IRIS Institutional Research Information System - OPENBS Open Archive UniBS

GAZZURELLI, Luisa
 Distribuzione geografica
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Continente #
NA - Nord America 1.140
EU - Europa 494
AS - Asia 181
AF - Africa 2
OC - Oceania 2
SA - Sud America 1
Totale 1.820
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Nazione #
US - Stati Uniti d'America 1.138
PL - Polonia 200
CN - Cina 98
IT - Italia 90
UA - Ucraina 65
HK - Hong Kong 41
FI - Finlandia 36
DE - Germania 34
IE - Irlanda 23
SG - Singapore 21
GB - Regno Unito 18
VN - Vietnam 12
SE - Svezia 8
FR - Francia 5
RO - Romania 4
IN - India 3
NL - Olanda 3
AU - Australia 2
BE - Belgio 2
CA - Canada 2
GR - Grecia 2
HR - Croazia 2
KZ - Kazakistan 2
TR - Turchia 2
AZ - Azerbaigian 1
BR - Brasile 1
ES - Italia 1
JP - Giappone 1
MU - Mauritius 1
PT - Portogallo 1
ZA - Sudafrica 1
Totale 1.820
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Città #
Warsaw 200
Fairfield 192
Ashburn 120
Seattle 100
Woodbridge 98
Chandler 84
Wilmington 71
Cambridge 70
Houston 69
Jacksonville 58
New York 49
Brescia 44
Princeton 42
Hong Kong 40
Helsinki 34
Ann Arbor 28
Beijing 28
Dublin 23
Nanjing 18
Shanghai 16
Dong Ket 12
Singapore 11
Dearborn 9
San Diego 9
Des Moines 8
Changsha 6
Jinan 5
Shenyang 5
Alessandria 4
Hebei 4
London 4
Boardman 3
Casoria 3
Lancaster 3
Nanchang 3
Redmond 3
San Francisco 3
Astana 2
Brussels 2
Castenedolo 2
Chicago 2
Cluj-Napoca 2
Core 2
Florence 2
Fort Worth 2
Guangzhou 2
Haikou 2
Islington 2
Kilburn 2
Lappeenranta 2
Monmouth Junction 2
Munich 2
Olginate 2
Phoenix 2
Rome 2
San Benedetto Po 2
Taiyuan 2
Toronto 2
Verona 2
Washington 2
Amsterdam 1
Augusta 1
Borås 1
Brooklyn 1
Central 1
Centurion 1
Duncan 1
Ergolding 1
Frankfurt am Main 1
Glendale 1
Hangzhou 1
Iasi 1
Jiaxing 1
Kocaeli 1
Lanzhou 1
Leawood 1
Magdeburg 1
Melbourne 1
Mountain View 1
New Bedfont 1
Ningbo 1
Orange 1
Pune 1
Redwood City 1
Rho 1
San Mateo 1
Sydney 1
Taizhou 1
Taormina 1
Tianjin 1
Tokyo 1
Vigo 1
Totale 1.557
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Nome #
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 186
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. 183
The RAC2-PI3K axis regulates human NK cell maturation and function 150
CTLA-4 regulates human Natural Killer cell effector functions 131
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 124
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 122
The atypical receptor CCRL2 is required for CXCR2-dependent neutrophil recruitment and tissue damage 113
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 99
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential 65
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
Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS) 48
RAC2 and primary human immune deficiencies 47
The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019) 42
Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations 40
Fatal SARS-CoV-2 infection in a male patient with Good's syndrome 38
Lack of DOCK8 impairs the primary biologic functions of human NK cells and abrogates CCR7 surface expression in a WASP-independent manner 32
A CVID-associated variant in the ciliogenesis protein CCDC28B disrupts immune synapse assembly 30
null 28
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 28
Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations 22
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 21
Paediatric MAS/HLH caused by a novel monoallelic activating mutation in p110δ 20
null 12
Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations 3
Rituximab Monotherapy Is Effective as First-Line Treatment for Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) in CVID Patients 2
Totale 1.882
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Categoria #
all - tutte 9.101
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 9.101
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020440 46 21 22 37 34 44 43 48 42 53 30 20
2020/2021545 14 23 23 145 34 26 22 68 38 67 57 28
2021/2022251 19 43 6 11 6 7 10 13 25 33 23 55
2022/2023209 34 2 4 14 19 51 3 33 21 0 13 15
2023/2024265 16 5 34 19 17 72 10 17 44 0 3 28
2024/20252 2 0 0 0 0 0 0 0 0 0 0 0
Totale 1.882