IRIS Institutional Research Information System - OPENBS Open Archive UniBS

BADOLATO, RAFFAELE
 Distribuzione geografica
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Continente #
NA - Nord America 13.564
AS - Asia 7.821
EU - Europa 5.420
SA - Sud America 1.676
AF - Africa 144
OC - Oceania 19
Continente sconosciuto - Info sul continente non disponibili 14
Totale 28.658
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Nazione #
US - Stati Uniti d'America 13.327
CN - Cina 2.812
SG - Singapore 2.592
BR - Brasile 1.425
UA - Ucraina 1.327
DE - Germania 1.012
HK - Hong Kong 1.006
IT - Italia 689
FI - Finlandia 548
VN - Vietnam 459
GB - Regno Unito 424
RU - Federazione Russa 347
TR - Turchia 319
PL - Polonia 281
IE - Irlanda 260
IN - India 174
FR - Francia 155
CA - Canada 122
SE - Svezia 106
AR - Argentina 104
BD - Bangladesh 93
MX - Messico 80
JP - Giappone 65
IQ - Iraq 52
ZA - Sudafrica 51
AT - Austria 48
ES - Italia 47
ID - Indonesia 46
CZ - Repubblica Ceca 36
EC - Ecuador 35
NL - Olanda 33
CO - Colombia 31
UZ - Uzbekistan 25
SA - Arabia Saudita 24
BE - Belgio 23
MA - Marocco 20
PK - Pakistan 20
PY - Paraguay 20
LT - Lituania 17
VE - Venezuela 17
AU - Australia 16
EG - Egitto 16
IL - Israele 16
KZ - Kazakistan 16
PE - Perù 16
IR - Iran 15
KE - Kenya 15
TN - Tunisia 14
AE - Emirati Arabi Uniti 13
EU - Europa 13
NP - Nepal 11
UY - Uruguay 11
AZ - Azerbaigian 9
CL - Cile 8
DZ - Algeria 8
PT - Portogallo 8
LB - Libano 7
PS - Palestinian Territory 7
BO - Bolivia 6
JM - Giamaica 6
LA - Repubblica Popolare Democratica del Laos 6
RO - Romania 6
SN - Senegal 6
AL - Albania 5
CH - Svizzera 5
CR - Costa Rica 5
DK - Danimarca 5
EE - Estonia 5
HN - Honduras 5
JO - Giordania 5
MU - Mauritius 5
SK - Slovacchia (Repubblica Slovacca) 5
ET - Etiopia 4
GE - Georgia 4
LV - Lettonia 4
TT - Trinidad e Tobago 4
AM - Armenia 3
BA - Bosnia-Erzegovina 3
BG - Bulgaria 3
GR - Grecia 3
GY - Guiana 3
HU - Ungheria 3
KW - Kuwait 3
LK - Sri Lanka 3
LU - Lussemburgo 3
MY - Malesia 3
NI - Nicaragua 3
OM - Oman 3
PA - Panama 3
RS - Serbia 3
BB - Barbados 2
BN - Brunei Darussalam 2
BY - Bielorussia 2
CI - Costa d'Avorio 2
DO - Repubblica Dominicana 2
NZ - Nuova Zelanda 2
PH - Filippine 2
SV - El Salvador 2
AO - Angola 1
BH - Bahrain 1
Totale 28.642
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Città #
Fairfield 1.587
Singapore 1.240
Ashburn 1.147
Woodbridge 1.123
Hong Kong 1.002
Jacksonville 957
Houston 906
Seattle 624
Cambridge 615
Beijing 550
Wilmington 550
Chandler 538
Ann Arbor 518
Princeton 500
New York 426
Shenzhen 404
Nanjing 364
Los Angeles 277
Helsinki 276
Warsaw 272
Dublin 260
Istanbul 246
Munich 223
The Dalles 185
Ho Chi Minh City 165
Des Moines 156
Dallas 150
Nanchang 145
Brescia 138
Moscow 130
Buffalo 115
São Paulo 113
Redondo Beach 111
Shanghai 102
Turku 102
Hanoi 100
Shenyang 99
San Francisco 95
Dearborn 94
London 87
San Diego 85
Jinan 79
Changsha 77
Milan 75
Chicago 66
Hebei 63
Tianjin 61
Rio de Janeiro 59
Santa Clara 54
Boardman 53
Hangzhou 52
Montreal 47
Jiaxing 45
Tokyo 45
Verona 42
Zhengzhou 42
Toronto 41
Denver 39
Nuremberg 38
Atlanta 35
Phoenix 34
Brooklyn 33
Romola 33
Chennai 32
Kunming 32
Johannesburg 31
Ningbo 30
Poplar 30
Haikou 28
Rome 28
Stockholm 28
Brasília 27
Kocaeli 27
Lancaster 27
Boston 26
Guangzhou 25
Brno 24
Frankfurt am Main 24
Lanzhou 24
Tashkent 24
San Mateo 23
Mexico City 22
New Delhi 22
Porto Alegre 22
Belo Horizonte 21
Brussels 21
Charlotte 21
Da Nang 20
Düsseldorf 20
Orem 20
Guarulhos 19
Manchester 19
Taizhou 18
Baghdad 17
Campinas 17
Salt Lake City 17
Vienna 17
Ankara 16
Dhaka 16
Leawood 16
Totale 18.741
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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. 560
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 335
Neutropenia da mielocatessi 264
Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis 211
Clinical, laboratory and molecular signs of immunodeficiency in patients with partial oculo-cutaneous albinism. 199
Activin A as a Mediator of NK-Dendritic Cell Functional Interactions. 183
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 177
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 172
α- and β-Papillomavirus infection in a young patient with an unclassified primary T-cell immunodeficiency and multiple mucosal and cutaneous lesions 171
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 168
G-CSF treatment of Severe Congenital Neutropenia reverses neutropenia but does not correct the underlying functional deficiency of the neutrophil in defending against microorganisms. 167
Altered leukocyte response to CXCL12 in patients with Warts Hypogammaglobulinemia, Infections, Myelokathexis (WHIM) syndrome 164
AIRE deficiency in thymus of 2 patients with Omenn syndrome. 164
Monocytes from Wiskott-Aldrich patients differentiate in functional mature dendritic cells with a defect in CD83 expression 163
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 159
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 158
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 158
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 157
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 156
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency 155
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 155
Functional defects of dendritic cells in patients with CD40 deficiency. 153
Interferon-α Production by Plasmacytoid Dendritic Cells Is Dispensable for an Effective Anti-Cytomegalovirus Response in Adaptor Protein-3-Deficient Mice. 153
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 153
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 153
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 153
Role of dendritic cell-derived CXCL13 in the pathogenesis of Bartonella henselae B-rich granuloma. 152
A new case of IPEX receiving bone marrow transplantation 151
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 151
A robust immunoassay for anti-interferon autoantibodies that is highly specific for patients with autoimmune polyglandular syndrome type 1 149
Long-Term Survival After Hematopoietic Stem Cell Transplantation for Complete STAT1 Deficiency 146
Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. 145
STAT mutations as program switchers: Turning primary immunodeficiencies into autoimmune diseases 145
Antiretroviral use in Italian children with perinatal HIV infection over a 14-year period. 142
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 142
Immune response in children with COVID-19 is characterized by lower levels of T-cell activation than infected adults 142
Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome. 141
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 140
How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome 140
A robust immunoassay for anti-interferon autoantibodies that is highly specific for patients with autoimmune polyglandular syndrome type 1 139
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 138
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis 136
Heterozygous mutation in adenosine deaminase gene in a patient with severe lymphopenia following corticosteroid treatment of autoimmune hemolytic anemia 136
Toll-like receptor-4 genotype in children with respiratory infections 135
Structural and functional basis for JAK3-deficient severe combined immunodeficiency. 134
Novel insights from adaptor protein 3 complex deficiency 134
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. 133
Diagnostics of primary immunodeficiencies through next-generation sequencing 133
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. 132
The CXCR4 mutations in WHIM syndrome impair the stability of the T-cell immunologic synapse. 132
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 132
Novel STAT1 gain-of-function mutation and suppurative infections 132
Signal transducer and activator of transcription gain-of-function primary immunodeficiency/immunodysregulation disorders 131
Primary immunodeficiencies appearing as combined lymphopenia, neutropenia, and monocytopenia. 130
Missed opportunities to prevent mother-to-child transmission of HIV in Italy 129
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function. 128
Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism. 126
Resolution of pulmonary and vertebral aspergillosis in a child with CGD following combined use of granulocyte transfusions and voriconazole 126
Tetralogy of Fallot is an Uncommon Manifestation of Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome. 125
Ureteral obstruction in a patient with chronic granulomatous disease, receiving combined prophylaxis with IFN-gamma and antibiotics 124
Five-year follow-up of children with perinatal HIV-1 infection receiving early highly active antiretroviral therapy. 124
Serum amyloid A is a chemoattractant: induction of migration, adhesion and tissue infiltration of monocytes and polymorphonuclear leukocytes 123
Albinismo oculocutaneo e immunodeficienza 123
Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome 123
Disseminated Mycobacterium genavense infection after immunosuppressive therapy shows underlying new composite heterozygous mutations of β1 subunit of IL-12 receptor gene. 123
Perinatally HIV-Infected Youths After Transition from Pediatric to Adult Care, a Single-Center Experience from Northern Italy 123
Differential expression of surface membrane growth hormone receptor on human peripheral blood lymphocytes detected by dual-fluorochrome flow cytometry 122
Leukocyte trafficking in primary immunodeficiencies. 122
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 122
A novel biological function of serum amyloid A: induction of T lymphocyte migration and adhesion 121
Development of systemic lupus erythematosus in a young child affected with chronic granulomatous disease following withdrawal of treatment with interferon-gamma 121
Poor health-related quality of life and abnormal psychosocial adjustment in Italian children with perinatal HIV infection receiving highly active antiretroviral treatment. 121
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 121
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 121
Toll receptor-mediated regulation of NADPH oxidase in human dendritic cells 121
X-chromosome inactivation analysis in a female carrier of FOXP3 mutation 120
Expression of inducible nitric oxide synthase in human granulomas and histiocytic reactions 120
Decreased type I interferon receptor-soluble isoform in antiretroviral-treated HIV-positive children. 120
Defect of regulatory T cells in patients with Omenn syndrome 120
Italian consensus statement on paediatric HIV infection 120
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 120
Innate immunity defects in Hermansky-Pudlak type 2 syndrome 119
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. 119
Epigenetic Regulation of Protein-Coding and MicroRNA Genes by the Gfi1-Interacting Tumor Suppressor PRDM5 118
Risk of perinatal HIV infection in infants born in Italy to immigrant mothers. 118
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 117
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 117
Interleukin-15 (IL-15) induces IL-8 and monocyte chemotactic protein 1 production in human monocytes. 116
Primary immunodeficiences - options for the future. 116
Severe impairment of IFN-γ and IFN-α responses in cells of a patient with a novel STAT1 splicing mutation. 115
Serum Amyloid A is an activator of PMN antimicrobial functions: induction of degranulation, phagocytosis and enhancement of anti-Candida activity. 114
SARS-CoV-2 infection in dialysis and kidney transplant patients: immunological and serological response 113
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 113
Immunodeficiencies with autoimmune consequences. 112
IL-10 enhances CCL2 release and chemotaxis induced by CCL16 in human monocytes 112
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients. 112
Psychosocial issues in children and adolescents with HIV infection evaluated with a World Health Organization age-specific descriptor system. 111
Expression of inducible Nitric Oxide Synthase (iNOS) in monocytic cells from children with infections by intracellular pathogens 111
Transient Decrease of Circulating and Tissular Dendritic Cells in Patients With Mycobacterial Disease and With Partial Dominant IFNγR1 Deficiency 111
Congenital neutropenia: advances in diagnosis and treatment 110
Totale 14.337
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Categoria #
all - tutte 154.925
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 154.925
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.503 0 0 0 0 0 341 230 594 420 368 408 142
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
2025/20266.288 1.004 1.532 915 1.698 1.046 93 0 0 0 0 0 0
Totale 29.080