Doç. Dr. Aydilek Dağdeviren Çakır

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

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

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

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

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

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

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

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

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

Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study

Journal of clinical research in pediatric endocrinology, 2024

DOI 10.4274/jcrpe.galenos.2024.2024-1-3 PMID 38664994 10 citations (Europe PMC) Open-access full textSource: Europe PMC

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

A Rare Presentation of Homozygous Pathogenic Variant in MC2R Gene with Salt-Wasting Crisis in a Neonate

Molecular Syndromology, 2024

DOI 10.1159/000533986 PMID 38357256 3 citations (Europe PMC) Open-access full textSource: ORCID

Cinsiyet Gelişim Bozuklukları

2024

DOI 10.5152/6800 Source: OpenAlex

Cinsel Gelişim Bozukluklarında Tanı

2024

DOI 10.5152/6805 Source: OpenAlex

Clinical indicators that influence a clinician’s decision to start L-thyroxine treatment in prematurity with transient hypothyroxinemia

The Italian Journal of Pediatrics/Italian journal of pediatrics, 2023

DOI 10.1186/s13052-023-01516-6 PMID 37644575 2 citations (Europe PMC) Open-access full textSource: OpenAlex

Left Ventricular Systolic Dysfunction Related to Adrenal Insufficiency in a Case due to Autoimmune Polyendocrine Syndrome Type 1 with a Novel Variant

Molecular Syndromology, 2023

DOI 10.1159/000526221 PMID 36777707 5 citations (Europe PMC) Open-access full textSource: ORCID

Thyroid Nodules in Children and Adolescents: A Single Institution’s Experience

Turkish Archives of Pediatrics, 2023

DOI 10.5152/turkarchpediatr.2023.22302 PMID 37317576 5 citations (Europe PMC) Open-access full textSource: ORCID

A Case with Alstrom Syndrome with a Novel Pathogenic Variant In ALMS1 gene as a Rare Cause of Diabetes Mellitus

Hormone Research in Paediatrics, 2023

Source: ORCID

Comparative analyses of surrogates of metabolic syndrome in children and adolescents with metabolically healthy obesity vs. metabolically unhealthy obesity according to Damanhoury's criteria

Journal of Pediatric Endocrinology and Metabolism, 2023

DOI 10.1515/jpem-2022-0484 PMID 37017079 2 citations (Europe PMC) Source: ORCID

Differentiated Thyroid Cancer in Children and Adolescents: Clinicopathological Characteristics of 32 Patients Followed up in our Pediatric Endocrinology Unit

Sisli Etfal Hastanesi Tip Bülteni, 2023

DOI 10.14744/semb.2023.09216 PMID 37899815 2 citations (Europe PMC) Open-access full textSource: ORCID

Evaluation of the Frequency and Time Course of Side Effects Asscociated With Metformin Use In Obese Adolescents As Related to Weight Loss: A Prospective Single-Centre Observational Study

Hormone Research in Paediatrics, 2023

Source: ORCID

Prolonged Bleeding after Dental Extraction Due to Decreased Serum Level of von Willebrand Factor Caused by Untreated Profound Hypothyroidism

Journal of Pediatric Hematology/Oncology, 2023

DOI 10.1097/mph.0000000000002617 PMID 36706297 2 citations (Europe PMC) Source: ORCID

The association of metabolic syndrome status with sensorineural hearing loss in pediatric obese patients

International Journal of Pediatric Otorhinolaryngology, 2023

DOI 10.1016/j.ijporl.2023.111454 PMID 36696712 Source: ORCID

Effect of Different Treatment Protocols on Clinical Parameters in Diabetic Ketoacidosis: A Multicenter Study

Kocaeli Üniversitesi - AVESİS, 2022

Source: OpenAlex

Elevated Urinary VEGF-A, Transferrin, and Angiotensinogen Levels in Normoalbuminuric Children and Adolescents with Type 1 Diabetes: Can They Be Early Markers of Diabetic Kidney Disease?

Hormone Research in Paediatrics, 2022

DOI 10.1159/000521447 PMID 34915504 8 citations (Europe PMC) Source: ORCID

A rare cause of acquired von Willebrand factor deficiency: Primary hypothyroidism due to autoimmune thyroiditis

Hormone Research in Paediatrics, 2022

Source: ORCID

Assessment of Serum Spexin Levels in Obese Adolescents with Metabolic Syndrome Antecedents: Preliminary Results

Hormone Research in Paediatrics, 2022

DOI 10.1159/000521180 PMID 34839286 4 citations (Europe PMC) Source: ORCID

Increased Circulating Levels of Myo-inositol in Girls with Polycystic Ovary Syndrome

Hormone Research in Paediatrics, 2022

Source: ORCID

Premature ovarian failure in a tall adolescent

Hormone Research in Paediatrics, 2022

Source: ORCID

Results of Gonadotropin and Testosterone Treatments in Male Cases Diagnosed with Hypogonadotropic Hypogonadism: A Single Center Experience

Hormone Research in Paediatrics, 2022

Source: ORCID

Evaluation of Thyroid Nodules in Children and Adolescents: Multicenter Study in Turkey

Güncel Pediatri, 2021

DOI 10.4274/jcp.2021.43926 1 citation (OpenAlex) Open-access full textSource: OpenAlex

Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2

Journal of clinical research in pediatric endocrinology, 2021

DOI 10.4274/jcrpe.galenos.2020.2019.0216 PMID 32539318 5 citations (Europe PMC) Open-access full textSource: Europe PMC

Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome

Journal of clinical research in pediatric endocrinology, 2021

DOI 10.4274/jcrpe.galenos.2021.2020.0228 PMID 33565750 11 citations (Europe PMC) Open-access full textSource: Europe PMC

Different clinical entities of the same mutation: a case report of three sisters with Wolfram syndrome and efficacy of dipeptidyl peptidase-4 inhibitor therapy

Journal of Pediatric Endocrinology and Metabolism, 2021

DOI 10.1515/jpem-2020-0699 PMID 33882198 3 citations (Europe PMC) Source: ORCID

Are Serum Spexin Levels Associated With Metabolic Syndrome Antecedents In Obese Adolescents?

Hormone Research in Paediatrics, 2021

Source: ORCID

Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

Genetics in Medicine, 2021

DOI 10.1038/s41436-020-01087-5 PMID 33495532 28 citations (Europe PMC) Open-access full textSource: ORCID

Hipogonadotropik Hipogonadizm Tanılı Erkek Olgularda Gonadotropin ve Testosteron Tedavilerinin Birlikte Kullanımının Sonuçları: Tek Merkez Deneyimi

Kocaeli Üniversitesi - AVESİS, 2021

Source: OpenAlex

Evaluation of the thyroid disorders in children with familial Mediterranean fever

Clinical Rheumatology, 2020

DOI 10.1007/s10067-020-05430-8 PMID 32996072 4 citations (Europe PMC) Source: ORCID

Factors influencing blood pressure and microalbuminuria in children with type 1 diabetes mellitus: salt or sugar?

Pediatric Nephrology, 2020

DOI 10.1007/s00467-020-04526-2 PMID 32211992 7 citations (Europe PMC) Source: ORCID

An Unusual Presentation of Carney Complex

Journal of Clinical Research in Pediatric Endocrinology, 2020

DOI 10.4274/jcrpe.galenos.2019.2019.0043 PMID 31117334 6 citations (Europe PMC) Open-access full textSource: ORCID

Two Novel Variants and One Previously Reported Variant in the Insulin Receptor Gene in Two Cases with Severe Insulin Resistance Syndrome

Molecular Syndromology, 2020

DOI 10.1159/000506722 PMID 32655340 1 citation (Europe PMC) Open-access full textSource: ORCID

Iodine Status and Thyroid Functions of Turkish and Syrian Mother-Newborn Dyads in a County of Istanbul

SSRN Electronic Journal, 2020

DOI 10.2139/ssrn.3685940 Open-access full textSource: OpenAlex

Proteinuria in a patient with Graves’ disease: Answers

Pediatric Nephrology, 2019

DOI 10.1007/s00467-019-04221-x PMID 30843111 2 citations (Europe PMC) Source: ORCID

Proteinuria in a patient with Graves’ disease: Questions

Pediatric Nephrology, 2019

DOI 10.1007/s00467-019-04220-y PMID 30843109 Source: ORCID

SUN-624 Occurrence Of Papillary Thyroid Cancer During Treatment Of Thyroid Dysfunction

Journal of the Endocrine Society, 2019

DOI 10.1210/js.2019-sun-624 Open-access full textSource: OpenAlex

Incidence of Type 1 Diabetes in Children Aged Below 18 Years During 2013-2015 in Northwest Turkey

Journal of Clinical Research in Pediatric Endocrinology, 2018

DOI 10.4274/jcrpe.0025 PMID 29789274 8 citations (Europe PMC) Open-access full textSource: OpenAlex

Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation

Journal of Clinical Research in Pediatric Endocrinology, 2018

DOI 10.4274/jcrpe.5078 PMID 29022557 8 citations (Europe PMC) Open-access full textSource: ORCID

Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation

JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2018

DOI 10.4274/jcrpe.5162 PMID 28943513 18 citations (Europe PMC) Open-access full textSource: ORCID

FACTORS INFLUENCING BLOOD PRESSURE IN CHILDREN WITH DIABETES MELLITUS TYPE 1: SALT OR SUGAR?

2018

Source: OpenAlex

A Novel Mutation of AMHR2 In Two Siblings with Persistent Müllerian Duct Syndrome

Sexual Development, 2017

DOI 10.1159/000485882 PMID 29332065 4 citations (Europe PMC) Source: ORCID