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Biologics for the Treatment of Juvenile Idiopathic Arthritis

Current medicinal chemistry, 2018-01, Vol.25 (42), p.5860-5893

2018

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New Horizons in the Genetic Etiology of Systemic Lupus Erythematosus and Lupus-Like Disease: Monogenic Lupus and Beyond

Journal of clinical medicine, 2020-03, Vol.9 (3), p.712

2020

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The Effect of Corrected Inflammation, Oxidative Stress and Endothelial Dysfunction on Fmd Levels in Patients with Selected Chronic Diseases: A Quasi-Experimental Study

Scientific reports, 2020-06, Vol.10 (1), p.9018-9018, Article 9018

2020

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The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology Points to Consider for Diagnosis and Management of Autoinflammatory Type I Interferonopathies: CANDLE/PRAAS, SAVI, and AGS

Arthritis & rheumatology (Hoboken, N.J.), 2022-05, Vol.74 (5), p.735-751

2022

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Current State of Precision Medicine in Primary Systemic Vasculitides

Frontiers in immunology, 2019-12, Vol.10, p.2813-2813

2019

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Cardiovascular disease risk assessment in patients with familial Mediterranean fever related renal amyloidosis

Scientific reports, 2020-10, Vol.10 (1), p.18374-18374, Article 18374

2020

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Next Generation Sequencing Based Multiplex Long-Range PCR for Routine Genotyping of Autoinflammatory Disorders

Frontiers in immunology, 2021-06, Vol.12, p.666273-666273

2021

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Celiac Disease in Juvenile Idiopathic Arthritis and Other Pediatric Rheumatic Disorders

Journal of clinical medicine, 2022-02, Vol.11 (4), p.1089

2022

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Paediatric Behçet's Disease: A Comprehensive Review with an Emphasis on Monogenic Mimics

Journal of clinical medicine, 2022-02, Vol.11 (5), p.1278

2022

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Long Term Experience in Patients With JIA-Associated Uveitis in a Large Referral Center

Frontiers in pediatrics, 2021-06, Vol.9, p.682327-682327

2021

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Assessment of Surrogate Markers for Cardiovascular Disease in Familial Mediterranean Fever-Related Amyloidosis Patients Homozygous for M694V Mutation in MEFV Gene

Life (Basel, Switzerland), 2022-04, Vol.12 (5), p.631

2022

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Evaluation of E148Q and Concomitant AA Amyloidosis in Patients with Familial Mediterranean Fever

Journal of clinical medicine, 2021-08, Vol.10 (16), p.3511

2021

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Anti-Inflammatory, Antioxidant, and Anti-Atherosclerotic Effects of Natural Supplements on Patients with FMF-Related AA Amyloidosis: A Non-Randomized 24-Week Open-Label Interventional Study

Life (Basel, Switzerland), 2022-06, Vol.12 (6), p.896

2022

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Number of Episodes Can Be Used as a Disease Activity Measure in Familial Mediterranean Fever

Frontiers in pediatrics, 2022-04, Vol.10, p.822473-822473

2022

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Absence of Severe Complications From SARS-CoV-2 Infection in Children With Rheumatic Diseases Treated With Biologic Drugs

Journal of rheumatology, 2021-08, Vol.48 (8), p.1343-1344

2021

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Mycoplasma pneumoniae Infections and Primary Immune Deficiencies

International journal of clinical practice (Esher), 2022-07, Vol.2022, p.1-6

2022

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Patients with juvenile idiopathic arthritis on TNF inhibitors exposed to COVID-19 family members

Seminars in arthritis and rheumatism, 2020-12, Vol.50 (6), p.1214-1215

2020

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Conventional and novel therapeutic options in children with familial Mediterranean fever: A rare autoinflammatory disease

British journal of clinical pharmacology, 2022-06, Vol.88 (6), p.2484-2499

2022

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Time for a new approach to drug development for rare systemic autoinflammatory diseases

Nature reviews. Rheumatology, 2024-06, Vol.20 (6), p.317-318

2024

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Pharmacokinetics of Baricitinib in Cerebrospinal Fluid and Plasma in a Patient with SPENCD

Journal of clinical immunology, 2024-03, Vol.44 (3), p.78-78, Article 78

2024

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Developing guidelines for ultrarare rheumatic disorders: a bumpy ride

Annals of the rheumatic diseases, 2022-09, Vol.81 (9), p.1203-1205

2022

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Baseline ultrasound examination as possible predictor of relapse in patients affected by juvenile idiopathic arthritis (JIA)

Annals of the rheumatic diseases, 2018-10, Vol.77 (10), p.1426-1431

2018

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The 2021 EULAR/American College of Rheumatology points to consider for diagnosis, management and monitoring of the interleukin-1 mediated autoinflammatory diseases: cryopyrin-associated periodic syndromes, tumour necrosis factor receptor-associated periodic syndrome, mevalonate kinase deficiency, and deficiency of the interleukin-1 receptor antagonist

Annals of the rheumatic diseases, 2022-07, Vol.81 (7), p.907-921

2022

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Childhood Sjogren's syndrome: An Italian case series and a literature review-based cohort

Seminars in arthritis and rheumatism, 2021-08, Vol.51 (4), p.903-910

2021

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The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology points to consider for diagnosis and management of autoinflammatory type I interferonopathies: CANDLE/PRAAS, SAVI and AGS

Annals of the rheumatic diseases, 2022-05, Vol.81 (5), p.601-613

2022

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Biologics for the Treatment of Juvenile Idiopathic Arthritis

New Horizons in the Genetic Etiology of Systemic Lupus Erythematosus and Lupus-Like Disease: Monogenic Lupus and Beyond

The Effect of Corrected Inflammation, Oxidative Stress and Endothelial Dysfunction on Fmd Levels in Patients with Selected Chronic Diseases: A Quasi-Experimental Study

The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology Points to Consider for Diagnosis and Management of Autoinflammatory Type I Interferonopathies: CANDLE/PRAAS, SAVI, and AGS

Current State of Precision Medicine in Primary Systemic Vasculitides

Cardiovascular disease risk assessment in patients with familial Mediterranean fever related renal amyloidosis

Next Generation Sequencing Based Multiplex Long-Range PCR for Routine Genotyping of Autoinflammatory Disorders

Celiac Disease in Juvenile Idiopathic Arthritis and Other Pediatric Rheumatic Disorders

Paediatric Behçet's Disease: A Comprehensive Review with an Emphasis on Monogenic Mimics

Long Term Experience in Patients With JIA-Associated Uveitis in a Large Referral Center

Assessment of Surrogate Markers for Cardiovascular Disease in Familial Mediterranean Fever-Related Amyloidosis Patients Homozygous for M694V Mutation in MEFV Gene

Evaluation of E148Q and Concomitant AA Amyloidosis in Patients with Familial Mediterranean Fever

Anti-Inflammatory, Antioxidant, and Anti-Atherosclerotic Effects of Natural Supplements on Patients with FMF-Related AA Amyloidosis: A Non-Randomized 24-Week Open-Label Interventional Study

Number of Episodes Can Be Used as a Disease Activity Measure in Familial Mediterranean Fever

Absence of Severe Complications From SARS-CoV-2 Infection in Children With Rheumatic Diseases Treated With Biologic Drugs

Mycoplasma pneumoniae Infections and Primary Immune Deficiencies

Patients with juvenile idiopathic arthritis on TNF inhibitors exposed to COVID-19 family members

Conventional and novel therapeutic options in children with familial Mediterranean fever: A rare autoinflammatory disease

Time for a new approach to drug development for rare systemic autoinflammatory diseases

Pharmacokinetics of Baricitinib in Cerebrospinal Fluid and Plasma in a Patient with SPENCD

Developing guidelines for ultrarare rheumatic disorders: a bumpy ride

Baseline ultrasound examination as possible predictor of relapse in patients affected by juvenile idiopathic arthritis (JIA)

Childhood Sjogren's syndrome: An Italian case series and a literature review-based cohort

The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology points to consider for diagnosis and management of autoinflammatory type I interferonopathies: CANDLE/PRAAS, SAVI and AGS

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