Scientific work

Uzm. Dr. Hilal Sekizkardeş

15 publications. The source of the information is stated next to each publication.

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  1. Diagnostic Utility of Genetic Testing in Hyperthyroxinemia With Non‐Suppressed TSH

    Clinical Endocrinology, 2026

    DOI 10.1111/cen.70126 PMID 41800491 Source: OpenAlex

  2. Serum Homocysteine, Insulin Resistance, and Metabolic Risk Factors in Children and Adolescents with Obesity: A Retrospective Cross-Sectional Study

    Journal of Clinical Medicine, 2026

    DOI 10.3390/jcm15062216 PMID 41899140 Open-access full textSource: ORCID

  3. Effects of Different Insulin Treatment Approaches on Metabolic Parameters and Quality of Life in Children with Type 1 Diabetes

    Diabetes & its Complications, 2026

    DOI 10.33425/2639-9326.1135 Open-access full textSource: OpenAlex

  4. Novel IGF1R Variants in Short Stature: Lessons from Two Patients and Outcome of Growth Hormone Therapy

    Journal of Clinical Research in Pediatric Endocrinology, 2025

    DOI 10.4274/jcrpe.galenos.2025.2024-12-7 PMID 40269620 2 citations (Europe PMC) Open-access full textSource: OpenAlex

  5. Lipodystrophy Severity Score to Assess Disease Burden in Lipodystrophy

    The Journal of Clinical Endocrinology & Metabolism, 2025

    DOI 10.1210/clinem/dgaf103 PMID 39970125 10 citations (Europe PMC) Open-access full textSource: OpenAlex

  6. Phenotypic Differences Among Familial Partial Lipodystrophy Due to LMNA or PPARG Variants

    Journal of the Endocrine Society, 2022

    DOI 10.1210/jendso/bvac155 PMID 36397776 29 citations (Europe PMC) Open-access full textSource: ORCID

  7. Heterozygous Deletions in MKRN3 Cause Central Precocious Puberty Without Prader-Willi Syndrome.

    The Journal of clinical endocrinology and metabolism, 2020

    DOI 10.1210/clinem/dgaa331 PMID 32480405 17 citations (Europe PMC) Open-access full textSource: ORCID

  8. Diagnostic Value of Anthropometric Measurements for Familial Partial Lipodystrophy, Dunnigan Variety.

    The Journal of clinical endocrinology and metabolism, 2020

    DOI 10.1210/clinem/dgaa137 PMID 32193531 30 citations (Europe PMC) Open-access full textSource: ORCID

  9. Free fatty acid processing diverges in human pathologic insulin resistance conditions.

    The Journal of clinical investigation, 2020

    DOI 10.1172/jci135431 PMID 32191645 55 citations (Europe PMC) Open-access full textSource: ORCID

  10. Thyroid Hormone Effects on Glucose Disposal in Patients With Insulin Receptor Mutations.

    The Journal of clinical endocrinology and metabolism, 2020

    DOI 10.1210/clinem/dgz079 PMID 31588494 12 citations (Europe PMC) Open-access full textSource: ORCID

  11. SUN-LB111 Comparison of Phenotype and Metabolic Abnormalities Among Familial Partial Lipodystrophy Due to LMNA or PPARG Variants

    Journal of the Endocrine Society, 2020

    DOI 10.1210/jendso/bvaa046.2312 2 citations (OpenAlex) Open-access full textSource: OpenAlex

  12. Clinical and laboratory characteristics and follow up of 62 cases of ketotic hypoglycemia: a retrospective study.

    International journal of pediatric endocrinology, 2019

    DOI 10.1186/s13633-019-0066-9 PMID 31700521 9 citations (Europe PMC) Open-access full textSource: ORCID

  13. Efficacy of Metreleptin Treatment in Familial Partial Lipodystrophy Due to PPARG vs LMNA Pathogenic Variants.

    The Journal of clinical endocrinology and metabolism, 2019

    DOI 10.1210/jc.2018-02787 PMID 31194872 39 citations (Europe PMC) Open-access full textSource: ORCID

  14. MON-159 Increased Gluconeogenesis and Lower Glycogenolysis in Patients with Non-Selective Compared Selective Insulin Resistance

    Journal of the Endocrine Society, 2019

    DOI 10.1210/js.2019-mon-159 Open-access full textSource: OpenAlex

  15. Effect of Educational Intervention on Adherence Estimator™ Scores and Asthma Control in Pediatric Patients

    Journal of Allergy and Clinical Immunology, 2015

    DOI 10.1016/j.jaci.2014.12.1092 1 citation (OpenAlex) Source: OpenAlex