IRIS Institutional Research Information System - OPENBS Open Archive UniBS

PLEBANI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 17.410
EU - Europa 6.033
AS - Asia 3.544
OC - Oceania 27
Continente sconosciuto - Info sul continente non disponibili 21
AF - Africa 15
SA - Sud America 10
Totale 27.060
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Nazione #
US - Stati Uniti d'America 17.382
CN - Cina 2.389
UA - Ucraina 2.223
DE - Germania 855
PL - Polonia 716
HK - Hong Kong 587
IT - Italia 549
FI - Finlandia 520
GB - Regno Unito 367
IE - Irlanda 351
SG - Singapore 340
FR - Francia 253
IN - India 92
SE - Svezia 83
TR - Turchia 45
NL - Olanda 28
VN - Vietnam 28
BE - Belgio 27
AU - Australia 25
CA - Canada 25
KR - Corea 23
EU - Europa 21
RU - Federazione Russa 14
IR - Iran 13
MU - Mauritius 13
CZ - Repubblica Ceca 10
JP - Giappone 10
BR - Brasile 7
ES - Italia 7
RO - Romania 7
CH - Svizzera 4
GR - Grecia 3
HR - Croazia 3
SK - Slovacchia (Repubblica Slovacca) 3
AR - Argentina 2
AZ - Azerbaigian 2
BD - Bangladesh 2
ID - Indonesia 2
IL - Israele 2
KZ - Kazakistan 2
MX - Messico 2
NZ - Nuova Zelanda 2
PT - Portogallo 2
SA - Arabia Saudita 2
AE - Emirati Arabi Uniti 1
BA - Bosnia-Erzegovina 1
BO - Bolivia 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EG - Egitto 1
HU - Ungheria 1
JO - Giordania 1
LV - Lettonia 1
MD - Moldavia 1
MK - Macedonia 1
MN - Mongolia 1
MY - Malesia 1
PK - Pakistan 1
RS - Serbia 1
SI - Slovenia 1
ZA - Sudafrica 1
Totale 27.060
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Città #
Fairfield 2.746
Woodbridge 2.424
Houston 1.576
Jacksonville 1.559
Ashburn 1.325
Ann Arbor 1.268
Cambridge 1.091
Seattle 1.058
Wilmington 941
Warsaw 715
Princeton 645
Chandler 644
Hong Kong 584
Nanjing 512
Beijing 420
New York 353
Dublin 349
Helsinki 237
Nanchang 205
Singapore 189
Brescia 179
Shenyang 161
Des Moines 146
San Diego 137
Hebei 134
Changsha 132
Jinan 114
Tianjin 107
Milan 96
Lancaster 92
Shanghai 88
Jiaxing 82
Dearborn 80
Kunming 66
Hangzhou 64
London 63
Boardman 57
Zhengzhou 46
Verona 43
Lanzhou 42
San Francisco 40
Ningbo 39
Haikou 35
Taizhou 35
Dong Ket 28
Kocaeli 28
San Mateo 27
Brussels 24
Norwalk 23
Washington 23
Orange 20
Seongnam 19
Toronto 18
Changchun 16
Leawood 16
Augusta 15
Redwood City 15
Fuzhou 14
Guangzhou 14
Los Angeles 13
Casoria 11
Taiyuan 11
Kilburn 10
New Bedfont 10
Rome 10
Brno 9
Chiswick 9
Prescot 9
Acton 8
Amsterdam 8
Ardabil 8
Munich 8
Sydney 8
Bologna 7
Canberra 7
Melbourne 7
Busto Arsizio 6
Phoenix 6
Pune 6
Tokyo 6
Brooklyn 5
Florence 5
Frankfurt am Main 5
Walnut 5
Alessandria 4
Chicago 4
Gunzenhausen 4
Hamburg 4
Hanover 4
Hefei 4
Islington 4
Lappeenranta 4
Montichiari 4
Wandsworth 4
Auburn Hills 3
Bratislava 3
Castenedolo 3
Castiglione Delle Stiviere 3
Falkenstein 3
Markham 3
Totale 21.474
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Nome #
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP 287
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 282
NFKB1 regulates human NK cell maturation and effector functions 274
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 186
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 183
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 183
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 180
Acral lympho-histiocytic dermatitis in X-linked agammaglobulinemia: A case report showing clonal CD8+ T cells with indolent clinical behaviour 163
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder? 161
Different molecular behavior of CD40 mutants causing hyper-IgM syndrome. 151
The RAC2-PI3K axis regulates human NK cell maturation and function 151
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 138
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 137
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome. 132
Evidence for antigenic selection of large granular lymphocytes in a patient with Wiskott-Aldrich syndrome 131
CTLA-4 regulates human Natural Killer cell effector functions 131
Pancreatitis in systemic lupus erythematosus. 129
T cell activity and cytokine production in X-linked agammaglobulinemia: implications for vaccination strategies 126
IgG subclass deficiency in patients with Down's syndrome and aberrant hepatitis B vaccine response. 126
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 125
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 124
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty. 124
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages. 123
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 123
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 122
The change in Ig regulation from children to adults disconnects the correlation with the 3'RR hs1.2 polymorphism 122
BAFF-R mutations in Good's syndrome. 122
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 121
Functional defects of dendritic cells in patients with CD40 deficiency. 120
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 120
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 116
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 116
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 115
Body experiences, emotional competence, and psychosocial functioning in juvenile idiopathic arthritis. 114
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 113
Profound T-cell defects in Dubowitz syndrome 113
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 113
Western Blot technique in the serological evaluation of three LAV/HTLV III-infected Italian families. 111
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 111
A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life. 110
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 110
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. 109
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 109
Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders 109
Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients. 108
Different role of secretory IgA in the pathogenesis of RAST-positive and RAST-negative atopic dermatitis. 108
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. 107
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 107
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration. 107
An avidin/biotin ELISA for the measurement of serum and secretory IgD. 106
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. 106
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 106
A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection 105
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 105
Serum immunoglobulin levels in heterozygous subjects with immunoglobulin heavy chain constant region gene deletions. 105
Recurrent infections with IgG2 deficiency. 105
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 105
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 105
Memory B-cell subsets as a predictive marker of outcome in hypogammaglobulinemia during infancy. 104
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy children. 104
Diagnostics of primary immunodeficiencies through next-generation sequencing 104
Evaluation by SDS-PAGE and immunoblotting of residual antigenicity in hydrolysed protein formulas. 104
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper IgM syndrome (HIGM2). 103
Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterization 103
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. 103
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunction. 103
C4bBinding Protein (C4BP) activates B cells through the CD40 receptor. 102
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 102
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations 102
Recurrent Bleedings in Newborn: A Factor VII Deficiency Case Report 102
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 101
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 100
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function. 100
Valutazione dell'allergenicità dei peptidi contenuti negli idrolizzati delle proteine del latte vaccino 100
Intravenous gammaglobulin therapy for prophylaxis of infection in high-risk neonates. 100
Activity of classical and alternative pathways of complement in preterm and small for gestational age infants. 100
Beta2 integrins are required for follicular helper T cell differentiation in humans 100
Neurovisual Assessment in Children with Ataxia Telangiectasia 100
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 100
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 100
BTK: 22 novel and 25 recurrent mutations in European patients with X-linked agammaglobulinemia. 99
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency. 99
Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome 99
Ontogeny of secretory immunity: levels of secretory IgA and natural antibodies in saliva 99
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 99
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 99
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 99
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world 99
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 99
Recurrent extended HLA haplotypes in children with selective IgA deficiency. 98
Defect of regulatory T cells in patients with Omenn syndrome 97
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 97
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 97
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 97
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 97
Hyper IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination. 96
Characterization of Ig gene somatic hypermutation in the absence of activation-induced cytidine deaminase. 96
Extensive deletion of immunoglobulin heavy chain constant region genes in the absence of recurrent infections: when is IgG subclass deficiency clinically relevant? 96
Impaired platelet activation in patients with hereditary deficiency of p47(phox) 96
ICOS deficiency in patients with common variable immunodeficiency 95
Totale 11.841
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Categoria #
all - tutte 124.383
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 124.383
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20207.929 1.142 253 285 1.002 473 812 746 829 582 1.100 245 460
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
2024/202515 15 0 0 0 0 0 0 0 0 0 0 0
Totale 27.686