IRIS Institutional Research Information System - OPENBS Open Archive UniBS

PLEBANI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 17.382
EU - Europa 5.997
AS - Asia 3.215
OC - Oceania 27
Continente sconosciuto - Info sul continente non disponibili 21
AF - Africa 15
SA - Sud America 10
Totale 26.667
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Nazione #
US - Stati Uniti d'America 17.354
CN - Cina 2.366
UA - Ucraina 2.221
DE - Germania 843
PL - Polonia 716
HK - Hong Kong 587
IT - Italia 541
FI - Finlandia 520
GB - Regno Unito 367
IE - Irlanda 351
FR - Francia 253
IN - India 92
SE - Svezia 83
TR - Turchia 45
SG - Singapore 34
VN - Vietnam 28
BE - Belgio 27
NL - Olanda 27
AU - Australia 25
CA - Canada 25
KR - Corea 23
EU - Europa 21
IR - Iran 13
MU - Mauritius 13
RU - Federazione Russa 13
JP - Giappone 10
BR - Brasile 7
RO - Romania 7
ES - Italia 5
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 26.667
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Città #
Fairfield 2.746
Woodbridge 2.424
Houston 1.576
Jacksonville 1.559
Ashburn 1.322
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
Brescia 179
Shenyang 161
Des Moines 146
San Diego 137
Hebei 134
Changsha 132
Jinan 114
Tianjin 107
Lancaster 92
Milan 91
Jiaxing 82
Dearborn 80
Shanghai 67
Kunming 66
Hangzhou 63
London 63
Zhengzhou 46
Lanzhou 42
Boardman 41
Verona 41
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
Chiswick 9
Prescot 9
Acton 8
Ardabil 8
Sydney 8
Amsterdam 7
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
Monmouth Junction 3
Mumbai 3
Padova 3
Totale 21.228
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Nome #
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP 284
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 280
NFKB1 regulates human NK cell maturation and effector functions 273
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 183
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. 182
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 178
Acral lympho-histiocytic dermatitis in X-linked agammaglobulinemia: A case report showing clonal CD8+ T cells with indolent clinical behaviour 159
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder? 159
Different molecular behavior of CD40 mutants causing hyper-IgM syndrome. 150
The RAC2-PI3K axis regulates human NK cell maturation and function 149
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 136
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 135
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome. 131
Evidence for antigenic selection of large granular lymphocytes in a patient with Wiskott-Aldrich syndrome 130
CTLA-4 regulates human Natural Killer cell effector functions 129
Pancreatitis in systemic lupus erythematosus. 127
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. 125
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 124
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty. 123
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages. 122
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 122
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 121
The change in Ig regulation from children to adults disconnects the correlation with the 3'RR hs1.2 polymorphism 121
BAFF-R mutations in Good's syndrome. 121
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 120
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 119
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 118
Functional defects of dendritic cells in patients with CD40 deficiency. 117
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 115
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 114
Body experiences, emotional competence, and psychosocial functioning in juvenile idiopathic arthritis. 113
Profound T-cell defects in Dubowitz syndrome 113
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 112
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 112
Western Blot technique in the serological evaluation of three LAV/HTLV III-infected Italian families. 110
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 110
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 110
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. 109
A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life. 109
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 108
Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders 108
Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients. 107
Different role of secretory IgA in the pathogenesis of RAST-positive and RAST-negative atopic dermatitis. 107
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. 106
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 106
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration. 106
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 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. 105
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 105
A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection 104
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 104
Serum immunoglobulin levels in heterozygous subjects with immunoglobulin heavy chain constant region gene deletions. 104
Recurrent infections with IgG2 deficiency. 104
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 104
Evaluation by SDS-PAGE and immunoblotting of residual antigenicity in hydrolysed protein formulas. 104
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 104
Memory B-cell subsets as a predictive marker of outcome in hypogammaglobulinemia during infancy. 103
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy children. 103
An avidin/biotin ELISA for the measurement of serum and secretory IgD. 103
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper IgM syndrome (HIGM2). 102
Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterization 102
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. 102
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunction. 102
Diagnostics of primary immunodeficiencies through next-generation sequencing 102
C4bBinding Protein (C4BP) activates B cells through the CD40 receptor. 101
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 101
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations 101
Recurrent Bleedings in Newborn: A Factor VII Deficiency Case Report 101
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 100
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 100
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function. 99
Valutazione dell'allergenicità dei peptidi contenuti negli idrolizzati delle proteine del latte vaccino 99
Intravenous gammaglobulin therapy for prophylaxis of infection in high-risk neonates. 99
Activity of classical and alternative pathways of complement in preterm and small for gestational age infants. 99
Beta2 integrins are required for follicular helper T cell differentiation in humans 99
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 99
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 99
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 99
BTK: 22 novel and 25 recurrent mutations in European patients with X-linked agammaglobulinemia. 98
Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome 98
Ontogeny of secretory immunity: levels of secretory IgA and natural antibodies in saliva 98
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 98
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 98
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency. 97
Recurrent extended HLA haplotypes in children with selective IgA deficiency. 97
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world 97
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 97
Defect of regulatory T cells in patients with Omenn syndrome 96
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 96
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 96
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 96
Neurovisual Assessment in Children with Ataxia Telangiectasia 96
Hyper IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination. 95
Characterization of Ig gene somatic hypermutation in the absence of activation-induced cytidine deaminase. 95
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 95
Extensive deletion of immunoglobulin heavy chain constant region genes in the absence of recurrent infections: when is IgG subclass deficiency clinically relevant? 95
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia 95
ICOS deficiency in patients with common variable immunodeficiency 94
Totale 11.708
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Categoria #
all - tutte 116.648
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 116.648
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20191.545 0 0 0 0 0 0 0 0 0 0 809 736
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
2023/20241.970 131 48 202 187 108 491 83 91 604 21 4 0
Totale 27.292