• Bloom's syndrome in a Turkish individual
• Clinical features and accompanying findings of Pseudo-Bartter Syndrome in cystic fibrosis
• Clinical Profile and Renal Ultrasound Characteristics of Children With Nutcracker Syndrome in Turkey
• Cystic fibrosis in Turkey: First data from the national registry
• Differences and similarities of multisystem inflammatory syndrome in children, Kawasaki disease and macrophage activating syndrome due to systemic juvenile idiopathic arthritis: a comparative study
• Evaluation of coronary artery abnormalities in Williams syndrome patients using myocardial perfusion scintigraphy and CT angiography
• Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome
• Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment
• Interferon alfa-2a in the treatment of Behçet disease: a randomized placebo-controlled and double-blind study
• Interferon therapy for Behçet's disease
• Keratoderma, hypotrichosis and leukonychia totalis: a new syndrome?
• Novel Gene Variants Associated with Primary Ciliary Dyskinesia
• Prognostic importance of predischarged troponin T levels in acute anterior myocardial infarction
• The mean platelet volume and neutrophil to lymphocyte ratio in obese and lean patients with polycystic ovary syndrome
• The success of the Cystic Fibrosis Registry of Turkey for improvement of patient care