PLEBANI, Alessandro
 Distribuzione geografica
Continente #
NA - Nord America 17.369
EU - Europa 6.059
AS - Asia 2.614
OC - Oceania 27
Continente sconosciuto - Info sul continente non disponibili 21
AF - Africa 15
SA - Sud America 10
Totale 26.115
Nazione #
US - Stati Uniti d'America 17.341
CN - Cina 2.347
UA - Ucraina 2.221
DE - Germania 848
PL - Polonia 716
IT - Italia 534
FI - Finlandia 518
GB - Regno Unito 403
IE - Irlanda 354
FR - Francia 253
IN - India 92
SE - Svezia 83
BE - Belgio 53
TR - Turchia 45
SG - Singapore 34
VN - Vietnam 28
NL - Olanda 27
AU - Australia 25
CA - Canada 25
KR - Corea 23
EU - Europa 21
IR - Iran 13
MU - Mauritius 13
RU - Federazione Russa 13
JP - Giappone 10
BR - Brasile 7
RO - Romania 7
ES - Italia 5
HK - Hong Kong 5
CH - Svizzera 4
GR - Grecia 3
HR - Croazia 3
SK - Slovacchia (Repubblica Slovacca) 3
AR - Argentina 2
AZ - Azerbaigian 2
BD - Bangladesh 2
ID - Indonesia 2
IL - Israele 2
KZ - Kazakistan 2
MX - Messico 2
NZ - Nuova Zelanda 2
PT - Portogallo 2
SA - Arabia Saudita 2
AE - Emirati Arabi Uniti 1
BA - Bosnia-Erzegovina 1
BO - Bolivia 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EG - Egitto 1
HU - Ungheria 1
JO - Giordania 1
LV - Lettonia 1
MD - Moldavia 1
MK - Macedonia 1
MN - Mongolia 1
MY - Malesia 1
PK - Pakistan 1
RS - Serbia 1
SI - Slovenia 1
ZA - Sudafrica 1
Totale 26.115
Città #
Fairfield 2.746
Woodbridge 2.424
Houston 1.576
Jacksonville 1.559
Ashburn 1.318
Ann Arbor 1.268
Cambridge 1.091
Seattle 1.058
Wilmington 941
Warsaw 715
Princeton 645
Chandler 644
Nanjing 512
Beijing 418
New York 353
Dublin 352
Helsinki 236
Nanchang 205
Brescia 175
Shenyang 161
Des Moines 146
San Diego 137
Hebei 134
Changsha 132
Jinan 114
Tianjin 107
Lancaster 92
Milan 91
London 84
Jiaxing 82
Dearborn 80
Kunming 66
Hangzhou 63
Brussels 50
Shanghai 50
Zhengzhou 46
Lanzhou 42
Boardman 41
Verona 41
San Francisco 40
Ningbo 39
Haikou 35
Taizhou 35
Dong Ket 28
Kocaeli 28
San Mateo 27
Norwalk 23
Washington 23
Orange 20
Seongnam 19
Toronto 18
Changchun 16
Leawood 16
Augusta 15
Redwood City 15
Chiswick 14
Fuzhou 14
Guangzhou 14
Casoria 11
Taiyuan 11
Acton 10
Kilburn 10
New Bedfont 10
Prescot 10
Rome 10
Hanover 9
Ardabil 8
Sydney 8
Amsterdam 7
Bologna 7
Canberra 7
Melbourne 7
Busto Arsizio 6
Islington 6
Phoenix 6
Pune 6
Tokyo 6
Brooklyn 5
Frankfurt am Main 5
Walnut 5
Alessandria 4
Chicago 4
Gunzenhausen 4
Hamburg 4
Hefei 4
Montichiari 4
Wandsworth 4
Auburn Hills 3
Bratislava 3
Castenedolo 3
Castiglione Delle Stiviere 3
Falkenstein 3
Florence 3
Lappeenranta 3
Los Angeles 3
Markham 3
Monmouth Junction 3
Mumbai 3
Padova 3
Pavia 3
Totale 20.671
Nome #
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP 283
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations 279
NFKB1 regulates human NK cell maturation and effector functions 271
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 187
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 180
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 180
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group 176
Acral lympho-histiocytic dermatitis in X-linked agammaglobulinemia: A case report showing clonal CD8+ T cells with indolent clinical behaviour 161
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder? 157
Different molecular behavior of CD40 mutants causing hyper-IgM syndrome. 148
The RAC2-PI3K axis regulates human NK cell maturation and function 147
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 134
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease 133
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome. 129
CTLA-4 regulates human Natural Killer cell effector functions 129
Evidence for antigenic selection of large granular lymphocytes in a patient with Wiskott-Aldrich syndrome 128
T cell activity and cytokine production in X-linked agammaglobulinemia: implications for vaccination strategies 126
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 126
Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages. 125
IgG subclass deficiency in patients with Down's syndrome and aberrant hepatitis B vaccine response. 125
Pancreatitis in systemic lupus erythematosus. 125
B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen. 123
The change in Ig regulation from children to adults disconnects the correlation with the 3'RR hs1.2 polymorphism 123
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty. 123
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 121
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 120
BAFF-R mutations in Good's syndrome. 119
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease 117
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 117
Functional defects of dendritic cells in patients with CD40 deficiency. 115
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 113
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 113
Body experiences, emotional competence, and psychosocial functioning in juvenile idiopathic arthritis. 111
Profound T-cell defects in Dubowitz syndrome 111
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 110
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. 110
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects 110
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 110
A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life. 109
Western Blot technique in the serological evaluation of three LAV/HTLV III-infected Italian families. 108
Different role of secretory IgA in the pathogenesis of RAST-positive and RAST-negative atopic dermatitis. 107
Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders 107
Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients. 106
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity 106
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography 106
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency 106
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. 105
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients. 104
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration. 104
Serum immunoglobulin levels in heterozygous subjects with immunoglobulin heavy chain constant region gene deletions. 104
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content. 103
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 103
Evaluation by SDS-PAGE and immunoblotting of residual antigenicity in hydrolysed protein formulas. 103
Mycoplasma infection may complicate the clinical course of SARS-Co-V-2 associated Kawasaki-like disease in children 103
Autosomal recessive agammaglobulinemia: novel insights from mutations in Ig-beta 102
Recurrent infections with IgG2 deficiency. 102
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome: time to review diagnostic criteria? 102
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper IgM syndrome (HIGM2). 101
A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection 101
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy children. 101
Recurrent Bleedings in Newborn: A Factor VII Deficiency Case Report 101
Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterization 100
Type I interferon-dependent gene MxA in perinatal HIV-infected patients under antiretroviral therapy as marker for therapy failure and blood plasmacytoid dendritic cells depletion. 100
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunction. 100
An avidin/biotin ELISA for the measurement of serum and secretory IgD. 100
Diagnostics of primary immunodeficiencies through next-generation sequencing 100
Memory B-cell subsets as a predictive marker of outcome in hypogammaglobulinemia during infancy. 99
C4bBinding Protein (C4BP) activates B cells through the CD40 receptor. 99
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients 99
Intravenous gammaglobulin therapy for prophylaxis of infection in high-risk neonates. 99
Activity of classical and alternative pathways of complement in preterm and small for gestational age infants. 99
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations 99
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study 99
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG 98
SH2-domain mutations in STAT3 in hyper-IgE syndrome patients result in impairment of IL-10 function. 98
Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome 98
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 98
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 98
Beta2 integrins are required for follicular helper T cell differentiation in humans 98
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world 98
Recurrent extended HLA haplotypes in children with selective IgA deficiency. 97
Ontogeny of secretory immunity: levels of secretory IgA and natural antibodies in saliva 97
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency 97
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 97
BTK: 22 novel and 25 recurrent mutations in European patients with X-linked agammaglobulinemia. 96
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 96
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly 96
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency. 95
Valutazione dell'allergenicità dei peptidi contenuti negli idrolizzati delle proteine del latte vaccino 95
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. 95
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects. 95
Neurovisual Assessment in Children with Ataxia Telangiectasia 95
ICOS deficiency in patients with common variable immunodeficiency 94
The EUROclass trial: defining subgroups in common variable immunodeficiency. 94
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. 94
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. 94
Intra-erythrocyte infusion of dexamethasone reduces neurological symptoms in ataxia teleangiectasia patients: results of a phase 2 trial. 94
Impaired platelet activation in patients with hereditary deficiency of p47(phox) 94
Hyper IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination. 93
Characterization of Ig gene somatic hypermutation in the absence of activation-induced cytidine deaminase. 93
Totale 11.589
Categoria #
all - tutte 107.371
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 107.371


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20192.305 0 0 0 0 0 0 0 314 27 419 809 736
2019/20207.929 1.142 253 285 1.002 473 812 746 829 582 1.100 245 460
2020/20215.161 89 547 103 697 176 576 253 682 634 621 600 183
2021/20222.825 174 633 59 179 47 83 148 186 183 339 227 567
2022/20232.168 379 15 34 142 202 621 5 232 306 15 107 110
2023/20241.369 133 53 209 190 120 491 83 90 0 0 0 0
Totale 26.738