Ozturk Ozdemir
Canakkale, Turkey
Last Updated: 09/26/2026
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Found 54 publications
The effect of retinopathy of prematurity on visual acuity, refraction, biometric values, retinal and choroidal thickness in school-aged children.
Journal: BMC ophthalmology
Published: December 28, 2024
HLA-DQ2 and HLA-DQ8 Haplotypes in Heart Failure Patients with Reduced Ejection Fraction.
Journal: Oman medical journal
Published: November 21, 2024
Could subcutaneous rifampicin administration be an effective approach for reducing episiotomy infections?
Journal: European review for medical and pharmacological sciences
Published: January 18, 2024
Re-evaluation of Genetic Variants in Parkinson's Disease Using Targeted Panel and Next-Generation Sequencing.
Journal: Twin research and human genetics : the official journal of the International Society for Twin Studies
Published: May 04, 2023
Evaluating of colchicine use patterns and attack frequency of familial Mediterranean fever patients in the COVID-19 pandemic.
Journal: International journal of rheumatic diseases
Published: September 04, 2022
A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels.
Journal: Hemoglobin
Published: August 05, 2022
Prognostic Prediction of BRCA Mutations by 18F-FDG PET/CT SUVmax in Breast Cancer
Journal: Molecular imaging and radionuclide therapy
Published: October 18, 2021
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Journal: Functional & integrative genomics
Published: July 09, 2021
A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation.
Journal: Molecular syndromology
Published: March 18, 2021
Copy number variations in patients with idiopathic recurrent pregnancy loss: an arrayCGH approach.
Journal: Turkish journal of medical sciences
Published: December 23, 2020
The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients.
Journal: Clinical neurology and neurosurgery
Published: July 09, 2020
The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas.
Journal: The journal of international advanced otology
Published: December 18, 2019
Last Updated: 09/26/2026