IRIS Institutional Research Information System - OPENBS Open Archive UniBS

LORENZINI, TIZIANA
 Distribuzione geografica
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Continente #
NA - Nord America 892
EU - Europa 359
AS - Asia 124
AF - Africa 2
OC - Oceania 1
Totale 1.378
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Nazione #
US - Stati Uniti d'America 890
PL - Polonia 130
CN - Cina 93
UA - Ucraina 66
IT - Italia 56
FI - Finlandia 33
DE - Germania 27
GB - Regno Unito 17
HK - Hong Kong 15
IE - Irlanda 13
VN - Vietnam 8
FR - Francia 6
SE - Svezia 6
IN - India 3
BE - Belgio 2
CA - Canada 2
RO - Romania 2
AU - Australia 1
GR - Grecia 1
IL - Israele 1
IR - Iran 1
JP - Giappone 1
MU - Mauritius 1
SG - Singapore 1
TR - Turchia 1
ZA - Sudafrica 1
Totale 1.378
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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 30
Princeton 26
New York 25
Nanjing 24
Beijing 19
Brescia 16
Dearborn 15
Hong Kong 14
Dublin 13
Dong Ket 8
Shanghai 8
Des Moines 7
Changsha 6
Jinan 6
Lancaster 6
London 6
Nanchang 6
Rome 5
Verona 5
San Diego 4
Shenyang 4
Casoria 3
Haikou 3
Jiaxing 3
Marina Di Gioiosa Jonica 3
San Francisco 3
Bologna 2
Brussels 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
Melbourne 1
Milan 1
Monmouth Junction 1
Montichiari 1
New Bedfont 1
Norwalk 1
Redwood City 1
Rio Saliceto 1
San Mateo 1
Shaoxing 1
Southwark 1
Torino 1
Valea Lupului 1
Zhengzhou 1
Totale 1.186
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Nome #
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 183
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 182
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
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) 112
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 110
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 100
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 99
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 99
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 98
STAT mutations as program switchers: Turning primary immunodeficiencies into autoimmune diseases 96
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 55
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) 53
Totale 1.428
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Categoria #
all - tutte 5.492
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 5.492
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201997 0 0 0 0 0 0 0 0 0 0 51 46
2019/2020466 56 23 23 51 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
2023/2024125 12 4 19 16 2 41 6 10 15 0 0 0
Totale 1.428