IRIS Institutional Research Information System - OPENBS Open Archive UniBS

LOUGARIS, VASSILIOS
 Distribuzione geografica
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Continente #
NA - Nord America 9.850
AS - Asia 4.237
EU - Europa 3.629
SA - Sud America 836
AF - Africa 101
OC - Oceania 23
Continente sconosciuto - Info sul continente non disponibili 11
Totale 18.687
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Nazione #
US - Stati Uniti d'America 9.683
SG - Singapore 1.442
CN - Cina 1.407
PL - Polonia 745
BR - Brasile 685
UA - Ucraina 666
IT - Italia 464
HK - Hong Kong 458
DE - Germania 445
VN - Vietnam 340
FI - Finlandia 309
GB - Regno Unito 248
FR - Francia 224
TR - Turchia 152
RU - Federazione Russa 146
IE - Irlanda 137
BD - Bangladesh 105
IN - India 96
CA - Canada 85
AR - Argentina 78
MX - Messico 50
SE - Svezia 47
NL - Olanda 42
IQ - Iraq 39
AT - Austria 35
ES - Italia 34
ZA - Sudafrica 34
JP - Giappone 33
ID - Indonesia 26
AU - Australia 21
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
LT - Lituania 11
SA - Arabia Saudita 11
BO - Bolivia 9
EU - Europa 9
JM - Giamaica 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
LA - Repubblica Popolare Democratica del Laos 4
LB - Libano 4
MU - Mauritius 4
CR - Costa Rica 3
EE - Estonia 3
ET - Etiopia 3
GR - Grecia 3
NI - Nicaragua 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
GE - Georgia 2
HU - Ungheria 2
LU - Lussemburgo 2
LV - Lettonia 2
MY - Malesia 2
OM - Oman 2
PA - Panama 2
PR - Porto Rico 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
KR - Corea 1
KW - Kuwait 1
LK - Sri Lanka 1
MN - Mongolia 1
MT - Malta 1
Totale 18.679
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Città #
Fairfield 1.220
Ashburn 961
Woodbridge 852
Singapore 792
Warsaw 741
Houston 607
Jacksonville 503
Seattle 481
Cambridge 465
Hong Kong 456
Wilmington 436
Ann Arbor 370
Beijing 368
San Jose 368
New York 310
Chandler 303
The Dalles 271
Princeton 245
Helsinki 196
Los Angeles 163
Nanjing 154
Brescia 151
Dublin 135
Lauterbourg 122
Istanbul 120
Ho Chi Minh City 94
Munich 92
Dallas 89
Des Moines 87
Hanoi 67
Shanghai 65
São Paulo 65
San Diego 64
Buffalo 57
Moscow 57
Council Bluffs 54
Milan 54
Redondo Beach 53
San Francisco 53
Chicago 49
Changsha 47
Nanchang 47
Santa Clara 45
Shenyang 45
Dearborn 42
London 41
Lancaster 39
Turku 39
Hebei 36
Montreal 34
Orem 34
Jinan 32
Jiaxing 28
Tokyo 27
Dong Ket 26
Phoenix 26
Johannesburg 25
Atlanta 24
Chennai 24
Nuremberg 23
Stockholm 23
Boardman 22
Guangzhou 22
Tianjin 22
Denver 21
Poplar 21
Toronto 21
Brooklyn 19
Mexico City 19
Frankfurt am Main 18
Hangzhou 18
Rio de Janeiro 18
Tashkent 18
Brasília 16
Haikou 16
Haiphong 16
Kunming 16
Boston 15
Da Nang 15
Indianapolis 15
Vienna 15
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 13.078
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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 384
NFKB1 regulates human NK cell maturation and effector functions 341
Congenital cystic lung disease: prenatal ultrasound and postnatal multidetector computer tomography evaluation. Correlation with surgical and pathological data 340
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 274
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 267
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 263
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 249
CTLA-4 regulates human Natural Killer cell effector functions 211
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 210
The RAC2-PI3K axis regulates human NK cell maturation and function 208
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 205
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 202
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 199
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 198
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 196
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 194
BAFF-R mutations in Good's syndrome. 194
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 187
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 185
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 185
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 183
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 180
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 177
CONGENITAL CYSTIC LUNG DISEASE: PRENATAL ULTRASOUND AND POSTNATAL MULTIDETECTOR COMPUTER TOMOGRAPHY EVALUATION. CORRELATION WITH SURGICAL AND PATHOLOGICAL DATA 177
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 176
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 176
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 175
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 174
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 174
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 173
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 168
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 164
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 163
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 162
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency 157
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 157
The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers 156
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. 155
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 153
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 153
Diagnostics of primary immunodeficiencies through next-generation sequencing 152
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 151
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 150
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 145
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 143
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 143
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study 142
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 142
Beta2 integrins are required for follicular helper T cell differentiation in humans 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. 139
Allergen immunotherapy, routes of administration and cytokine networks: An update 139
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 138
Screening of functional and positional candidate genes in families with common variable immunodeficiency 137
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 137
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency 136
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 135
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 134
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 134
Mutational analysis of human BAFF Receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency. 133
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations 133
Double-blind, placebo-controlled, randomized trial on low-dose azithromycin prophylaxis in patients with primary antibody deficiencies 133
Importance of B cell co-stimulation in CD4(+) T cell differentiation: X-linked agammaglobulinaemia, a human model. 131
Circulating follicular helper and follicular regulatory T cells are severely compromised in human CD40 deficiency: A case report 131
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 131
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis. 130
Regulation of the germinal center gene program by interferon (IFN) regulatory factor 8/IFN consensus sequence-binding protein. 128
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 128
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency 128
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 127
Mutational analysis of human BLyS in patients with common variable immunodeficiency. 126
Thymic and bone marrow output in patients with common variable immunodeficiency 125
Breastfeeding and IL-10 levels in children affected by cow's milk protein allergy: A restrospective study 125
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency. 124
Mutations of the Igb gene cause agammaglobulinemia in man 122
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients. 122
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. 121
Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor κB kinase alpha (IKKα) 121
Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency 120
Diagnostic approach of hypogammaglobulinemia in infancy 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
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 116
Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features. 116
CXCL12 mediates aberrant costimulation of B lymphocytes in warts, hypogammaglobulinemia, infections, myelokathexis immunodeficiency 116
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects 115
The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019) 115
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study 115
Response to the Letter to the Editor Regarding “Functional evaluation of natural killer cell cytotoxic activity in NFKB-2 mutated patients” 114
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 114
Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS) 114
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 113
P85α is an intrinsic regulator of human natural killer cell effector functions 113
When a Nontuberculous Mycobacterial Infection Reveals an Error of Immunity: A Single Center's Experience 112
RAC2 and primary human immune deficiencies 111
Proteus syndrome: evaluation of the immunological profile 109
Maternal T-cell engraftment impedes with diagnosis of a SCID-ADA patient 107
Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients 107
Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency 106
Screening of 181 Patients With Antibody Deficiency for Deficiency of Adenosine Deaminase 2 Sheds New Light on the Disease in Adulthood 105
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study 105
Totale 15.622
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Categoria #
all - tutte 89.083
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 89.083
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021112 0 0 0 0 0 0 0 0 0 0 0 112
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
2025/20265.308 486 682 443 789 539 402 759 191 268 443 217 89
Totale 19.017