Ayse D. Bulus

Ankara, Turkey

Last Updated: 09/26/2026

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Found 27 publications

Association of GSTM1, GSTT1, and TP53 Genetic Variants with Obesity in Children.

Association of GSTM1, GSTT1, and TP53 Genetic Variants with Obesity in Children.

Journal: Turkish archives of pediatrics

Published: April 27, 2026

ACAN-Related Short Stature and Skeletal Dysplasia: Expanding the Phenotypic and Genotypic Spectrum in a 47 Patient Cohort From Turkey.

ACAN-Related Short Stature and Skeletal Dysplasia: Expanding the Phenotypic and Genotypic Spectrum in a 47 Patient Cohort From Turkey.

Journal: American journal of medical genetics. Part A

Published: March 13, 2026

Genotype-Phenotype Spectrum of Non-Syndromic Monogenic Obesity in a National Paediatric Cohort.

Genotype-Phenotype Spectrum of Non-Syndromic Monogenic Obesity in a National Paediatric Cohort.

Journal: Pediatric obesity

Published: November 25, 2025

Serum uric acid level as a marker associated with microalbuminuria in pediatric patients with type 1 diabetes mellitus.

Serum uric acid level as a marker associated with microalbuminuria in pediatric patients with type 1 diabetes mellitus.

Journal: European journal of pediatrics

Published: September 04, 2025

Is Serum Uric Acid to Creatinine Ratio Associated with Hypertension and Metabolic Syndrome in Children with Obesity?

Is Serum Uric Acid to Creatinine Ratio Associated with Hypertension and Metabolic Syndrome in Children with Obesity?

Journal: Klinische Padiatrie

Published: February 04, 2025

Treatment and Follow-up of Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency in Childhood and Adolescence

Treatment and Follow-up of Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency in Childhood and Adolescence

Journal: Journal of clinical research in pediatric endocrinology

Published: December 23, 2024

Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency

Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency

Journal: Journal of clinical research in pediatric endocrinology

Published: December 23, 2024

A New Case with Weaver Syndrome: Delineating Natural Course and Growth Pattern, Further Clarifying Clinical Phenotype.

A New Case with Weaver Syndrome: Delineating Natural Course and Growth Pattern, Further Clarifying Clinical Phenotype.

Journal: Molecular syndromology

Published: July 23, 2024

Sonographic cortical bone thickness measurement: can it predict bone mineral density in the pediatric population?

Sonographic cortical bone thickness measurement: can it predict bone mineral density in the pediatric population?

Journal: Diagnostic and interventional radiology (Ankara, Turkey)

Published: December 04, 2023

Cases of hypogonadotropic hypogonadism: A single-center experience.

Cases of hypogonadotropic hypogonadism: A single-center experience.

Journal: Nigerian journal of clinical practice

Published: November 06, 2023

Clinical and laboratory predictors of long-COVID in children: a single center retrospective study.

Clinical and laboratory predictors of long-COVID in children: a single center retrospective study.

Journal: European review for medical and pharmacological sciences

Published: October 31, 2022

Hyponatremia in a patient with diabetic ketosis: Answers.

Hyponatremia in a patient with diabetic ketosis: Answers.

Journal: Pediatric nephrology (Berlin, Germany)

Published: July 27, 2022

Showing 1-12 of 27

Last Updated: 09/26/2026