IRIS Institutional Research Information System - OPENBS Open Archive UniBS

LOUGARIS, VASSILIOS
 Distribuzione geografica
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Continente #
NA - Nord America 7.061
EU - Europa 2.585
AS - Asia 1.094
Continente sconosciuto - Info sul continente non disponibili 9
OC - Oceania 8
AF - Africa 7
SA - Sud America 5
Totale 10.769
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Nazione #
US - Stati Uniti d'America 7.049
CN - Cina 756
PL - Polonia 714
UA - Ucraina 650
IT - Italia 297
DE - Germania 295
HK - Hong Kong 243
FI - Finlandia 194
GB - Regno Unito 144
IE - Irlanda 131
FR - Francia 75
IN - India 27
VN - Vietnam 26
SE - Svezia 23
NL - Olanda 14
BE - Belgio 13
RU - Federazione Russa 13
CA - Canada 12
SG - Singapore 10
EU - Europa 9
JP - Giappone 9
AU - Australia 8
TR - Turchia 8
RO - Romania 6
ES - Italia 4
IR - Iran 4
MU - Mauritius 4
BR - Brasile 3
AE - Emirati Arabi Uniti 2
AR - Argentina 2
CH - Svizzera 2
DZ - Algeria 2
HR - Croazia 2
ID - Indonesia 2
KZ - Kazakistan 2
SK - Slovacchia (Repubblica Slovacca) 2
AZ - Azerbaigian 1
BD - Bangladesh 1
DK - Danimarca 1
GR - Grecia 1
HU - Ungheria 1
JO - Giordania 1
LV - Lettonia 1
MN - Mongolia 1
MY - Malesia 1
PT - Portogallo 1
RS - Serbia 1
ZA - Sudafrica 1
Totale 10.769
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Città #
Fairfield 1.220
Woodbridge 852
Warsaw 714
Ashburn 620
Houston 588
Jacksonville 501
Seattle 477
Cambridge 465
Wilmington 434
Ann Arbor 370
Chandler 303
Princeton 245
Hong Kong 242
New York 217
Beijing 207
Nanjing 150
Brescia 131
Dublin 129
Helsinki 127
San Diego 63
Des Moines 50
Nanchang 46
Shenyang 43
Dearborn 42
Shanghai 42
Changsha 39
Lancaster 37
Hebei 36
Jinan 30
Jiaxing 27
Dong Ket 26
London 25
Milan 21
Tianjin 20
Haikou 16
San Francisco 14
Casoria 13
Ningbo 13
Kunming 12
Hangzhou 11
Brussels 10
Taizhou 10
Toronto 10
Zhengzhou 10
Leawood 9
Orange 9
San Mateo 9
Guangzhou 8
Redwood City 8
Norwalk 7
Phoenix 7
Verona 7
Busto Arsizio 6
Lanzhou 6
Taiyuan 6
Boardman 5
Chiswick 5
Kilburn 5
Prescot 5
Alessandria 4
Frankfurt am Main 4
Rome 4
Tokyo 4
Acton 3
Augusta 3
Castenedolo 3
Changchun 3
Chicago 3
Falkenstein 3
Fuzhou 3
Gunzenhausen 3
Hanover 3
Los Angeles 3
Melbourne 3
Montichiari 3
Washington 3
Amsterdam 2
Astana 2
Blida 2
Bratislava 2
Brooklyn 2
Canberra 2
Castiglione Delle Stiviere 2
Cluj-Napoca 2
Core 2
Erlangen 2
Florence 2
Hefei 2
Kocaeli 2
Lappeenranta 2
Mantova 2
Markham 2
Mumbai 2
New Bedfont 2
New Delhi 2
Nürnberg 2
Olginate 2
Palazzolo 2
Rezzato 2
San Benedetto Po 2
Totale 8.863
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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 280
Congenital cystic lung disease: prenatal ultrasound and postnatal multidetector computer tomography evaluation. Correlation with surgical and pathological data 280
NFKB1 regulates human NK cell maturation and effector functions 273
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 183
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 183
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 182
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 178
The RAC2-PI3K axis regulates human NK cell maturation and function 149
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 136
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 135
CTLA-4 regulates human Natural Killer cell effector functions 129
CONGENITAL CYSTIC LUNG DISEASE: PRENATAL ULTRASOUND AND POSTNATAL MULTIDETECTOR COMPUTER TOMOGRAPHY EVALUATION. CORRELATION WITH SURGICAL AND PATHOLOGICAL DATA 125
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 124
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 122
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 121
BAFF-R mutations in Good's syndrome. 121
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 120
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 119
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency 117
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 115
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 114
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 112
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 112
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 110
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 110
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 108
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 106
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. 105
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 105
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 104
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 104
Diagnostics of primary immunodeficiencies through next-generation sequencing 102
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 101
Allergen immunotherapy, routes of administration and cytokine networks: An update 101
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 100
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 100
Beta2 integrins are required for follicular helper T cell differentiation in humans 99
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 99
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 99
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 99
Importance of B cell co-stimulation in CD4(+) T cell differentiation: X-linked agammaglobulinaemia, a human model. 98
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 98
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 98
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency. 97
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 97
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 96
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 96
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 96
The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers 96
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 95
Breastfeeding and IL-10 levels in children affected by cow's milk protein allergy: A restrospective study 94
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia. 94
Regulation of the germinal center gene program by interferon (IFN) regulatory factor 8/IFN consensus sequence-binding protein. 93
Mutational analysis of human BAFF Receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency. 93
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 93
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. 92
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study 92
Thymic and bone marrow output in patients with common variable immunodeficiency 91
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 91
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis. 91
Screening of functional and positional candidate genes in families with common variable immunodeficiency 90
Clinical, immunological, and molecular features of typical and atypical severe combined immunodeficiency: Report of the italian primary immunodeficiency network 90
Double-blind, placebo-controlled, randomized trial on low-dose azithromycin prophylaxis in patients with primary antibody deficiencies 90
Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency 89
Mutations of the Igb gene cause agammaglobulinemia in man 89
Circulating follicular helper and follicular regulatory T cells are severely compromised in human CD40 deficiency: A case report 89
Mutational analysis of human BLyS in patients with common variable immunodeficiency. 88
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients. 88
Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features. 84
Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: Neuroimaging and clinical findings 84
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency 83
Proteus syndrome: evaluation of the immunological profile 80
Different clinical and immunological presentation of Ataxia Telangiectasia within the same family. 79
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 78
CXCL12 mediates aberrant costimulation of B lymphocytes in warts, hypogammaglobulinemia, infections, myelokathexis immunodeficiency 76
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 75
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations 75
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency 75
Maternal T-cell engraftment impedes with diagnosis of a SCID-ADA patient 75
Screening of 181 Patients With Antibody Deficiency for Deficiency of Adenosine Deaminase 2 Sheds New Light on the Disease in Adulthood 73
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects 72
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 70
Response to the Letter to the Editor Regarding “Functional evaluation of natural killer cell cytotoxic activity in NFKB-2 mutated patients” 69
Clinical manifestations and gastrointestinal pathology in 40 patients with autoimmune enteropathy 69
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. 66
P85α is an intrinsic regulator of human natural killer cell effector functions 66
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 63
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study 61
Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency 59
Characterization of the clinical and immunological phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations 58
Long term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality 57
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 56
Expansion of somatically reverted memory CD8+ T cells in X-linked lymphoproliferative disease is due to selective pressure from Epstein Barr virus. 54
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Diagnostic approach of hypogammaglobulinemia in infancy 53
GENETIC ANALYSIS OF THE TNFRSF13B GENE IN A LARGE ITALIAN CVID COHORT 49
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 49
Glossotillomania as cause of Riga-Fede syndrome 48
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study 48
• Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes. 47
Totale 9.991
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Categoria #
all - tutte 48.070
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 48.070
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019648 0 0 0 0 0 0 0 0 0 0 339 309
2019/20203.118 379 126 140 339 205 316 302 340 258 403 132 178
2020/20212.363 50 201 58 356 90 230 136 306 232 336 256 112
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
2023/2024970 71 25 116 85 44 270 35 56 256 12 0 0
Totale 11.086