Engin Yılmaz

Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population

Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia

Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever.

Neuronal Organization in Area 17 of Cat Visual Cortex

Detection of Mycobacterium tuberculosis in sputum samples by polymerase chain reaction using a simplified procedure

Effects of Regular Kefir Consumption on Gut Microbiota in Patients with Metabolic Syndrome: A Parallel-Group, Randomized, Controlled Study

Mutations in the gene for familial Mediterranean fever: do they predispose to inflammation?

Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome

Exome Sequencing Reveals Cubilin Mutation as a Single-Gene Cause of Proteinuria

MEFV mutations in systemic onset juvenile idiopathic arthritis

Primitive persistent carotid‐basilar and carotid‐vertebral anastomoses: A report of seven gases and a review of the literature

Genetic Evidence for <i>PLASMINOGEN</i> as a Shared Genetic Risk Factor of Coronary Artery Disease and Periodontitis