IRIS Institutional Research Information System - OPENBS Open Archive UniBS

PLEBANI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 20.538
AS - Asia 8.650
EU - Europa 7.201
SA - Sud America 1.849
AF - Africa 155
OC - Oceania 31
Continente sconosciuto - Info sul continente non disponibili 24
Totale 38.448
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Nazione #
US - Stati Uniti d'America 20.284
CN - Cina 3.303
SG - Singapore 2.714
UA - Ucraina 2.262
BR - Brasile 1.592
HK - Hong Kong 1.097
DE - Germania 1.049
PL - Polonia 761
IT - Italia 617
FI - Finlandia 606
GB - Regno Unito 520
VN - Vietnam 506
TR - Turchia 369
IE - Irlanda 356
RU - Federazione Russa 341
FR - Francia 290
IN - India 188
CA - Canada 129
SE - Svezia 115
AR - Argentina 106
BD - Bangladesh 95
MX - Messico 84
IQ - Iraq 69
ZA - Sudafrica 59
ES - Italia 55
NL - Olanda 52
AT - Austria 48
JP - Giappone 45
ID - Indonesia 36
EC - Ecuador 34
BE - Belgio 30
CO - Colombia 30
PK - Pakistan 29
VE - Venezuela 28
UZ - Uzbekistan 27
AU - Australia 26
KR - Corea 26
SA - Arabia Saudita 23
EU - Europa 21
AZ - Azerbaigian 19
MA - Marocco 19
IR - Iran 17
KE - Kenya 15
PY - Paraguay 15
EG - Egitto 14
JO - Giordania 14
CL - Cile 13
CZ - Repubblica Ceca 13
LT - Lituania 13
MU - Mauritius 13
PE - Perù 13
TN - Tunisia 12
IL - Israele 11
KZ - Kazakistan 11
AE - Emirati Arabi Uniti 10
LB - Libano 10
UY - Uruguay 10
CH - Svizzera 9
BO - Bolivia 8
DK - Danimarca 8
DZ - Algeria 8
JM - Giamaica 8
RO - Romania 8
HN - Honduras 7
NP - Nepal 7
ET - Etiopia 6
PS - Palestinian Territory 6
GR - Grecia 5
SK - Slovacchia (Repubblica Slovacca) 5
AL - Albania 4
BG - Bulgaria 4
CR - Costa Rica 4
DO - Repubblica Dominicana 4
HR - Croazia 4
NI - Nicaragua 4
NZ - Nuova Zelanda 4
PA - Panama 4
PT - Portogallo 4
BA - Bosnia-Erzegovina 3
HU - Ungheria 3
LA - Repubblica Popolare Democratica del Laos 3
LV - Lettonia 3
RS - Serbia 3
SN - Senegal 3
TT - Trinidad e Tobago 3
XK - ???statistics.table.value.countryCode.XK??? 3
BB - Barbados 2
BF - Burkina Faso 2
BY - Bielorussia 2
EE - Estonia 2
KG - Kirghizistan 2
KW - Kuwait 2
LU - Lussemburgo 2
MD - Moldavia 2
MN - Mongolia 2
OM - Oman 2
SV - El Salvador 2
TH - Thailandia 2
AO - Angola 1
CI - Costa d'Avorio 1
Totale 38.435
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Città #
Fairfield 2.746
Woodbridge 2.424
Ashburn 1.664
Houston 1.598
Jacksonville 1.562
Singapore 1.301
Ann Arbor 1.268
Hong Kong 1.092
Cambridge 1.091
Seattle 1.066
Wilmington 945
Warsaw 754
Beijing 686
Chandler 645
Princeton 645
Nanjing 514
New York 467
Dublin 354
Istanbul 291
Los Angeles 288
Helsinki 266
Nanchang 208
Des Moines 198
Brescia 193
Moscow 174
Ho Chi Minh City 173
The Dalles 170
Shenyang 167
Munich 142
Changsha 140
San Diego 137
Buffalo 134
Hebei 134
Dallas 128
São Paulo 123
Redondo Beach 119
Jinan 114
Tianjin 111
Milan 105
San Francisco 105
Shanghai 105
Hanoi 101
Lancaster 98
London 85
Chicago 84
Jiaxing 83
Dearborn 80
Hangzhou 70
Kunming 69
Boardman 57
Santa Clara 56
Turku 53
Zhengzhou 53
Rio de Janeiro 51
Montreal 50
Lanzhou 45
Verona 43
Brooklyn 42
Ningbo 41
Belo Horizonte 40
Tokyo 40
Guangzhou 37
Johannesburg 37
Phoenix 36
Haikou 35
Taizhou 35
Denver 34
Mexico City 33
Stockholm 32
Toronto 31
Dong Ket 28
Kocaeli 28
Nuremberg 28
San Mateo 27
Brussels 26
Tashkent 26
Brasília 25
Atlanta 24
Dhaka 24
Washington 24
Campinas 23
Curitiba 23
Norwalk 23
Poplar 23
Charlotte 22
Chennai 22
Da Nang 21
Orange 21
Manchester 20
Orem 20
Guarulhos 19
Seongnam 19
Vienna 19
Augusta 18
Haiphong 18
Amsterdam 17
Ankara 17
Baghdad 17
Baku 17
Boston 17
Totale 26.754
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Nome #
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP 351
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 335
NFKB1 regulates human NK cell maturation and effector functions 316
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 243
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 238
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 230
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 226
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder? 213
Acral lympho-histiocytic dermatitis in X-linked agammaglobulinemia: A case report showing clonal CD8+ T cells with indolent clinical behaviour 199
Different molecular behavior of CD40 mutants causing hyper-IgM syndrome. 189
The RAC2-PI3K axis regulates human NK cell maturation and function 188
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 184
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 178
BAFF-R mutations in Good's syndrome. 178
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 177
CTLA-4 regulates human Natural Killer cell effector functions 176
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 174
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 173
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 172
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome. 169
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 169
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 168
IgG subclass deficiency in patients with Down's syndrome and aberrant hepatitis B vaccine response. 167
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 167
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages. 165
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 164
Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients. 163
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations 161
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration. 160
A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life. 159
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 159
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 158
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 156
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 155
Evidence for antigenic selection of large granular lymphocytes in a patient with Wiskott-Aldrich syndrome 154
T cell activity and cytokine production in X-linked agammaglobulinemia: implications for vaccination strategies 154
Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders 154
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 154
Functional defects of dendritic cells in patients with CD40 deficiency. 153
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 153
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 153
Pancreatitis in systemic lupus erythematosus. 152
The change in Ig regulation from children to adults disconnects the correlation with the 3'RR hs1.2 polymorphism 152
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 151
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 151
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 151
Body experiences, emotional competence, and psychosocial functioning in juvenile idiopathic arthritis. 150
A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection 149
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 149
Evaluation by SDS-PAGE and immunoblotting of residual antigenicity in hydrolysed protein formulas. 148
Different role of secretory IgA in the pathogenesis of RAST-positive and RAST-negative atopic dermatitis. 147
Recurrent Bleedings in Newborn: A Factor VII Deficiency Case Report 147
“Maturazione della risposta anticorpale: dal repertorio anticorpale primario a quello secondario”. 146
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 146
Recurrent infections with IgG2 deficiency. 145
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. 145
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty. 145
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 144
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 142
Profound T-cell defects in Dubowitz syndrome 141
Activity of classical and alternative pathways of complement in preterm and small for gestational age infants. 141
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 141
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 140
Neurovisual Assessment in Children with Ataxia Telangiectasia 140
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 140
An avidin/biotin ELISA for the measurement of serum and secretory IgD. 139
C4bBinding Protein (C4BP) activates B cells through the CD40 receptor. 138
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 138
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. 138
Intravenous gammaglobulin therapy for prophylaxis of infection in high-risk neonates. 138
Western Blot technique in the serological evaluation of three LAV/HTLV III-infected Italian families. 136
Positive effect of erythrocyte-delivered dexamethasone in ataxia-telangiectasia 135
Serum immunoglobulin levels in heterozygous subjects with immunoglobulin heavy chain constant region gene deletions. 134
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity 134
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 134
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. 133
The tec kinase-regulated phosphoproteome reveals a mechanism for the regulation of inhibitory signals in murine macrophages 133
Diagnostics of primary immunodeficiencies through next-generation sequencing 133
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. 132
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 132
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy children. 132
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 132
A homozygous CARD9 mutation in a family with susceptibility to fungal infections. 131
Valutazione dell'allergenicità dei peptidi contenuti negli idrolizzati delle proteine del latte vaccino 131
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 131
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper IgM syndrome (HIGM2). 130
Screening of functional and positional candidate genes in families with common variable immunodeficiency 130
Extensive deletion of immunoglobulin heavy chain constant region genes in the absence of recurrent infections: when is IgG subclass deficiency clinically relevant? 130
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 130
A case of lymphoproliferative disease presenting with a clinical and immunological phenotype of common variable immunodeficiency. 129
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects. 129
Missed opportunities to prevent mother-to-child transmission of HIV in Italy 129
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function. 128
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 128
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 128
Variability of the immunoglobulin heavy chain constant region locus: a population study. 127
Ontogeny of secretory immunity: levels of secretory IgA and natural antibodies in saliva 127
Beta2 integrins are required for follicular helper T cell differentiation in humans 127
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world 127
Memory B-cell subsets as a predictive marker of outcome in hypogammaglobulinemia during infancy. 126
Totale 15.767
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Categoria #
all - tutte 188.272
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 188.272
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20213.549 0 0 0 0 0 576 253 682 634 621 600 183
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
2024/20254.954 23 19 13 602 571 445 428 154 552 415 1.012 720
2025/20266.451 1.037 1.592 884 1.689 1.083 166 0 0 0 0 0 0
Totale 39.076