IRIS Institutional Research Information System - OPENBS Open Archive UniBS

BADOLATO, RAFFAELE
 Distribuzione geografica
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Continente #
NA - Nord America 13.844
AS - Asia 7.966
EU - Europa 5.466
SA - Sud America 1.715
AF - Africa 151
OC - Oceania 19
Continente sconosciuto - Info sul continente non disponibili 14
Totale 29.175
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Nazione #
US - Stati Uniti d'America 13.591
CN - Cina 2.823
SG - Singapore 2.626
BR - Brasile 1.452
UA - Ucraina 1.328
DE - Germania 1.013
HK - Hong Kong 1.006
IT - Italia 696
FI - Finlandia 548
VN - Vietnam 525
GB - Regno Unito 439
RU - Federazione Russa 348
TR - Turchia 322
PL - Polonia 289
IE - Irlanda 260
IN - India 181
FR - Francia 155
CA - Canada 129
AR - Argentina 111
SE - Svezia 108
BD - Bangladesh 99
MX - Messico 86
JP - Giappone 70
IQ - Iraq 54
ZA - Sudafrica 54
AT - Austria 50
ES - Italia 47
ID - Indonesia 46
CZ - Repubblica Ceca 36
EC - Ecuador 36
NL - Olanda 36
CO - Colombia 33
UZ - Uzbekistan 27
SA - Arabia Saudita 24
BE - Belgio 23
PK - Pakistan 22
LT - Lituania 21
MA - Marocco 21
PY - Paraguay 21
VE - Venezuela 18
EG - Egitto 17
IL - Israele 17
AU - Australia 16
KZ - Kazakistan 16
PE - Perù 16
IR - Iran 15
KE - Kenya 15
TN - Tunisia 15
AE - Emirati Arabi Uniti 13
EU - Europa 13
NP - Nepal 13
UY - Uruguay 11
AZ - Azerbaigian 9
DZ - Algeria 9
CL - Cile 8
LB - Libano 8
PT - Portogallo 8
PS - Palestinian Territory 7
BO - Bolivia 6
JM - Giamaica 6
JO - Giordania 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
MU - Mauritius 5
SK - Slovacchia (Repubblica Slovacca) 5
BG - Bulgaria 4
DO - Repubblica Dominicana 4
ET - Etiopia 4
GE - Georgia 4
LV - Lettonia 4
OM - Oman 4
PA - Panama 4
TT - Trinidad e Tobago 4
AM - Armenia 3
BA - Bosnia-Erzegovina 3
BY - Bielorussia 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
RS - Serbia 3
BB - Barbados 2
BN - Brunei Darussalam 2
CI - Costa d'Avorio 2
NZ - Nuova Zelanda 2
PH - Filippine 2
SV - El Salvador 2
AO - Angola 1
BH - Bahrain 1
Totale 29.158
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Città #
Fairfield 1.587
Singapore 1.272
Ashburn 1.201
Woodbridge 1.123
Hong Kong 1.002
Jacksonville 957
Houston 909
Seattle 627
Cambridge 615
Beijing 550
Wilmington 550
Chandler 538
Ann Arbor 518
Princeton 500
New York 439
Shenzhen 405
Nanjing 364
The Dalles 297
Los Angeles 285
Warsaw 279
Helsinki 276
Dublin 260
Istanbul 246
Munich 223
Ho Chi Minh City 186
Des Moines 156
Dallas 150
Nanchang 145
Brescia 138
Moscow 130
São Paulo 121
Hanoi 117
Buffalo 115
Redondo Beach 111
Shanghai 102
Turku 102
Shenyang 99
San Francisco 96
Dearborn 94
London 89
San Diego 85
Jinan 79
Changsha 77
Milan 77
Chicago 68
Hebei 63
Tianjin 61
Rio de Janeiro 60
Santa Clara 58
Boardman 53
Hangzhou 52
Montreal 51
Tokyo 50
Jiaxing 45
Denver 42
Toronto 42
Verona 42
Zhengzhou 42
Nuremberg 39
Chennai 37
Poplar 37
Atlanta 36
Phoenix 35
Brooklyn 34
Johannesburg 33
Romola 33
Kunming 32
Ningbo 30
Orem 30
Stockholm 30
Rome 29
Boston 28
Haikou 28
Brasília 27
Guangzhou 27
Kocaeli 27
Lancaster 27
Tashkent 26
Mexico City 25
Brno 24
Frankfurt am Main 24
Lanzhou 24
Belo Horizonte 23
Da Nang 23
Manchester 23
New Delhi 23
San Mateo 23
Porto Alegre 22
Brussels 21
Charlotte 21
Düsseldorf 20
Ankara 19
Baghdad 19
Guarulhos 19
Haiphong 19
Taizhou 18
Vienna 18
Amsterdam 17
Campinas 17
Salt Lake City 17
Totale 19.105
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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. 563
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 340
Neutropenia da mielocatessi 271
Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis 214
Clinical, laboratory and molecular signs of immunodeficiency in patients with partial oculo-cutaneous albinism. 204
Activin A as a Mediator of NK-Dendritic Cell Functional Interactions. 186
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 181
α- and β-Papillomavirus infection in a young patient with an unclassified primary T-cell immunodeficiency and multiple mucosal and cutaneous lesions 174
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 174
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 170
G-CSF treatment of Severe Congenital Neutropenia reverses neutropenia but does not correct the underlying functional deficiency of the neutrophil in defending against microorganisms. 168
Altered leukocyte response to CXCL12 in patients with Warts Hypogammaglobulinemia, Infections, Myelokathexis (WHIM) syndrome 167
AIRE deficiency in thymus of 2 patients with Omenn syndrome. 167
Monocytes from Wiskott-Aldrich patients differentiate in functional mature dendritic cells with a defect in CD83 expression 165
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 164
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 164
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 162
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 160
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency 159
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 159
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 157
Role of dendritic cell-derived CXCL13 in the pathogenesis of Bartonella henselae B-rich granuloma. 157
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 157
Interferon-α Production by Plasmacytoid Dendritic Cells Is Dispensable for an Effective Anti-Cytomegalovirus Response in Adaptor Protein-3-Deficient Mice. 156
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 156
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 156
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 156
A new case of IPEX receiving bone marrow transplantation 154
A robust immunoassay for anti-interferon autoantibodies that is highly specific for patients with autoimmune polyglandular syndrome type 1 153
Functional defects of dendritic cells in patients with CD40 deficiency. 153
Long-Term Survival After Hematopoietic Stem Cell Transplantation for Complete STAT1 Deficiency 149
STAT mutations as program switchers: Turning primary immunodeficiencies into autoimmune diseases 148
Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. 147
Immune response in children with COVID-19 is characterized by lower levels of T-cell activation than infected adults 145
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 144
Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome. 143
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 143
Heterozygous mutation in adenosine deaminase gene in a patient with severe lymphopenia following corticosteroid treatment of autoimmune hemolytic anemia 143
Antiretroviral use in Italian children with perinatal HIV infection over a 14-year period. 142
A robust immunoassay for anti-interferon autoantibodies that is highly specific for patients with autoimmune polyglandular syndrome type 1 142
How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome 142
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 141
Primary immunodeficiencies appearing as combined lymphopenia, neutropenia, and monocytopenia. 138
Signal transducer and activator of transcription gain-of-function primary immunodeficiency/immunodysregulation disorders 138
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis 137
Toll-like receptor-4 genotype in children with respiratory infections 137
Diagnostics of primary immunodeficiencies through next-generation sequencing 137
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. 136
Structural and functional basis for JAK3-deficient severe combined immunodeficiency. 135
Novel STAT1 gain-of-function mutation and suppurative infections 135
Novel insights from adaptor protein 3 complex deficiency 134
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. 133
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
Missed opportunities to prevent mother-to-child transmission of HIV in Italy 130
Decreased type I interferon receptor-soluble isoform in antiretroviral-treated HIV-positive children. 128
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function. 128
Resolution of pulmonary and vertebral aspergillosis in a child with CGD following combined use of granulocyte transfusions and voriconazole 127
A novel biological function of serum amyloid A: induction of T lymphocyte migration and adhesion 126
Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism. 126
Ureteral obstruction in a patient with chronic granulomatous disease, receiving combined prophylaxis with IFN-gamma and antibiotics 125
Albinismo oculocutaneo e immunodeficienza 125
Tetralogy of Fallot is an Uncommon Manifestation of Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome. 125
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 125
Perinatally HIV-Infected Youths After Transition from Pediatric to Adult Care, a Single-Center Experience from Northern Italy 125
Serum amyloid A is a chemoattractant: induction of migration, adhesion and tissue infiltration of monocytes and polymorphonuclear leukocytes 124
Five-year follow-up of children with perinatal HIV-1 infection receiving early highly active antiretroviral therapy. 124
Differential expression of surface membrane growth hormone receptor on human peripheral blood lymphocytes detected by dual-fluorochrome flow cytometry 123
Leukocyte trafficking in primary immunodeficiencies. 123
X-chromosome inactivation analysis in a female carrier of FOXP3 mutation 123
Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome 123
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. 123
Disseminated Mycobacterium genavense infection after immunosuppressive therapy shows underlying new composite heterozygous mutations of β1 subunit of IL-12 receptor gene. 123
Expression of inducible nitric oxide synthase in human granulomas and histiocytic reactions 122
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 122
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 122
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
Toll receptor-mediated regulation of NADPH oxidase in human dendritic cells 121
Innate immunity defects in Hermansky-Pudlak type 2 syndrome 120
Defect of regulatory T cells in patients with Omenn syndrome 120
Italian consensus statement on paediatric HIV infection 120
Risk of perinatal HIV infection in infants born in Italy to immigrant mothers. 120
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 120
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 120
Epigenetic Regulation of Protein-Coding and MicroRNA Genes by the Gfi1-Interacting Tumor Suppressor PRDM5 118
Interleukin-15 (IL-15) induces IL-8 and monocyte chemotactic protein 1 production in human monocytes. 117
Primary immunodeficiences - options for the future. 117
SARS-CoV-2 infection in dialysis and kidney transplant patients: immunological and serological response 117
Severe impairment of IFN-γ and IFN-α responses in cells of a patient with a novel STAT1 splicing mutation. 116
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 116
Serum Amyloid A is an activator of PMN antimicrobial functions: induction of degranulation, phagocytosis and enhancement of anti-Candida activity. 115
Expression of inducible Nitric Oxide Synthase (iNOS) in monocytic cells from children with infections by intracellular pathogens 114
Transient Decrease of Circulating and Tissular Dendritic Cells in Patients With Mycobacterial Disease and With Partial Dominant IFNγR1 Deficiency 114
Inducible nitric oxide synthase expression on human monocyte-derived cells in granulomatous reactions. 113
Virologic, immunologic, and clinical benefits from early combined antiretroviral therapy in infants with perinatal HIV-1 infection 112
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
Totale 14.571
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Categoria #
all - tutte 156.797
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 156.797
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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
2025/20266.805 1.004 1.532 915 1.698 1.046 610 0 0 0 0 0 0
Totale 29.597