Doç. Dr. Aydilek Dağdeviren Çakır
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Which diseases does this doctor work on?
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Diabetes Mellitus, Type 1 3 publicationsSource: OpenAlex / PubMed MeSHView publications
- Hypothyroidism 2 publications
- Infant, Newborn, Diseases 2 publications
- Familial Mediterranean Fever 2 publications
- Proteinuria 2 publications
- Graves Disease 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
- InstitutionŞişli Hamidiye Etfal Eğitim ve Araştırma Hastanesisaglik.gov.trFrom source
- Area of workDiabetes Mellitus, Type 1Extracted from 3 publications · Model version —From source
- Publications53 publicationsOpenAlex, ORCIDFrom source
- ORCID0000-0001-7136-9241ORCIDFrom source
- Last synchronised5 November 2026 08:56https://sislietfaleah.saglik.gov.tr/TR-1434007/doktorlarimiz.html#aydilek-dagdeviren-cakirsaglik.gov.tr
Scientific work
Publications on Diabetes Mellitus, Type 1
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Early dextrose and lower-chloride fluids in pediatric diabetic ketoacidosis: a faster and safer approach? - A multicenter cohort study
BMC Endocrine Disorders, 2026
DOI 10.1186/s12902-026-02555-w Open-access full textSource: OpenAlex
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Baseline and 3-Year Follow-Up Changes in Retinal Neurovascular Structures Assessed by OCT and OCTA in Pediatric Type 1 Diabetes Without Retinopathy
Journal of VitreoRetinal Diseases, 2026
DOI 10.1177/24741264261484021 PMID 42756149 Open-access full textSource: ORCID
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Serum Netrin-1 and ultrasonographic hepatic steatosis severity in obese children and adolescents with metabolic dysfunction–associated steatotic liver disease: a preliminary study
European Journal of Pediatrics, 2026
DOI 10.1007/s00431-026-07566-2 PMID 42925329 Source: ORCID
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A Rare Cause of Thyroid Hormone Abnormalities in an Adolescent: A Case Report of SBP2 (SECISBP2) Deficiency
Molecular Syndromology, 2026
DOI 10.1159/000551282 PMID 42238688 Open-access full textSource: ORCID
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The first report of a gross deletion in the SCNN1G gene in a case presenting with hyponatremic convulsion at fifth year of treatment
Journal of Pediatric Endocrinology and Metabolism, 2026
DOI 10.1515/jpem-2025-0372 PMID 41275343 Source: ORCID
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Case Reports: Exploring the Varied Presentations and Clinical Features of Carney Complex, A Detailed Report on Three Distinct Cases
Journal of Clinical Research in Pediatric Endocrinology, 2026
DOI 10.4274/jcrpe.galenos.2026.2025-8-10 PMID 41486943 2 citations (OpenAlex) Open-access full textSource: OpenAlex
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Current Practices in Hashimoto's Thyroiditis: Differences in Attitudes Between Pediatric and Adult Endocrinologists in Türkiye: A National Survey
Journal of Clinical Research in Pediatric Endocrinology, 2025
DOI 10.4274/jcrpe.galenos.2025.2024-9-12 PMID 39849667 Open-access full textSource: OpenAlex
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Attitudes Towards the Management of Congenital Hypothyroidism in Türkiye: National Survey Study
Journal of Clinical Research in Pediatric Endocrinology, 2025
DOI 10.4274/jcrpe.galenos.2025.2024-9-18 PMID 39885770 1 citation (Europe PMC) Open-access full textSource: OpenAlex
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Testicular growth and sperm detection rates following combined hcg and rfsh therapy in adolescents with congenital and acquired hypogonadotropic hypogonadism
Kocaeli Üniversitesi - AVESİS, 2025
Source: OpenAlex
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Temporary Thyroid Dysfunction and Catecholamine Excess Due to Mercury Poisoning in 6 Cases
Turkish Archives of Pediatrics, 2024
DOI 10.5152/turkarchpediatr.2023.23150 PMID 37818842 2 citations (Europe PMC) Open-access full textSource: ORCID