Scientific work
Uzm. Dr. Hilal Sekizkardeş
15 publications. The source of the information is stated next to each publication.
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Diagnostic Utility of Genetic Testing in Hyperthyroxinemia With Non‐Suppressed TSH
Clinical Endocrinology, 2026
DOI 10.1111/cen.70126 PMID 41800491 Source: OpenAlex
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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