IRIS Institutional Research Information System - OPENBS Open Archive UniBS

LOUGARIS, VASSILIOS
 Distribuzione geografica
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Continente #
NA - Nord America 8.756
AS - Asia 3.606
EU - Europa 3.282
SA - Sud America 782
AF - Africa 76
Continente sconosciuto - Info sul continente non disponibili 11
OC - Oceania 10
Totale 16.523
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Nazione #
US - Stati Uniti d'America 8.627
SG - Singapore 1.223
CN - Cina 1.222
PL - Polonia 743
UA - Ucraina 664
BR - Brasile 659
HK - Hong Kong 445
DE - Germania 434
IT - Italia 365
VN - Vietnam 267
FI - Finlandia 264
GB - Regno Unito 223
TR - Turchia 145
RU - Federazione Russa 144
IE - Irlanda 135
FR - Francia 99
IN - India 70
CA - Canada 68
AR - Argentina 65
BD - Bangladesh 43
SE - Svezia 43
MX - Messico 41
AT - Austria 35
NL - Olanda 34
IQ - Iraq 32
ZA - Sudafrica 31
ES - Italia 30
JP - Giappone 28
ID - Indonesia 23
UZ - Uzbekistan 16
BE - Belgio 15
CO - Colombia 13
EC - Ecuador 12
MA - Marocco 12
PK - Pakistan 12
AZ - Azerbaigian 11
DZ - Algeria 9
EU - Europa 9
JO - Giordania 9
SA - Arabia Saudita 9
AU - Australia 8
LT - Lituania 8
VE - Venezuela 8
RO - Romania 7
TN - Tunisia 7
AE - Emirati Arabi Uniti 6
BO - Bolivia 6
CH - Svizzera 6
DK - Danimarca 6
IR - Iran 6
PY - Paraguay 6
CZ - Repubblica Ceca 5
HN - Honduras 5
IL - Israele 5
KZ - Kazakistan 5
NP - Nepal 5
UY - Uruguay 5
BG - Bulgaria 4
CL - Cile 4
EG - Egitto 4
LA - Repubblica Popolare Democratica del Laos 4
LB - Libano 4
MU - Mauritius 4
PE - Perù 4
PS - Palestinian Territory 4
DO - Repubblica Dominicana 3
EE - Estonia 3
JM - Giamaica 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
LU - Lussemburgo 2
LV - Lettonia 2
NI - Nicaragua 2
OM - Oman 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
PR - Porto Rico 1
PT - Portogallo 1
PW - Palau 1
RS - Serbia 1
SN - Senegal 1
SV - El Salvador 1
TH - Thailandia 1
Totale 16.523
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Città #
Fairfield 1.220
Woodbridge 852
Ashburn 807
Warsaw 739
Houston 601
Singapore 598
Jacksonville 502
Seattle 481
Cambridge 465
Hong Kong 444
Wilmington 436
Ann Arbor 370
Beijing 364
Chandler 303
New York 283
Princeton 245
Helsinki 151
Nanjing 150
Brescia 147
Los Angeles 142
Dublin 133
The Dalles 127
Istanbul 119
Munich 92
Des Moines 86
Dallas 80
Ho Chi Minh City 78
San Diego 63
Shanghai 60
São Paulo 59
Moscow 57
Redondo Beach 53
Buffalo 52
Hanoi 50
San Francisco 49
Chicago 47
Nanchang 46
Changsha 45
Shenyang 45
Dearborn 42
Lancaster 39
Turku 39
London 37
Hebei 36
Milan 33
Jinan 30
Santa Clara 30
Jiaxing 28
Montreal 27
Dong Ket 26
Nuremberg 23
Phoenix 23
Johannesburg 22
Tianjin 22
Tokyo 22
Stockholm 19
Denver 18
Rio de Janeiro 18
Boardman 17
Guangzhou 17
Mexico City 17
Toronto 17
Brooklyn 16
Haikou 16
Hangzhou 16
Atlanta 15
Brasília 15
Kunming 15
Orem 15
Poplar 15
Tashkent 15
Vienna 15
Boston 14
Chennai 14
Haiphong 14
Jakarta 14
Ningbo 14
Casoria 13
Da Nang 13
Zhengzhou 13
Belo Horizonte 12
Brussels 11
Frankfurt am Main 11
Indianapolis 11
Amsterdam 10
Ankara 10
Baku 10
Glasgow 10
Manchester 10
Taizhou 10
Baghdad 9
Buenos Aires 9
Elk Grove Village 9
Leawood 9
Orange 9
San Mateo 9
Verona 9
Amman 8
Charlotte 8
Curitiba 8
Totale 11.697
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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 337
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 318
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 246
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 239
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. 227
The RAC2-PI3K axis regulates human NK cell maturation and function 189
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 185
BAFF-R mutations in Good's syndrome. 180
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 179
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 177
CTLA-4 regulates human Natural Killer cell effector functions 177
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 175
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 174
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 173
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 171
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 169
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 169
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 166
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 162
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 160
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 157
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 157
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 156
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 155
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 153
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 152
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 152
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 151
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. 147
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 146
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 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
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 142
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 142
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 141
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. 139
Diagnostics of primary immunodeficiencies through next-generation sequencing 135
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
Allergen immunotherapy, routes of administration and cytokine networks: An update 130
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 130
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 129
Beta2 integrins are required for follicular helper T cell differentiation in humans 128
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 128
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 127
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study 127
Mutational analysis of human BAFF Receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency. 126
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency 126
Importance of B cell co-stimulation in CD4(+) T cell differentiation: X-linked agammaglobulinaemia, a human model. 124
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 122
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 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
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
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 120
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
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations 119
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency 118
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 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
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 114
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients. 112
Diagnostic approach of hypogammaglobulinemia in infancy 110
CXCL12 mediates aberrant costimulation of B lymphocytes in warts, hypogammaglobulinemia, infections, myelokathexis immunodeficiency 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
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 107
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. 105
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 104
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 103
Maternal T-cell engraftment impedes with diagnosis of a SCID-ADA patient 101
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study 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” 100
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
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
When a Nontuberculous Mycobacterial Infection Reveals an Error of Immunity: A Single Center's Experience 97
The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019) 96
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) 96
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 95
RAC2 and primary human immune deficiencies 95
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
Totale 14.026
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Categoria #
all - tutte 80.621
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 80.621
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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
2025/20263.141 486 682 443 789 539 202 0 0 0 0 0 0
Totale 16.850