IRIS Institutional Research Information System - OPENBS Open Archive UniBS

LOUGARIS, VASSILIOS
 Distribuzione geografica
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Continente #
NA - Nord America 7.239
EU - Europa 2.798
AS - Asia 1.658
Continente sconosciuto - Info sul continente non disponibili 9
AF - Africa 8
OC - Oceania 8
SA - Sud America 5
Totale 11.725
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Nazione #
US - Stati Uniti d'America 7.223
CN - Cina 776
PL - Polonia 714
UA - Ucraina 650
SG - Singapore 421
DE - Germania 333
IT - Italia 325
HK - Hong Kong 243
FI - Finlandia 220
GB - Regno Unito 144
IE - Irlanda 131
TR - Turchia 127
RU - Federazione Russa 120
FR - Francia 75
IN - India 28
VN - Vietnam 26
SE - Svezia 23
CA - Canada 16
NL - Olanda 15
ID - Indonesia 14
BE - Belgio 13
JP - Giappone 10
ES - Italia 9
EU - Europa 9
AU - Australia 8
RO - Romania 6
CZ - Repubblica Ceca 4
IR - Iran 4
MU - Mauritius 4
BR - Brasile 3
AE - Emirati Arabi Uniti 2
AR - Argentina 2
CH - Svizzera 2
DK - Danimarca 2
DZ - Algeria 2
HR - Croazia 2
KZ - Kazakistan 2
LT - Lituania 2
SK - Slovacchia (Repubblica Slovacca) 2
AZ - Azerbaigian 1
BD - Bangladesh 1
EE - Estonia 1
GR - Grecia 1
HU - Ungheria 1
JO - Giordania 1
LV - Lettonia 1
MA - Marocco 1
MN - Mongolia 1
MY - Malesia 1
PT - Portogallo 1
RS - Serbia 1
ZA - Sudafrica 1
Totale 11.725
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Città #
Fairfield 1.220
Woodbridge 852
Warsaw 714
Ashburn 622
Houston 588
Jacksonville 501
Seattle 477
Cambridge 465
Wilmington 434
Ann Arbor 370
Singapore 360
Chandler 303
Princeton 245
Hong Kong 242
New York 217
Beijing 207
Nanjing 150
Helsinki 149
Brescia 136
Dublin 129
Istanbul 119
San Diego 63
Moscow 56
Shanghai 54
Des Moines 50
Nanchang 46
Shenyang 43
Dearborn 42
Changsha 39
Lancaster 37
Hebei 36
Jinan 30
Munich 29
Milan 28
Jiaxing 27
Dong Ket 26
London 25
Tianjin 20
Boardman 17
Haikou 16
San Francisco 14
Casoria 13
Jakarta 13
Ningbo 13
Toronto 13
Kunming 12
Hangzhou 11
Brussels 10
Taizhou 10
Zhengzhou 10
Leawood 9
Orange 9
San Mateo 9
Verona 9
Guangzhou 8
Redwood City 8
Falkenstein 7
Norwalk 7
Phoenix 7
Busto Arsizio 6
Lanzhou 6
Los Angeles 6
Taiyuan 6
Barcelona 5
Chiswick 5
Kilburn 5
Prescot 5
Alessandria 4
Frankfurt am Main 4
Rome 4
Santa Clara 4
Tokyo 4
Acton 3
Augusta 3
Brno 3
Castenedolo 3
Changchun 3
Chicago 3
Espoo 3
Fuzhou 3
Gunzenhausen 3
Hanover 3
Lappeenranta 3
Melbourne 3
Montichiari 3
Washington 3
Amsterdam 2
Astana 2
Blida 2
Bratislava 2
Brooklyn 2
Canberra 2
Castiglione Delle Stiviere 2
Cluj-Napoca 2
Core 2
Erlangen 2
Florence 2
Hefei 2
Hyderabad 2
Kocaeli 2
Totale 9.510
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Nome #
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 288
Congenital cystic lung disease: prenatal ultrasound and postnatal multidetector computer tomography evaluation. Correlation with surgical and pathological data 285
NFKB1 regulates human NK cell maturation and effector functions 281
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 193
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 193
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 189
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 185
The RAC2-PI3K axis regulates human NK cell maturation and function 155
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 145
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 143
CTLA-4 regulates human Natural Killer cell effector functions 138
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 132
BAFF-R mutations in Good's syndrome. 132
CONGENITAL CYSTIC LUNG DISEASE: PRENATAL ULTRASOUND AND POSTNATAL MULTIDETECTOR COMPUTER TOMOGRAPHY EVALUATION. CORRELATION WITH SURGICAL AND PATHOLOGICAL DATA 131
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 130
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 130
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 129
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 129
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 128
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 126
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 123
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency 122
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 121
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 120
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 117
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 117
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 113
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 113
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 111
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. 110
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 110
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 109
Diagnostics of primary immunodeficiencies through next-generation sequencing 109
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 109
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 107
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 107
Allergen immunotherapy, routes of administration and cytokine networks: An update 106
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 106
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 105
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 105
Beta2 integrins are required for follicular helper T cell differentiation in humans 105
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 105
The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers 104
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 103
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency. 102
Importance of B cell co-stimulation in CD4(+) T cell differentiation: X-linked agammaglobulinaemia, a human model. 102
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 102
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 101
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 101
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 101
Breastfeeding and IL-10 levels in children affected by cow's milk protein allergy: A restrospective study 101
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 101
Thymic and bone marrow output in patients with common variable immunodeficiency 100
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 100
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 100
Mutational analysis of human BAFF Receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency. 98
Regulation of the germinal center gene program by interferon (IFN) regulatory factor 8/IFN consensus sequence-binding protein. 97
Mutational analysis of human BLyS in patients with common variable immunodeficiency. 97
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study 97
Reduced germinal center follicular helper T cells but normal follicular regulatory T cells in the tonsils of a patient with a mutation in the PI3KR1 gene 96
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 96
Double-blind, placebo-controlled, randomized trial on low-dose azithromycin prophylaxis in patients with primary antibody deficiencies 96
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis. 96
Screening of functional and positional candidate genes in families with common variable immunodeficiency 94
Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency 94
Mutations of the Igb gene cause agammaglobulinemia in man 94
Circulating follicular helper and follicular regulatory T cells are severely compromised in human CD40 deficiency: A case report 94
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients. 93
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 92
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency 89
Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features. 88
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 86
Proteus syndrome: evaluation of the immunological profile 85
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 84
Different clinical and immunological presentation of Ataxia Telangiectasia within the same family. 83
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations 82
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency 82
CXCL12 mediates aberrant costimulation of B lymphocytes in warts, hypogammaglobulinemia, infections, myelokathexis immunodeficiency 81
Maternal T-cell engraftment impedes with diagnosis of a SCID-ADA patient 80
Screening of 181 Patients With Antibody Deficiency for Deficiency of Adenosine Deaminase 2 Sheds New Light on the Disease in Adulthood 79
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 78
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects 77
Response to the Letter to the Editor Regarding “Functional evaluation of natural killer cell cytotoxic activity in NFKB-2 mutated patients” 75
Clinical manifestations and gastrointestinal pathology in 40 patients with autoimmune enteropathy 73
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. 72
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 72
P85α is an intrinsic regulator of human natural killer cell effector functions 70
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study 66
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 65
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 65
Characterization of the clinical and immunological phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations 64
Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency 64
Diagnostic approach of hypogammaglobulinemia in infancy 61
Expansion of somatically reverted memory CD8+ T cells in X-linked lymphoproliferative disease is due to selective pressure from Epstein Barr virus. 59
Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity 57
Glossotillomania as cause of Riga-Fede syndrome 55
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study 55
null 54
GENETIC ANALYSIS OF THE TNFRSF13B GENE IN A LARGE ITALIAN CVID COHORT 54
RAC2 and primary human immune deficiencies 54
Totale 10.673
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Categoria #
all - tutte 61.534
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 61.534
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.929 0 0 0 0 0 316 302 340 258 403 132 178
2020/20212.363 50 201 58 356 90 230 136 306 232 336 256 112
2021/20221.244 116 213 48 57 20 40 45 86 105 145 102 267
2022/2023896 156 5 13 51 77 238 5 123 132 5 39 52
2023/20241.133 71 25 116 85 44 270 35 56 256 12 15 148
2024/2025796 9 10 13 323 239 202 0 0 0 0 0 0
Totale 12.045