verona 11
Genoa 10
Modena 10
Phoenix 10
Queens 10
Bern 9
Boydton 9
Bắc Ninh 9
Can Tho 9
Woodbridge 9
Amsterdam 8
Atlanta 8
Jinan 8
Las Vegas 8
Orem 8
Palermo 8
Pittsburgh 8
Santiago 8
Thái Nguyên 8
Biên Hòa 7
Chennai 7
Denver 7
Groningen 7
Johannesburg 7
Managua 7
Memphis 7
Ottawa 7
Quận Bình Thạnh 7
Rio de Janeiro 7
San Francisco 7
Shenzhen 7
Toronto 7
Berlin 6
Des Moines 6
Guatemala City 6
Kingston 6
Manchester 6
Qingdao 6
Tianjin 6
Xi'an 6
Totale 4.514
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Nome #
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) 258
Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children 234
Anti-Inflammatory and Immunomodulatory Effect of High-Dose Immunoglobulins in Children: From Approved Indications to Off-Label Use 224
Immune response against adenovirus in acute upper respiratory tract infections in immunocompetent children 211
Unraveling the Genetic Predisposition on Respiratory Infections: From Single Nucleotide Polymorphisms to Inborn Errors of Immunity 207
In‐Depth Immunological Typization of Children with Sickle Cell Disease: A Preliminary Insight into Its Plausible Correlation with Clinical Course and Hydroxyurea Therapy 197
Immune dysregulation associated with co-occurring germline CBL and SH2B3 variants 191
Cannabidiol in the acute phase of febrile infection-related epilepsy syndrome (FIRES) 191
Activated phosphoinositde 3-kinase (PI3Kδ) syndrome: an Italian point of view on diagnosis and new advances in treatment 178
Expanding phenotype of schimke immuno-osseous dysplasia: Congenital anomalies of the kidneys and of the urinary tract and alteration of nk cells 170
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 163
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 163
Expert insights on Hodgkin’s lymphoma development in an activated PI3K delta syndrome patient undergoing leniolisib treatment 160
Diagnosis, treatment, and follow-up of a case of Wolman disease with hemophagocytic lymphohistiocytosis 153
MicroRNA dysregulation in ataxia telangiectasia 148
Case Report: Hereditary Alpha Tryptasemia in Children: A Pediatric Case Series and a Brief Overview of Literature 148
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 146
Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient 146
Immune dysregulation in Kabuki syndrome: a case report of Evans syndrome and hypogammaglobulinemia 144
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) 143
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 141
Auto-Abs neutralizing type I IFNs in patients with severe Powassan, Usutu, or Ross River virus disease 138
Immune cytopenias as a continuum in inborn errors of immunity: An in-depth clinical and immunological exploration 137
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunity 135
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet) 133
Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation 129
Imiquimod cream in pediatric patients: Recommendations, adverse events, and controversies 129
Autoantibodies neutralizing type I IFNs underlie West Nile virus encephalitis in ∼40% of patients 128
The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase 127
Early bone marrow alterations in patients with adenosine deaminase 2 deficiency across disease phenotypes and severities 127
Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children 124
Neuroinflammation in CTLA-4 Haploinsufficiency: Case Report of a New Variant with Remarkable Response to Targeted Therapy 122
SARS-CoV-2 infection and treatment in a cohort of patients with inborn errors of immunity 120
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature 117
A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association 114
How to: Diagnose inborn errors of intrinsic and innate immunity to viral, bacterial, mycobacterial, and fungal infections 112
Lentiviral correction of enzymatic activity restrains macrophage inflammation in adenosine deaminase 2 deficiency 105
Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity 104
Refractory immune thrombocytopenia successfully treated with bortezomib in a child with 22q11.2 deletion syndrome, complicated by Evans syndrome and hypogammaglobulinemia 103
MOG IgG3-Subclass Antibodies in MOG-Associated Disease: Insights From a Pediatric Case With IgG1 Deficiency and Literature Review 103
Italian pediatric experts' consensus statement on diagnosis and management of primary atopic disorders 101
Exploring Factors Influencing Changes in Incidence and Severity of Multisystem Inflammatory Syndrome in Children 96
Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up 95
Inborn errors of immunity and cancer 95
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function 93
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function 93
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 89
Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 82
First case of patient with two homozygous mutations in MYD88 and CARD9 genes presenting with pyogenic bacterial infections, elevated IgE, and persistent EBV viremia 80
NEONATAL INVASIVE HERPES INFECTIONS. INBORN ERRORS OF IMMUNITY AND PHENOCOPIES AS PREDISPOSING FACTORS 76
Clinical Manifestations and Treatment Response of Patients With Syndrome of Undifferentiated Recurrent Fever (SURF) 74
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 64
Immunological Aspects of Kabuki Syndrome: A Retrospective Multicenter Study of the Italian Primary Immunodeficiency Network (IPINet) 64
Spectrum of Cardiovascular Diseases in Children during High Peak Coronavirus Disease 2019 Period Infection in Northern Italy: Is There a Link? 63
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 60
Inborn errors of immunity underlying a susceptibility to pyogenic infections: from innate immune system deficiency to complex phenotypes 58
Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases 58
Gene therapy supports long-term reconstitution of patient hematopoietic stem cells in deficiency of adenosine deaminase 2 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) 57
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome 56
Theophylline as a precision therapy in a young girl with PIK3R1 immunodeficiency 54
Neonatal Erythroderma as an Early Sign of Primary Immunodeficiency 52
Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia 49
The impact of taci mutations: From hypogammaglobulinemia in infancy to autoimmunity in adulthood 46
Chronic granulomatous disease in Morocco: Genetic, immunological, and clinical features of 12 patients from 10 kindreds 39
Seletalisib for Activated PI3Kδ Syndromes: Open-Label Phase 1b and Extension Studies 37
Mycobacterium simiae Infection in Two Unrelated Patients with Different Forms of Inherited IFN-γR2 Deficiency 37
Cardiofaciocutaneous syndrome and immunodeficiency: data from an international multicenter cohort 36
Transient hypogammaglobulinemia of infancy 33
Chilblains in a child with confirmed SARS-CoV-2 infection: a red flag for late-onset skin manifestation in previously infected individuals 31
A 23-Year Follow-Up of a Patient with Gain-of-Function IkB-Alpha Mutation and Stable Full Chimerism After Hematopoietic Stem Cell Transplantation 27
Thymic epithelium abnormalities in DiGeorge and Down syndrome patients contribute to dysregulation in T cell development 27
Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency 23
Totale 8.025
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Categoria #
all - tutte 23.610
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 23.610
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202289 0 0 0 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
2026/2027844 166 327 293 58 0 0 0 0 0 0 0 0
Totale 8.025