2016 classification criteria for macrophage activation syndrome complicating systemic juvenile idiopathic arthritis: a European League Against Rheumatism/American …

…, A Aggarwal, J Akikusa, SM AlMayouf… - Arthritis & …, 2016 - Wiley Online Library
Objective To develop criteria for the classification of macrophage activation syndrome (MAS)
in patients with systemic juvenile idiopathic arthritis (JIA). Methods A multistep process, …

Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus

SM Al-Mayouf, A Sunker, R Abdwani, SA Abrawi… - Nature …, 2011 - nature.com
Systemic lupus erythematosus (SLE) is a complex autoimmune disease that causes substantial
morbidity. As is typical for many other multifactorial disorders, much of the heritability of …

[HTML][HTML] Epidemiology and demographics of juvenile idiopathic arthritis in Africa and Middle East

SM Al-Mayouf, M Al Mutairi, K Bouayed… - Pediatric …, 2021 - Springer
Juvenile Idiopathic Arthritis (JIA) is a group of chronic heterogenous disorders that manifests
as joint inflammation in patients aged <16 years. Globally, approximately 3 million children …

Treating juvenile idiopathic arthritis to target: recommendations of an international task force

…, NM Wulffraat, JD Akikusa, SM Al-Mayouf… - Annals of the …, 2018 - ard.bmj.com
Recent therapeutic advances in juvenile idiopathic arthritis (JIA) have made remission an
achievable goal for most patients. Reaching this target leads to improved outcomes. The …

[HTML][HTML] The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

…, MH Hamad, L Szonyi, F Abaalkhail, SM Al-Mayouf… - Human genetics, 2017 - Springer
In this study, we report the experience of the only reference clinical next-generation sequencing
lab in Saudi Arabia with the first 1000 families who span a wide-range of suspected …

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

…, B Bader-Meunier, A Insalaco, SM Al-Mayouf… - Annals of the …, 2015 - ard.bmj.com
Objective To evaluate genetic, demographic and clinical features in patients with cryopyrin-associated
periodic syndrome (CAPS) from the Eurofever Registry, with a focus on genotype-…

Systemic sclerosis in childhood: clinical and immunologic features of 153 patients in an international database

…, F Sztajnbok, SM AlMayouf… - … : Official Journal of …, 2006 - Wiley Online Library
Objective To determine the clinical and immunologic features of systemic sclerosis (SSc) in
a large group of children and describe the clinical evolution of the disease and compare it …

Phenotypic variability and disparities in treatment and outcomes of childhood arthritis throughout the world: an observational cohort study

…, A Aggarwal, SM Al-Mayouf… - The Lancet Child & …, 2019 - thelancet.com
Background To our knowledge, the characteristics and burden of childhood arthritis have
never been studied on a worldwide basis. We aimed to investigate, with a cross-sectional study…

Results from a multicentre international registry of familial Mediterranean fever: impact of environment on the expression of a monogenic disease in children

…, E Papadopoulou-Alataki, SM Al-Mayouf… - Annals of the …, 2014 - ard.bmj.com
Background and aim Familial Mediterranean fever (FMF) is an autoinflammatory disease
caused by mutations of the MEFV gene. We analyse the impact of ethnic, environmental and …

Intravenous immunoglobulin therapy for juvenile dermatomyositis: efficacy and safety.

SM Al-Mayouf, RM Laxer, R Schneider… - The Journal of …, 2000 - europepmc.org
Objective To assess the efficacy of intravenous immunoglobulin (IVIG) for the treatment of
juvenile dermatomyositis (JDM) in patients who were unresponsive to corticosteroids (steroid …