GATTORNO, MARCO
 Distribuzione geografica
Continente #
EU - Europa 4.170
Totale 4.170
Nazione #
IT - Italia 4.170
Totale 4.170
Città #
Genova 2.720
Rapallo 773
Genoa 649
Bordighera 28
Totale 4.170
Nome #
ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study 138
T cell defects in patients with ARPC1B germline mutations account for their combined immunodeficiency 134
CD70 deficiency due to a novel mutation in a patient with severe chronic EBV infection presenting as a periodic fever 122
Analysis of pulmonary features and treatment approaches in the COPA syndrome 118
Type I interferon pathway activation in COPA syndrome 116
Type i interferon-mediated autoinflammation due to DNase II deficiency 104
A circulating reservoir of pathogenic-like CD4+ T cells shares a genetic and phenotypic signature with the inflamed synovial micro-environment 103
Cryopyrin-associated periodic syndromes in Italian Patients: Evaluation of the rate of somatic NLRP3 mosaicism and phenotypic characterization 101
HLA-DRB1∗11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis 101
Disease-associated mutations identify a novel region in human STING necessary for the control of type I interferon signaling 100
Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome 95
Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: Clinical and therapeutic implications 95
Performance of different diagnostic criteria for familial Mediterranean fever in children with periodic fevers: Results from a multicenter international registry 91
Evidence-based recommendations for genetic diagnosis of familial Mediterranean fever 91
Dysregulation in B-cell responses and T follicular helper cell function in ADA2 deficiency patients 90
Type I interferonopathies in pediatric rheumatology 89
EULAR recommendations for the management of familial Mediterranean fever 84
A child with a novel ACAN missense variant mimicking a septic arthritis 83
A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency 82
A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry 81
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome 81
Distinct expression pattern of IFN-α and TNF-α in juvenile idiopathic arthritis synovial tissue 77
Murine Rankl−/− Mesenchymal Stromal Cells Display an Osteogenic Differentiation Defect Improved by a RANKL-Expressing Lentiviral Vector 75
Canakinumab treatment for patients with active recurrent or chronic TNF receptor-associated periodic syndrome (TRAPS): An open-label, phase II study 74
The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever Registry 73
When neonatal inflammation does not mean infection: an early-onset mevalonate kinase deficiency with interstitial lung disease 72
Anakinra: An emerging option for refractory idiopathic recurrent pericarditis: A systematic review of published evidence 71
An international delphi survey for the definition of new classification criteria for familial mediterranean fever, mevalonate kinase deficiency, TNF receptor-associated periodic fever syndromes, and cryopyrin-associated periodic syndrome 71
In silico validation of the autoinflammatory disease damage index 70
Clinical and genetic characterization of Italian patients affected by CINCA syndrome 70
The multifaceted presentation of chronic recurrent multifocal osteomyelitis: a series of 486 cases from the Eurofever international registry 69
Recurrent pericarditis in children and adolescents: A multicentre cohort study 66
Management of idiopathic recurrent pericarditis in adults and in children: a role for IL-1 receptor antagonism 66
Molecular mechanisms of autophagic memory in pathogenic T cells in human arthritis 65
An international delphi survey for the definition of the variables for the development of new classification criteria for periodic fever aphtous stomatitis pharingitis cervical adenitis (PFAPA) 65
Overview of STING-Associated Vasculopathy with Onset in Infancy (SAVI) Among 21 Patients 63
The Ped-APS registry: The antiphospholipid syndrome in childhood 60
Development of the autoinflammatory disease damage index (ADDI) 59
IL1RN Variation Influences Both Disease Susceptibility and Response to Recombinant Human Interleukin-1 Receptor Antagonist Therapy in Systemic Juvenile Idiopathic Arthritis 58
Critical role of STIR MRI in early detection of post-streptococcal periostitis with dysproteinaemia (Goldbloom's syndrome) 55
Reply to: About the AIRTRIP randomised clinical trial 49
Safety and efficacy of early high-dose IV anakinra in severe COVID-19 lung disease 49
Juvenile eosinophilic fasciitis: three case reports with review of the literature 46
Successful treatment of refractory hyperferritinemic syndromes with canakinumab: A report of two cases 45
Efficacy of early anti-inflammatory treatment with high doses of intravenous anakinra with or without glucocorticoids in patients with severe COVID-19 pneumonia 43
Neutrophil Extracellular Traps in Systemic Lupus Erythematosus Stimulate IgG2 Production From B Lymphocytes 41
Monogenetic causes of chilblains, panniculitis and vasculopathy: the Type I interferonopathies 40
Neutrophil extracellular traps-dnase balance and autoimmunity 40
Failure of anti Interleukin-1 β monoclonal antibody in the treatment of recurrent pericarditis in two children 39
Contact tracing, use of surgical masks, hand hygiene and social distancing represent a bundle of effective measures to control SARS-CoV-2 spreading among healthcare workers in a paediatric hospital 36
On the Alert for Cytokine Storm: Immunopathology in COVID-19 35
Timely Recognition and Early Multi-Step Antinflammatory Therapy May Prevent ICU Admission of Patients With MIS-C: Proposal for a Severity Score 33
A novel LC–MS/MS-based method for the diagnosis of ADA2 deficiency from dried plasma spot 33
Clinical characterization, long-term follow-up, and response to treatment of patients with syndrome of undifferentiated recurrent fever (SURF) 32
Syndrome of undifferentiated recurrent fever (Surf): An emerging group of autoinflammatory recurrent fevers 30
Actin Remodeling Defects Leading to Autoinflammation and Immune Dysregulation 29
Effect of anakinra on mortality in patients with COVID-19: a systematic review and patient-level meta-analysis 27
Haploidentical α/β T-cell and B-cell depleted stem cell transplantation in severe mevalonate kinase deficiency 27
Cardiovascular Manifestations in Multisystem Inflammatory Syndrome in Children (MIS-C) Associated with COVID-19 According to Age 26
Type I interferon activation in RAS-associated autoimmune leukoproliferative disease (RALD) 26
Erratum: Haploidentical α/β T-cell and B-cell depleted stem cell transplantation in severe mevalonate kinase deficiency (Rheumatology (2021) DOI: 10.1093/rheumatology/keaa912) 25
Erratum: Next generation sequencing panel in undifferentiated autoinflammatory diseases identifies patients with colchicine-responder recurrent fevers (Rheumatology (2020) 59 (344-60) DOI: 10.1093/rheumatology/kez270) 25
Intravenous immunoglobulin for corticosteroid-resistant intestinal Henoch-Schönlein purpura: worth a controlled trial against corticosteroids? 24
Spontaneous NLRP3 inflammasome-driven IL-1-β secretion is induced in severe COVID-19 patients and responds to anakinra treatment 21
Targeted ngs yields plentiful ultra-rare variants in inborn errors of immunity patients 19
Cerebrovascular disease and varicella in children 16
Disparities in the prevalence of clinical features between systemic juvenile idiopathic arthritis and adult-onset Still's disease 15
Paediatric recurrent pericarditis: Appropriateness of the standard of care and response to IL1-blockade 14
The Notch1/CD22 signaling axis disrupts Treg function in SARS-CoV-2-associated multisystem inflammatory syndrome in children 14
LONG-TERM OUTCOME IN CEREBRAL ARTERIA ISCHEMIC STROKE (AIS) DUE TO VARICELLA ZOSTER VIRUS (VZV) IN CHILDREN 10
Adenosine Deaminase 2 Deficiency (DADA2): A Crosstalk Between Innate and Adaptive Immunity 9
Evidence-based provisional clinical classification criteria for autoinflammatory periodic fevers 8
Protection against MIS-C outweighs the risk of myocarditis after Covid-19 vaccination in children 7
DADA-ism (2) 7
Proteomic Signatures of Monocytes in Hereditary Recurrent Fevers 6
A Report of 2 Cases of Kidney Involvement in ADA2 Deficiency: Different Disease Phenotypes and the Tissue Response to Type I Interferon 6
New monogenic autoinflammatory diseases: 2021 year in review 5
Remission of eczema and recovery of Th1 polarization following treatment with Dupilumab in STAT3 hyper IgE syndrome 4
Vasculitis and vasculopathy associated with inborn errors of immunity: an overview 3
Epidemiological and clinical evolution of multisystem inflammatory syndrome in children throughout the SARS-CoV-2 pandemic in a tertiary Italian children's hospital 3
Hematopoietic Stem Cell Transplantation in ARPC1B Deficiency 3
Notch1-CD22-Dependent Immune Dysregulation in the SARS-CoV2-Associated Multisystem Inflammatory Syndrome in Children 3
An Update on Familial Mediterranean Fever 3
Early anakinra treatment improves cardiac outcome of multisystem inflammatory syndrome in children, regardless of disease severity 2
ARF1 prevents aberrant type I interferon induction by regulating STING activation and recycling 2
Expert Perspective: Diagnostic Approach to the Autoinflammatory Diseases 2
Novel heterozygous TREX1 mutation in a juvenile systemic lupus erythematosus patient with severe cutaneous involvement treated successfully with Jak-inhibitors: a case report 2
The Inborn Errors of Immunity—Virtual Consultation System Platform in Service for the Italian Primary Immunodeficiency Network: Results from the Validation Phase 2
Case Report: Susceptibility to viral infections and secondary hemophagocytic lymphohistiocytosis responsive to intravenous immunoglobulin as primary manifestations of adenosine deaminase 2 deficiency 2
Pyrin Inflammasome Activation Defines Colchicine-Responsive SURF Patients from FMF and Other Recurrent Fevers 2
Corrigendum to “Clinical characterization, long-term follow-up, and response to treatment of patients with syndrome of undifferentiated recurrent fever (SURF)” Seminars in Arthritis and Rheumatism 55 (2022) 152024 (Seminars in Arthritis and Rheumatism (2022) 55, (S0049017222000750), (10.1016/j.semarthrit.2022.152024)) 2
Interface Gain-of-Function Mutations in TLR7 Cause Systemic and Neuro-inflammatory Disease 2
A Novel LC-MS/MS Method for Therapeutic Drug Monitoring of Baricitinib in Plasma of Pediatric Patients 1
Hematopoietic stem cell transplantation for inborn errors of immunity: 30-year single-center experience 1
Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait? 1
Validation of the PEDiatric Behçet’s Disease classification criteria: an evidence-based approach 1
Microvascular status in juvenile Sjögren's disease: the first nailfold videocapillaroscopy investigation 1
HSP90β controls NLRP3 autoactivation 1
Performance of the EULAR/ACR 2019 classification criteria for systemic lupus erythematous in monogenic lupus 1
Deficiency in coatomer complex I causes aberrant activation of STING signalling 1
Totale 4.380
Categoria #
all - tutte 17.562
article - articoli 17.562
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 35.124


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019105 0 0 0 0 0 0 0 0 0 0 43 62
2019/20201.385 89 50 20 95 114 160 222 132 152 196 124 31
2020/2021637 27 48 67 87 16 30 79 61 42 82 44 54
2021/2022699 31 20 34 59 30 71 29 139 63 91 39 93
2022/2023925 79 77 15 79 152 125 14 78 153 6 124 23
2023/2024588 30 46 23 84 67 113 63 53 58 50 1 0
Totale 4.380