IRIS Institutional Research Information System - OPENBS Open Archive UniBS

LOUGARIS, VASSILIOS
 Distribuzione geografica
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Continente #
NA - Nord America 10.138
AS - Asia 4.283
EU - Europa 3.679
SA - Sud America 843
Continente sconosciuto - Info sul continente non disponibili 341
AF - Africa 104
OC - Oceania 23
Totale 19.411
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Nazione #
US - Stati Uniti d'America 9.952
SG - Singapore 1.450
CN - Cina 1.409
PL - Polonia 745
BR - Brasile 686
UA - Ucraina 666
IT - Italia 502
HK - Hong Kong 461
DE - Germania 445
VN - Vietnam 341
FI - Finlandia 309
GB - Regno Unito 248
FR - Francia 226
TR - Turchia 152
RU - Federazione Russa 146
IE - Irlanda 137
BD - Bangladesh 134
IN - India 96
CA - Canada 91
AR - Argentina 81
MX - Messico 50
NL - Olanda 47
SE - Svezia 47
IQ - Iraq 39
ES - Italia 38
AT - Austria 35
JP - Giappone 34
ZA - Sudafrica 34
ID - Indonesia 27
AU - Australia 21
UZ - Uzbekistan 20
CO - Colombia 18
PK - Pakistan 18
BE - Belgio 15
MA - Marocco 15
EC - Ecuador 14
JO - Giordania 13
VE - Venezuela 13
AZ - Azerbaigian 12
JM - Giamaica 12
CZ - Repubblica Ceca 11
DZ - Algeria 11
LT - Lituania 11
SA - Arabia Saudita 11
BO - Bolivia 9
EU - Europa 9
NG - Nigeria 9
RO - Romania 9
EG - Egitto 8
HN - Honduras 8
TN - Tunisia 8
AE - Emirati Arabi Uniti 7
IL - Israele 7
CH - Svizzera 6
CL - Cile 6
CR - Costa Rica 6
DK - Danimarca 6
IR - Iran 6
NP - Nepal 6
PH - Filippine 6
PY - Paraguay 6
BG - Bulgaria 5
KE - Kenya 5
KZ - Kazakistan 5
PE - Perù 5
PS - Palestinian Territory 5
UY - Uruguay 5
DO - Repubblica Dominicana 4
HR - Croazia 4
LA - Repubblica Popolare Democratica del Laos 4
LB - Libano 4
MU - Mauritius 4
NI - Nicaragua 4
EE - Estonia 3
ET - Etiopia 3
GR - Grecia 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
GE - Georgia 2
GT - Guatemala 2
HU - Ungheria 2
KR - Corea 2
LU - Lussemburgo 2
LV - Lettonia 2
MY - Malesia 2
OM - Oman 2
PA - Panama 2
PR - Porto Rico 2
PT - Portogallo 2
XK - ???statistics.table.value.countryCode.XK??? 2
AL - Albania 1
BB - Barbados 1
BH - Bahrain 1
BW - Botswana 1
CI - Costa d'Avorio 1
CM - Camerun 1
CY - Cipro 1
HT - Haiti 1
KG - Kirghizistan 1
KW - Kuwait 1
Totale 19.068
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Città #
Fairfield 1.220
Ashburn 972
Woodbridge 852
Singapore 797
Warsaw 741
Houston 610
Jacksonville 503
Seattle 481
Cambridge 465
Hong Kong 459
Wilmington 436
San Jose 372
Ann Arbor 370
Beijing 368
New York 311
Chandler 303
The Dalles 271
Princeton 245
Helsinki 196
Los Angeles 165
Nanjing 154
Brescia 152
Dublin 135
Lauterbourg 122
Istanbul 120
Council Bluffs 107
Ho Chi Minh City 94
Munich 92
Dallas 91
Des Moines 87
Hanoi 68
São Paulo 66
Columbus 65
Shanghai 65
San Diego 64
Buffalo 61
Moscow 57
Milan 55
San Francisco 55
Santa Clara 54
Redondo Beach 53
Chicago 50
Changsha 47
Nanchang 47
Shenyang 45
Dearborn 42
London 41
Lancaster 39
Phoenix 39
Turku 39
Hebei 36
Montreal 34
Orem 34
Jinan 32
Jiaxing 28
Atlanta 27
Tokyo 27
Dong Ket 26
Johannesburg 25
Chennai 24
Nuremberg 23
Stockholm 23
Boardman 22
Brooklyn 22
Denver 22
Guangzhou 22
Tianjin 22
Poplar 21
Toronto 21
Mexico City 19
Frankfurt am Main 18
Hangzhou 18
Rio de Janeiro 18
Tashkent 18
Boston 16
Brasília 16
Haikou 16
Haiphong 16
Kunming 16
Da Nang 15
Indianapolis 15
Vienna 15
Jakarta 14
Manchester 14
Ningbo 14
Zhengzhou 14
Amsterdam 13
Casoria 13
Rome 13
Belo Horizonte 12
Amman 11
Ankara 11
Baghdad 11
Baku 11
Brussels 11
Charlotte 11
Buenos Aires 10
Elk Grove Village 10
Glasgow 10
Mumbai 10
Totale 13.263
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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 388
NFKB1 regulates human NK cell maturation and effector functions 347
Congenital cystic lung disease: prenatal ultrasound and postnatal multidetector computer tomography evaluation. Correlation with surgical and pathological data 341
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 278
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 271
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 270
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 249
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 227
CTLA-4 regulates human Natural Killer cell effector functions 212
The RAC2-PI3K axis regulates human NK cell maturation and function 210
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 206
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 204
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 204
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 201
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 199
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 197
BAFF-R mutations in Good's syndrome. 196
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 191
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 189
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 188
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 186
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 184
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 180
CONGENITAL CYSTIC LUNG DISEASE: PRENATAL ULTRASOUND AND POSTNATAL MULTIDETECTOR COMPUTER TOMOGRAPHY EVALUATION. CORRELATION WITH SURGICAL AND PATHOLOGICAL DATA 179
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 178
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 177
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 177
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 177
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 176
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 175
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 169
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 169
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 165
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 164
The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers 158
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency 158
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 158
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. 157
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 156
Diagnostics of primary immunodeficiencies through next-generation sequencing 153
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 153
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 152
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 151
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 148
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 147
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 147
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 145
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 145
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 145
Allergen immunotherapy, routes of administration and cytokine networks: An update 143
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study 142
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 142
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 141
Beta2 integrins are required for follicular helper T cell differentiation in humans 141
Screening of functional and positional candidate genes in families with common variable immunodeficiency 140
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 139
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 138
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency 137
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 136
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations 136
Double-blind, placebo-controlled, randomized trial on low-dose azithromycin prophylaxis in patients with primary antibody deficiencies 136
Mutational analysis of human BAFF Receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency. 135
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 135
Importance of B cell co-stimulation in CD4(+) T cell differentiation: X-linked agammaglobulinaemia, a human model. 134
Circulating follicular helper and follicular regulatory T cells are severely compromised in human CD40 deficiency: A case report 133
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency 131
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis. 131
Regulation of the germinal center gene program by interferon (IFN) regulatory factor 8/IFN consensus sequence-binding protein. 130
Thymic and bone marrow output in patients with common variable immunodeficiency 130
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 130
Mutational analysis of human BLyS in patients with common variable immunodeficiency. 128
Breastfeeding and IL-10 levels in children affected by cow's milk protein allergy: A restrospective study 128
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 128
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients. 127
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency. 125
Mutations of the Igb gene cause agammaglobulinemia in man 124
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. 124
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 122
Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency 122
Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor κB kinase alpha (IKKα) 122
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects 120
Diagnostic approach of hypogammaglobulinemia in infancy 119
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 119
Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features. 117
CXCL12 mediates aberrant costimulation of B lymphocytes in warts, hypogammaglobulinemia, infections, myelokathexis immunodeficiency 117
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 117
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study 116
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 115
Response to the Letter to the Editor Regarding “Functional evaluation of natural killer cell cytotoxic activity in NFKB-2 mutated patients” 115
The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019) 115
Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS) 115
P85α is an intrinsic regulator of human natural killer cell effector functions 114
RAC2 and primary human immune deficiencies 113
Rituximab Monotherapy Is Effective as First-Line Treatment for Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) in CVID Patients 113
When a Nontuberculous Mycobacterial Infection Reveals an Error of Immunity: A Single Center's Experience 112
Proteus syndrome: evaluation of the immunological profile 111
Maternal T-cell engraftment impedes with diagnosis of a SCID-ADA patient 109
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study 109
Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients 108
Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency 108
Totale 15.889
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Categoria #
all - tutte 93.043
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 93.043
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.128 0 213 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
2024/20252.460 9 10 13 323 239 202 177 122 279 197 515 374
2025/20265.339 486 682 443 789 539 402 759 191 268 443 217 120
2026/2027363 208 155 0 0 0 0 0 0 0 0 0 0
Totale 19.411