IRIS Institutional Research Information System - OPENBS Open Archive UniBS

PLEBANI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 23.430
AS - Asia 9.997
EU - Europa 7.968
SA - Sud America 1.975
Continente sconosciuto - Info sul continente non disponibili 654
AF - Africa 293
OC - Oceania 44
Totale 44.361
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Nazione #
US - Stati Uniti d'America 23.067
CN - Cina 3.687
SG - Singapore 3.162
UA - Ucraina 2.268
BR - Brasile 1.658
HK - Hong Kong 1.145
DE - Germania 1.074
IT - Italia 800
PL - Polonia 767
FI - Finlandia 710
VN - Vietnam 672
FR - Francia 614
GB - Regno Unito 567
TR - Turchia 380
IE - Irlanda 361
RU - Federazione Russa 345
IN - India 239
BD - Bangladesh 225
CA - Canada 178
AR - Argentina 127
SE - Svezia 122
MX - Messico 100
NG - Nigeria 96
IQ - Iraq 84
NL - Olanda 67
ZA - Sudafrica 67
ES - Italia 66
JP - Giappone 60
AT - Austria 49
ID - Indonesia 41
PK - Pakistan 41
CO - Colombia 40
VE - Venezuela 40
AU - Australia 39
EC - Ecuador 38
UZ - Uzbekistan 33
KR - Corea 31
BE - Belgio 30
SA - Arabia Saudita 29
JO - Giordania 23
MA - Marocco 23
AZ - Azerbaigian 22
KE - Kenya 22
EU - Europa 21
CL - Cile 19
EG - Egitto 19
CZ - Repubblica Ceca 18
LT - Lituania 18
IR - Iran 17
PY - Paraguay 17
TN - Tunisia 16
JM - Giamaica 15
PE - Perù 15
CH - Svizzera 13
KZ - Kazakistan 13
LB - Libano 13
MU - Mauritius 13
HN - Honduras 12
IL - Israele 12
NP - Nepal 12
AE - Emirati Arabi Uniti 11
RO - Romania 11
UY - Uruguay 11
BO - Bolivia 10
CR - Costa Rica 10
DZ - Algeria 10
ET - Etiopia 9
NI - Nicaragua 9
PS - Palestinian Territory 9
DK - Danimarca 8
PH - Filippine 8
SN - Senegal 8
TT - Trinidad e Tobago 8
GR - Grecia 7
BG - Bulgaria 6
AL - Albania 5
DO - Repubblica Dominicana 5
HR - Croazia 5
PA - Panama 5
RS - Serbia 5
SK - Slovacchia (Repubblica Slovacca) 5
GT - Guatemala 4
MD - Moldavia 4
MY - Malesia 4
NZ - Nuova Zelanda 4
PR - Porto Rico 4
PT - Portogallo 4
BA - Bosnia-Erzegovina 3
BB - Barbados 3
CI - Costa d'Avorio 3
HU - Ungheria 3
LA - Repubblica Popolare Democratica del Laos 3
LV - Lettonia 3
MN - Mongolia 3
TH - Thailandia 3
XK - ???statistics.table.value.countryCode.XK??? 3
BF - Burkina Faso 2
BH - Bahrain 2
BY - Bielorussia 2
CY - Cipro 2
Totale 43.696
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Città #
Fairfield 2.747
Woodbridge 2.424
Ashburn 2.015
Singapore 1.693
Houston 1.615
Jacksonville 1.565
Ann Arbor 1.268
Hong Kong 1.136
Cambridge 1.091
Seattle 1.066
Wilmington 945
Warsaw 760
Beijing 693
San Jose 686
The Dalles 655
Princeton 646
Chandler 645
New York 521
Nanjing 519
Helsinki 369
Dublin 359
Los Angeles 332
Lauterbourg 304
Istanbul 294
Columbus 261
Ho Chi Minh City 227
Nanchang 209
Des Moines 199
Brescia 198
Moscow 174
Shenyang 167
Dallas 156
Milan 147
Buffalo 144
Munich 142
Changsha 141
San Diego 140
Hanoi 135
Hebei 134
São Paulo 134
Redondo Beach 119
Council Bluffs 116
Jinan 115
Tianjin 112
San Francisco 111
Shanghai 110
Lancaster 99
Abuja 96
London 95
Chicago 94
Santa Clara 91
Jiaxing 83
Dearborn 80
Hangzhou 74
Kunming 70
Orem 65
Montreal 64
Boardman 62
Phoenix 55
Tokyo 54
Zhengzhou 54
Turku 53
Rio de Janeiro 51
Brooklyn 48
Guangzhou 47
Denver 45
Lanzhou 45
Verona 43
Johannesburg 42
Ningbo 42
Atlanta 40
Belo Horizonte 40
Chennai 40
Stockholm 39
Mexico City 37
Toronto 36
Haikou 35
Taizhou 35
Poplar 34
Nuremberg 33
Frankfurt am Main 31
Tashkent 30
Da Nang 29
Manchester 29
Dong Ket 28
Kocaeli 28
Amsterdam 27
Charlotte 27
Haiphong 27
Rome 27
San Mateo 27
Brasília 26
Brussels 26
Dhaka 25
Washington 25
Campinas 24
Curitiba 24
Baghdad 23
Norwalk 23
Boston 22
Totale 30.188
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Nome #
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP 394
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 388
NFKB1 regulates human NK cell maturation and effector functions 347
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 278
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 271
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 269
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 249
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder? 237
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 227
Acral lympho-histiocytic dermatitis in X-linked agammaglobulinemia: A case report showing clonal CD8+ T cells with indolent clinical behaviour 216
CTLA-4 regulates human Natural Killer cell effector functions 212
The RAC2-PI3K axis regulates human NK cell maturation and function 209
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 206
Different molecular behavior of CD40 mutants causing hyper-IgM syndrome. 204
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 204
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 204
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 200
A case of lymphoproliferative disease presenting with a clinical and immunological phenotype of common variable immunodeficiency. 198
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 198
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 197
BAFF-R mutations in Good's syndrome. 196
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 191
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 188
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome. 187
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 187
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 185
IgG subclass deficiency in patients with Down's syndrome and aberrant hepatitis B vaccine response. 184
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 184
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages. 183
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 180
A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life. 179
Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients. 179
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 177
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 177
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration. 177
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 177
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 177
Body experiences, emotional competence, and psychosocial functioning in juvenile idiopathic arthritis. 176
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 176
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 175
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 174
Functional defects of dendritic cells in patients with CD40 deficiency. 172
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations 172
Evidence for antigenic selection of large granular lymphocytes in a patient with Wiskott-Aldrich syndrome 169
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 169
Evaluation by SDS-PAGE and immunoblotting of residual antigenicity in hydrolysed protein formulas. 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 168
Different role of secretory IgA in the pathogenesis of RAST-positive and RAST-negative atopic dermatitis. 166
T cell activity and cytokine production in X-linked agammaglobulinemia: implications for vaccination strategies 164
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 164
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 164
A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection 163
The change in Ig regulation from children to adults disconnects the correlation with the 3'RR hs1.2 polymorphism 163
“Maturazione della risposta anticorpale: dal repertorio anticorpale primario a quello secondario”. 162
Intravenous gammaglobulin therapy for prophylaxis of infection in high-risk neonates. 162
Activity of classical and alternative pathways of complement in preterm and small for gestational age infants. 162
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty. 162
Pancreatitis in systemic lupus erythematosus. 160
Recurrent infections with IgG2 deficiency. 159
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 158
Neurovisual Assessment in Children with Ataxia Telangiectasia 158
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 158
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 156
An avidin/biotin ELISA for the measurement of serum and secretory IgD. 156
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. 155
Profound T-cell defects in Dubowitz syndrome 154
Recurrent Bleedings in Newborn: A Factor VII Deficiency Case Report 154
Diagnostics of primary immunodeficiencies through next-generation sequencing 153
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity 153
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 153
A homozygous CARD9 mutation in a family with susceptibility to fungal infections. 152
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 152
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. 151
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 151
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world 151
Extensive deletion of immunoglobulin heavy chain constant region genes in the absence of recurrent infections: when is IgG subclass deficiency clinically relevant? 149
C4bBinding Protein (C4BP) activates B cells through the CD40 receptor. 148
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 147
Serum immunoglobulin levels in heterozygous subjects with immunoglobulin heavy chain constant region gene deletions. 147
Positive effect of erythrocyte-delivered dexamethasone in ataxia-telangiectasia 147
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 147
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 146
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy children. 146
Western Blot technique in the serological evaluation of three LAV/HTLV III-infected Italian families. 146
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. 145
Valutazione dell'allergenicità dei peptidi contenuti negli idrolizzati delle proteine del latte vaccino 145
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 145
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 145
Missed opportunities to prevent mother-to-child transmission of HIV in Italy 145
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. 144
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper IgM syndrome (HIGM2). 144
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 144
Variability of the immunoglobulin heavy chain constant region locus: a population study. 144
The tec kinase-regulated phosphoproteome reveals a mechanism for the regulation of inhibitory signals in murine macrophages 144
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 144
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects. 141
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 141
Ontogeny of secretory immunity: levels of secretory IgA and natural antibodies in saliva 141
Beta2 integrins are required for follicular helper T cell differentiation in humans 141
Totale 17.796
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Categoria #
all - tutte 215.018
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 215.018
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.651 0 633 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
2025/202611.016 1.037 1.592 884 1.689 1.083 760 1.721 407 552 789 350 152
2026/2027720 509 211 0 0 0 0 0 0 0 0 0 0
Totale 44.361