Travaux scientifiques

Uzm. Dr. Mehmet Eltan

48 publications. La source de l’information est indiquée à côté de chaque publication.

Retour au profil

  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. Targeting Hypercalciuria in SLC34A1-Related Disorders: Impact of Oral Phosphate Therapy and Novel Genetic Insights in Pediatric Case Series

    Calcified tissue international, 2026

    DOI 10.1007/s00223-025-01462-x PMID 41543768 Texte intégral en libre accèsSource : Europe PMC

  3. Isolated Hyperchlorhidrosis Caused by Novel Biallelic CA12 Variants Mimicking Pseudohypoaldosteronism

    2026

    DOI 10.1159/hrp/adaag054 Source : ORCID

  4. Determinants of pubertal progression and final height in premature pubarche

    Journal of Endocrinological Investigation, 2026

    DOI 10.1007/s40618-026-02957-6 PMID 42340620 Texte intégral en libre accèsSource : ORCID

  5. Adrenal androgens as predictors of growth characteristics in premature pubarche

    European journal of endocrinology, 2026

    DOI 10.1093/ejendo/lvag024 PMID 41637567 1 citation (Europe PMC) Source : Europe PMC

  6. How Accurate is Self-Reported Parental Height? Evidence From a Tertiary Pediatric Endocrinology

    Southern Clinics of Istanbul Eurasia, 2026

    DOI 10.14744/scie.2026.51333 Texte intégral en libre accèsSource : OpenAlex

  7. Clinical Correlates of Adrenal Zona Reticularis Function in Turner Syndrome

    Figshare, 2026

    DOI 10.6084/m9.figshare.32780793 Texte intégral en libre accèsSource : OpenAlex

  8. Clinical Correlates of Adrenal Zona Reticularis Function in Turner Syndrome

    Figshare, 2026

    DOI 10.6084/m9.figshare.32780751 Texte intégral en libre accèsSource : OpenAlex

  9. Functional Impact of a Novel Intronic TG Variant in Congenital Goiter and Thyroid Dyshormonogenesis

    Hormone Research in Paediatrics, 2026

    DOI 10.1159/000553376 PMID 42378173 Source : ORCID

  10. Serum selenium and urinary iodine status in children and adolescents with autoimmune thyroiditis and mild subclinical hypothyroidism

    Endocrinología Diabetes y Nutrición, 2026

    DOI 10.1016/j.endinu.2026.501856 Source : OpenAlex

  11. 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) Texte intégral en libre accèsSource : OpenAlex

  12. Clinical and Molecular Spectrum of Infantile Hypercalcemia Type I: Insights Into CYP24A1 Variants

    Clinical Endocrinology, 2025

    DOI 10.1111/cen.70064 PMID 41327588 Source : OpenAlex

  13. The role of FGF23 in phosphorus and calcium metabolism: lessons from diseases affecting serum phosphate levels

    Endocrine Abstracts, 2025

    DOI 10.1530/endoabs.110.p225 Source : OpenAlex

  14. Expanding the Clinical Features of Schimke Immuno-osseous Dysplasia: a New Patient with a Novel Variant and Novel Clinical Findings

    Journal of clinical research in pediatric endocrinology, 2025

    DOI 10.4274/jcrpe.galenos.2024.2024-1-17 PMID 39113392 2 citations (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  15. Comprehensive clinical and genetic characterization of Bardet-Biedl Syndrome: insights from the largest Turkish cohort

    European Journal of Pediatrics, 2025

    DOI 10.1007/s00431-025-06592-w PMID 41219488 1 citation (OpenAlex) Source : OpenAlex

  16. Assessing Physical Activity in Obese Children: Reliability and Validity of the PAQ-C

    Comprehensive Medicine, 2025

    DOI 10.14744/cm.2024.73745 Texte intégral en libre accèsSource : OpenAlex

  17. Triiodothyronine/Thyroxine Ratio and Metabolic Connections: Exploring Hyperthyrotropinemia in Childhood Obesity

    Southern Clinics of Istanbul Eurasia, 2025

    DOI 10.14744/scie.2025.97830 Texte intégral en libre accèsSource : OpenAlex

  18. A novel biallelic intronic variant in the TG gene associated with thyroid dyshormonogenesis and fetal goiter

    Endocrine Abstracts, 2025

    DOI 10.1530/endoabs.110.p1143 Source : OpenAlex

  19. Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia

    The Journal of Clinical Endocrinology & Metabolism, 2024

    DOI 10.1210/clinem/dgae868 PMID 39700445 3 citations (Europe PMC) Source : OpenAlex

  20. Presentation and outcome in carriers of pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter NPT 2a and 2c

    Kidney International, 2024

    DOI 10.1016/j.kint.2024.08.035 PMID 39461557 31 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  21. Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the Literature

    Hormone Research in Paediatrics, 2023

    DOI 10.1159/000529070 PMID 36630941 1 citation (Europe PMC) Source : OpenAlex

  22. Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty

    Journal of Pediatric Endocrinology and Metabolism, 2023

    DOI 10.1515/jpem-2022-0645 PMID 36883204 7 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  23. Late-effects of Chemoradiotherapy on Growth and Puberty in Survivors of Childhood Acute Lymphoblastic Leukemia

    Trends in Pediatrics, 2022

    DOI 10.4274/tp.2022.43043 Texte intégral en libre accèsSource : ORCID

  24. Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with One Year of IDegAsp Therapy in Poorly Controlled and Non-compliant Patients

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2022

    DOI 10.4274/jcrpe.galenos.2021.2021.0113 PMID 34355879 4 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  25. Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features

    Calcified Tissue International, 2021

    DOI 10.1007/s00223-021-00928-y PMID 34761296 4 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  26. A rare cause of hypercalcemia: Congenital Lactase Deficiency

    59th ESPE Annual Meeting (ESPE 2021 Online), 2021

    Source : OpenAlex

  27. Does Genotype–Phenotype Correlation Exist in Vitamin D-Dependent Rickets Type IA: Report of 13 New Cases and Review of the Literature

    Calcified Tissue International, 2021

    DOI 10.1007/s00223-020-00784-2 PMID 33386952 20 citations (Europe PMC) Source : ORCID

  28. mTOR-Activating mutations in RRAGD are causative for kidney tubulopathy and cardiomyopathy

    Journal of the American Society of Nephrology, 2021

    DOI 10.1681/asn.2021030333 PMID 34607910 53 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  29. Acetazolamide treatment in a patient with pseudohypoparathyroidism with venous calcification

    59th ESPE Annual Meeting (ESPE 2021 Online), 2021

    Source : OpenAlex

  30. 46,XY DSD due to biallelic DHX37 gene mutations

    59th ESPE Annual Meeting (ESPE 2021 Online), 2021

    Source : OpenAlex

  31. Biallelic PPP2R3C mutations are associated with partial and complete gonadal dysgenesis in 46,XY and 46,XX individuals

    59th ESPE Annual Meeting (ESPE 2021 Online), 2021

    Source : OpenAlex

  32. Correlation of 11-oxygenated C19 androgens with the clinical and biochemical characteristics in premature adrenarche

    2021

    Source : OpenAlex

  33. A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age

    Calcified Tissue International, 2020

    DOI 10.1007/s00223-020-00694-3 PMID 32337609 14 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  34. Low DHEAS Concentration in a Girl Presenting with Short Stature and Premature Pubarche: A Novel PAPSS2 Gene Mutation

    Hormone Research in Paediatrics, 2020

    DOI 10.1159/000502114 PMID 31461705 8 citations (Europe PMC) Source : ORCID

  35. Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) Mutation

    Hormone Research in Paediatrics, 2020

    DOI 10.1159/000510623 PMID 33147586 14 citations (Europe PMC) Source : ORCID

  36. Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees

    Dspace Repository (Marmara Üniversitesi), 2019

    Texte intégral en libre accèsSource : OpenAlex

  37. Hypergonadotropic Hypogonadism in 46, XX Adolescents Without Gonadotoxic Therapy: Clinical Features and Molecular Etiologies

    Dspace Repository (Marmara Üniversitesi), 2019

    Texte intégral en libre accèsSource : OpenAlex

  38. A Case Of Syndromic Hypopituitarism

    Dspace Repository (Marmara Üniversitesi), 2019

    Texte intégral en libre accèsSource : OpenAlex

  39. Adrenocortical carcinoma in atypical Beckwith‐Wiedemann syndrome due to loss of methylation at imprinting control region 2

    Pediatric Blood & Cancer, 2019

    DOI 10.1002/pbc.28042 PMID 31612591 11 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  40. MON-LB061 Cushing Syndrome Due to an Adrenocortical Carcinoma in a Baby with Atypical Beckwith-Wiedemann Syndrome

    Journal of the Endocrine Society, 2019

    DOI 10.1210/js.2019-mon-lb061 Texte intégral en libre accèsSource : OpenAlex

  41. Cushing Syndrome due to an Adrenacortical Carcinoma in a Baby with Atypical Beckwith-Wiedemann Syndrome

    Dspace Repository (Marmara Üniversitesi), 2019

    Texte intégral en libre accèsSource : OpenAlex

  42. Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature

    Hormones, 2019

    DOI 10.1007/s42000-019-00096-7 PMID 30747411 9 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  43. A Real-Life Experience with a New Insulin Co-Formulation Degludec/Aspart for one Year in Poorly Controlled Children and Adolescents with Type 1 Diabetes

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Source : OpenAlex

  44. A rare cause of hypophosphatemia: Raine Syndrome

    Dspace Repository (Marmara Üniversitesi), 2019

    Texte intégral en libre accèsSource : OpenAlex

  45. Simplifying the Interpretation of Steroid Metabolome Data by a Machine-Learning Approach

    Dspace Repository (Marmara Üniversitesi), 2019

    Texte intégral en libre accèsSource : OpenAlex

  46. Evaluation of Brain Mri Lesions in 381 Girls with Central Precocious Puberty

    Dspace Repository (Marmara Üniversitesi), 2019

    Texte intégral en libre accèsSource : OpenAlex

  47. Genotype and Phenotype Characterization of Turkish Patients with Vitamin D Dependent Rickets Type IA

    Dspace Repository (Marmara Üniversitesi), 2019

    Texte intégral en libre accèsSource : OpenAlex

  48. Çocukluk Çağı Hodgkin Lenfoma Nedeniyle Tedavi Gören Hastalarda Tiroid Fonksiyonlarının Değerlendirilmesi

    Çocuk Dergisi / Journal of Child, 2019

    DOI 10.5222/j.child.2019.45822 1 citation (OpenAlex) Texte intégral en libre accèsSource : OpenAlex