IRIS Institutional Research Information System - OPENBS Open Archive UniBS

BARONIO, Manuela
 Distribuzione geografica
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Continente #
NA - Nord America 1.650
EU - Europa 517
AS - Asia 266
AF - Africa 3
OC - Oceania 1
SA - Sud America 1
Totale 2.438
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Nazione #
US - Stati Uniti d'America 1.643
CN - Cina 204
UA - Ucraina 168
IT - Italia 101
DE - Germania 67
FI - Finlandia 55
GB - Regno Unito 51
HK - Hong Kong 41
IE - Irlanda 28
FR - Francia 23
IN - India 12
BE - Belgio 7
CA - Canada 7
NL - Olanda 5
RO - Romania 4
MU - Mauritius 3
SE - Svezia 3
TR - Turchia 3
HR - Croazia 2
IR - Iran 2
SG - Singapore 2
AU - Australia 1
AZ - Azerbaigian 1
BR - Brasile 1
HU - Ungheria 1
JP - Giappone 1
PL - Polonia 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 2.438
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Città #
Fairfield 222
Woodbridge 201
Jacksonville 125
Ashburn 119
Chandler 111
Wilmington 106
Ann Arbor 105
Houston 105
Seattle 97
Cambridge 94
New York 77
Beijing 56
Princeton 52
Brescia 48
Nanjing 47
Hong Kong 40
Helsinki 34
Dublin 28
San Diego 17
Shenyang 17
Lancaster 15
Changsha 14
Des Moines 11
Dearborn 9
Nanchang 9
Shanghai 9
San Mateo 8
Haikou 7
London 7
Milan 7
Taizhou 7
Jiaxing 6
Leawood 6
Hangzhou 5
Tianjin 5
Brussels 4
Hebei 4
Jinan 4
San Francisco 4
Toronto 4
Frankfurt am Main 3
Montichiari 3
Ningbo 3
Orange 3
Turin 3
Augusta 2
Boardman 2
Chiswick 2
Cluj-Napoca 2
Core 2
Hanover 2
Los Angeles 2
Mantova 2
Markham 2
Norwalk 2
Redwood City 2
Rome 2
Waanrode 2
Wandsworth 2
Zhengzhou 2
Amsterdam 1
Bratislava 1
Budapest 1
Central 1
Changchun 1
Chicago 1
Falkenstein 1
Fuzhou 1
Gent 1
Glendale 1
Grosio 1
Gunzenhausen 1
Hyderabad 1
Iasi 1
Isfahan 1
Jesi 1
Kilburn 1
Kunming 1
Lanzhou 1
Las Vegas 1
Melbourne 1
Nave 1
New Bedfont 1
New Delhi 1
Nichelino 1
Ottawa 1
Poncarale 1
Prato 1
Prescot 1
Sabz 1
Silvi 1
Taiyuan 1
Tokyo 1
Valea Lupului 1
Verona 1
Walnut 1
Warsaw 1
Xian 1
Totale 1.929
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Nome #
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 136
CTLA-4 regulates human Natural Killer cell effector functions 129
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
HIV-1 matrix protein p17 increases the production of proinflammatory cytokines and counteracts IL-4 activity by binding to a cellular receptor. 119
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
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 110
Espansione di una rara popolazione linfocitaria con fenotipo CD8+CD28-CD11b- in pazienti sieropositivi per HIV. 103
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 100
Beta2 integrins are required for follicular helper T cell differentiation in humans 99
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 98
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 95
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 93
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
Proteus syndrome: evaluation of the immunological profile 80
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 78
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
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
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
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 56
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 20
Totale 2.533
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Categoria #
all - tutte 10.491
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 10.491
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019127 0 0 0 0 0 0 0 0 0 0 66 61
2019/2020673 93 22 25 72 38 72 65 74 47 101 27 37
2020/2021438 5 49 11 60 13 44 21 44 53 48 77 13
2021/2022274 26 29 6 15 1 10 9 20 13 48 24 73
2022/2023292 37 2 3 24 30 63 0 43 57 2 9 22
2023/2024250 20 9 38 17 13 87 7 17 41 1 0 0
Totale 2.533