Paediatric Endocrinology

Uzm. Dr. Zeynep Donbaloğlu

Doctor and researcher Antalya Şehir Hastanesi Antalya
Adrenal InsufficiencyInfant, Newborn, DiseasesDiabetes Mellitus, Type 1Congenital Hypothyroidism

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Person ↔ Disease

Which diseases does this doctor work on?

From source
  • Adrenal Insufficiency 2 publications
    Source: OpenAlex / PubMed MeSHView publications
  • Infant, Newborn, Diseases 2 publications
  • Diabetes Mellitus, Type 1 2 publications
  • Congenital Hypothyroidism 2 publications

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Where does this information come from?

The source is stated next to each piece of information. If you see something wrong, you can suggest a correction.

  • SpecialtyPaediatric Endocrinologysaglik.gov.trFrom source
  • Department name at the sourceÇocuk Endokrinoloji ve Metabolizmasaglik.gov.trFrom source
  • InstitutionAntalya Şehir Hastanesisaglik.gov.trFrom source
  • Area of workAdrenal InsufficiencyExtracted from 2 publications · Model version —From source
  • Publications29 publicationsORCID, Europe PMC, OpenAlexFrom source
  • ORCID0000-0003-0605-3229ORCIDFrom source
  • Last synchronised7 November 2026 00:03https://antalyasehir.saglik.gov.tr/TR-1059999/doktorlarimiz.html#zeynep-donbaloglusaglik.gov.tr

Scientific work

Publications on Adrenal Insufficiency

29 publications
Publications by year Most: 8, in 2025
  1. 2019: 1 publication
  2. 2020: 0 publications
  3. 2021: 0 publications
  4. 2022: 4 publications
  5. 2023: 1 publication
  6. 2024: 7 publications
  7. 2025: 8 publications
  8. 2026: 8 publications
  1. Can uric acid levels be helpful for the diagnosis of CPP in girls?

    Journal of Pediatric Endocrinology and Metabolism, 2026

    DOI 10.1515/jpem-2025-0492 PMID 41392030 Source: ORCID

  2. Investigating the Role of <i>LRG1</i> in Hepatosteatosis and Insulin Resistance in Obese Children

    Journal of clinical research in pediatric endocrinology, 2026

    DOI 10.4274/jcrpe.galenos.2026.2025-11-5 PMID 41521682 Open-access full textSource: Europe PMC

  3. Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder

    Journal of clinical research in pediatric endocrinology, 2026

    DOI 10.4274/jcrpe.galenos.2025.2024-12-4 PMID 40103355 4 citations (Europe PMC) Open-access full textSource: Europe PMC

  4. A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism due to a Novel Homozygous Variant in the <i>SCNN1B</i> Gene

    Journal of clinical research in pediatric endocrinology, 2026

    DOI 10.4274/jcrpe.galenos.2024.2024-10-5 PMID 39723761 1 citation (Europe PMC) Open-access full textSource: Europe PMC

  5. Longitudinal changes in nonfunctioning pituitary neuroendocrine tumors in children receiving growth hormone therapy: A comparison with untreated patients

    Archivos argentinos de pediatria, 2026

    DOI 10.5546/aap.2026-11133.eng PMID 42517616 Open-access full textSource: Europe PMC

  6. Evaluation of Muscle Mass and Strength in Children and Adolescents with Disorders of Sex Development

    Journal of Clinical Research in Pediatric Endocrinology, 2026

    DOI 10.4274/jcrpe.galenos.2026.2025-12-1 PMID 41498263 Open-access full textSource: OpenAlex

  7. Single-Center Experience in Five Patients Diagnosed with Lipoid Congenital Adrenal Hyperplasia due to <i>Steroidogenic Acute Regulatory Protein (STAR)</i> Gene Variants: A Rare Cause of Adrenal Insufficiency

    Journal of clinical research in pediatric endocrinology, 2026

    DOI 10.4274/jcrpe.galenos.2025.2025-9-15 PMID 41261870 Open-access full textSource: Europe PMC

  8. Assessing the effectiveness of written educational materials on parental knowledge of childhood constipation

    Medicine Science | International Medical Journal, 2026

    DOI 10.5455/medscience.2025.12.336 Open-access full textSource: OpenAlex

  9. Evaluation of the genetic alterations landscape of differentiated thyroid cancer in children

    Journal of Pediatric Endocrinology and Metabolism, 2025

    DOI 10.1515/jpem-2025-0443 PMID 41176785 Source: ORCID

  10. Changes in body composition and muscle strength in girls with idiopathic central precocious puberty during gonadotropin-releasing hormone agonist therapy

    Journal of Health Sciences and Medicine, 2025

    DOI 10.32322/jhsm.1557045 1 citation (OpenAlex) Open-access full textSource: ORCID

View all 29 publications