IRIS Institutional Research Information System - OPENBS Open Archive UniBS

PLEBANI, Alessandro
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 22.812
AS - Asia 9.929
EU - Europa 7.914
SA - Sud America 1.964
AF - Africa 290
OC - Oceania 44
Continente sconosciuto - Info sul continente non disponibili 26
Totale 42.979
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 22.489
CN - Cina 3.682
SG - Singapore 3.147
UA - Ucraina 2.268
BR - Brasile 1.653
HK - Hong Kong 1.136
DE - Germania 1.074
PL - Polonia 767
IT - Italia 759
FI - Finlandia 710
VN - Vietnam 671
FR - Francia 611
GB - Regno Unito 567
TR - Turchia 380
IE - Irlanda 361
RU - Federazione Russa 345
IN - India 239
BD - Bangladesh 190
CA - Canada 163
AR - Argentina 125
SE - Svezia 122
MX - Messico 100
NG - Nigeria 96
IQ - Iraq 84
ZA - Sudafrica 67
NL - Olanda 66
ES - Italia 59
JP - Giappone 59
AT - Austria 49
PK - Pakistan 41
ID - Indonesia 40
AU - Australia 39
CO - Colombia 39
VE - Venezuela 39
EC - Ecuador 37
UZ - Uzbekistan 33
BE - Belgio 30
KR - Corea 30
SA - Arabia Saudita 29
JO - Giordania 23
MA - Marocco 23
AZ - Azerbaigian 22
KE - Kenya 22
EU - Europa 21
CL - Cile 19
CZ - Repubblica Ceca 18
EG - Egitto 17
IR - Iran 17
LT - Lituania 17
PY - Paraguay 16
TN - Tunisia 16
PE - Perù 15
CH - Svizzera 13
JM - Giamaica 13
KZ - Kazakistan 13
LB - Libano 13
MU - Mauritius 13
IL - Israele 12
NP - Nepal 12
AE - Emirati Arabi Uniti 11
RO - Romania 11
UY - Uruguay 11
BO - Bolivia 10
DZ - Algeria 10
HN - Honduras 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
CR - Costa Rica 5
DO - Repubblica Dominicana 5
HR - Croazia 5
PA - Panama 5
RS - Serbia 5
SK - Slovacchia (Repubblica Slovacca) 5
TT - Trinidad e Tobago 5
MD - Moldavia 4
MY - Malesia 4
NZ - Nuova Zelanda 4
PT - Portogallo 4
BA - Bosnia-Erzegovina 3
CI - Costa d'Avorio 3
HU - Ungheria 3
LA - Repubblica Popolare Democratica del Laos 3
LV - Lettonia 3
MN - Mongolia 3
PR - Porto Rico 3
TH - Thailandia 3
XK - ???statistics.table.value.countryCode.XK??? 3
BB - Barbados 2
BF - Burkina Faso 2
BH - Bahrain 2
BY - Bielorussia 2
CY - Cipro 2
EE - Estonia 2
Totale 42.949
Salva come PNG Salva come JPEG
Città #
Fairfield 2.747
Woodbridge 2.424
Ashburn 1.994
Singapore 1.686
Houston 1.612
Jacksonville 1.565
Ann Arbor 1.268
Hong Kong 1.127
Cambridge 1.091
Seattle 1.066
Wilmington 945
Warsaw 760
Beijing 692
San Jose 681
The Dalles 655
Princeton 646
Chandler 645
Nanjing 519
New York 519
Helsinki 369
Dublin 359
Los Angeles 325
Lauterbourg 304
Istanbul 294
Ho Chi Minh City 227
Nanchang 209
Des Moines 198
Brescia 197
Moscow 174
Shenyang 167
Dallas 148
Milan 143
Munich 142
Changsha 141
Buffalo 140
San Diego 139
Hanoi 134
Hebei 134
São Paulo 133
Redondo Beach 119
Jinan 115
Tianjin 112
San Francisco 111
Shanghai 110
Lancaster 99
Abuja 96
London 95
Chicago 92
Jiaxing 83
Dearborn 80
Santa Clara 78
Hangzhou 74
Kunming 70
Orem 65
Montreal 64
Boardman 62
Tokyo 54
Zhengzhou 54
Council Bluffs 53
Turku 53
Rio de Janeiro 51
Guangzhou 47
Brooklyn 46
Lanzhou 45
Denver 44
Verona 43
Johannesburg 42
Ningbo 42
Belo Horizonte 40
Chennai 40
Phoenix 40
Stockholm 39
Atlanta 37
Mexico City 37
Haikou 35
Taizhou 35
Poplar 34
Toronto 34
Nuremberg 33
Frankfurt am Main 31
Tashkent 30
Da Nang 29
Manchester 29
Dong Ket 28
Kocaeli 28
Amsterdam 27
Haiphong 27
San Mateo 27
Brasília 26
Brussels 26
Charlotte 25
Dhaka 25
Washington 25
Campinas 24
Baghdad 23
Curitiba 23
Norwalk 23
Rome 23
Amman 21
Boston 21
Totale 29.763
Salva come PNG Salva come JPEG
Nome #
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP 388
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 384
NFKB1 regulates human NK cell maturation and effector functions 341
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 274
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 267
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 263
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? 233
Acral lympho-histiocytic dermatitis in X-linked agammaglobulinemia: A case report showing clonal CD8+ T cells with indolent clinical behaviour 215
CTLA-4 regulates human Natural Killer cell effector functions 211
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 210
The RAC2-PI3K axis regulates human NK cell maturation and function 208
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 205
Different molecular behavior of CD40 mutants causing hyper-IgM syndrome. 202
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 202
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 199
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 198
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 196
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 194
BAFF-R mutations in Good's syndrome. 194
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
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 185
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome. 184
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 183
A case of lymphoproliferative disease presenting with a clinical and immunological phenotype of common variable immunodeficiency. 182
IgG subclass deficiency in patients with Down's syndrome and aberrant hepatitis B vaccine response. 181
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages. 180
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 180
Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients. 178
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 177
A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life. 177
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 176
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration. 176
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 176
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 175
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 174
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 174
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 173
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 173
Body experiences, emotional competence, and psychosocial functioning in juvenile idiopathic arthritis. 173
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations 172
Functional defects of dendritic cells in patients with CD40 deficiency. 171
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 168
Evaluation by SDS-PAGE and immunoblotting of residual antigenicity in hydrolysed protein formulas. 168
Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders 167
Different role of secretory IgA in the pathogenesis of RAST-positive and RAST-negative atopic dermatitis. 165
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 164
Evidence for antigenic selection of large granular lymphocytes in a patient with Wiskott-Aldrich syndrome 163
T cell activity and cytokine production in X-linked agammaglobulinemia: implications for vaccination strategies 163
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 163
The change in Ig regulation from children to adults disconnects the correlation with the 3'RR hs1.2 polymorphism 163
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 162
“Maturazione della risposta anticorpale: dal repertorio anticorpale primario a quello secondario”. 161
A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection 161
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty. 160
Intravenous gammaglobulin therapy for prophylaxis of infection in high-risk neonates. 158
Pancreatitis in systemic lupus erythematosus. 158
Recurrent infections with IgG2 deficiency. 158
Activity of classical and alternative pathways of complement in preterm and small for gestational age infants. 157
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 157
Neurovisual Assessment in Children with Ataxia Telangiectasia 157
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 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
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 153
Profound T-cell defects in Dubowitz syndrome 153
An avidin/biotin ELISA for the measurement of serum and secretory IgD. 153
Recurrent Bleedings in Newborn: A Factor VII Deficiency Case Report 153
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 153
Diagnostics of primary immunodeficiencies through next-generation sequencing 152
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity 152
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 151
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. 150
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 150
A homozygous CARD9 mutation in a family with susceptibility to fungal infections. 148
Extensive deletion of immunoglobulin heavy chain constant region genes in the absence of recurrent infections: when is IgG subclass deficiency clinically relevant? 147
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world 147
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 145
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
Positive effect of erythrocyte-delivered dexamethasone in ataxia-telangiectasia 145
C4bBinding Protein (C4BP) activates B cells through the CD40 receptor. 144
Valutazione dell'allergenicità dei peptidi contenuti negli idrolizzati delle proteine del latte vaccino 144
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy children. 144
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 144
Missed opportunities to prevent mother-to-child transmission of HIV in Italy 144
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 143
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 143
The tec kinase-regulated phosphoproteome reveals a mechanism for the regulation of inhibitory signals in murine macrophages 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
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 142
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. 141
Variability of the immunoglobulin heavy chain constant region locus: a population study. 141
Beta2 integrins are required for follicular helper T cell differentiation in humans 141
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 141
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 139
Ontogeny of secretory immunity: levels of secretory IgA and natural antibodies in saliva 139
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 138
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 138
Totale 17.544
Salva come PNG Salva come JPEG
Categoria #
all - tutte 207.149
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 207.149
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021183 0 0 0 0 0 0 0 0 0 0 0 183
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
2025/202610.982 1.037 1.592 884 1.689 1.083 760 1.721 407 552 789 350 118
Totale 43.607