IRIS Institutional Research Information System - OPENBS Open Archive UniBS

GAZZURELLI, Luisa
 Distribuzione geografica
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Continente #
NA - Nord America 1.137
EU - Europa 489
AS - Asia 158
AF - Africa 2
OC - Oceania 2
SA - Sud America 1
Totale 1.789
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Nazione #
US - Stati Uniti d'America 1.135
PL - Polonia 200
CN - Cina 94
IT - Italia 88
UA - Ucraina 65
HK - Hong Kong 41
FI - Finlandia 36
DE - Germania 31
IE - Irlanda 23
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
SG - Singapore 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 1.789
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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
Dong Ket 12
Shanghai 12
Dearborn 9
San Diego 9
Des Moines 8
Changsha 6
Jinan 5
Shenyang 5
Alessandria 4
Hebei 4
London 4
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
Olginate 2
Phoenix 2
Rome 2
San Benedetto Po 2
Taiyuan 2
Toronto 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
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 1.534
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Nome #
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
The RAC2-PI3K axis regulates human NK cell maturation and function 149
CTLA-4 regulates human Natural Killer cell effector functions 129
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 121
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 120
The atypical receptor CCRL2 is required for CXCR2-dependent neutrophil recruitment and tissue damage 112
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 63
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
RAC2 and primary human immune deficiencies 47
Complete CD95/FAS deficiency due to complex homozygous germline TNFRSF6 mutations in an adult patient with mild autoimmune lymphoproliferative syndrome (ALPS) 47
The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019) 41
Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations 39
Fatal SARS-CoV-2 infection in a male patient with Good's syndrome 36
Lack of DOCK8 impairs the primary biologic functions of human NK cells and abrogates CCR7 surface expression in a WASP-independent manner 31
null 28
A CVID-associated variant in the ciliogenesis protein CCDC28B disrupts immune synapse assembly 28
Activated Phosphoinositide 3-Kinase Delta Syndrome 1: Clinical and Immunological Data from an Italian Cohort of Patients 26
Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations 21
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 20
Paediatric MAS/HLH caused by a novel monoallelic activating mutation in p110δ 19
null 12
Totale 1.849
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Categoria #
all - tutte 8.493
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 8.493
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201990 0 0 0 0 0 0 0 0 0 0 44 46
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
2023/2024234 16 5 34 19 17 72 10 17 44 0 0 0
Totale 1.849