IRIS Institutional Research Information System - OPENBS Open Archive UniBS

LOUGARIS, VASSILIOS
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 8.713
AS - Asia 3.541
EU - Europa 3.278
SA - Sud America 768
AF - Africa 74
Continente sconosciuto - Info sul continente non disponibili 11
OC - Oceania 10
Totale 16.395
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 8.588
CN - Cina 1.222
SG - Singapore 1.214
PL - Polonia 742
UA - Ucraina 664
BR - Brasile 650
HK - Hong Kong 445
DE - Germania 434
IT - Italia 365
FI - Finlandia 264
VN - Vietnam 228
GB - Regno Unito 220
RU - Federazione Russa 144
TR - Turchia 143
IE - Irlanda 135
FR - Francia 99
IN - India 70
CA - Canada 66
AR - Argentina 61
SE - Svezia 43
MX - Messico 40
BD - Bangladesh 38
AT - Austria 35
NL - Olanda 34
ZA - Sudafrica 31
ES - Italia 30
IQ - Iraq 30
JP - Giappone 27
ID - Indonesia 23
UZ - Uzbekistan 16
BE - Belgio 15
CO - Colombia 12
EC - Ecuador 12
AZ - Azerbaigian 11
MA - Marocco 11
PK - Pakistan 11
DZ - Algeria 9
EU - Europa 9
SA - Arabia Saudita 9
AU - Australia 8
LT - Lituania 8
VE - Venezuela 8
JO - Giordania 7
RO - Romania 7
AE - Emirati Arabi Uniti 6
BO - Bolivia 6
CH - Svizzera 6
DK - Danimarca 6
IR - Iran 6
PY - Paraguay 6
TN - Tunisia 6
CZ - Repubblica Ceca 5
HN - Honduras 5
IL - Israele 5
KZ - Kazakistan 5
UY - Uruguay 5
BG - Bulgaria 4
CL - Cile 4
EG - Egitto 4
LA - Repubblica Popolare Democratica del Laos 4
MU - Mauritius 4
NP - Nepal 4
PE - Perù 4
PS - Palestinian Territory 4
DO - Repubblica Dominicana 3
EE - Estonia 3
KE - Kenya 3
SK - Slovacchia (Repubblica Slovacca) 3
CR - Costa Rica 2
ET - Etiopia 2
GE - Georgia 2
GR - Grecia 2
HR - Croazia 2
HU - Ungheria 2
JM - Giamaica 2
LB - Libano 2
LU - Lussemburgo 2
LV - Lettonia 2
NI - Nicaragua 2
PA - Panama 2
PH - Filippine 2
XK - ???statistics.table.value.countryCode.XK??? 2
BW - Botswana 1
CI - Costa d'Avorio 1
CM - Camerun 1
GT - Guatemala 1
KG - Kirghizistan 1
KW - Kuwait 1
LK - Sri Lanka 1
MN - Mongolia 1
MY - Malesia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PR - Porto Rico 1
PT - Portogallo 1
PW - Palau 1
RS - Serbia 1
SN - Senegal 1
SV - El Salvador 1
TH - Thailandia 1
Totale 16.395
Salva come PNG Salva come JPEG
Città #
Fairfield 1.220
Woodbridge 852
Ashburn 803
Warsaw 738
Houston 601
Singapore 590
Jacksonville 502
Seattle 481
Cambridge 465
Hong Kong 444
Wilmington 436
Ann Arbor 370
Beijing 364
Chandler 303
New York 282
Princeton 245
Helsinki 151
Nanjing 150
Brescia 147
Los Angeles 139
Dublin 133
Istanbul 119
The Dalles 106
Munich 92
Des Moines 86
Dallas 80
Ho Chi Minh City 68
San Diego 63
Shanghai 60
Moscow 57
São Paulo 57
Redondo Beach 53
Buffalo 52
San Francisco 49
Chicago 46
Nanchang 46
Changsha 45
Shenyang 45
Dearborn 42
Hanoi 40
Lancaster 39
Turku 39
London 37
Hebei 36
Milan 33
Jinan 30
Santa Clara 30
Jiaxing 28
Dong Ket 26
Montreal 26
Nuremberg 23
Phoenix 23
Johannesburg 22
Tianjin 22
Tokyo 21
Stockholm 19
Rio de Janeiro 18
Boardman 17
Denver 17
Guangzhou 17
Mexico City 17
Toronto 17
Brooklyn 16
Haikou 16
Hangzhou 16
Brasília 15
Kunming 15
Tashkent 15
Vienna 15
Atlanta 14
Chennai 14
Jakarta 14
Ningbo 14
Orem 14
Boston 13
Casoria 13
Poplar 13
Zhengzhou 13
Belo Horizonte 12
Brussels 11
Da Nang 11
Frankfurt am Main 11
Indianapolis 11
Amsterdam 10
Baku 10
Glasgow 10
Taizhou 10
Baghdad 9
Elk Grove Village 9
Haiphong 9
Leawood 9
Manchester 9
Orange 9
San Mateo 9
Verona 9
Ankara 8
Buenos Aires 8
Charlotte 8
Curitiba 8
Redwood City 8
Totale 11.617
Salva come PNG Salva come JPEG
Nome #
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 335
Congenital cystic lung disease: prenatal ultrasound and postnatal multidetector computer tomography evaluation. Correlation with surgical and pathological data 323
NFKB1 regulates human NK cell maturation and effector functions 316
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 242
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 238
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 230
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 226
The RAC2-PI3K axis regulates human NK cell maturation and function 188
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 184
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 178
BAFF-R mutations in Good's syndrome. 178
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 177
CTLA-4 regulates human Natural Killer cell effector functions 176
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 174
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 173
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 172
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 169
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 168
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 167
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 164
CONGENITAL CYSTIC LUNG DISEASE: PRENATAL ULTRASOUND AND POSTNATAL MULTIDETECTOR COMPUTER TOMOGRAPHY EVALUATION. CORRELATION WITH SURGICAL AND PATHOLOGICAL DATA 162
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 159
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 159
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 156
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 155
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 154
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 153
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 151
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 151
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 151
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 149
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 146
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. 145
The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers 144
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency 144
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 144
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 142
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 141
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 140
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 140
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 138
Diagnostics of primary immunodeficiencies through next-generation sequencing 133
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 132
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 131
Screening of functional and positional candidate genes in families with common variable immunodeficiency 130
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 130
Allergen immunotherapy, routes of administration and cytokine networks: An update 129
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 128
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 128
Beta2 integrins are required for follicular helper T cell differentiation in humans 127
Mutational analysis of human BAFF Receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency. 126
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 126
Importance of B cell co-stimulation in CD4(+) T cell differentiation: X-linked agammaglobulinaemia, a human model. 124
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency 124
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study 124
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 122
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis. 122
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 121
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 121
Circulating follicular helper and follicular regulatory T cells are severely compromised in human CD40 deficiency: A case report 121
Double-blind, placebo-controlled, randomized trial on low-dose azithromycin prophylaxis in patients with primary antibody deficiencies 121
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 120
Regulation of the germinal center gene program by interferon (IFN) regulatory factor 8/IFN consensus sequence-binding protein. 119
Mutational analysis of human BLyS in patients with common variable immunodeficiency. 119
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 118
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency. 117
Thymic and bone marrow output in patients with common variable immunodeficiency 117
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency 117
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 117
Breastfeeding and IL-10 levels in children affected by cow's milk protein allergy: A restrospective study 116
Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency 115
Mutations of the Igb gene cause agammaglobulinemia in man 114
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 113
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients. 112
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations 112
CXCL12 mediates aberrant costimulation of B lymphocytes in warts, hypogammaglobulinemia, infections, myelokathexis immunodeficiency 109
Diagnostic approach of hypogammaglobulinemia in infancy 109
Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features. 108
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 108
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. 104
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 102
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 102
Maternal T-cell engraftment impedes with diagnosis of a SCID-ADA patient 101
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 101
Proteus syndrome: evaluation of the immunological profile 100
Response to the Letter to the Editor Regarding “Functional evaluation of natural killer cell cytotoxic activity in NFKB-2 mutated patients” 99
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects 99
Clinical manifestations and gastrointestinal pathology in 40 patients with autoimmune enteropathy 99
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study 99
Screening of 181 Patients With Antibody Deficiency for Deficiency of Adenosine Deaminase 2 Sheds New Light on the Disease in Adulthood 98
Different clinical and immunological presentation of Ataxia Telangiectasia within the same family. 97
Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS) 96
Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor κB kinase alpha (IKKα) 95
When a Nontuberculous Mycobacterial Infection Reveals an Error of Immunity: A Single Center's Experience 95
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 94
The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019) 94
Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency 94
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study 94
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 93
RAC2 and primary human immune deficiencies 93
Totale 13.931
Salva come PNG Salva come JPEG
Categoria #
all - tutte 80.393
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 80.393
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.608 0 0 0 0 0 230 136 306 232 336 256 112
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
2024/20252.460 9 10 13 323 239 202 177 122 279 197 515 374
2025/20263.013 486 682 443 789 539 74 0 0 0 0 0 0
Totale 16.722