Ayse N. Cebeci
Istanbul, Turkey
Last Updated: 09/26/2026
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Found 27 publications
Association Between Pediatric Obesity and Ocular Structural Parameters: A Cross-Sectional Study.
Journal: Children (Basel, Switzerland)
Published: May 17, 2026
The clinical picture of symptomatic Rathke cleft cysts in children.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: April 28, 2026
The clinical picture of symptomatic Rathke cleft cysts in children.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: July 20, 2025
SIADH as a Rare Complication of Foramen Magnum Stenosis in an Infant With Achondroplasia.
Journal: JCEM case reports
Published: April 27, 2024
Neutropenia Occurs More Often Under Carbimazole than Under Methimazole Treatment in Pediatric Graves' Disease Patients.
Journal: Thyroid : official journal of the American Thyroid Association
Published: April 13, 2024
A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome.
Journal: Anatolian journal of cardiology
Published: February 22, 2022
Impact of eating habits and nutritional status on children with autism spectrum disorder.
Journal: Journal of Taibah University Medical Sciences
Published: October 02, 2020
Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis
Journal: Journal of clinical research in pediatric endocrinology
Published: September 17, 2020
Evaluation of hydration status of children with obesity-a pilot study.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: August 24, 2020
A Rare Cause of Autistic Regression in a Boy with Down Syndrome: Hashimoto Encephalopathy.
Journal: Journal of pediatric neurosciences
Published: December 21, 2019
Mutation of SGK3, a Novel Regulator of Renal Phosphate Transport, Causes Autosomal Dominant Hypophosphatemic Rickets.
Journal: The Journal of clinical endocrinology and metabolism
Published: July 02, 2019
Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey.
Journal: Journal of clinical immunology
Published: April 30, 2016
Last Updated: 09/26/2026