IRIS Institutional Research Information System - OPENBS Open Archive UniBS

LORENZINI, TIZIANA
 Distribuzione geografica
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Continente #
NA - Nord America 914
EU - Europa 364
AS - Asia 175
AF - Africa 2
OC - Oceania 1
Totale 1.456
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Nazione #
US - Stati Uniti d'America 912
PL - Polonia 130
CN - Cina 96
UA - Ucraina 66
IT - Italia 58
SG - Singapore 36
FI - Finlandia 34
DE - Germania 29
GB - Regno Unito 17
HK - Hong Kong 15
IE - Irlanda 13
TR - Turchia 12
VN - Vietnam 8
FR - Francia 6
SE - Svezia 6
IN - India 3
BE - Belgio 2
CA - Canada 2
ID - Indonesia 2
RO - Romania 2
AU - Australia 1
GR - Grecia 1
IL - Israele 1
IR - Iran 1
JP - Giappone 1
MU - Mauritius 1
ZA - Sudafrica 1
Totale 1.456
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Città #
Fairfield 158
Warsaw 130
Ashburn 87
Woodbridge 86
Houston 76
Seattle 74
Cambridge 64
Wilmington 61
Jacksonville 57
Chandler 47
Ann Arbor 31
Helsinki 31
Singapore 30
Princeton 26
New York 25
Nanjing 24
Beijing 19
Brescia 16
Dearborn 15
Hong Kong 14
Dublin 13
Istanbul 11
Shanghai 11
Dong Ket 8
Des Moines 7
Verona 7
Changsha 6
Jinan 6
Lancaster 6
London 6
Nanchang 6
Rome 5
San Diego 4
Shenyang 4
Casoria 3
Haikou 3
Jiaxing 3
Marina Di Gioiosa Jonica 3
San Francisco 3
Boardman 2
Bologna 2
Brussels 2
Jakarta 2
Munich 2
Ningbo 2
Olginate 2
Phoenix 2
Pune 2
Taiyuan 2
Tianjin 2
Toronto 2
Carrù 1
Central 1
Chicago 1
Como 1
Duncan 1
Esslingen am Neckar 1
Frankfurt am Main 1
Fuzhou 1
Guangzhou 1
Hebei 1
Iasi 1
Isfahan 1
Islington 1
Jerusalem 1
Kunming 1
Los Angeles 1
Melbourne 1
Milan 1
Monmouth Junction 1
Montichiari 1
New Bedfont 1
Norwalk 1
Redwood City 1
Rio Saliceto 1
San Mateo 1
Santa Clara 1
Shaoxing 1
Southwark 1
Torino 1
Valea Lupului 1
Zhengzhou 1
Totale 1.241
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Nome #
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 191
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 190
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 128
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 127
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 120
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 118
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 104
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 104
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 104
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 102
STAT mutations as program switchers: Turning primary immunodeficiencies into autoimmune diseases 102
Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgE 59
Corrigendum to: “Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET)” [Vaccine 36 (2018) Pages 3541–3542](S0264410X1830121X)(10.1016/j.vaccine.2018.01.061) 57
Totale 1.506
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Categoria #
all - tutte 6.629
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 6.629
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020313 0 0 0 0 36 52 44 51 40 50 21 19
2020/2021352 8 25 8 33 20 20 32 85 26 52 25 18
2021/2022149 19 8 2 11 0 10 3 7 11 33 15 30
2022/2023106 18 1 3 8 9 27 1 16 12 0 4 7
2023/2024146 12 4 19 16 2 41 6 10 15 0 4 17
2024/202557 3 1 0 37 16 0 0 0 0 0 0 0
Totale 1.506