IRIS Institutional Research Information System - OPENBS Open Archive UniBS

PLEBANI, Alessandro
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 26.231
AS - Asia 10.037
EU - Europa 8.170
SA - Sud America 2.067
Continente sconosciuto - Info sul continente non disponibili 661
AF - Africa 296
OC - Oceania 46
Totale 47.508
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 25.624
CN - Cina 3.689
SG - Singapore 3.167
UA - Ucraina 2.268
BR - Brasile 1.725
HK - Hong Kong 1.146
DE - Germania 1.081
IT - Italia 931
PL - Polonia 767
FI - Finlandia 710
VN - Vietnam 679
FR - Francia 622
GB - Regno Unito 597
TR - Turchia 383
IE - Irlanda 362
RU - Federazione Russa 345
CA - Canada 297
IN - India 244
BD - Bangladesh 228
AR - Argentina 129
SE - Svezia 122
MX - Messico 105
NG - Nigeria 96
IQ - Iraq 84
ES - Italia 70
NL - Olanda 69
ZA - Sudafrica 67
JP - Giappone 61
CO - Colombia 51
AT - Austria 49
EC - Ecuador 46
ID - Indonesia 42
VE - Venezuela 42
AU - Australia 41
PK - Pakistan 41
JM - Giamaica 33
UZ - Uzbekistan 33
BE - Belgio 32
KR - Corea 32
SA - Arabia Saudita 31
NI - Nicaragua 26
HN - Honduras 25
KE - Kenya 24
MA - Marocco 24
JO - Giordania 23
AZ - Azerbaigian 22
GT - Guatemala 22
CR - Costa Rica 21
EU - Europa 21
LT - Lituania 21
TT - Trinidad e Tobago 20
CL - Cile 19
EG - Egitto 19
CZ - Repubblica Ceca 18
IR - Iran 17
PY - Paraguay 17
SV - El Salvador 17
PE - Perù 16
TN - Tunisia 16
CH - Svizzera 14
KZ - Kazakistan 14
AE - Emirati Arabi Uniti 13
LB - Libano 13
MU - Mauritius 13
IL - Israele 12
NP - Nepal 12
UY - Uruguay 12
PR - Porto Rico 11
RO - Romania 11
BO - Bolivia 10
DZ - Algeria 10
EE - Estonia 10
ET - Etiopia 9
PS - Palestinian Territory 9
CW - ???statistics.table.value.countryCode.CW??? 8
DK - Danimarca 8
GR - Grecia 8
MY - Malesia 8
PH - Filippine 8
SN - Senegal 8
AL - Albania 6
BG - Bulgaria 6
HR - Croazia 6
BB - Barbados 5
DO - Repubblica Dominicana 5
MD - Moldavia 5
PA - Panama 5
RS - Serbia 5
SK - Slovacchia (Repubblica Slovacca) 5
HU - Ungheria 4
NZ - Nuova Zelanda 4
PT - Portogallo 4
BA - Bosnia-Erzegovina 3
CI - Costa d'Avorio 3
GP - Guadalupe 3
LA - Repubblica Popolare Democratica del Laos 3
LC - Santa Lucia 3
LV - Lettonia 3
MN - Mongolia 3
TH - Thailandia 3
Totale 46.834
Salva come PNG Salva come JPEG
Città #
Fairfield 2.747
Ashburn 2.677
Woodbridge 2.424
Singapore 1.694
Houston 1.617
Jacksonville 1.567
Ann Arbor 1.268
San Jose 1.154
Hong Kong 1.137
Cambridge 1.091
Seattle 1.067
Wilmington 945
Warsaw 760
Beijing 693
The Dalles 660
Princeton 646
Chandler 645
Council Bluffs 592
New York 540
Nanjing 519
Helsinki 369
Dublin 359
Los Angeles 349
Lauterbourg 304
Istanbul 294
Columbus 264
Ho Chi Minh City 228
Nanchang 209
Brescia 201
Des Moines 200
São Paulo 184
Dallas 181
Moscow 174
Shenyang 167
Milan 151
Buffalo 150
San Diego 143
Munich 142
Changsha 141
Hanoi 136
Hebei 134
San Francisco 125
Santa Clara 125
Redondo Beach 119
Chicago 115
Jinan 115
Shanghai 112
Tianjin 112
London 101
Lancaster 99
Abuja 96
Jiaxing 83
Phoenix 82
Dearborn 80
Hangzhou 74
Montreal 74
Toronto 71
Kunming 70
Orem 68
Boardman 65
Tokyo 55
Atlanta 54
Zhengzhou 54
Brooklyn 53
Denver 53
Turku 53
Rio de Janeiro 51
Guangzhou 47
Lanzhou 45
Verona 44
Johannesburg 42
Ningbo 42
Rome 41
Belo Horizonte 40
Chennai 40
Stockholm 40
Mexico City 37
Haikou 35
Taizhou 35
Poplar 34
North Bergen 33
Nuremberg 33
Frankfurt am Main 31
Tashkent 30
Brasília 29
Da Nang 29
Haiphong 29
Manchester 29
Amsterdam 28
Charlotte 28
Dong Ket 28
Kocaeli 28
Naples 28
Washington 28
Brussels 27
San Mateo 27
Managua 26
Boston 25
Dhaka 25
Campinas 24
Totale 32.169
Salva come PNG Salva come JPEG
Nome #
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP 417
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 397
NFKB1 regulates human NK cell maturation and effector functions 353
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 288
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 283
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 277
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 255
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder? 249
A case of lymphoproliferative disease presenting with a clinical and immunological phenotype of common variable immunodeficiency. 240
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 236
Acral lympho-histiocytic dermatitis in X-linked agammaglobulinemia: A case report showing clonal CD8+ T cells with indolent clinical behaviour 224
CTLA-4 regulates human Natural Killer cell effector functions 220
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 219
The RAC2-PI3K axis regulates human NK cell maturation and function 216
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 214
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 213
Different molecular behavior of CD40 mutants causing hyper-IgM syndrome. 209
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 207
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 205
BAFF-R mutations in Good's syndrome. 205
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 204
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 203
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 202
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 200
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages. 197
IgG subclass deficiency in patients with Down's syndrome and aberrant hepatitis B vaccine response. 195
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 194
A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life. 193
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 192
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome. 191
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration. 189
Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients. 189
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 189
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 189
Application of common recommendations for diagnosis and treatment of Wiskott-Aldrich syndrome and X-recessive piastrinopenia: clinical and immunological characteristics of 65 patients with WAS/XLT 188
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 188
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 187
Functional defects of dendritic cells in patients with CD40 deficiency. 186
Body experiences, emotional competence, and psychosocial functioning in juvenile idiopathic arthritis. 185
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 184
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 183
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 182
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 182
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 181
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations 180
Evaluation by SDS-PAGE and immunoblotting of residual antigenicity in hydrolysed protein formulas. 179
Evidence for antigenic selection of large granular lymphocytes in a patient with Wiskott-Aldrich syndrome 178
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity 178
Different role of secretory IgA in the pathogenesis of RAST-positive and RAST-negative atopic dermatitis. 177
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 176
Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders 174
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 172
T cell activity and cytokine production in X-linked agammaglobulinemia: implications for vaccination strategies 171
Intravenous gammaglobulin therapy for prophylaxis of infection in high-risk neonates. 171
The change in Ig regulation from children to adults disconnects the correlation with the 3'RR hs1.2 polymorphism 171
“Maturazione della risposta anticorpale: dal repertorio anticorpale primario a quello secondario”. 169
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 169
Pancreatitis in systemic lupus erythematosus. 169
Recurrent infections with IgG2 deficiency. 169
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 169
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty. 168
A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection 167
Profound T-cell defects in Dubowitz syndrome 167
Activity of classical and alternative pathways of complement in preterm and small for gestational age infants. 167
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 167
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 167
A homozygous CARD9 mutation in a family with susceptibility to fungal infections. 166
CASE REPORT: IDENTIFICATION OF A PATIENT WITH FAMILIAR MUTATIONS AFFECTING BOTH WASP AND FOXP3 GENES 166
Neurovisual Assessment in Children with Ataxia Telangiectasia 166
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 165
An avidin/biotin ELISA for the measurement of serum and secretory IgD. 164
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. 163
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world 163
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 162
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 161
Western Blot technique in the serological evaluation of three LAV/HTLV III-infected Italian families. 161
Diagnostics of primary immunodeficiencies through next-generation sequencing 161
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 161
X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease. 160
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 159
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 159
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. 158
Recurrent Bleedings in Newborn: A Factor VII Deficiency Case Report 158
Positive effect of erythrocyte-delivered dexamethasone in ataxia-telangiectasia 158
Serum immunoglobulin levels in heterozygous subjects with immunoglobulin heavy chain constant region gene deletions. 157
Variability of the immunoglobulin heavy chain constant region locus: a population study. 157
Clustering of immunoglobulin heavy chain constant region gene deletions and duplications in one family: functional and molecular analysis. 156
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 156
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 155
C4bBinding Protein (C4BP) activates B cells through the CD40 receptor. 154
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 154
Extensive deletion of immunoglobulin heavy chain constant region genes in the absence of recurrent infections: when is IgG subclass deficiency clinically relevant? 154
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 153
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. 151
Memory B-cell subsets as a predictive marker of outcome in hypogammaglobulinemia during infancy. 151
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy children. 151
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects. 151
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 151
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper IgM syndrome (HIGM2). 150
Valutazione dell'allergenicità dei peptidi contenuti negli idrolizzati delle proteine del latte vaccino 150
Totale 18.837
Salva come PNG Salva come JPEG
Categoria #
all - tutte 227.001
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 227.001
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.959 0 0 0 179 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
2025/202611.016 1.037 1.592 884 1.689 1.083 760 1.721 407 552 789 350 152
2026/20273.867 509 539 1.001 1.818 0 0 0 0 0 0 0 0
Totale 47.508