IRIS Institutional Research Information System - OPENBS Open Archive UniBS

PLEBANI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 20.772
AS - Asia 8.808
EU - Europa 7.240
SA - Sud America 1.869
AF - Africa 161
OC - Oceania 31
Continente sconosciuto - Info sul continente non disponibili 24
Totale 38.905
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Nazione #
US - Stati Uniti d'America 20.502
CN - Cina 3.318
SG - Singapore 2.752
UA - Ucraina 2.262
BR - Brasile 1.603
HK - Hong Kong 1.098
DE - Germania 1.051
PL - Polonia 767
IT - Italia 622
FI - Finlandia 606
VN - Vietnam 577
GB - Regno Unito 535
TR - Turchia 371
IE - Irlanda 356
RU - Federazione Russa 341
FR - Francia 291
IN - India 194
CA - Canada 138
SE - Svezia 120
AR - Argentina 113
BD - Bangladesh 101
MX - Messico 89
IQ - Iraq 73
ZA - Sudafrica 61
ES - Italia 56
NL - Olanda 52
AT - Austria 49
JP - Giappone 48
ID - Indonesia 36
EC - Ecuador 34
CO - Colombia 32
PK - Pakistan 31
BE - Belgio 30
UZ - Uzbekistan 29
VE - Venezuela 28
AU - Australia 26
KR - Corea 26
SA - Arabia Saudita 23
EU - Europa 21
MA - Marocco 20
AZ - Azerbaigian 19
IR - Iran 17
JO - Giordania 16
EG - Egitto 15
KE - Kenya 15
LT - Lituania 15
PY - Paraguay 15
TN - Tunisia 14
CL - Cile 13
CZ - Repubblica Ceca 13
MU - Mauritius 13
PE - Perù 13
KZ - Kazakistan 12
LB - Libano 12
IL - Israele 11
AE - Emirati Arabi Uniti 10
UY - Uruguay 10
CH - Svizzera 9
JM - Giamaica 9
NP - Nepal 9
BO - Bolivia 8
DK - Danimarca 8
DZ - Algeria 8
RO - Romania 8
HN - Honduras 7
ET - Etiopia 6
PS - Palestinian Territory 6
BG - Bulgaria 5
GR - Grecia 5
NI - Nicaragua 5
SK - Slovacchia (Repubblica Slovacca) 5
AL - Albania 4
CR - Costa Rica 4
DO - Repubblica Dominicana 4
HR - Croazia 4
NZ - Nuova Zelanda 4
PA - Panama 4
PT - Portogallo 4
BA - Bosnia-Erzegovina 3
HU - Ungheria 3
LA - Repubblica Popolare Democratica del Laos 3
LV - Lettonia 3
RS - Serbia 3
SN - Senegal 3
TT - Trinidad e Tobago 3
XK - ???statistics.table.value.countryCode.XK??? 3
BB - Barbados 2
BF - Burkina Faso 2
BY - Bielorussia 2
EE - Estonia 2
KG - Kirghizistan 2
KW - Kuwait 2
LU - Lussemburgo 2
MD - Moldavia 2
MN - Mongolia 2
OM - Oman 2
SV - El Salvador 2
TH - Thailandia 2
AO - Angola 1
CI - Costa d'Avorio 1
Totale 38.891
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Città #
Fairfield 2.746
Woodbridge 2.424
Ashburn 1.715
Houston 1.602
Jacksonville 1.562
Singapore 1.338
Ann Arbor 1.268
Hong Kong 1.093
Cambridge 1.091
Seattle 1.066
Wilmington 945
Warsaw 760
Beijing 687
Chandler 645
Princeton 645
Nanjing 514
New York 475
Dublin 354
Los Angeles 297
Istanbul 291
Helsinki 266
The Dalles 252
Nanchang 208
Ho Chi Minh City 200
Des Moines 198
Brescia 193
Moscow 174
Shenyang 167
Munich 142
Changsha 140
San Diego 137
Buffalo 134
Hebei 134
Dallas 128
São Paulo 125
Redondo Beach 119
Hanoi 115
Jinan 114
Tianjin 112
Milan 108
San Francisco 105
Shanghai 105
Lancaster 98
London 88
Chicago 85
Jiaxing 83
Dearborn 80
Hangzhou 70
Kunming 69
Boardman 57
Santa Clara 56
Montreal 55
Turku 53
Zhengzhou 53
Rio de Janeiro 51
Lanzhou 45
Tokyo 43
Verona 43
Brooklyn 42
Denver 41
Ningbo 41
Belo Horizonte 40
Guangzhou 39
Johannesburg 38
Stockholm 37
Phoenix 36
Haikou 35
Mexico City 35
Taizhou 35
Poplar 34
Toronto 31
Nuremberg 30
Chennai 28
Dong Ket 28
Kocaeli 28
Tashkent 28
Atlanta 27
Da Nang 27
San Mateo 27
Brussels 26
Brasília 25
Dhaka 24
Haiphong 24
Orem 24
Washington 24
Campinas 23
Curitiba 23
Norwalk 23
Charlotte 22
Boston 21
Manchester 21
Orange 21
Augusta 20
Vienna 20
Ankara 19
Guarulhos 19
Seongnam 19
Fuzhou 18
Amsterdam 17
Baghdad 17
Totale 27.080
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Nome #
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP 356
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 340
NFKB1 regulates human NK cell maturation and effector functions 318
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 248
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 245
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 232
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 227
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder? 217
Acral lympho-histiocytic dermatitis in X-linked agammaglobulinemia: A case report showing clonal CD8+ T cells with indolent clinical behaviour 201
The RAC2-PI3K axis regulates human NK cell maturation and function 192
Different molecular behavior of CD40 mutants causing hyper-IgM syndrome. 190
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 185
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 181
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 181
BAFF-R mutations in Good's syndrome. 180
CTLA-4 regulates human Natural Killer cell effector functions 178
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 175
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 175
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 174
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 172
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome. 170
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 170
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 170
IgG subclass deficiency in patients with Down's syndrome and aberrant hepatitis B vaccine response. 168
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages. 167
Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients. 166
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 166
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
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration. 163
A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life. 163
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations 163
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 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
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 157
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
Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders 156
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 156
Evidence for antigenic selection of large granular lymphocytes in a patient with Wiskott-Aldrich syndrome 155
T cell activity and cytokine production in X-linked agammaglobulinemia: implications for vaccination strategies 155
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 154
A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection 153
Functional defects of dendritic cells in patients with CD40 deficiency. 153
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 152
Body experiences, emotional competence, and psychosocial functioning in juvenile idiopathic arthritis. 152
Pancreatitis in systemic lupus erythematosus. 152
The change in Ig regulation from children to adults disconnects the correlation with the 3'RR hs1.2 polymorphism 152
“Maturazione della risposta anticorpale: dal repertorio anticorpale primario a quello secondario”. 150
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty. 150
Evaluation by SDS-PAGE and immunoblotting of residual antigenicity in hydrolysed protein formulas. 150
Intravenous gammaglobulin therapy for prophylaxis of infection in high-risk neonates. 149
Different role of secretory IgA in the pathogenesis of RAST-positive and RAST-negative atopic dermatitis. 149
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content. 148
Recurrent Bleedings in Newborn: A Factor VII Deficiency Case Report 148
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 146
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 146
Recurrent infections with IgG2 deficiency. 145
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 144
Activity of classical and alternative pathways of complement in preterm and small for gestational age infants. 143
Neurovisual Assessment in Children with Ataxia Telangiectasia 143
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 143
Profound T-cell defects in Dubowitz syndrome 142
An avidin/biotin ELISA for the measurement of serum and secretory IgD. 142
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 142
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 141
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 141
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. 139
C4bBinding Protein (C4BP) activates B cells through the CD40 receptor. 138
The tec kinase-regulated phosphoproteome reveals a mechanism for the regulation of inhibitory signals in murine macrophages 137
Diagnostics of primary immunodeficiencies through next-generation sequencing 137
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity 137
Western Blot technique in the serological evaluation of three LAV/HTLV III-infected Italian families. 136
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 136
Positive effect of erythrocyte-delivered dexamethasone in ataxia-telangiectasia 136
A homozygous CARD9 mutation in a family with susceptibility to fungal infections. 134
Serum immunoglobulin levels in heterozygous subjects with immunoglobulin heavy chain constant region gene deletions. 134
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. 133
A case of lymphoproliferative disease presenting with a clinical and immunological phenotype of common variable immunodeficiency. 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. 133
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 133
Valutazione dell'allergenicità dei peptidi contenuti negli idrolizzati delle proteine del latte vaccino 133
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy children. 133
Extensive deletion of immunoglobulin heavy chain constant region genes in the absence of recurrent infections: when is IgG subclass deficiency clinically relevant? 133
Screening of functional and positional candidate genes in families with common variable immunodeficiency 132
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 132
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper IgM syndrome (HIGM2). 131
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 131
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 131
Missed opportunities to prevent mother-to-child transmission of HIV in Italy 130
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 129
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects. 129
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 129
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function. 128
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 128
Variability of the immunoglobulin heavy chain constant region locus: a population study. 128
Ontogeny of secretory immunity: levels of secretory IgA and natural antibodies in saliva 128
Beta2 integrins are required for follicular helper T cell differentiation in humans 128
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world 128
Totale 15.994
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Categoria #
all - tutte 189.906
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 189.906
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20213.549 0 0 0 0 0 576 253 682 634 621 600 183
2021/20222.825 174 633 59 179 47 83 148 186 183 339 227 567
2022/20232.121 379 15 34 142 202 621 4 227 292 10 93 102
2023/20242.349 131 48 202 187 108 491 83 91 604 21 21 362
2024/20254.954 23 19 13 602 571 445 428 154 552 415 1.012 720
2025/20266.908 1.037 1.592 884 1.689 1.083 623 0 0 0 0 0 0
Totale 39.533