Gulay Ceylaner
Ankara, Turkey
Last Updated: 09/26/2026
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Found 18 publications
Neonatal Aicardi-Goutières syndrome presenting with macrophage activation syndrome-like hyperinflammation and severe congenital glaucoma: a case report.
Journal: Pediatric rheumatology online journal
Published: June 08, 2026
Exploratory Associations of Targeted Genetic Variants with Cephalometric Airway Parameters in Children with Skeletal Class II Sleep-Disordered Breathing Symptoms.
Journal: Children (Basel, Switzerland)
Published: January 09, 2026
Correction to: A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature.
Journal: Journal of clinical immunology
Published: January 15, 2024
A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature.
Journal: Journal of clinical immunology
Published: January 25, 2023
Specific Granule Deficiency Due To Novel Homozygote SMARCD2 Variant.
Journal: Pediatric allergy, immunology, and pulmonology
Published: March 23, 2022
The outcome of 41 Late-Diagnosed Turkish GA-1 Patients: A Candidate for the Turkish NBS.
Journal: Neuropediatrics
Published: February 12, 2021
Isolated congenital diaphragm hernia associated with homozygous SLIT3 gene variant in dizygous twins.
Journal: European journal of medical genetics
Published: June 04, 2020
Fabry Disease Screening in Patients With Kidney Transplant: A Single-Center Study in Turkey.
Journal: Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation
Published: April 14, 2020
Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty
Journal: Journal of clinical research in pediatric endocrinology
Published: March 15, 2018
Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations.
Journal: The Turkish journal of pediatrics
Published: January 01, 2017
A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus.
Journal: European journal of medical genetics
Published: May 21, 2016
Congenital Glucose-Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene.
Journal: Digestive diseases and sciences
Published: May 03, 2016
Last Updated: 09/26/2026