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The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registry

Annals of the rheumatic diseases, 2014-12, Vol.73 (12), p.2160-2167

2014

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Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry

Annals of the rheumatic diseases, 2015-11, Vol.74 (11), p.2043-2049

2015

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Widening the Neuroimaging Features of Adenosine Deaminase 2 Deficiency

American journal of neuroradiology : AJNR, 2021-05, Vol.42 (5), p.975-979

2021

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Widening the Neuroimaging Features of Adenosine Deaminase 2 Deficiency

American journal of neuroradiology : AJNR, 2021-05, Vol.42 (5), p.975-979

2021

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Phase 3 Trial of Interleukin-1 Trap Rilonacept in Recurrent Pericarditis

The New England journal of medicine, 2021-01, Vol.384 (1), p.31-41

2021

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Severe osteoarticular involvement in isotretinoin‐triggered acne fulminans: two cases successfully treated with anakinra

Journal of the European Academy of Dermatology and Venereology, 2017-06, Vol.31 (6), p.e277-e279

2017

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S10.3 Genetical and phenotypical findings of childhood-onset systemic lupus erythematosus

Lupus science & medicine, 2022-10, Vol.9 (Suppl 2), p.A14-A15

2022

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PO.6.141 Efficacy of mycophenolate mofetil (MMF) in pediatric patients with defined and undefined type I interferonopathies

Lupus science & medicine, 2022-10, Vol.9 (Suppl 2), p.A106-A106

2022

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OP0008 Single Center Experience in Next Generation Sequencing for Genetic Diagnosis of Autoinflammatory Disorders (AIDS)

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.67-67

2015

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FRI0323 Cronic Non-Bacterial Osteomyelitis (CNO) in a Cohort of Pediatric Patients: Clinical, Biological and Radiological Response to Treatment with Anakinra

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.541-541

2015

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SAT0484 Prevalence of Cecr1 Mutations in Pediatric Patients with Polyarteritis Nodosa, Livedo Reticularis and/or Stroke

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.835-835

2015

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SAT0325 Chronic Recurrent Multifocal Osteomyelitis (CRMO): Typical Patterns of Bone Involvement on MRI with Particular Emphasis on Whole Body MRI (WBMRI)

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.776-776

2015

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SAT0486 Macrophage Activation Syndrome and Familial Hemophagocytic Lymphohistiocytosis: Is Their Clinical Phenotype Really Similar?

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.836-836

2015

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AB1115 A novel mutation in the CIAS1/NLRP3 gene associated with an unexpected phenotype of caps

Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.701-701

2013

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OP0280 Recurrent Pericarditis in Children and Adolescents: A Large, Multicentric Case-Series and Implications for the Pediatric Rheumatologist

Annals of the rheumatic diseases, 2014-06, Vol.73 (Suppl 2), p.168-168

2014

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AB1020 Evaluation of the Disease Course of Italian Children with Juvenile Idiopathic Arthritis Treated with Etanercept: Preliminary Results in 1019 Patients

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.1239-1240

2015

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The phenotypic variability of PAPA syndrome: evidence from the Eurofever Registry

Pediatric rheumatology online journal, 2015-09, Vol.13 (Suppl 1), p.O8-O8, Article O8

2015

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Cronic non-bacterial osteomyelitis (CNO) in a cohort of pediatric patients: clinical, biological and radiological response to treatment with Anakinra

Pediatric rheumatology online journal, 2015-09, Vol.13 (Suppl 1), p.P168-P168, Article P168

2015

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The multifaceted presentation of chronic recurrent multifocal osteomyelitis: a series of 486 cases from the Eurofever international registry

Rheumatology (Oxford, England), 2018-07, Vol.57 (7), p.1203-1211

2018

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Single center experience in Next Generation Sequencing for genetic diagnosis of Autoinflammatory Disorders (AIDs)

Pediatric rheumatology online journal, 2015-09, Vol.13 (99), p.P52-P52, Article P52

2015

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Identification of three ADA2 deficiency families with novel CECR1 mutations

Pediatric rheumatology online journal, 2015-09, Vol.13 (Suppl 1), p.P153-P153, Article P153

2015

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Inflammatory Cytokine response in a cohort of patients carrying novel NLRP12 variants

Pediatric rheumatology online journal, 2015-09, Vol.13 (Suppl 1), p.O23-O23, Article O23

2015

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THU0334 Differences in the features of familial mediterranean fever among patients from europe as compared to those from the eastern mediterranean countries

Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.268-269

2013

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Rapid and sustained effect of anti-TNF treatment in patients with ADA2 deficiency

Pediatric rheumatology online journal, 2015-09, Vol.13 (Suppl 1), p.O80-O80, Article O80

2015

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The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registry

Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry

Widening the Neuroimaging Features of Adenosine Deaminase 2 Deficiency

Widening the Neuroimaging Features of Adenosine Deaminase 2 Deficiency

Phase 3 Trial of Interleukin-1 Trap Rilonacept in Recurrent Pericarditis

Severe osteoarticular involvement in isotretinoin‐triggered acne fulminans: two cases successfully treated with anakinra

S10.3 Genetical and phenotypical findings of childhood-onset systemic lupus erythematosus

PO.6.141 Efficacy of mycophenolate mofetil (MMF) in pediatric patients with defined and undefined type I interferonopathies

OP0008 Single Center Experience in Next Generation Sequencing for Genetic Diagnosis of Autoinflammatory Disorders (AIDS)

FRI0323 Cronic Non-Bacterial Osteomyelitis (CNO) in a Cohort of Pediatric Patients: Clinical, Biological and Radiological Response to Treatment with Anakinra

SAT0484 Prevalence of Cecr1 Mutations in Pediatric Patients with Polyarteritis Nodosa, Livedo Reticularis and/or Stroke

SAT0325 Chronic Recurrent Multifocal Osteomyelitis (CRMO): Typical Patterns of Bone Involvement on MRI with Particular Emphasis on Whole Body MRI (WBMRI)

SAT0486 Macrophage Activation Syndrome and Familial Hemophagocytic Lymphohistiocytosis: Is Their Clinical Phenotype Really Similar?

AB1115 A novel mutation in the CIAS1/NLRP3 gene associated with an unexpected phenotype of caps

OP0280 Recurrent Pericarditis in Children and Adolescents: A Large, Multicentric Case-Series and Implications for the Pediatric Rheumatologist

AB1020 Evaluation of the Disease Course of Italian Children with Juvenile Idiopathic Arthritis Treated with Etanercept: Preliminary Results in 1019 Patients

The phenotypic variability of PAPA syndrome: evidence from the Eurofever Registry

Cronic non-bacterial osteomyelitis (CNO) in a cohort of pediatric patients: clinical, biological and radiological response to treatment with Anakinra

ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study

The multifaceted presentation of chronic recurrent multifocal osteomyelitis: a series of 486 cases from the Eurofever international registry

Single center experience in Next Generation Sequencing for genetic diagnosis of Autoinflammatory Disorders (AIDs)

Identification of three ADA2 deficiency families with novel CECR1 mutations

Inflammatory Cytokine response in a cohort of patients carrying novel NLRP12 variants

THU0334 Differences in the features of familial mediterranean fever among patients from europe as compared to those from the eastern mediterranean countries

Rapid and sustained effect of anti-TNF treatment in patients with ADA2 deficiency

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