MORATTO, Daniele
 Distribuzione geografica
Continente #
NA - Nord America 3.280
EU - Europa 1.591
AS - Asia 1.193
SA - Sud America 124
AF - Africa 11
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 2
Totale 6.208
Nazione #
US - Stati Uniti d'America 3.260
SG - Singapore 411
CN - Cina 388
PL - Polonia 324
UA - Ucraina 253
DE - Germania 245
IT - Italia 243
HK - Hong Kong 232
FI - Finlandia 169
BR - Brasile 110
GB - Regno Unito 83
RU - Federazione Russa 76
TR - Turchia 67
IE - Irlanda 57
FR - Francia 40
VN - Vietnam 21
SE - Svezia 20
IN - India 19
AT - Austria 18
CZ - Repubblica Ceca 14
CA - Canada 13
NL - Olanda 10
AR - Argentina 8
BE - Belgio 8
ES - Italia 8
ID - Indonesia 8
IL - Israele 7
AU - Australia 6
BD - Bangladesh 5
MX - Messico 5
RO - Romania 5
IQ - Iraq 4
PT - Portogallo 4
UZ - Uzbekistan 4
AE - Emirati Arabi Uniti 3
AZ - Azerbaigian 3
GR - Grecia 3
HR - Croazia 3
JP - Giappone 3
ZA - Sudafrica 3
CH - Svizzera 2
CL - Cile 2
DK - Danimarca 2
DZ - Algeria 2
EG - Egitto 2
EU - Europa 2
IR - Iran 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
MU - Mauritius 2
PE - Perù 2
PH - Filippine 2
SA - Arabia Saudita 2
BO - Bolivia 1
ET - Etiopia 1
GT - Guatemala 1
HN - Honduras 1
HU - Ungheria 1
JO - Giordania 1
KG - Kirghizistan 1
KR - Corea 1
KW - Kuwait 1
LK - Sri Lanka 1
LT - Lituania 1
LV - Lettonia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PK - Pakistan 1
PS - Palestinian Territory 1
SK - Slovacchia (Repubblica Slovacca) 1
TN - Tunisia 1
VE - Venezuela 1
Totale 6.208
Città #
Fairfield 391
Warsaw 317
Singapore 277
Woodbridge 264
Houston 246
Hong Kong 230
Ashburn 228
Chandler 202
Jacksonville 194
Seattle 176
Cambridge 167
Wilmington 156
Ann Arbor 148
Beijing 124
New York 119
Helsinki 103
Princeton 101
Brescia 85
Munich 59
Istanbul 58
Dublin 57
Des Moines 52
Nanjing 51
Chicago 42
Los Angeles 39
Shanghai 39
Turku 38
Dearborn 30
The Dalles 27
Lancaster 24
Changsha 23
Boardman 22
Dong Ket 20
Moscow 20
Buffalo 19
London 18
Salt Lake City 18
Hebei 17
Milan 16
Nanchang 16
Shenyang 16
Jinan 15
San Diego 15
San Francisco 15
Elk Grove Village 11
Nuremberg 11
Brno 10
Haikou 10
Hangzhou 10
Frankfurt am Main 9
Tampa 9
Tianjin 9
Toronto 8
Verona 8
Vienna 8
Assemini 7
Jakarta 7
Miami 7
Redwood City 7
Romola 7
Santa Clara 7
São Paulo 7
Belo Horizonte 6
Brussels 6
Cremona 6
Dallas 6
Jiaxing 6
Lanzhou 6
Ningbo 6
Taiyuan 6
Düsseldorf 5
Falkenstein 5
Leawood 5
Mazzano 5
Norwalk 5
Barlassina 4
Casoria 4
Genoa 4
Phoenix 4
Rende 4
Rome 4
Sydney 4
Trieste 4
Zhengzhou 4
Amsterdam 3
Athens 3
Aubervilliers 3
Barcelona 3
Brooklyn 3
Espoo 3
Kunming 3
Las Vegas 3
Lauterbourg 3
Leipzig 3
New Bedfont 3
Newark 3
Salò 3
Tashkent 3
Wroclaw 3
Ankara 2
Totale 4.602
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 237
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. 209
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) 206
A distinct human cell type expressing MHCII and RORγt with dual characteristics of dendritic cells and type 3 innate lymphoid cells 205
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. 197
Collapse of the Plasmacytoid Dendritic Cells compartment in advanced cutaneous melanomas by components of the tumor cell secretome 167
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 160
α- and β-Papillomavirus infection in a young patient with an unclassified primary T-cell immunodeficiency and multiple mucosal and cutaneous lesions 145
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency 145
Stem cell transplantation for the Wiskott-Aldrich syndrome: a single-center experience confirms efficacy of matched unrelated donor transplantation 141
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 140
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 138
Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency 137
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 137
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 136
Functional defects of dendritic cells in patients with CD40 deficiency. 135
Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia 131
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency 130
Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications 127
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions 124
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 123
Immune response in children with COVID-19 is characterized by lower levels of T-cell activation than infected adults 121
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. 118
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome 115
Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. 114
The Wiskott-Aldrich syndrome: From genotype-phenotype correlation to treatment 105
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity 104
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) 96
Low WASp expression in patients with no apparent mutation in the WASP gene 94
Long-term outcome and lineage-specific chimerism in 194 Wiskott-Aldrich Syndrome patients treated by hematopoietic celltransplantation between 1980-2009: an international collaborative study. 94
Plasmacytoid dendritic cell impairment in metastatic melanoma by lactic acidosis 92
Proteus syndrome: evaluation of the immunological profile 91
WASP-WIP DEFICIENCIES: NEW INSIGHTS IN WASP-WIP INTERACTION 87
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 87
CASE REPORT: IDENTIFICATION OF A PATIENT WITH FAMILIAR MUTATIONS AFFECTING BOTH WASP AND FOXP3 GENES 84
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 81
Multi-lineage analysis of X-inactivation in female carriers of genetic alterations in the Wiskott-Aldrich syndrome protein (WASP) gene locus 78
Flow Cytometry Identifies Risk Factors and Dynamic Changes in Patients with COVID-19 78
Successful hematopoietic stem cell transplantation for complete CTLA-4 haploinsufficiency due to a de novo monoallelic 2q33.2-2q33.3 deletion 76
P1450: AUTOLOGOUS STEM CELL TRANSPLANTATION INDUCES HIGHER LEVEL OF EXHAUSTED T-CELLS IN DLBCL PATIENTS BEFORE LEUKAPHERESIS FOR CAR-T CELL THERAPY 74
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections. 72
Transient Decrease of Circulating and Tissular Dendritic Cells in Patients With Mycobacterial Disease and With Partial Dominant IFNγR1 Deficiency 72
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 68
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency 67
Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related Malignancies 65
Immunologic characterization of a immunosuppressed multiple sclerosis patient that recovered from SARS-CoV-2 infection 64
Two X-linked agammaglobulinemia patients develop pneumonia as COVID-19 manifestation but recover 62
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections 55
Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis 53
Inflammatory pathways signal transducers analysis in iPSC-derived neurons and 3D cerebral organoids 51
Multisystem autoimmune disease caused by increased STAT3 phosphorylation and dysregulated gene expression 51
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 50
Timely Leukapheresis May Interfere with the “Fitness” of Lymphocytes Collected for CAR-T Treatment in High Risk DLBCL Patients 47
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 47
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 43
Pseudomonas aeruginosa severe skin infection in a toddler with X-linked agammaglobulinemia due to a novel BTK mutation 42
Longitudinal Characterization of Immune Response in a Cohort of Children Hospitalized with Multisystem Inflammatory Syndrome 41
Plasmacytoid Dendritic Cells Depletion and Elevation of IFN-γ Dependent Chemokines CXCL9 and CXCL10 in Children With Multisystem Inflammatory Syndrome 38
Abnormal B-Cell Maturation and Increased Transitional B Cells in CBL Syndrome 38
Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations 37
Identical EP300 variant leading to Rubinstein–Taybi syndrome with different clinical and immunologic phenotype 37
Clinical and transcriptomic characteristics of a novel SMARCD2 mutation that disrupts neutrophil maturation and function 33
Rituximab Monotherapy Is Effective as First-Line Treatment for Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) in CVID Patients 32
Immune Reconstitution after Allogenic Stem Cell Transplantation in Patients with Myelofibrosis 32
Reduced G protein signaling despite impaired internalization and β-arrestin recruitment in patients carrying a CXCR4Leu317fsX3 mutation causing WHIM syndrome 28
Transient Decrease of Circulating and Tissular Dendritic Cells in Patients With Mycobacterial Disease and With Partial Dominant IFNγR1 Deficiency 26
Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations 25
Patients with STAT1 Gain-of-function Mutations Display Increased Apoptosis which is Reversed by the JAK Inhibitor Ruxolitinib 23
Case Report: A Case of X-Linked Agammaglobulinemia With High Serum IgE Levels and Allergic Rhinitis 20
Totale 6.378
Categoria #
all - tutte 33.710
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 33.710


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202061 0 0 0 0 0 0 0 0 0 0 0 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
2024/20251.633 23 17 15 210 125 109 131 96 209 114 445 139
Totale 6.378