Uzm. Dr. Hilal Sekizkardeş
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Which diseases does this doctor work on?
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Insulin Resistance 2 publicationsSource: OpenAlex / PubMed MeSHView publications
- Lipodystrophy 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 Endokrinolojisaglik.gov.trFrom source
- InstitutionSancaktepe Şehit Prof. Dr. İlhan Varank Eğitim ve Araştırma Hastanesisaglik.gov.trFrom source
- Area of workInsulin ResistanceExtracted from 2 publications · Model version —From source
- Publications15 publicationsOpenAlex, ORCIDFrom source
- ORCID0000-0002-6482-870XORCIDFrom source
- Last synchronised5 November 2026 08:56https://sancaktepeah.saglik.gov.tr/TR-1485776/doktorlarimiz.html#hilal-sekizkardessaglik.gov.tr
Scientific work
Publications on Insulin Resistance
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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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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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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