IRIS Institutional Research Information System - OPENBS Open Archive UniBS

MORATTO, Daniele
 Distribuzione geografica
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Continente #
NA - Nord America 4.891
AS - Asia 2.285
EU - Europa 1.981
SA - Sud America 315
AF - Africa 51
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 2
Totale 9.533
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Nazione #
US - Stati Uniti d'America 4.803
SG - Singapore 869
CN - Cina 644
PL - Polonia 343
DE - Germania 305
IT - Italia 302
UA - Ucraina 266
HK - Hong Kong 264
BR - Brasile 253
FI - Finlandia 213
VN - Vietnam 172
GB - Regno Unito 133
FR - Francia 107
RU - Federazione Russa 84
TR - Turchia 81
IN - India 72
IE - Irlanda 59
CA - Canada 50
BD - Bangladesh 45
SE - Svezia 33
ES - Italia 31
AR - Argentina 26
MX - Messico 25
ZA - Sudafrica 22
AT - Austria 20
IQ - Iraq 19
CZ - Repubblica Ceca 18
NL - Olanda 18
JP - Giappone 16
ID - Indonesia 12
IL - Israele 11
PK - Pakistan 11
UZ - Uzbekistan 10
EC - Ecuador 9
AZ - Azerbaigian 8
BE - Belgio 8
NG - Nigeria 8
AU - Australia 7
PE - Perù 7
VE - Venezuela 7
CO - Colombia 6
LT - Lituania 6
PH - Filippine 6
RO - Romania 6
SA - Arabia Saudita 6
AE - Emirati Arabi Uniti 5
CL - Cile 5
JO - Giordania 5
MA - Marocco 5
DO - Repubblica Dominicana 4
GR - Grecia 4
HR - Croazia 4
KZ - Kazakistan 4
PT - Portogallo 4
CH - Svizzera 3
DK - Danimarca 3
DZ - Algeria 3
EG - Egitto 3
IR - Iran 3
KE - Kenya 3
LB - Libano 3
OM - Oman 3
AL - Albania 2
BY - Bielorussia 2
EU - Europa 2
HN - Honduras 2
JM - Giamaica 2
KG - Kirghizistan 2
LA - Repubblica Popolare Democratica del Laos 2
MU - Mauritius 2
NP - Nepal 2
PA - Panama 2
PS - Palestinian Territory 2
TN - Tunisia 2
AM - Armenia 1
AO - Angola 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CI - Costa d'Avorio 1
CY - Cipro 1
ET - Etiopia 1
GT - Guatemala 1
HU - Ungheria 1
KH - Cambogia 1
KR - Corea 1
KW - Kuwait 1
LK - Sri Lanka 1
LV - Lettonia 1
MD - Moldavia 1
MK - Macedonia 1
MT - Malta 1
MY - Malesia 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PR - Porto Rico 1
SK - Slovacchia (Repubblica Slovacca) 1
UY - Uruguay 1
Totale 9.533
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Città #
Ashburn 523
Singapore 485
Fairfield 391
Warsaw 334
San Jose 301
Houston 265
Woodbridge 264
Hong Kong 261
Chandler 202
Jacksonville 195
New York 187
Seattle 183
Beijing 168
Cambridge 167
Wilmington 156
Ann Arbor 148
The Dalles 136
Helsinki 130
Los Angeles 125
Munich 110
Dallas 105
Princeton 101
Brescia 88
Chicago 66
Lauterbourg 62
Dublin 59
Istanbul 59
Des Moines 52
Ho Chi Minh City 51
Nanjing 51
Turku 51
Shanghai 45
Buffalo 40
San Francisco 39
Hanoi 37
São Paulo 37
Santa Clara 36
Milan 33
Dearborn 30
Changsha 29
Redondo Beach 27
Chennai 26
Council Bluffs 26
Orem 26
Lancaster 24
London 24
Boardman 23
Poplar 23
Phoenix 22
Dong Ket 20
Montreal 20
Moscow 20
Salt Lake City 19
Atlanta 18
Denver 18
Hebei 17
Nanchang 16
Shenyang 16
Brooklyn 15
Frankfurt am Main 15
Jinan 15
San Diego 15
Elk Grove Village 14
Johannesburg 14
Stockholm 14
Tokyo 14
Toronto 14
Hangzhou 13
Boston 12
Nuremberg 12
Miami 11
Mumbai 11
Tampa 11
Ankara 10
Baghdad 10
Brno 10
Haikou 10
Charlotte 9
Cremona 9
Manchester 9
Tashkent 9
Tianjin 9
Belo Horizonte 8
Haiphong 8
Verona 8
Vienna 8
Abuja 7
Amsterdam 7
Assemini 7
Brasília 7
Jakarta 7
Lanzhou 7
Mexico City 7
Redwood City 7
Rio de Janeiro 7
Romola 7
Zhengzhou 7
Baku 6
Barcelona 6
Brussels 6
Totale 6.599
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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 286
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 274
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 266
A distinct human cell type expressing MHCII and RORγt with dual characteristics of dendritic cells and type 3 innate lymphoid cells 258
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 248
Collapse of the Plasmacytoid Dendritic Cells compartment in advanced cutaneous melanomas by components of the tumor cell secretome 231
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 205
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 204
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 194
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 185
Stem cell transplantation for the Wiskott-Aldrich syndrome: a single-center experience confirms efficacy of matched unrelated donor transplantation 184
Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia 183
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 183
α- and β-Papillomavirus infection in a young patient with an unclassified primary T-cell immunodeficiency and multiple mucosal and cutaneous lesions 181
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 180
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency 179
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 176
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 174
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 173
Functional defects of dendritic cells in patients with CD40 deficiency. 169
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 168
Immune response in children with COVID-19 is characterized by lower levels of T-cell activation than infected adults 167
Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. 159
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. 155
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity 152
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 151
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 143
Plasmacytoid dendritic cell impairment in metastatic melanoma by lactic acidosis 139
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 138
Low WASp expression in patients with no apparent mutation in the WASP gene 137
Flow Cytometry Identifies Risk Factors and Dynamic Changes in Patients with COVID-19 137
CASE REPORT: IDENTIFICATION OF A PATIENT WITH FAMILIAR MUTATIONS AFFECTING BOTH WASP AND FOXP3 GENES 136
The Wiskott-Aldrich syndrome: From genotype-phenotype correlation to treatment 132
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 132
Transient Decrease of Circulating and Tissular Dendritic Cells in Patients With Mycobacterial Disease and With Partial Dominant IFNγR1 Deficiency 131
Long-term outcome and lineage-specific chimerism in 194 Wiskott-Aldrich Syndrome patients treated by hematopoietic celltransplantation between 1980-2009: an international collaborative study. 130
P1450: AUTOLOGOUS STEM CELL TRANSPLANTATION INDUCES HIGHER LEVEL OF EXHAUSTED T-CELLS IN DLBCL PATIENTS BEFORE LEUKAPHERESIS FOR CAR-T CELL THERAPY 128
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 127
Multi-lineage analysis of X-inactivation in female carriers of genetic alterations in the Wiskott-Aldrich syndrome protein (WASP) gene locus 125
Two X-linked agammaglobulinemia patients develop pneumonia as COVID-19 manifestation but recover 125
WASP-WIP DEFICIENCIES: NEW INSIGHTS IN WASP-WIP INTERACTION 123
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency 122
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 120
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 116
Immunologic characterization of a immunosuppressed multiple sclerosis patient that recovered from SARS-CoV-2 infection 113
Proteus syndrome: evaluation of the immunological profile 109
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections. 108
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 106
Timely Leukapheresis May Interfere with the “Fitness” of Lymphocytes Collected for CAR-T Treatment in High Risk DLBCL Patients 105
Multisystem autoimmune disease caused by increased STAT3 phosphorylation and dysregulated gene expression 105
Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis 105
Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related Malignancies 104
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 97
Immune Reconstitution after Allogenic Stem Cell Transplantation in Patients with Myelofibrosis 95
Longitudinal Characterization of Immune Response in a Cohort of Children Hospitalized with Multisystem Inflammatory Syndrome 91
Identical EP300 variant leading to Rubinstein–Taybi syndrome with different clinical and immunologic phenotype 90
Clinical and transcriptomic characteristics of a novel SMARCD2 mutation that disrupts neutrophil maturation and function 86
Rituximab Monotherapy Is Effective as First-Line Treatment for Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) in CVID Patients 86
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections 85
Case Report: A Case of X-Linked Agammaglobulinemia With High Serum IgE Levels and Allergic Rhinitis 85
Abnormal B-Cell Maturation and Increased Transitional B Cells in CBL Syndrome 83
Plasmacytoid Dendritic Cells Depletion and Elevation of IFN-γ Dependent Chemokines CXCL9 and CXCL10 in Children With Multisystem Inflammatory Syndrome 81
Reduced G protein signaling despite impaired internalization and β-arrestin recruitment in patients carrying a CXCR4Leu317fsX3 mutation causing WHIM syndrome 79
Inflammatory pathways signal transducers analysis in iPSC-derived neurons and 3D cerebral organoids 76
Patients with STAT1 Gain-of-function Mutations Display Increased Apoptosis which is Reversed by the JAK Inhibitor Ruxolitinib 73
Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations 72
Transient Decrease of Circulating and Tissular Dendritic Cells in Patients With Mycobacterial Disease and With Partial Dominant IFNγR1 Deficiency 70
Pseudomonas aeruginosa severe skin infection in a toddler with X-linked agammaglobulinemia due to a novel BTK mutation 62
Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations 58
Mapping of RORγt+ dendritic cells in human tissues establishes their preferential niche in adult lymph nodes 41
Low Th17 cells in patients with cystic fibrosis and allergic broncho-pulmonary aspergillosis 9
Long-term outcome in Wiskott-Aldrich syndrome and X-linked thrombocytopenia patients: an observational -prospective multi-center study of the Italian Primary Immune Deficiency Network (IPINET) 6
Totale 9.706
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Categoria #
all - tutte 43.742
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 43.742
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202141 0 0 0 0 0 0 0 0 0 0 0 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
2024/20251.722 23 17 15 210 125 109 131 96 209 114 445 228
2025/20263.239 306 349 242 460 409 274 508 120 163 286 120 2
Totale 9.706