Kenan Kocabay
Duzce, Turkey
Last Updated: 09/26/2026
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Found 16 publications
The rising threat of antibiotic and multidrug resistance in neonatal urinary tract infections.
Journal: BMC pediatrics
Published: May 13, 2025
The Evaluation of the Genetic Variation Types of the Uridine Diphosphate Glucuronosyl Transferase 1A1 Gene by Next-Generation Sequencing and Their Effects on Bilirubin Levels in Obese Children.
Journal: Genetic testing and molecular biomarkers
Published: June 25, 2024
Heightened Serum Mitochondrial Biomarkers; FGF21 and NOS in Pediatric Anemia and a Negative Correlation between GDF15 and Serum Ferritin.
Journal: Journal of clinical medicine
Published: June 06, 2024
Refugee and asylum-seeker children and health problems in the city of Duzce, Türkiye.
Journal: Child: care, health and development
Published: November 22, 2023
Low-carb Diet in Hospitalized Late Pubertal Type 1 Diabetic Girls: A Short-Term CGM Study.
Journal: Indian journal of endocrinology and metabolism
Published: April 22, 2021
Clinical and molecular findings in a Turkish family with an ultra-rare condition, ELP2-related neurodevelopmental disorder.
Journal: Molecular biology reports
Published: October 11, 2020
Serum 25-hydroxyvitamin D is associated with insulin resistance independently of obesity in children ages 5-17.
Journal: Primary care diabetes
Published: February 27, 2020
Use of Intravenous Lipid Emulsion Therapy in a Case of Atomoxetine (Strattera®) Toxicity.
Journal: The Journal of emergency medicine
Published: January 24, 2020
Short Term Unscheduled Revisits to Paediatric Emergency Department - A Six Year Data.
Journal: Journal of clinical and diagnostic research : JCDR
Published: October 28, 2016
Basal Cell Nevus (Gorlin) Syndrome with a Novel Heterozygous Deletion Frameshift Mutation (C.959delc, P.val322 Phe Fsx2) in the Ptch1 Gene Associated with Epiretinal Membrane, Odontogenic Keratocysts and without Skin Lesions and Falx Cerebri Calcification.
Journal: Genetic counseling (Geneva, Switzerland)
Published: January 01, 2016
A NOVEL MUTATION K447M (P.LYS447MET, C.1340 A>T) IDENTIFIED IN EXON 4 OF THE MEFV GENE.
Journal: Genetic counseling (Geneva, Switzerland)
Published: January 01, 2016
Last Updated: 09/26/2026