IRIS Institutional Research Information System - OPENBS Open Archive UniBS

BADOLATO, RAFFAELE
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 15.341
AS - Asia 9.005
EU - Europa 6.012
SA - Sud America 1.820
AF - Africa 225
OC - Oceania 33
Continente sconosciuto - Info sul continente non disponibili 14
Totale 32.450
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 15.056
CN - Cina 3.214
SG - Singapore 2.991
BR - Brasile 1.508
UA - Ucraina 1.332
HK - Hong Kong 1.044
DE - Germania 1.036
IT - Italia 814
VN - Vietnam 616
FI - Finlandia 591
GB - Regno Unito 468
FR - Francia 429
RU - Federazione Russa 351
TR - Turchia 330
PL - Polonia 291
IE - Irlanda 262
IN - India 227
CA - Canada 137
AR - Argentina 123
BD - Bangladesh 119
SE - Svezia 111
MX - Messico 96
JP - Giappone 76
IQ - Iraq 75
ZA - Sudafrica 61
AT - Austria 53
ES - Italia 53
ID - Indonesia 51
NG - Nigeria 49
NL - Olanda 46
CZ - Repubblica Ceca 40
EC - Ecuador 40
CO - Colombia 38
VE - Venezuela 32
SA - Arabia Saudita 31
AU - Australia 30
UZ - Uzbekistan 29
MA - Marocco 27
PK - Pakistan 27
BE - Belgio 24
LT - Lituania 22
PY - Paraguay 21
EG - Egitto 19
KE - Kenya 19
IL - Israele 18
KZ - Kazakistan 18
PE - Perù 18
AE - Emirati Arabi Uniti 16
TN - Tunisia 16
CL - Cile 15
IR - Iran 15
EU - Europa 13
JO - Giordania 13
NP - Nepal 13
UY - Uruguay 12
AZ - Azerbaigian 11
DZ - Algeria 11
PT - Portogallo 11
PS - Palestinian Territory 10
BO - Bolivia 9
JM - Giamaica 9
LB - Libano 9
PH - Filippine 8
RO - Romania 8
CH - Svizzera 7
HN - Honduras 7
SK - Slovacchia (Repubblica Slovacca) 7
SN - Senegal 7
AL - Albania 6
CR - Costa Rica 6
DK - Danimarca 6
DO - Repubblica Dominicana 6
ET - Etiopia 6
LA - Repubblica Popolare Democratica del Laos 6
OM - Oman 6
TT - Trinidad e Tobago 6
EE - Estonia 5
MU - Mauritius 5
NI - Nicaragua 5
PA - Panama 5
RS - Serbia 5
BG - Bulgaria 4
BY - Bielorussia 4
GE - Georgia 4
GR - Grecia 4
GY - Guiana 4
LV - Lettonia 4
MY - Malesia 4
AM - Armenia 3
BA - Bosnia-Erzegovina 3
CI - Costa d'Avorio 3
CY - Cipro 3
HR - Croazia 3
HU - Ungheria 3
KW - Kuwait 3
LK - Sri Lanka 3
LU - Lussemburgo 3
BB - Barbados 2
BH - Bahrain 2
BN - Brunei Darussalam 2
Totale 32.424
Salva come PNG Salva come JPEG
Città #
Fairfield 1.587
Singapore 1.586
Ashburn 1.431
Woodbridge 1.123
Hong Kong 1.039
Jacksonville 958
Houston 909
The Dalles 683
Seattle 627
Cambridge 615
San Jose 563
Beijing 559
Wilmington 550
Chandler 538
Ann Arbor 518
Princeton 500
New York 465
Shenzhen 406
Nanjing 365
Helsinki 319
Los Angeles 300
Warsaw 281
Lauterbourg 264
Dublin 262
Istanbul 249
Munich 223
Ho Chi Minh City 210
Dallas 158
Des Moines 157
Nanchang 146
Brescia 142
Hanoi 139
Moscow 130
São Paulo 128
Buffalo 118
Milan 112
Redondo Beach 111
Shanghai 104
Turku 102
Shenyang 99
San Francisco 98
Dearborn 94
London 92
San Diego 85
Jinan 81
Changsha 79
Orem 73
Chicago 69
Santa Clara 69
Hebei 63
Rio de Janeiro 62
Tianjin 61
Hangzhou 57
Tokyo 56
Montreal 55
Boardman 53
Council Bluffs 53
Chennai 52
Abuja 48
Jiaxing 46
Zhengzhou 46
Denver 43
Toronto 42
Verona 42
Nuremberg 41
Frankfurt am Main 40
Atlanta 39
Johannesburg 38
Poplar 37
Rome 37
Phoenix 36
Manchester 35
Brooklyn 34
Kunming 33
Romola 33
Baghdad 32
Stockholm 32
Guangzhou 30
Ningbo 30
Boston 29
Brasília 29
Haikou 28
Kocaeli 27
Lancaster 27
Amsterdam 26
Da Nang 26
Tashkent 26
Mexico City 25
New Delhi 25
Belo Horizonte 24
Brno 24
Haiphong 24
Lanzhou 24
San Mateo 23
Brussels 22
Porto Alegre 22
Ankara 21
Charlotte 21
Düsseldorf 20
Mumbai 20
Totale 21.335
Salva come PNG Salva come JPEG
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. 577
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 379
Neutropenia da mielocatessi 301
Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis 227
Clinical, laboratory and molecular signs of immunodeficiency in patients with partial oculo-cutaneous albinism. 220
Activin A as a Mediator of NK-Dendritic Cell Functional Interactions. 198
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 196
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 192
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 186
α- and β-Papillomavirus infection in a young patient with an unclassified primary T-cell immunodeficiency and multiple mucosal and cutaneous lesions 181
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 180
G-CSF treatment of Severe Congenital Neutropenia reverses neutropenia but does not correct the underlying functional deficiency of the neutrophil in defending against microorganisms. 178
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency 178
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 178
AIRE deficiency in thymus of 2 patients with Omenn syndrome. 177
Altered leukocyte response to CXCL12 in patients with Warts Hypogammaglobulinemia, Infections, Myelokathexis (WHIM) syndrome 175
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 175
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 174
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 173
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 173
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 172
Monocytes from Wiskott-Aldrich patients differentiate in functional mature dendritic cells with a defect in CD83 expression 171
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 171
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 170
Functional defects of dendritic cells in patients with CD40 deficiency. 169
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 168
Interferon-α Production by Plasmacytoid Dendritic Cells Is Dispensable for an Effective Anti-Cytomegalovirus Response in Adaptor Protein-3-Deficient Mice. 167
Role of dendritic cell-derived CXCL13 in the pathogenesis of Bartonella henselae B-rich granuloma. 165
Immune response in children with COVID-19 is characterized by lower levels of T-cell activation than infected adults 165
A new case of IPEX receiving bone marrow transplantation 164
A robust immunoassay for anti-interferon autoantibodies that is highly specific for patients with autoimmune polyglandular syndrome type 1 163
Long-Term Survival After Hematopoietic Stem Cell Transplantation for Complete STAT1 Deficiency 163
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 160
Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. 159
A robust immunoassay for anti-interferon autoantibodies that is highly specific for patients with autoimmune polyglandular syndrome type 1 159
How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome 158
Heterozygous mutation in adenosine deaminase gene in a patient with severe lymphopenia following corticosteroid treatment of autoimmune hemolytic anemia 158
STAT mutations as program switchers: Turning primary immunodeficiencies into autoimmune diseases 157
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 152
Antiretroviral use in Italian children with perinatal HIV infection over a 14-year period. 152
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 151
Diagnostics of primary immunodeficiencies through next-generation sequencing 150
Primary immunodeficiencies appearing as combined lymphopenia, neutropenia, and monocytopenia. 149
Structural and functional basis for JAK3-deficient severe combined immunodeficiency. 148
Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome. 148
Signal transducer and activator of transcription gain-of-function primary immunodeficiency/immunodysregulation disorders 147
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis 143
Toll-like receptor-4 genotype in children with respiratory infections 143
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 143
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. 142
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. 142
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 142
Novel STAT1 gain-of-function mutation and suppurative infections 142
Albinismo oculocutaneo e immunodeficienza 141
Perinatally HIV-Infected Youths After Transition from Pediatric to Adult Care, a Single-Center Experience from Northern Italy 141
Missed opportunities to prevent mother-to-child transmission of HIV in Italy 141
Decreased type I interferon receptor-soluble isoform in antiretroviral-treated HIV-positive children. 140
A novel biological function of serum amyloid A: induction of T lymphocyte migration and adhesion 139
Novel insights from adaptor protein 3 complex deficiency 139
Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism. 138
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. 138
The CXCR4 mutations in WHIM syndrome impair the stability of the T-cell immunologic synapse. 138
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 137
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function. 136
Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome 136
Resolution of pulmonary and vertebral aspergillosis in a child with CGD following combined use of granulocyte transfusions and voriconazole 136
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 135
Tetralogy of Fallot is an Uncommon Manifestation of Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome. 134
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 134
SARS-CoV-2 infection in dialysis and kidney transplant patients: immunological and serological response 134
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 133
Five-year follow-up of children with perinatal HIV-1 infection receiving early highly active antiretroviral therapy. 133
Differential expression of surface membrane growth hormone receptor on human peripheral blood lymphocytes detected by dual-fluorochrome flow cytometry 132
Ureteral obstruction in a patient with chronic granulomatous disease, receiving combined prophylaxis with IFN-gamma and antibiotics 131
X-chromosome inactivation analysis in a female carrier of FOXP3 mutation 130
Disseminated Mycobacterium genavense infection after immunosuppressive therapy shows underlying new composite heterozygous mutations of β1 subunit of IL-12 receptor gene. 130
La sindrome emofagocitica: dai sintomi alle cause genetiche 129
Leukocyte trafficking in primary immunodeficiencies. 129
Innate immunity defects in Hermansky-Pudlak type 2 syndrome 129
Defect of regulatory T cells in patients with Omenn syndrome 129
Inducible nitric oxide synthase expression on human monocyte-derived cells in granulomatous reactions. 129
Transient Decrease of Circulating and Tissular Dendritic Cells in Patients With Mycobacterial Disease and With Partial Dominant IFNγR1 Deficiency 129
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 128
Serum amyloid A is a chemoattractant: induction of migration, adhesion and tissue infiltration of monocytes and polymorphonuclear leukocytes 127
Severe impairment of IFN-γ and IFN-α responses in cells of a patient with a novel STAT1 splicing mutation. 127
Expression of inducible nitric oxide synthase in human granulomas and histiocytic reactions 126
Poor health-related quality of life and abnormal psychosocial adjustment in Italian children with perinatal HIV infection receiving highly active antiretroviral treatment. 126
Risk of perinatal HIV infection in infants born in Italy to immigrant mothers. 126
Toll receptor-mediated regulation of NADPH oxidase in human dendritic cells 126
Development of systemic lupus erythematosus in a young child affected with chronic granulomatous disease following withdrawal of treatment with interferon-gamma 125
Epigenetic Regulation of Protein-Coding and MicroRNA Genes by the Gfi1-Interacting Tumor Suppressor PRDM5 125
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 125
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 124
Italian consensus statement on paediatric HIV infection 123
Primary immunodeficiences - options for the future. 123
Expression of inducible Nitric Oxide Synthase (iNOS) in monocytic cells from children with infections by intracellular pathogens 123
Serum Amyloid A is an activator of PMN antimicrobial functions: induction of degranulation, phagocytosis and enhancement of anti-Candida activity. 122
Interleukin-15 (IL-15) induces IL-8 and monocyte chemotactic protein 1 production in human monocytes. 122
Virologic, immunologic, and clinical benefits from early combined antiretroviral therapy in infants with perinatal HIV-1 infection 121
AIRE modulates IFN- expression in T lymphocytes. 121
Totale 15.711
Salva come PNG Salva come JPEG
Categoria #
all - tutte 163.677
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 163.677
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021918 0 0 0 0 0 0 0 0 0 368 408 142
2021/20222.080 112 372 31 127 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
2025/202610.084 1.004 1.532 915 1.698 1.046 733 1.453 405 568 730 0 0
Totale 32.876