Ozlem Unal-Uzun

Kosekoy, Turkey

Last Updated: 09/26/2026

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Found 18 publications

The relationship between appetite hormones and body mass index in children with intoxication type metabolic diseases.

The relationship between appetite hormones and body mass index in children with intoxication type metabolic diseases.

Journal: Orphanet journal of rare diseases

Published: April 23, 2025

Cord blood metabolomic profiling in high risk newborns born to diabetic, obese, and overweight mothers: preliminary report.

Cord blood metabolomic profiling in high risk newborns born to diabetic, obese, and overweight mothers: preliminary report.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: December 15, 2024

Expert opinion on clinical presentation, diagnosis, and treatment of infantile-onset Pompe disease: a Delphi study in Türkiye.

Expert opinion on clinical presentation, diagnosis, and treatment of infantile-onset Pompe disease: a Delphi study in Türkiye.

Journal: Turkish journal of medical sciences

Published: May 23, 2024

Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency.

Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency.

Journal: European journal of pediatrics

Published: September 04, 2023

Difficult to think about but easy to treat: scurvy.

Difficult to think about but easy to treat: scurvy.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: March 23, 2023

Two cases of MEGDHEL syndrome diagnosed with hyperammonemia.

Two cases of MEGDHEL syndrome diagnosed with hyperammonemia.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: August 31, 2022

Molecular and clinical findings of Turkish patients with hereditary fructose intolerance.

Molecular and clinical findings of Turkish patients with hereditary fructose intolerance.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: April 28, 2021

Proteinuria and progressive kidney failure due to an inborn error of metabolism: Answers.

Proteinuria and progressive kidney failure due to an inborn error of metabolism: Answers.

Journal: Pediatric nephrology (Berlin, Germany)

Published: November 11, 2020

Proteinuria and progressive kidney failure due to an inborn error of metabolism: Questions.

Proteinuria and progressive kidney failure due to an inborn error of metabolism: Questions.

Journal: Pediatric nephrology (Berlin, Germany)

Published: November 11, 2020

Evaluation of nutritional status in pediatric patients diagnosed with Covid-19 infection.

Evaluation of nutritional status in pediatric patients diagnosed with Covid-19 infection.

Journal: Clinical nutrition ESPEN

Published: October 31, 2020

A novel etiologic factor of highly elevated cholestanol levels: progressive familial intrahepatic cholestasis.

A novel etiologic factor of highly elevated cholestanol levels: progressive familial intrahepatic cholestasis.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: July 11, 2019

Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation.

Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation.

Journal: The Turkish journal of pediatrics

Published: May 18, 2016

Showing 1-12 of 18

Last Updated: 09/26/2026