IRIS Institutional Research Information System - OPENBS Open Archive UniBS

LOUGARIS, VASSILIOS
 Distribuzione geografica
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Continente #
NA - Nord America 9.556
AS - Asia 4.154
EU - Europa 3.590
SA - Sud America 836
AF - Africa 101
OC - Oceania 22
Continente sconosciuto - Info sul continente non disponibili 11
Totale 18.270
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Nazione #
US - Stati Uniti d'America 9.406
SG - Singapore 1.427
CN - Cina 1.392
PL - Polonia 745
BR - Brasile 685
UA - Ucraina 666
HK - Hong Kong 458
DE - Germania 445
IT - Italia 429
VN - Vietnam 338
FI - Finlandia 309
GB - Regno Unito 247
FR - Francia 224
TR - Turchia 152
RU - Federazione Russa 146
IE - Irlanda 137
IN - India 96
AR - Argentina 78
CA - Canada 77
BD - Bangladesh 55
MX - Messico 48
SE - Svezia 47
NL - Olanda 41
IQ - Iraq 39
AT - Austria 35
ZA - Sudafrica 34
ES - Italia 33
JP - Giappone 33
ID - Indonesia 26
AU - Australia 20
UZ - Uzbekistan 20
PK - Pakistan 18
CO - Colombia 17
BE - Belgio 15
MA - Marocco 15
EC - Ecuador 13
JO - Giordania 13
AZ - Azerbaigian 12
VE - Venezuela 12
CZ - Repubblica Ceca 11
DZ - Algeria 11
SA - Arabia Saudita 11
LT - Lituania 10
BO - Bolivia 9
EU - Europa 9
NG - Nigeria 9
RO - Romania 9
TN - Tunisia 8
AE - Emirati Arabi Uniti 7
HN - Honduras 7
IL - Israele 7
CH - Svizzera 6
CL - Cile 6
DK - Danimarca 6
EG - Egitto 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
JM - Giamaica 4
LA - Repubblica Popolare Democratica del Laos 4
LB - Libano 4
MU - Mauritius 4
EE - Estonia 3
ET - Etiopia 3
GR - Grecia 3
NI - Nicaragua 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
CR - Costa Rica 2
GE - Georgia 2
HU - Ungheria 2
LU - Lussemburgo 2
LV - Lettonia 2
MY - Malesia 2
OM - Oman 2
PA - Panama 2
XK - ???statistics.table.value.countryCode.XK??? 2
AL - Albania 1
BH - Bahrain 1
BW - Botswana 1
CI - Costa d'Avorio 1
CM - Camerun 1
CY - Cipro 1
GT - Guatemala 1
KG - Kirghizistan 1
KW - Kuwait 1
LK - Sri Lanka 1
MN - Mongolia 1
MT - Malta 1
NZ - Nuova Zelanda 1
PR - Porto Rico 1
Totale 18.263
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Città #
Fairfield 1.220
Ashburn 944
Woodbridge 852
Singapore 791
Warsaw 741
Houston 604
Jacksonville 502
Seattle 481
Cambridge 465
Hong Kong 456
Wilmington 436
Ann Arbor 370
Beijing 367
San Jose 305
Chandler 303
New York 294
The Dalles 271
Princeton 245
Helsinki 196
Nanjing 154
Brescia 151
Los Angeles 150
Dublin 135
Lauterbourg 122
Istanbul 120
Ho Chi Minh City 94
Munich 92
Des Moines 87
Dallas 82
Hanoi 66
São Paulo 65
San Diego 64
Shanghai 64
Moscow 57
Buffalo 53
Redondo Beach 53
Council Bluffs 50
Milan 50
San Francisco 49
Chicago 48
Nanchang 47
Changsha 46
Shenyang 45
Dearborn 42
London 41
Lancaster 39
Turku 39
Hebei 36
Santa Clara 36
Jinan 32
Montreal 32
Orem 31
Jiaxing 28
Tokyo 27
Dong Ket 26
Johannesburg 25
Chennai 24
Nuremberg 23
Phoenix 23
Stockholm 23
Guangzhou 22
Tianjin 22
Boardman 21
Poplar 21
Atlanta 20
Denver 19
Frankfurt am Main 18
Rio de Janeiro 18
Tashkent 18
Mexico City 17
Toronto 17
Brasília 16
Brooklyn 16
Haikou 16
Haiphong 16
Hangzhou 16
Kunming 16
Boston 15
Da Nang 15
Vienna 15
Indianapolis 14
Jakarta 14
Manchester 14
Ningbo 14
Zhengzhou 14
Amsterdam 13
Casoria 13
Belo Horizonte 12
Amman 11
Ankara 11
Baghdad 11
Baku 11
Brussels 11
Buenos Aires 10
Elk Grove Village 10
Glasgow 10
Mumbai 10
Paris 10
Taizhou 10
Abuja 9
Totale 12.900
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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 379
Congenital cystic lung disease: prenatal ultrasound and postnatal multidetector computer tomography evaluation. Correlation with surgical and pathological data 337
NFKB1 regulates human NK cell maturation and effector functions 333
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 270
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 263
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 260
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 246
CTLA-4 regulates human Natural Killer cell effector functions 206
The RAC2-PI3K axis regulates human NK cell maturation and function 206
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 201
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 201
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 198
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 197
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 196
BAFF-R mutations in Good's syndrome. 193
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 192
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 191
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 186
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 183
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 181
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 179
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 178
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 174
CONGENITAL CYSTIC LUNG DISEASE: PRENATAL ULTRASOUND AND POSTNATAL MULTIDETECTOR COMPUTER TOMOGRAPHY EVALUATION. CORRELATION WITH SURGICAL AND PATHOLOGICAL DATA 172
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 172
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 171
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 170
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 170
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 168
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 163
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 162
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 159
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 159
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 158
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 155
The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers 154
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency 154
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. 154
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 152
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 152
Diagnostics of primary immunodeficiencies through next-generation sequencing 150
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 149
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 149
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 142
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 142
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study 142
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 141
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 141
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 138
Allergen immunotherapy, routes of administration and cytokine networks: An update 138
Beta2 integrins are required for follicular helper T cell differentiation in humans 138
Screening of functional and positional candidate genes in families with common variable immunodeficiency 137
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency 135
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 134
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 134
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 134
Mutational analysis of human BAFF Receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency. 133
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 133
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations 132
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 132
Importance of B cell co-stimulation in CD4(+) T cell differentiation: X-linked agammaglobulinaemia, a human model. 130
Circulating follicular helper and follicular regulatory T cells are severely compromised in human CD40 deficiency: A case report 130
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency 128
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis. 128
Regulation of the germinal center gene program by interferon (IFN) regulatory factor 8/IFN consensus sequence-binding protein. 127
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 127
Double-blind, placebo-controlled, randomized trial on low-dose azithromycin prophylaxis in patients with primary antibody deficiencies 127
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency. 124
Mutational analysis of human BLyS in patients with common variable immunodeficiency. 124
Thymic and bone marrow output in patients with common variable immunodeficiency 124
Breastfeeding and IL-10 levels in children affected by cow's milk protein allergy: A restrospective study 123
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 123
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 122
Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency 120
Mutations of the Igb gene cause agammaglobulinemia in man 120
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. 118
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients. 118
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 118
Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor κB kinase alpha (IKKα) 118
CXCL12 mediates aberrant costimulation of B lymphocytes in warts, hypogammaglobulinemia, infections, myelokathexis immunodeficiency 116
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study 115
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 114
Diagnostic approach of hypogammaglobulinemia in infancy 114
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 113
Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features. 113
Response to the Letter to the Editor Regarding “Functional evaluation of natural killer cell cytotoxic activity in NFKB-2 mutated patients” 113
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 112
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 112
The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019) 112
P85α is an intrinsic regulator of human natural killer cell effector functions 111
Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS) 111
When a Nontuberculous Mycobacterial Infection Reveals an Error of Immunity: A Single Center's Experience 109
Proteus syndrome: evaluation of the immunological profile 108
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects 108
RAC2 and primary human immune deficiencies 108
Maternal T-cell engraftment impedes with diagnosis of a SCID-ADA patient 107
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study 105
Screening of 181 Patients With Antibody Deficiency for Deficiency of Adenosine Deaminase 2 Sheds New Light on the Disease in Adulthood 104
Clinical manifestations and gastrointestinal pathology in 40 patients with autoimmune enteropathy 104
Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency 104
Totale 15.331
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Categoria #
all - tutte 84.560
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 84.560
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021704 0 0 0 0 0 0 0 0 0 336 256 112
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
2024/20252.460 9 10 13 323 239 202 177 122 279 197 515 374
2025/20264.889 486 682 443 789 539 402 759 191 268 330 0 0
Totale 18.598