IRIS Institutional Research Information System - OPENBS Open Archive UniBS

PLEBANI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 22.333
AS - Asia 9.811
EU - Europa 7.867
SA - Sud America 1.963
AF - Africa 290
OC - Oceania 43
Continente sconosciuto - Info sul continente non disponibili 24
Totale 42.331
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Nazione #
US - Stati Uniti d'America 22.034
CN - Cina 3.664
SG - Singapore 3.126
UA - Ucraina 2.268
BR - Brasile 1.652
HK - Hong Kong 1.133
DE - Germania 1.074
PL - Polonia 767
IT - Italia 717
FI - Finlandia 710
VN - Vietnam 670
FR - Francia 611
GB - Regno Unito 567
TR - Turchia 380
IE - Irlanda 361
RU - Federazione Russa 345
IN - India 238
CA - Canada 148
AR - Argentina 125
SE - Svezia 122
BD - Bangladesh 120
MX - Messico 99
NG - Nigeria 96
IQ - Iraq 84
ZA - Sudafrica 67
NL - Olanda 65
ES - Italia 59
JP - Giappone 58
AT - Austria 49
PK - Pakistan 41
ID - Indonesia 40
CO - Colombia 39
VE - Venezuela 39
AU - Australia 38
EC - Ecuador 37
UZ - Uzbekistan 33
BE - Belgio 30
KR - Corea 29
SA - Arabia Saudita 29
MA - Marocco 23
AZ - Azerbaigian 22
JO - Giordania 22
KE - Kenya 22
EU - Europa 21
CL - Cile 19
CZ - Repubblica Ceca 18
EG - Egitto 17
IR - Iran 17
LT - Lituania 16
PY - Paraguay 16
TN - Tunisia 16
PE - Perù 15
KZ - Kazakistan 13
LB - Libano 13
MU - Mauritius 13
IL - Israele 12
NP - Nepal 12
AE - Emirati Arabi Uniti 11
CH - Svizzera 11
RO - Romania 11
UY - Uruguay 11
BO - Bolivia 10
DZ - Algeria 10
HN - Honduras 10
JM - Giamaica 10
ET - Etiopia 9
PS - Palestinian Territory 9
DK - Danimarca 8
PH - Filippine 8
SN - Senegal 8
GR - Grecia 7
NI - Nicaragua 6
AL - Albania 5
BG - Bulgaria 5
DO - Repubblica Dominicana 5
HR - Croazia 5
PA - Panama 5
RS - Serbia 5
SK - Slovacchia (Repubblica Slovacca) 5
CR - Costa Rica 4
MY - Malesia 4
NZ - Nuova Zelanda 4
PT - Portogallo 4
TT - Trinidad e Tobago 4
BA - Bosnia-Erzegovina 3
CI - Costa d'Avorio 3
HU - Ungheria 3
LA - Repubblica Popolare Democratica del Laos 3
LV - Lettonia 3
MD - Moldavia 3
MN - Mongolia 3
TH - Thailandia 3
XK - ???statistics.table.value.countryCode.XK??? 3
BB - Barbados 2
BF - Burkina Faso 2
BH - Bahrain 2
BY - Bielorussia 2
EE - Estonia 2
KG - Kirghizistan 2
KW - Kuwait 2
Totale 42.306
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Città #
Fairfield 2.746
Woodbridge 2.424
Ashburn 1.975
Singapore 1.684
Houston 1.607
Jacksonville 1.562
Ann Arbor 1.268
Hong Kong 1.124
Cambridge 1.091
Seattle 1.066
Wilmington 945
Warsaw 760
Beijing 692
The Dalles 655
Chandler 645
Princeton 645
San Jose 589
Nanjing 519
New York 491
Helsinki 369
Dublin 359
Los Angeles 310
Lauterbourg 304
Istanbul 294
Ho Chi Minh City 227
Nanchang 209
Des Moines 198
Brescia 197
Moscow 174
Shenyang 167
Munich 142
Changsha 141
Milan 139
San Diego 139
Dallas 138
Buffalo 135
Hanoi 134
Hebei 134
São Paulo 133
Redondo Beach 119
Jinan 115
Tianjin 112
Shanghai 109
San Francisco 106
Lancaster 98
Abuja 96
London 95
Chicago 89
Jiaxing 83
Dearborn 80
Hangzhou 71
Kunming 70
Santa Clara 67
Orem 63
Boardman 61
Montreal 59
Tokyo 53
Turku 53
Zhengzhou 53
Rio de Janeiro 51
Council Bluffs 48
Guangzhou 47
Lanzhou 45
Verona 43
Brooklyn 42
Johannesburg 42
Ningbo 42
Denver 41
Belo Horizonte 40
Chennai 40
Stockholm 39
Mexico City 36
Phoenix 36
Haikou 35
Taizhou 35
Poplar 34
Atlanta 33
Nuremberg 33
Frankfurt am Main 31
Toronto 31
Tashkent 30
Da Nang 29
Manchester 29
Dong Ket 28
Kocaeli 28
Amsterdam 27
Haiphong 27
San Mateo 27
Brasília 26
Brussels 26
Dhaka 25
Washington 25
Campinas 24
Baghdad 23
Charlotte 23
Curitiba 23
Norwalk 23
Boston 21
Nairobi 21
Orange 21
Totale 29.513
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Nome #
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP 384
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 379
NFKB1 regulates human NK cell maturation and effector functions 333
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 270
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 263
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 260
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 246
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder? 232
Acral lympho-histiocytic dermatitis in X-linked agammaglobulinemia: A case report showing clonal CD8+ T cells with indolent clinical behaviour 214
CTLA-4 regulates human Natural Killer cell effector functions 206
The RAC2-PI3K axis regulates human NK cell maturation and function 206
Different molecular behavior of CD40 mutants causing hyper-IgM syndrome. 201
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 201
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 201
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 198
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 197
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 196
BAFF-R mutations in Good's syndrome. 193
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 192
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
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome. 183
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 183
IgG subclass deficiency in patients with Down's syndrome and aberrant hepatitis B vaccine response. 181
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 181
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages. 180
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 180
Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients. 178
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 178
A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life. 177
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration. 175
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 175
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 173
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 171
Body experiences, emotional competence, and psychosocial functioning in juvenile idiopathic arthritis. 171
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations 171
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 170
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 170
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 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
Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders 166
Evaluation by SDS-PAGE and immunoblotting of residual antigenicity in hydrolysed protein formulas. 166
Different role of secretory IgA in the pathogenesis of RAST-positive and RAST-negative atopic dermatitis. 164
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 163
The change in Ig regulation from children to adults disconnects the correlation with the 3'RR hs1.2 polymorphism 163
T cell activity and cytokine production in X-linked agammaglobulinemia: implications for vaccination strategies 162
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 162
A case of lymphoproliferative disease presenting with a clinical and immunological phenotype of common variable immunodeficiency. 161
Evidence for antigenic selection of large granular lymphocytes in a patient with Wiskott-Aldrich syndrome 161
A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection 160
“Maturazione della risposta anticorpale: dal repertorio anticorpale primario a quello secondario”. 159
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 159
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 159
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 159
Recurrent infections with IgG2 deficiency. 158
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty. 158
Intravenous gammaglobulin therapy for prophylaxis of infection in high-risk neonates. 157
Activity of classical and alternative pathways of complement in preterm and small for gestational age infants. 157
Pancreatitis in systemic lupus erythematosus. 157
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 155
Neurovisual Assessment in Children with Ataxia Telangiectasia 155
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. 154
Profound T-cell defects in Dubowitz syndrome 153
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 153
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 152
Recurrent Bleedings in Newborn: A Factor VII Deficiency Case Report 152
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 152
An avidin/biotin ELISA for the measurement of serum and secretory IgD. 151
Diagnostics of primary immunodeficiencies through next-generation sequencing 150
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity 150
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. 149
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 149
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 149
A homozygous CARD9 mutation in a family with susceptibility to fungal infections. 147
Extensive deletion of immunoglobulin heavy chain constant region genes in the absence of recurrent infections: when is IgG subclass deficiency clinically relevant? 146
Serum immunoglobulin levels in heterozygous subjects with immunoglobulin heavy chain constant region gene deletions. 145
Western Blot technique in the serological evaluation of three LAV/HTLV III-infected Italian families. 145
C4bBinding Protein (C4BP) activates B cells through the CD40 receptor. 144
Positive effect of erythrocyte-delivered dexamethasone in ataxia-telangiectasia 144
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 143
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper IgM syndrome (HIGM2). 142
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
Valutazione dell'allergenicità dei peptidi contenuti negli idrolizzati delle proteine del latte vaccino 142
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 142
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy children. 142
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 142
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world 142
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. 141
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 141
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 141
Missed opportunities to prevent mother-to-child transmission of HIV in Italy 141
The tec kinase-regulated phosphoproteome reveals a mechanism for the regulation of inhibitory signals in murine macrophages 140
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 138
Ontogeny of secretory immunity: levels of secretory IgA and natural antibodies in saliva 138
Beta2 integrins are required for follicular helper T cell differentiation in humans 138
Update on treatment of Marshall's syndrome (PFAPA syndrome): report of five cases with review of the literature. 138
Screening of functional and positional candidate genes in families with common variable immunodeficiency 137
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects. 137
Variability of the immunoglobulin heavy chain constant region locus: a population study. 137
Totale 17.304
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Categoria #
all - tutte 196.896
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 196.896
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.404 0 0 0 0 0 0 0 0 0 621 600 183
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
2025/202610.334 1.037 1.592 884 1.689 1.083 760 1.721 407 552 609 0 0
Totale 42.959