Paediatric Endocrinology

Uzm. Dr. Berna Singin

Doctor and researcher Antalya Şehir Hastanesi Antalya
Congenital HypothyroidismDiabetes Mellitus, Type 1

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Person ↔ Disease

Which diseases does this doctor work on?

From source
  • Congenital Hypothyroidism 2 publications
    Source: OpenAlex / PubMed MeSHView publications
  • Diabetes Mellitus, Type 1 2 publications

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Where does this information come from?

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  • SpecialtyPaediatric Endocrinologysaglik.gov.trFrom source
  • Department name at the sourceÇocuk Endokrinoloji ve Metabolizmasaglik.gov.trFrom source
  • InstitutionAntalya Şehir Hastanesisaglik.gov.trFrom source
  • Area of workCongenital HypothyroidismExtracted from 2 publications · Model version —From source
  • Publications22 publicationsORCID, Europe PMC, OpenAlexFrom source
  • ORCID0000-0002-2204-5336ORCIDFrom source
  • Last synchronised7 November 2026 00:03https://antalyasehir.saglik.gov.tr/TR-1059999/doktorlarimiz.html#berna-singinsaglik.gov.tr

Scientific work

Publications on Congenital Hypothyroidism

22 publications
Publications by year Most: 6, in 2024
  1. 2022: 2 publications
  2. 2023: 2 publications
  3. 2024: 6 publications
  4. 2025: 6 publications
  5. 2026: 6 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. A Comparative Assessment of Large Language Models in Congenital Hypothyroidism: Reliability, Quality and Readability

    Journal of clinical research in pediatric endocrinology, 2026

    DOI 10.4274/jcrpe.galenos.2026.2026-1-15 PMID 42011955 Open-access full textSource: Europe PMC

  3. 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

  4. 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

  5. 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

  6. Evaluation of children with neurocutaneous diseases: A five-year clinical experience

    Medicine Science | International Medical Journal, 2026

    DOI 10.5455/medscience.2025.09.252 Open-access full textSource: OpenAlex

  7. 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

  8. 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

  9. Growth Hormone Therapy in Neurosecretory Dysfunction

    Turkish Archives of Pediatrics, 2025

    DOI 10.5152/turkarchpediatr.2025.24319 PMID 40353620 2 citations (OpenAlex) Open-access full textSource: OpenAlex

  10. A Case of Adolescent Girl with Hypercalcemia Resistant to Medical Treatment Due to Giant Breast Fibroadenoma

    Journal of Clinical Research in Pediatric Endocrinology, 2025

    DOI 10.4274/jcrpe.galenos.2025.2025-3-21 PMID 40501122 Open-access full textSource: OpenAlex

View all 22 publications