IRIS Institutional Research Information System - OPENBS Open Archive UniBS

MORATTO, Daniele
 Distribuzione geografica
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Continente #
NA - Nord America 2.807
EU - Europa 1.271
AS - Asia 545
OC - Oceania 6
SA - Sud America 3
AF - Africa 2
Continente sconosciuto - Info sul continente non disponibili 2
Totale 4.636
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Nazione #
US - Stati Uniti d'America 2.799
PL - Polonia 318
CN - Cina 314
UA - Ucraina 252
IT - Italia 197
DE - Germania 166
FI - Finlandia 113
HK - Hong Kong 112
GB - Regno Unito 76
SG - Singapore 74
IE - Irlanda 55
FR - Francia 23
VN - Vietnam 20
SE - Svezia 19
IN - India 13
CZ - Repubblica Ceca 11
RU - Federazione Russa 10
BE - Belgio 8
CA - Canada 8
AU - Australia 6
NL - Olanda 6
RO - Romania 5
ES - Italia 4
TR - Turchia 4
JP - Giappone 3
BR - Brasile 2
EU - Europa 2
GR - Grecia 2
HR - Croazia 2
MU - Mauritius 2
PT - Portogallo 2
AZ - Azerbaigian 1
CL - Cile 1
HU - Ungheria 1
ID - Indonesia 1
IL - Israele 1
IR - Iran 1
PS - Palestinian Territory 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 4.636
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Città #
Fairfield 391
Warsaw 314
Woodbridge 264
Houston 244
Ashburn 217
Chandler 202
Jacksonville 194
Seattle 175
Cambridge 167
Wilmington 155
Ann Arbor 148
New York 114
Hong Kong 110
Princeton 101
Helsinki 88
Brescia 79
Beijing 67
Dublin 55
Nanjing 51
Singapore 46
Shanghai 39
Dearborn 30
Changsha 23
Boardman 22
Des Moines 22
Lancaster 22
Dong Ket 20
Hebei 17
London 17
Nanchang 16
Shenyang 16
Jinan 15
San Diego 15
Brno 10
Haikou 10
Hangzhou 10
Milan 10
San Francisco 9
Munich 8
Tianjin 8
Assemini 7
Redwood City 7
Romola 7
Verona 7
Brussels 6
Jiaxing 6
Ningbo 6
Taiyuan 6
Toronto 6
Lanzhou 5
Leawood 5
Los Angeles 5
Barlassina 4
Casoria 4
Chicago 4
Norwalk 4
Rende 4
Rome 4
Sydney 4
Aubervilliers 3
Barcelona 3
Falkenstein 3
Kunming 3
Leipzig 3
New Bedfont 3
Phoenix 3
Zhengzhou 3
Amsterdam 2
Arezzo 2
Athens 2
Central 2
Cluj-Napoca 2
Core 2
Florence 2
Genoa 2
Guangzhou 2
Kilburn 2
Kocaeli 2
Lappeenranta 2
Mantova 2
Mazzano 2
Melbourne 2
Monmouth Junction 2
Montichiari 2
Nürnberg 2
Olginate 2
Orange 2
Palermo 2
Pavia 2
Prad am Stilfser Joch 2
Pune 2
Stuttgart 2
Waanrode 2
Acton 1
Airdrie 1
Augusta 1
Baotou 1
Borgosatollo 1
Bosio 1
Bratislava 1
Totale 3.705
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Nome #
Evaluation of a novel human IgG1 anti-claudin3 antibody that specifically recognizes its aberrantly localized antigen in ovarian cancer cells and that is suitable for selective drug delivery 219
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
Collapse of the Plasmacytoid Dendritic Cells compartment in advanced cutaneous melanomas by components of the tumor cell secretome 142
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 139
α- and β-Papillomavirus infection in a young patient with an unclassified primary T-cell immunodeficiency and multiple mucosal and cutaneous lesions 129
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 124
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 123
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 122
Functional defects of dendritic cells in patients with CD40 deficiency. 120
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 120
Stem cell transplantation for the Wiskott-Aldrich syndrome: a single-center experience confirms efficacy of matched unrelated donor transplantation 117
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 116
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 112
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency 111
Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia 110
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. 106
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 101
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 101
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 99
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 99
Immune response in children with COVID-19 is characterized by lower levels of T-cell activation than infected adults 94
The Wiskott-Aldrich syndrome: From genotype-phenotype correlation to treatment 93
Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. 90
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity 82
Proteus syndrome: evaluation of the immunological profile 81
Plasmacytoid dendritic cell impairment in metastatic melanoma by lactic acidosis 80
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 76
Low WASp expression in patients with no apparent mutation in the WASP gene 76
PROSPECTIVE STUDY OF 84 PATIENTS WITH WISKOTT-ALDRICH SYNDROME AND X-RECESSIVE PIASTRINOPENIA: RESULTS OF THE APPLICATION OF COMMON PROTOCOL FOR DIAGNOSIS AND TREATMENT OF WAS/XLT 73
Long-term outcome and lineage-specific chimerism in 194 Wiskott-Aldrich Syndrome patients treated by hematopoietic celltransplantation between 1980-2009: an international collaborative study. 71
CASE REPORT: IDENTIFICATION OF A PATIENT WITH FAMILIAR MUTATIONS AFFECTING BOTH WASP AND FOXP3 GENES 67
WASP-WIP DEFICIENCIES: NEW INSIGHTS IN WASP-WIP INTERACTION 65
Multi-lineage analysis of X-inactivation in female carriers of genetic alterations in the Wiskott-Aldrich syndrome protein (WASP) gene locus 63
Application of common recommendations for diagnosis and treatment of Wiskott-Aldrich syndrome and X-recessive piastrinopenia: clinical and immunological characteristics of 65 patients with WAS/XLT 61
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections. 59
Flow Cytometry Identifies Risk Factors and Dynamic Changes in Patients with COVID-19 59
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 59
Transient Decrease of Circulating and Tissular Dendritic Cells in Patients With Mycobacterial Disease and With Partial Dominant IFNγR1 Deficiency 57
P1450: AUTOLOGOUS STEM CELL TRANSPLANTATION INDUCES HIGHER LEVEL OF EXHAUSTED T-CELLS IN DLBCL PATIENTS BEFORE LEUKAPHERESIS FOR CAR-T CELL THERAPY 48
Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related Malignancies 45
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency 44
Two X-linked agammaglobulinemia patients develop pneumonia as COVID-19 manifestation but recover 42
Immunologic characterization of a immunosuppressed multiple sclerosis patient that recovered from SARS-CoV-2 infection 39
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections 38
Multisystem autoimmune disease caused by increased STAT3 phosphorylation and dysregulated gene expression 38
Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis 35
Pseudomonas aeruginosa severe skin infection in a toddler with X-linked agammaglobulinemia due to a novel BTK mutation 31
Identical EP300 variant leading to Rubinstein–Taybi syndrome with different clinical and immunologic phenotype 26
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 25
Case Report: Analysis of Inflammatory Cytokines IL-6, CCL2/MCP1, CCL5/RANTES, CXCL9/MIG, and CXCL10/IP10 in a Cystic Fibrosis Patient Cohort During the First Wave of the COVID-19 Pandemic 25
Plasmacytoid Dendritic Cells Depletion and Elevation of IFN-γ Dependent Chemokines CXCL9 and CXCL10 in Children With Multisystem Inflammatory Syndrome 25
Inflammatory pathways signal transducers analysis in iPSC-derived neurons and 3D cerebral organoids 23
Timely Leukapheresis May Interfere with the “Fitness” of Lymphocytes Collected for CAR-T Treatment in High Risk DLBCL Patients 22
Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations 22
Generation of induced Pluripotent Stem Cells (UNIBSi008-A, UNIBSi008-B, UNIBSi008-C) from an Ataxia-Telangiectasia (AT) patient carrying a novel homozygous deletion in ATM gene 20
Autologous Stem Cell Transplantation before Lymphocyte Apheresis for CAR-T Cells Therapy Negatively Impacts on T-Cells Fitness and NK Cell Levels in DLBCL Patients 19
Abnormal B-Cell Maturation and Increased Transitional B Cells in CBL Syndrome 13
Reduced G protein signaling despite impaired internalization and β-arrestin recruitment in patients carrying a CXCR4Leu317fsX3 mutation causing WHIM syndrome 12
Longitudinal Characterization of Immune Response in a Cohort of Children Hospitalized with Multisystem Inflammatory Syndrome 12
Clinical and transcriptomic characteristics of a novel SMARCD2 mutation that disrupts neutrophil maturation and function 8
Patients with STAT1 Gain-of-function Mutations Display Increased Apoptosis which is Reversed by the JAK Inhibitor Ruxolitinib 7
A distinct human cell type expressing MHCII and RORγt with dual characteristics of dendritic cells and type 3 innate lymphoid cells 6
Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations 4
Rituximab Monotherapy Is Effective as First-Line Treatment for Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) in CVID Patients 2
Totale 4.799
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Categoria #
all - tutte 24.889
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 24.889
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020986 0 0 54 129 80 132 105 128 90 148 59 61
2020/2021953 22 84 49 104 65 92 59 142 90 114 91 41
2021/2022499 43 58 5 30 10 25 15 31 33 73 58 118
2022/2023526 66 14 25 33 64 125 1 58 77 4 28 31
2023/2024675 34 14 78 50 30 163 27 43 120 4 10 102
2024/202554 23 17 14 0 0 0 0 0 0 0 0 0
Totale 4.799