Hayrullah Manyas
Sanliurfa, Turkey
Last Updated: 09/26/2026
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Found 10 publications
Genotype-Phenotype Spectrum of Non-Syndromic Monogenic Obesity in a National Paediatric Cohort.
Journal: Pediatric obesity
Published: November 25, 2025
Long-term Impact of Continuous Glucose Monitoring Assistance on Glycemic Control in Children and Adolescents with Type 1 Diabetes Following the 2023 Kahramanmaraş Earthquake
Journal: Journal of clinical research in pediatric endocrinology
Published: December 23, 2024
OBSESSIVE COMPULSIVE DISORDER AND CONSTITUTIONAL DELAY OF GROWTH AND PUBERTY IN WOLFRAM SYNDROME: NEW ASPECTS AND A NOVEL WFS1 MUTATION.
Journal: Acta endocrinologica (Bucharest, Romania : 2005)
Published: October 07, 2024
Androgen receptor CAG repeat polymorphism might be a possible cause of familial constitutional delay of growth and puberty.
Journal: Journal of endocrinological investigation
Published: August 16, 2024
A rare endocrinological complication of chronic kidney disease.
Journal: The Turkish journal of pediatrics
Published: May 25, 2022
Childhood-onset mild diabetes caused by a homozygous novel variant in the glucokinase gene.
Journal: Hormones (Athens, Greece)
Published: December 23, 2020
Can ocular changes be detected early in children and adolescents with type 1 diabetes mellitus without retinopathy by using optical biometry and optical coherence tomography?
Journal: International ophthalmology
Published: March 10, 2020
A Drug Reaction With Eosinophilia and Systemic Symptoms Syndrome Associated With Clobazam.
Journal: Pediatric emergency care
Published: March 15, 2019
Showing 1-10 of 10
Last Updated: 09/26/2026