Uzm. Dr. Mehmet Eltan

Diagnostic Utility of Genetic Testing in Hyperthyroxinemia With Non‐Suppressed TSH

Clinical Endocrinology, 2026

DOI 10.1111/cen.70126 PMID 41800491 Quelle: OpenAlex

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 Frei zugänglicher VolltextQuelle: Europe PMC

Isolated Hyperchlorhidrosis Caused by Novel Biallelic CA12 Variants Mimicking Pseudohypoaldosteronism

2026

DOI 10.1159/hrp/adaag054 Quelle: ORCID

Determinants of pubertal progression and final height in premature pubarche

Journal of Endocrinological Investigation, 2026

DOI 10.1007/s40618-026-02957-6 PMID 42340620 Frei zugänglicher VolltextQuelle: ORCID

Adrenal androgens as predictors of growth characteristics in premature pubarche

European journal of endocrinology, 2026

DOI 10.1093/ejendo/lvag024 PMID 41637567 1 Zitation (Europe PMC) Quelle: Europe PMC

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 Frei zugänglicher VolltextQuelle: OpenAlex

Clinical Correlates of Adrenal Zona Reticularis Function in Turner Syndrome

Figshare, 2026

DOI 10.6084/m9.figshare.32780793 Frei zugänglicher VolltextQuelle: OpenAlex

Clinical Correlates of Adrenal Zona Reticularis Function in Turner Syndrome

Figshare, 2026

DOI 10.6084/m9.figshare.32780751 Frei zugänglicher VolltextQuelle: OpenAlex

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 Quelle: ORCID

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 Quelle: OpenAlex

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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

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

Clinical Endocrinology, 2025

DOI 10.1111/cen.70064 PMID 41327588 Quelle: OpenAlex

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 Quelle: OpenAlex

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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

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 Zitation (OpenAlex) Quelle: OpenAlex

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

Comprehensive Medicine, 2025

DOI 10.14744/cm.2024.73745 Frei zugänglicher VolltextQuelle: OpenAlex

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

Southern Clinics of Istanbul Eurasia, 2025

DOI 10.14744/scie.2025.97830 Frei zugänglicher VolltextQuelle: OpenAlex

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 Quelle: OpenAlex

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 Zitationen (Europe PMC) Quelle: OpenAlex

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 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

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 Zitation (Europe PMC) Quelle: OpenAlex

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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

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 Frei zugänglicher VolltextQuelle: ORCID

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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

A rare cause of hypercalcemia: Congenital Lactase Deficiency

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

Quelle: OpenAlex

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 Zitationen (Europe PMC) Quelle: ORCID

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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

Acetazolamide treatment in a patient with pseudohypoparathyroidism with venous calcification

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

Quelle: OpenAlex

46,XY DSD due to biallelic DHX37 gene mutations

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

Quelle: OpenAlex

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

Quelle: OpenAlex

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

2021

Quelle: OpenAlex

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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

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 Zitationen (Europe PMC) Quelle: ORCID

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 Zitationen (Europe PMC) Quelle: ORCID

Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

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

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

A Case Of Syndromic Hypopituitarism

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

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 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

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 Frei zugänglicher VolltextQuelle: OpenAlex

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

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

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

Quelle: OpenAlex

A rare cause of hypophosphatemia: Raine Syndrome

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

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

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

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

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

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

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

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 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex