Spectrum of auto-inflammatory diseases in Morocco: a monocentric experience. Souali M, Sakhi A, Benbrahim Ansari G, Mikou N, Bousfiha AA, Bouayed K. https://pubmed.ncbi.nlm.nih.gov/36685993
Monogenic interferonopathies: Phenotypic and genotypic findings of CANDLE syndrome and its overlap with C1q deficient SLE. Al-Mayouf SM, AlSaleem A, AlMutairi N, AlSonbul...
Pattern and diagnostic evaluation of systemic autoinflammatory diseases other than familial Mediterranean fever among Arab children: a multicenter study from the Pediatric Rheumatology...
Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds Abderrahmane Errami, Jamila El Baghdadi,...
Second Report of Chronic Granulomatous Disease in Jordan: Clinical and Genetic Description of 31 Patients From 21 Different Families, Including Families From Lybia...
Chronic granulomatous disease in the United Arab Emirates: clinical and molecular characteristics in a single center Amna Ali Al Kuwaiti, Ahmed Darwaish Al...
A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families. Al-Sulaiman R, Othman A, El-Akouri K, Fareed S, AlMulla H,...
Immune Dysregulation in Monogenic Inborn Errors of Immunity in Oman: Over A Decade of Experience From a Single Tertiary Center. Al Farsi T,...
Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry. Jamee M, Azizi G, Baris S, Karakoc-Aydiner...
Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi Arabia. Sheikh F, Alajlan H, Albanyan M, Alruwaili H, Alawami F, Sumayli S, Al...