Area of research
Molecular Biology · Rheumatology
Research interest
Research interests include Medicine, Pediatrics, Familial Mediterranean fever, Adenosine deaminase, Vasculitis, and Internal medicine.
A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity
2023 ACR/EULAR antiphospholipid syndrome classification criteria
Evaluation and Management of Deficiency of Adenosine Deaminase 2
Pediatric respiratory admissions and related viral infections during the COVID‐19 pandemic
Platelet count and risk of severe illness in hospitalised children with <scp>Influenza‐Like</scp> illness
Tofacitinib-induced progressive multifocal leukoencephalopathy–immune reconstitution inflammatory syndrome
Outcomes of SARS-CoV-2 infection among children and young people with pre-existing rheumatic and musculoskeletal diseases
Six cases of pityriasis rosea following SARS‐CoV‐2 vaccination with BNT162b2
Risk factors for haemodynamic compromise in multisystem inflammatory syndrome in children: a multicentre retrospective study
Obstacles in Early Diagnosis of Children With Juvenile Idiopathic Arthritis: A Nationwide Israeli Retrospective Study
Multisystem inflammatory syndrome in children associated with COVID‐19 presenting as cervical inflammation
Minor Clinical Impact of COVID-19 Pandemic on Patients With Primary Immunodeficiency in Israel
Neurological and neurodevelopmental symptoms in children with familial Mediterranean fever and their siblings
Discontinuation of Colchicine Therapy in Children With Familial Mediterranean Fever
Increased prevalence of attention-deficit hyperactivity disorder symptomatology in patients with familial Mediterranean fever
POS1183 OUTCOMES OF COVID-19 INFECTION AMONG CHILDREN AND YOUNG PEOPLE WITH PRE-EXISTING RHEUMATIC AND MUSCULOSKELETAL DISEASES
JAK1/2 inhibition with baricitinib in the treatment of autoinflammatory interferonopathies
Adenosine Deaminase 2 Deficiency: More Than Monogenic Vasculitis.
PubMed 2017cited by 7position: first
Extending the Clinical Phenotype of Adenosine Deaminase 2 Deficiency
Sudden onset unexplained encephalopathy in infants: think of cannabis intoxication
Seasonality of birth of patients with juvenile idiopathic arthritis.
PubMed 2015cited by 17position: first
Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy
Pentraxin 3 is a marker of early joint inflammation in patients with juvenile idiopathic arthritis
NOD2/CARD15 Gene Mutations in Patients with Familial Mediterranean Fever
Pharmacokinetics and Colchicine in Pediatric and Adult Patients with Familial Mediterranean Fever