IRIS Institutional Research Information System - OPENBS Open Archive UniBS

BADOLATO, RAFFAELE
 Distribuzione geografica
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Continente #
NA - Nord America 10.352
EU - Europa 3.990
AS - Asia 2.946
OC - Oceania 14
Continente sconosciuto - Info sul continente non disponibili 13
SA - Sud America 11
AF - Africa 10
Totale 17.336
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Nazione #
US - Stati Uniti d'America 10.329
CN - Cina 1.948
UA - Ucraina 1.285
DE - Germania 695
IT - Italia 554
HK - Hong Kong 506
FI - Finlandia 398
SG - Singapore 314
GB - Regno Unito 273
IE - Irlanda 258
PL - Polonia 224
FR - Francia 104
SE - Svezia 77
IN - India 68
RU - Federazione Russa 38
TR - Turchia 37
CZ - Repubblica Ceca 25
CA - Canada 22
JP - Giappone 22
BE - Belgio 19
AU - Australia 14
IR - Iran 14
EU - Europa 13
VN - Vietnam 13
NL - Olanda 12
BR - Brasile 9
PT - Portogallo 6
RO - Romania 6
ID - Indonesia 5
MU - Mauritius 5
BD - Bangladesh 4
IL - Israele 4
SK - Slovacchia (Repubblica Slovacca) 4
KZ - Kazakistan 3
DZ - Algeria 2
ES - Italia 2
HU - Ungheria 2
LA - Repubblica Popolare Democratica del Laos 2
LU - Lussemburgo 2
AL - Albania 1
AZ - Azerbaigian 1
BN - Brunei Darussalam 1
BY - Bielorussia 1
CL - Cile 1
GR - Grecia 1
KR - Corea 1
LV - Lettonia 1
MD - Moldavia 1
MX - Messico 1
MY - Malesia 1
PE - Perù 1
RS - Serbia 1
SA - Arabia Saudita 1
SL - Sierra Leone 1
TH - Thailandia 1
TN - Tunisia 1
ZA - Sudafrica 1
Totale 17.336
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Città #
Fairfield 1.586
Woodbridge 1.123
Jacksonville 955
Houston 880
Ashburn 773
Cambridge 615
Seattle 614
Wilmington 547
Chandler 537
Ann Arbor 518
Hong Kong 502
Princeton 500
Shenzhen 403
Nanjing 362
New York 283
Beijing 270
Dublin 258
Helsinki 232
Warsaw 221
Singapore 172
Nanchang 144
Brescia 123
Des Moines 108
Shenyang 96
Dearborn 94
Shanghai 92
San Diego 85
Jinan 73
Changsha 69
London 66
Hebei 63
Milan 58
Tianjin 56
Boardman 51
Hangzhou 47
Jiaxing 43
Verona 42
Zhengzhou 34
Ningbo 29
Haikou 28
Kunming 28
Los Angeles 28
Kocaeli 27
Lancaster 25
San Francisco 25
Brno 24
San Mateo 23
Lanzhou 21
Rome 19
Toronto 19
Brussels 18
Taizhou 17
Leawood 16
Augusta 14
Norwalk 14
Munich 13
Dong Ket 12
Redwood City 12
Ardabil 11
Guangzhou 11
Kilburn 10
Washington 10
Changchun 9
Taiyuan 9
Fuzhou 8
Lappeenranta 8
Nürnberg 8
Orange 8
Prescot 8
Gunzenhausen 6
New Delhi 6
Alessandria 5
Falkenstein 5
Ferentino 5
Hefei 5
Pune 5
Sydney 5
Venezia 5
Acton 4
Bologna 4
Bratislava 4
Canberra 4
Casoria 4
Central 4
Chiswick 4
Dhaka 4
Flero 4
Florence 4
Hamburg 4
Leipzig 4
Melbourne 4
Monmouth Junction 4
Naples 4
Napoli 4
Origgio 4
Padova 4
Providence 4
São Paulo 4
Wandsworth 4
Amsterdam 3
Totale 13.341
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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. 514
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 282
Neutropenia da mielocatessi 231
Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis 154
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 137
Clinical, laboratory and molecular signs of immunodeficiency in patients with partial oculo-cutaneous albinism. 130
α- and β-Papillomavirus infection in a young patient with an unclassified primary T-cell immunodeficiency and multiple mucosal and cutaneous lesions 129
Monocytes from Wiskott-Aldrich patients differentiate in functional mature dendritic cells with a defect in CD83 expression 128
Activin A as a Mediator of NK-Dendritic Cell Functional Interactions. 127
Interferon-α Production by Plasmacytoid Dendritic Cells Is Dispensable for an Effective Anti-Cytomegalovirus Response in Adaptor Protein-3-Deficient Mice. 123
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 122
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 121
Role of dendritic cell-derived CXCL13 in the pathogenesis of Bartonella henselae B-rich granuloma. 121
Functional defects of dendritic cells in patients with CD40 deficiency. 120
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 120
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 117
G-CSF treatment of Severe Congenital Neutropenia reverses neutropenia but does not correct the underlying functional deficiency of the neutrophil in defending against microorganisms. 116
Antiretroviral use in Italian children with perinatal HIV infection over a 14-year period. 116
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 115
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 113
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis 111
AIRE deficiency in thymus of 2 patients with Omenn syndrome. 111
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency 111
A robust immunoassay for anti-interferon autoantibodies that is highly specific for patients with autoimmune polyglandular syndrome type 1 108
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 107
Novel insights from adaptor protein 3 complex deficiency 106
A new case of IPEX receiving bone marrow transplantation 105
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 105
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. 104
Diagnostics of primary immunodeficiencies through next-generation sequencing 104
Altered leukocyte response to CXCL12 in patients with Warts Hypogammaglobulinemia, Infections, Myelokathexis (WHIM) syndrome 103
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. 103
Resolution of pulmonary and vertebral aspergillosis in a child with CGD following combined use of granulocyte transfusions and voriconazole 103
Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism. 102
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 102
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 101
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function. 100
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 100
Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome 99
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 99
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 99
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 99
STAT mutations as program switchers: Turning primary immunodeficiencies into autoimmune diseases 99
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 99
Differential expression of surface membrane growth hormone receptor on human peripheral blood lymphocytes detected by dual-fluorochrome flow cytometry 98
Leukocyte trafficking in primary immunodeficiencies. 98
Primary immunodeficiencies appearing as combined lymphopenia, neutropenia, and monocytopenia. 98
Serum amyloid A is a chemoattractant: induction of migration, adhesion and tissue infiltration of monocytes and polymorphonuclear leukocytes 97
X-chromosome inactivation analysis in a female carrier of FOXP3 mutation 97
Defect of regulatory T cells in patients with Omenn syndrome 97
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 97
A robust immunoassay for anti-interferon autoantibodies that is highly specific for patients with autoimmune polyglandular syndrome type 1 97
The CXCR4 mutations in WHIM syndrome impair the stability of the T-cell immunologic synapse. 97
Poor health-related quality of life and abnormal psychosocial adjustment in Italian children with perinatal HIV infection receiving highly active antiretroviral treatment. 95
Tetralogy of Fallot is an Uncommon Manifestation of Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome. 95
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 94
Immune response in children with COVID-19 is characterized by lower levels of T-cell activation than infected adults 94
Structural and functional basis for JAK3-deficient severe combined immunodeficiency. 93
Ureteral obstruction in a patient with chronic granulomatous disease, receiving combined prophylaxis with IFN-gamma and antibiotics 92
Serum Amyloid A is an activator of PMN antimicrobial functions: induction of degranulation, phagocytosis and enhancement of anti-Candida activity. 92
Toll-like receptor-4 genotype in children with respiratory infections 92
Five-year follow-up of children with perinatal HIV-1 infection receiving early highly active antiretroviral therapy. 92
Primary immunodeficiences - options for the future. 92
Virologic, immunologic, and clinical benefits from early combined antiretroviral therapy in infants with perinatal HIV-1 infection 91
Expression of inducible nitric oxide synthase in human granulomas and histiocytic reactions 91
Risk of perinatal HIV infection in infants born in Italy to immigrant mothers. 91
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 91
Development of systemic lupus erythematosus in a young child affected with chronic granulomatous disease following withdrawal of treatment with interferon-gamma 90
Leukocyte circulation: one-way or round-trip? Lessons from primary immunodeficiency patients 90
Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. 90
Innate immunity defects in Hermansky-Pudlak type 2 syndrome 90
Signal transducer and activator of transcription gain-of-function primary immunodeficiency/immunodysregulation disorders 90
Interleukin-15 (IL-15) induces IL-8 and monocyte chemotactic protein 1 production in human monocytes. 89
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients. 89
Immunodeficiencies with autoimmune consequences. 88
Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome. 88
Long-Term Survival After Hematopoietic Stem Cell Transplantation for Complete STAT1 Deficiency 88
Toll receptor-mediated regulation of NADPH oxidase in human dendritic cells 88
Novel STAT1 gain-of-function mutation and suppurative infections 88
Italian consensus statement on paediatric HIV infection 87
Congenital neutropenia: advances in diagnosis and treatment 86
IL-10 enhances CCL2 release and chemotaxis induced by CCL16 in human monocytes 86
Inducible nitric oxide synthase expression on human monocyte-derived cells in granulomatous reactions. 86
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 86
Epigenetic Regulation of Protein-Coding and MicroRNA Genes by the Gfi1-Interacting Tumor Suppressor PRDM5 85
Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features. 85
Heterozygous mutation in adenosine deaminase gene in a patient with severe lymphopenia following corticosteroid treatment of autoimmune hemolytic anemia 85
Leishmania promastigotes selectively inhibits interleukin 12 induction in bone marrow-derived macrophages from susceptible and resistent mice. 84
Is the interruption of antiretroviral treatment during pregnancy an additional major risk factor for mother-to-child transmission of HIV type 1? 83
Five year follow-up of children with perinatal HIV-1 infection receiving early highly active antiretroviral therapy. 82
Psychosocial issues in children and adolescents with HIV infection evaluated with a World Health Organization age-specific descriptor system. 82
Disseminated Mycobacterium genavense infection after immunosuppressive therapy shows underlying new composite heterozygous mutations of β1 subunit of IL-12 receptor gene. 82
Decreased type I interferon receptor-soluble isoform in antiretroviral-treated HIV-positive children. 80
Combined decrease of defined B- and T-cell subsets in a group of common variable immunodeficiency patients. 80
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 79
Severe impairment of IFN-γ and IFN-α responses in cells of a patient with a novel STAT1 splicing mutation. 78
Lymphocyte trafficking: from immunology paradigms to disease mechanisms 77
CXCL12 mediates aberrant costimulation of B lymphocytes in warts, hypogammaglobulinemia, infections, myelokathexis immunodeficiency 77
Leishmania infection of human monocytes induces expression of IL-8 and MCAF 76
From Bone Marrow Transplantation to Cellular Therapies: Possible therapeutic strategies in managing autoimmune disorders. 76
Totale 10.577
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Categoria #
all - tutte 100.702
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 100.702
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.619 0 0 177 543 236 473 394 466 294 653 123 260
2020/20213.365 47 318 74 304 119 341 230 594 420 368 408 142
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
2024/202550 28 22 0 0 0 0 0 0 0 0 0 0
Totale 17.743