IRIS Institutional Research Information System - OPENBS Open Archive UniBS

LOUGARIS, VASSILIOS
 Distribuzione geografica
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Continente #
NA - Nord America 11.062
AS - Asia 4.305
EU - Europa 3.777
SA - Sud America 866
Continente sconosciuto - Info sul continente non disponibili 343
AF - Africa 104
OC - Oceania 24
Totale 20.481
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Nazione #
US - Stati Uniti d'America 10.808
SG - Singapore 1.452
CN - Cina 1.411
PL - Polonia 745
BR - Brasile 701
UA - Ucraina 666
IT - Italia 563
HK - Hong Kong 462
DE - Germania 449
VN - Vietnam 345
FI - Finlandia 309
GB - Regno Unito 262
FR - Francia 230
TR - Turchia 153
RU - Federazione Russa 146
IE - Irlanda 138
BD - Bangladesh 137
CA - Canada 127
IN - India 99
AR - Argentina 81
MX - Messico 54
NL - Olanda 48
SE - Svezia 47
ES - Italia 41
IQ - Iraq 39
AT - Austria 35
JP - Giappone 34
ZA - Sudafrica 34
ID - Indonesia 28
CO - Colombia 24
AU - Australia 22
UZ - Uzbekistan 20
JM - Giamaica 19
PK - Pakistan 18
BE - Belgio 15
EC - Ecuador 15
MA - Marocco 15
LT - Lituania 14
JO - Giordania 13
SA - Arabia Saudita 13
VE - Venezuela 13
AZ - Azerbaigian 12
CR - Costa Rica 11
CZ - Repubblica Ceca 11
DZ - Algeria 11
BO - Bolivia 9
EU - Europa 9
HN - Honduras 9
NG - Nigeria 9
RO - Romania 9
AE - Emirati Arabi Uniti 8
EE - Estonia 8
EG - Egitto 8
TN - Tunisia 8
CH - Svizzera 7
IL - Israele 7
NI - Nicaragua 7
CL - Cile 6
DK - Danimarca 6
IR - Iran 6
NP - Nepal 6
PE - Perù 6
PH - Filippine 6
PS - Palestinian Territory 6
PY - Paraguay 6
BG - Bulgaria 5
GT - Guatemala 5
KE - Kenya 5
KZ - Kazakistan 5
UY - Uruguay 5
DO - Repubblica Dominicana 4
GR - Grecia 4
HR - Croazia 4
LA - Repubblica Popolare Democratica del Laos 4
LB - Libano 4
MU - Mauritius 4
PR - Porto Rico 4
SV - El Salvador 4
ET - Etiopia 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
CW - ???statistics.table.value.countryCode.CW??? 2
GE - Georgia 2
HT - Haiti 2
HU - Ungheria 2
KR - Corea 2
LC - Santa Lucia 2
LU - Lussemburgo 2
LV - Lettonia 2
MY - Malesia 2
OM - Oman 2
PA - Panama 2
PT - Portogallo 2
TH - Thailandia 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
Totale 20.135
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Città #
Fairfield 1.220
Ashburn 1.085
Woodbridge 852
Singapore 798
Warsaw 741
Houston 612
San Jose 526
Jacksonville 503
Seattle 482
Cambridge 465
Hong Kong 460
Wilmington 436
Ann Arbor 370
Beijing 368
New York 320
Chandler 303
The Dalles 275
Council Bluffs 272
Princeton 245
Helsinki 196
Los Angeles 170
Nanjing 154
Brescia 152
Dublin 135
Lauterbourg 122
Istanbul 120
Dallas 98
Ho Chi Minh City 94
Munich 92
Des Moines 87
São Paulo 74
Santa Clara 72
Hanoi 68
Columbus 67
San Diego 67
Shanghai 65
Buffalo 64
Milan 59
San Francisco 58
Moscow 57
Chicago 56
Redondo Beach 53
Phoenix 48
Changsha 47
Nanchang 47
Shenyang 45
Dearborn 43
London 43
Lancaster 39
Montreal 39
Turku 39
Hebei 36
Atlanta 34
Orem 34
Jinan 32
Jiaxing 28
Toronto 28
Tokyo 27
Dong Ket 26
Brooklyn 25
Denver 25
Johannesburg 25
Chennai 24
Boardman 23
Nuremberg 23
Rome 23
Stockholm 23
Guangzhou 22
Tianjin 22
Poplar 21
Mexico City 20
Frankfurt am Main 18
Hangzhou 18
Rio de Janeiro 18
Tashkent 18
Boston 17
Brasília 17
Haiphong 17
Haikou 16
Kunming 16
Naples 16
Da Nang 15
Indianapolis 15
Vienna 15
Amsterdam 14
Jakarta 14
Kingston 14
Manchester 14
Ningbo 14
Zhengzhou 14
Casoria 13
Belo Horizonte 12
Amman 11
Ankara 11
Baghdad 11
Baku 11
Brussels 11
Charlotte 11
Elk Grove Village 11
Miami 11
Totale 13.837
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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 396
NFKB1 regulates human NK cell maturation and effector functions 352
Congenital cystic lung disease: prenatal ultrasound and postnatal multidetector computer tomography evaluation. Correlation with surgical and pathological data 345
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 288
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 282
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 277
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 254
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 235
CTLA-4 regulates human Natural Killer cell effector functions 219
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 217
The RAC2-PI3K axis regulates human NK cell maturation and function 215
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 213
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 212
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 205
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 204
BAFF-R mutations in Good's syndrome. 204
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 202
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 202
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 199
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 198
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 193
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 191
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 188
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 188
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 187
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 186
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 185
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 184
CONGENITAL CYSTIC LUNG DISEASE: PRENATAL ULTRASOUND AND POSTNATAL MULTIDETECTOR COMPUTER TOMOGRAPHY EVALUATION. CORRELATION WITH SURGICAL AND PATHOLOGICAL DATA 183
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 182
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 180
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 175
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 172
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 168
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 167
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 166
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 164
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency 163
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. 162
The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers 161
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 161
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 160
Diagnostics of primary immunodeficiencies through next-generation sequencing 160
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 159
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 158
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 158
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 155
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 153
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 153
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 150
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency 149
Beta2 integrins are required for follicular helper T cell differentiation in humans 148
Allergen immunotherapy, routes of administration and cytokine networks: An update 147
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study 146
Screening of functional and positional candidate genes in families with common variable immunodeficiency 145
Mutational analysis of human BAFF Receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency. 145
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 145
Double-blind, placebo-controlled, randomized trial on low-dose azithromycin prophylaxis in patients with primary antibody deficiencies 144
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 144
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 142
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 140
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 140
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 139
Importance of B cell co-stimulation in CD4(+) T cell differentiation: X-linked agammaglobulinaemia, a human model. 139
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations 139
Circulating follicular helper and follicular regulatory T cells are severely compromised in human CD40 deficiency: A case report 139
Mutational analysis of human BLyS in patients with common variable immunodeficiency. 138
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis. 138
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 136
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency 136
Regulation of the germinal center gene program by interferon (IFN) regulatory factor 8/IFN consensus sequence-binding protein. 135
Thymic and bone marrow output in patients with common variable immunodeficiency 135
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 135
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients. 133
Breastfeeding and IL-10 levels in children affected by cow's milk protein allergy: A restrospective study 133
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency. 132
Mutations of the Igb gene cause agammaglobulinemia in man 131
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. 131
Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency 129
CXCL12 mediates aberrant costimulation of B lymphocytes in warts, hypogammaglobulinemia, infections, myelokathexis immunodeficiency 128
Diagnostic approach of hypogammaglobulinemia in infancy 127
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 127
Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor κB kinase alpha (IKKα) 127
When a Nontuberculous Mycobacterial Infection Reveals an Error of Immunity: A Single Center's Experience 126
Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features. 124
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 123
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects 122
The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019) 122
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study 122
Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS) 121
Response to the Letter to the Editor Regarding “Functional evaluation of natural killer cell cytotoxic activity in NFKB-2 mutated patients” 120
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 119
P85α is an intrinsic regulator of human natural killer cell effector functions 118
Rituximab Monotherapy Is Effective as First-Line Treatment for Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) in CVID Patients 118
Proteus syndrome: evaluation of the immunological profile 117
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study 117
RAC2 and primary human immune deficiencies 116
Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients 116
Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related Malignancies 115
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 115
Totale 16.604
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Categoria #
all - tutte 97.780
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 97.780
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022867 0 0 0 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
2026/20271.433 208 244 371 610 0 0 0 0 0 0 0 0
Totale 20.481