IRIS Institutional Research Information System - OPENBS Open Archive UniBS

BADOLATO, RAFFAELE
 Distribuzione geografica
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Continente #
NA - Nord America 18.549
AS - Asia 9.252
EU - Europa 6.337
SA - Sud America 1.891
Continente sconosciuto - Info sul continente non disponibili 445
AF - Africa 229
OC - Oceania 35
Totale 36.738
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Nazione #
US - Stati Uniti d'America 18.073
CN - Cina 3.253
SG - Singapore 3.049
BR - Brasile 1.555
UA - Ucraina 1.335
HK - Hong Kong 1.056
DE - Germania 1.043
IT - Italia 1.037
VN - Vietnam 625
FI - Finlandia 591
GB - Regno Unito 504
FR - Francia 442
RU - Federazione Russa 353
TR - Turchia 331
PL - Polonia 292
IE - Irlanda 262
CA - Canada 235
IN - India 230
BD - Bangladesh 209
AR - Argentina 127
SE - Svezia 111
MX - Messico 104
JP - Giappone 84
IQ - Iraq 75
ZA - Sudafrica 62
ES - Italia 60
NL - Olanda 57
ID - Indonesia 56
AT - Austria 53
CO - Colombia 49
NG - Nigeria 49
EC - Ecuador 47
CZ - Repubblica Ceca 40
SA - Arabia Saudita 33
VE - Venezuela 33
AU - Australia 32
UZ - Uzbekistan 29
PK - Pakistan 28
MA - Marocco 27
BE - Belgio 25
JM - Giamaica 25
AE - Emirati Arabi Uniti 23
CR - Costa Rica 23
LT - Lituania 23
EG - Egitto 21
PY - Paraguay 21
IL - Israele 20
KE - Kenya 19
KZ - Kazakistan 19
PE - Perù 19
TN - Tunisia 16
CL - Cile 15
HN - Honduras 15
IR - Iran 15
NI - Nicaragua 14
TT - Trinidad e Tobago 14
EE - Estonia 13
EU - Europa 13
JO - Giordania 13
NP - Nepal 13
UY - Uruguay 12
AZ - Azerbaigian 11
CH - Svizzera 11
DZ - Algeria 11
PH - Filippine 11
PT - Portogallo 11
PS - Palestinian Territory 10
BO - Bolivia 9
LB - Libano 9
RO - Romania 8
SV - El Salvador 8
DK - Danimarca 7
LA - Repubblica Popolare Democratica del Laos 7
MY - Malesia 7
SK - Slovacchia (Repubblica Slovacca) 7
SN - Senegal 7
AL - Albania 6
DO - Repubblica Dominicana 6
ET - Etiopia 6
OM - Oman 6
PR - Porto Rico 6
RS - Serbia 6
BG - Bulgaria 5
BY - Bielorussia 5
GR - Grecia 5
MU - Mauritius 5
PA - Panama 5
BB - Barbados 4
CY - Cipro 4
GE - Georgia 4
GP - Guadalupe 4
GY - Guiana 4
HR - Croazia 4
LV - Lettonia 4
AM - Armenia 3
BA - Bosnia-Erzegovina 3
CI - Costa d'Avorio 3
GT - Guatemala 3
HU - Ungheria 3
KW - Kuwait 3
Totale 36.263
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Città #
Ashburn 1.909
Singapore 1.600
Fairfield 1.587
Woodbridge 1.123
Hong Kong 1.051
San Jose 998
Jacksonville 962
Houston 918
The Dalles 683
Seattle 630
Cambridge 619
Beijing 569
Wilmington 553
Chandler 539
Council Bluffs 536
Ann Arbor 518
New York 504
Princeton 501
Shenzhen 406
Nanjing 365
Los Angeles 330
Helsinki 319
Warsaw 282
Lauterbourg 264
Dublin 262
Istanbul 249
Munich 223
Columbus 216
Ho Chi Minh City 212
Dallas 195
Des Moines 158
São Paulo 156
Brescia 148
Nanchang 146
Hanoi 141
Moscow 130
Buffalo 129
Milan 128
Santa Clara 120
San Francisco 114
Redondo Beach 111
Shanghai 106
Turku 102
Shenyang 99
Dearborn 95
London 95
San Diego 86
Chicago 84
Jinan 81
Changsha 79
Phoenix 78
Orem 76
Montreal 69
Toronto 66
Hebei 63
Rio de Janeiro 63
Atlanta 62
Hangzhou 61
Tianjin 61
Tokyo 60
Boardman 57
Rome 55
Chennai 52
Denver 52
Abuja 48
Zhengzhou 47
Jiaxing 46
Nuremberg 44
Brooklyn 42
Verona 42
Frankfurt am Main 40
Manchester 39
Johannesburg 38
Poplar 37
Kunming 33
Naples 33
Romola 33
Baghdad 32
Brasília 32
Stockholm 32
Mexico City 31
Boston 30
Guangzhou 30
Ningbo 30
Amsterdam 28
Haikou 28
Lancaster 28
Charlotte 27
Kocaeli 27
Da Nang 26
Tashkent 26
Haiphong 25
New Delhi 25
Belo Horizonte 24
Brno 24
Lanzhou 24
San Mateo 23
Brussels 22
Porto Alegre 22
Ankara 21
Totale 23.445
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Nome #
Occurrence of nodular lymphocyte-predominant hodgkin lymphoma in hermansky-pudlak type 2 syndrome is associated to natural killer and natural killer T cell defects. 589
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 396
Neutropenia da mielocatessi 355
Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis 249
Clinical, laboratory and molecular signs of immunodeficiency in patients with partial oculo-cutaneous albinism. 231
Activin A as a Mediator of NK-Dendritic Cell Functional Interactions. 209
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 205
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 204
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 199
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 199
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency 193
Altered leukocyte response to CXCL12 in patients with Warts Hypogammaglobulinemia, Infections, Myelokathexis (WHIM) syndrome 190
G-CSF treatment of Severe Congenital Neutropenia reverses neutropenia but does not correct the underlying functional deficiency of the neutrophil in defending against microorganisms. 190
AIRE deficiency in thymus of 2 patients with Omenn syndrome. 188
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 188
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 188
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 187
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 186
α- and β-Papillomavirus infection in a young patient with an unclassified primary T-cell immunodeficiency and multiple mucosal and cutaneous lesions 185
Functional defects of dendritic cells in patients with CD40 deficiency. 184
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 184
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 183
Monocytes from Wiskott-Aldrich patients differentiate in functional mature dendritic cells with a defect in CD83 expression 180
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 179
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 177
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 175
Role of dendritic cell-derived CXCL13 in the pathogenesis of Bartonella henselae B-rich granuloma. 175
A robust immunoassay for anti-interferon autoantibodies that is highly specific for patients with autoimmune polyglandular syndrome type 1 174
A new case of IPEX receiving bone marrow transplantation 173
A robust immunoassay for anti-interferon autoantibodies that is highly specific for patients with autoimmune polyglandular syndrome type 1 173
Interferon-α Production by Plasmacytoid Dendritic Cells Is Dispensable for an Effective Anti-Cytomegalovirus Response in Adaptor Protein-3-Deficient Mice. 173
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 172
Long-Term Survival After Hematopoietic Stem Cell Transplantation for Complete STAT1 Deficiency 172
Immune response in children with COVID-19 is characterized by lower levels of T-cell activation than infected adults 172
How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome 171
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 168
Heterozygous mutation in adenosine deaminase gene in a patient with severe lymphopenia following corticosteroid treatment of autoimmune hemolytic anemia 167
STAT mutations as program switchers: Turning primary immunodeficiencies into autoimmune diseases 166
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 165
Incidence of acute respiratory infections in preschool children in an outpatient setting before and during Covid-19 pandemic in Lombardy Region, Italy 164
Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. 163
Albinismo oculocutaneo e immunodeficienza 162
Structural and functional basis for JAK3-deficient severe combined immunodeficiency. 160
Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome. 160
Diagnostics of primary immunodeficiencies through next-generation sequencing 160
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 159
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 158
Primary immunodeficiencies appearing as combined lymphopenia, neutropenia, and monocytopenia. 158
Antiretroviral use in Italian children with perinatal HIV infection over a 14-year period. 157
Assessment of red blood cell indexes in growth hormone treated children 156
A novel biological function of serum amyloid A: induction of T lymphocyte migration and adhesion 156
Signal transducer and activator of transcription gain-of-function primary immunodeficiency/immunodysregulation disorders 153
Toll-like receptor-4 genotype in children with respiratory infections 152
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 152
Novel STAT1 gain-of-function mutation and suppurative infections 152
Low prevalence of selective IgA deficiency in infected children born to HIV-seropositive mothers: an in vivo model for speculation on selective IgA deficiency pathogenesis. 151
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis 150
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency 150
A 17q25.3 duplication defines a new dosage-sensitive congenital neutropenia locus and implicates SOCS3 as a candidate gene for cases unexplained by ELA2 mutation. 149
Type I interferon-dependent gene MxA in perinatal HIV-infected patients under antiretroviral therapy as marker for therapy failure and blood plasmacytoid dendritic cells depletion. 148
Missed opportunities to prevent mother-to-child transmission of HIV in Italy 148
Decreased type I interferon receptor-soluble isoform in antiretroviral-treated HIV-positive children. 147
Poor health-related quality of life and abnormal psychosocial adjustment in Italian children with perinatal HIV infection receiving highly active antiretroviral treatment. 147
Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome 147
WHIM SYNDROME: CLINICAL AND GENETIC DIAGNOSIS 147
Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism. 145
The CXCR4 mutations in WHIM syndrome impair the stability of the T-cell immunologic synapse. 145
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 145
Perinatally HIV-Infected Youths After Transition from Pediatric to Adult Care, a Single-Center Experience from Northern Italy 145
X-chromosome inactivation analysis in a female carrier of FOXP3 mutation 144
Expression of inducible Nitric Oxide Synthase (iNOS) in monocytic cells from children with infections by intracellular pathogens 144
La sindrome emofagocitica: dai sintomi alle cause genetiche 143
La sindrome di Wiskott-Aldrich e piastrinopenia X-recessiva: dalla biologia alla clinica 143
Novel insights from adaptor protein 3 complex deficiency 143
Toll receptor-mediated regulation of NADPH oxidase in human dendritic cells 143
Resolution of pulmonary and vertebral aspergillosis in a child with CGD following combined use of granulocyte transfusions and voriconazole 142
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 142
Two X-linked agammaglobulinemia patients develop pneumonia as COVID-19 manifestation but recover 142
SARS-CoV-2 infection in dialysis and kidney transplant patients: immunological and serological response 142
Ureteral obstruction in a patient with chronic granulomatous disease, receiving combined prophylaxis with IFN-gamma and antibiotics 141
Tetralogy of Fallot is an Uncommon Manifestation of Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome. 141
Serum amyloid A is a chemoattractant: induction of migration, adhesion and tissue infiltration of monocytes and polymorphonuclear leukocytes 140
Defect of regulatory T cells in patients with Omenn syndrome 140
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 140
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 139
Leukocyte trafficking in primary immunodeficiencies. 139
Innate immunity defects in Hermansky-Pudlak type 2 syndrome 139
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function. 139
First-line antiretroviral therapy with a protease inhibitor versus non-nucleoside reverse transcriptase inhibitor and switch at higher versus low viral load in HIV-infected children: An open-label, randomised phase 2/3 trial 139
Differential expression of surface membrane growth hormone receptor on human peripheral blood lymphocytes detected by dual-fluorochrome flow cytometry 138
Five-year follow-up of children with perinatal HIV-1 infection receiving early highly active antiretroviral therapy. 138
Expression of inducible nitric oxide synthase in human granulomas and histiocytic reactions 137
Disseminated Mycobacterium genavense infection after immunosuppressive therapy shows underlying new composite heterozygous mutations of β1 subunit of IL-12 receptor gene. 137
Severe impairment of IFN-γ and IFN-α responses in cells of a patient with a novel STAT1 splicing mutation. 137
Epigenetic Regulation of Protein-Coding and MicroRNA Genes by the Gfi1-Interacting Tumor Suppressor PRDM5 136
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 136
Risk of perinatal HIV infection in infants born in Italy to immigrant mothers. 136
Transient Decrease of Circulating and Tissular Dendritic Cells in Patients With Mycobacterial Disease and With Partial Dominant IFNγR1 Deficiency 136
Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis 136
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 135
Totale 16.927
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Categoria #
all - tutte 190.819
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 190.819
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.565 0 0 0 127 38 100 112 128 135 285 180 460
2022/20231.623 279 19 28 103 147 460 4 193 225 8 73 84
2023/20242.544 108 42 626 177 81 367 89 131 526 26 27 344
2024/20255.099 28 22 68 604 538 449 435 221 596 424 999 715
2025/202610.763 1.004 1.532 915 1.698 1.046 733 1.453 405 568 858 366 185
2026/20273.183 443 428 909 1.403 0 0 0 0 0 0 0 0
Totale 36.738