IRIS Institutional Research Information System - OPENBS Open Archive UniBS

PLEBANI, Alessandro
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 18.425
EU - Europa 6.748
AS - Asia 5.863
SA - Sud America 653
AF - Africa 48
OC - Oceania 29
Continente sconosciuto - Info sul continente non disponibili 23
Totale 31.789
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 18.331
CN - Cina 2.603
UA - Ucraina 2.235
SG - Singapore 1.541
HK - Hong Kong 1.069
DE - Germania 965
PL - Polonia 730
BR - Brasile 604
FI - Finlandia 589
IT - Italia 589
GB - Regno Unito 409
IE - Irlanda 354
TR - Turchia 342
RU - Federazione Russa 323
FR - Francia 276
IN - India 102
SE - Svezia 88
CA - Canada 53
NL - Olanda 35
AT - Austria 32
MX - Messico 30
VN - Vietnam 30
BE - Belgio 29
AU - Australia 25
KR - Corea 24
BD - Bangladesh 22
EU - Europa 21
AR - Argentina 20
ES - Italia 19
UZ - Uzbekistan 16
JP - Giappone 15
IR - Iran 14
IQ - Iraq 13
MU - Mauritius 13
CZ - Repubblica Ceca 12
ID - Indonesia 12
ZA - Sudafrica 12
VE - Venezuela 10
AZ - Azerbaigian 9
MA - Marocco 9
DK - Danimarca 8
CH - Svizzera 7
RO - Romania 7
SA - Arabia Saudita 7
CO - Colombia 6
IL - Israele 6
KZ - Kazakistan 6
LT - Lituania 6
PK - Pakistan 6
GR - Grecia 5
BO - Bolivia 4
DZ - Algeria 4
EG - Egitto 4
HR - Croazia 4
JO - Giordania 4
NP - Nepal 4
NZ - Nuova Zelanda 4
PT - Portogallo 4
SK - Slovacchia (Repubblica Slovacca) 4
HU - Ungheria 3
LA - Repubblica Popolare Democratica del Laos 3
LV - Lettonia 3
PY - Paraguay 3
AE - Emirati Arabi Uniti 2
BF - Burkina Faso 2
BG - Bulgaria 2
EC - Ecuador 2
EE - Estonia 2
HN - Honduras 2
KE - Kenya 2
KG - Kirghizistan 2
LB - Libano 2
LU - Lussemburgo 2
OM - Oman 2
PA - Panama 2
PE - Perù 2
PS - Palestinian Territory 2
TH - Thailandia 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
XK - ???statistics.table.value.countryCode.XK??? 2
AL - Albania 1
BA - Bosnia-Erzegovina 1
CL - Cile 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
JM - Giamaica 1
LK - Sri Lanka 1
MD - Moldavia 1
MK - Macedonia 1
MN - Mongolia 1
MY - Malesia 1
NI - Nicaragua 1
RS - Serbia 1
SI - Slovenia 1
SV - El Salvador 1
UY - Uruguay 1
Totale 31.789
Salva come PNG Salva come JPEG
Città #
Fairfield 2.746
Woodbridge 2.424
Houston 1.578
Jacksonville 1.559
Ashburn 1.347
Ann Arbor 1.268
Cambridge 1.091
Hong Kong 1.065
Seattle 1.060
Singapore 1.059
Wilmington 941
Warsaw 724
Princeton 645
Chandler 644
Beijing 594
Nanjing 513
New York 362
Dublin 352
Istanbul 289
Helsinki 265
Nanchang 205
Des Moines 198
Brescia 191
Moscow 174
Shenyang 162
San Diego 137
Hebei 134
Changsha 132
Jinan 114
Tianjin 107
Milan 100
Lancaster 93
Shanghai 90
Jiaxing 82
Dearborn 80
The Dalles 78
London 70
Hangzhou 66
Kunming 66
Munich 66
Los Angeles 58
Boardman 57
San Francisco 53
Zhengzhou 46
Verona 43
Lanzhou 42
Ningbo 39
Turku 37
Haikou 35
Taizhou 35
São Paulo 33
Dong Ket 28
Kocaeli 28
San Mateo 27
Brussels 26
Toronto 25
Nuremberg 24
Washington 24
Belo Horizonte 23
Norwalk 23
Rio de Janeiro 21
Orange 20
Santa Clara 19
Seongnam 19
Mexico City 17
Changchun 16
Leawood 16
Augusta 15
Fuzhou 15
Redwood City 15
Tashkent 15
Brooklyn 14
Guangzhou 14
Campinas 12
Frankfurt am Main 12
Vienna 12
Casoria 11
Dallas 11
Dhaka 11
Phoenix 11
Taiyuan 11
Amsterdam 10
Jakarta 10
Kilburn 10
New Bedfont 10
Rome 10
Tokyo 10
Brno 9
Chiswick 9
Prescot 9
Acton 8
Ardabil 8
Düsseldorf 8
Sumaré 8
Sydney 8
Baku 7
Bologna 7
Brasília 7
Buenos Aires 7
Canberra 7
Totale 24.046
Salva come PNG Salva come JPEG
Nome #
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP 307
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 299
NFKB1 regulates human NK cell maturation and effector functions 290
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 208
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 206
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 197
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 191
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder? 183
Acral lympho-histiocytic dermatitis in X-linked agammaglobulinemia: A case report showing clonal CD8+ T cells with indolent clinical behaviour 177
Different molecular behavior of CD40 mutants causing hyper-IgM syndrome. 167
The RAC2-PI3K axis regulates human NK cell maturation and function 162
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 159
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 154
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome. 153
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 147
CTLA-4 regulates human Natural Killer cell effector functions 147
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 145
BAFF-R mutations in Good's syndrome. 145
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 143
IgG subclass deficiency in patients with Down's syndrome and aberrant hepatitis B vaccine response. 143
Evidence for antigenic selection of large granular lymphocytes in a patient with Wiskott-Aldrich syndrome 142
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 142
Pancreatitis in systemic lupus erythematosus. 141
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 140
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 139
T cell activity and cytokine production in X-linked agammaglobulinemia: implications for vaccination strategies 138
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 138
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages. 137
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 137
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 137
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 136
Functional defects of dendritic cells in patients with CD40 deficiency. 135
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty. 135
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 135
The change in Ig regulation from children to adults disconnects the correlation with the 3'RR hs1.2 polymorphism 132
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 130
Body experiences, emotional competence, and psychosocial functioning in juvenile idiopathic arthritis. 129
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration. 128
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 127
Profound T-cell defects in Dubowitz syndrome 127
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 127
Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients. 126
A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life. 125
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 125
Different role of secretory IgA in the pathogenesis of RAST-positive and RAST-negative atopic dermatitis. 124
Western Blot technique in the serological evaluation of three LAV/HTLV III-infected Italian families. 124
Recurrent infections with IgG2 deficiency. 124
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations 124
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 124
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 124
Evaluation by SDS-PAGE and immunoblotting of residual antigenicity in hydrolysed protein formulas. 123
C4bBinding Protein (C4BP) activates B cells through the CD40 receptor. 122
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 122
Serum immunoglobulin levels in heterozygous subjects with immunoglobulin heavy chain constant region gene deletions. 122
Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders 122
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 122
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 121
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. 120
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 119
Memory B-cell subsets as a predictive marker of outcome in hypogammaglobulinemia during infancy. 118
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. 118
Intravenous gammaglobulin therapy for prophylaxis of infection in high-risk neonates. 118
Diagnostics of primary immunodeficiencies through next-generation sequencing 118
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 118
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper IgM syndrome (HIGM2). 117
A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection 117
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 117
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. 117
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 117
Activity of classical and alternative pathways of complement in preterm and small for gestational age infants. 117
An avidin/biotin ELISA for the measurement of serum and secretory IgD. 117
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. 117
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy children. 116
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 116
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 116
Recurrent Bleedings in Newborn: A Factor VII Deficiency Case Report 115
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 115
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 114
Neurovisual Assessment in Children with Ataxia Telangiectasia 114
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 113
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 113
Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterization 112
Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome 112
Valutazione dell'allergenicità dei peptidi contenuti negli idrolizzati delle proteine del latte vaccino 112
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 112
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world 112
“Maturazione della risposta anticorpale: dal repertorio anticorpale primario a quello secondario”. 111
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 111
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunction. 111
Ontogeny of secretory immunity: levels of secretory IgA and natural antibodies in saliva 111
Beta2 integrins are required for follicular helper T cell differentiation in humans 111
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis. 111
A homozygous CARD9 mutation in a family with susceptibility to fungal infections. 110
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 110
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function. 110
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 110
Extensive deletion of immunoglobulin heavy chain constant region genes in the absence of recurrent infections: when is IgG subclass deficiency clinically relevant? 110
BTK: 22 novel and 25 recurrent mutations in European patients with X-linked agammaglobulinemia. 109
Hyper IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination. 109
Mutational analysis of human BAFF Receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency. 109
Totale 13.429
Salva come PNG Salva come JPEG
Categoria #
all - tutte 165.491
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 165.491
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020460 0 0 0 0 0 0 0 0 0 0 0 460
2020/20215.161 89 547 103 697 176 576 253 682 634 621 600 183
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
2024/20254.745 23 19 13 602 571 445 428 154 552 415 1.012 511
Totale 32.416