Wissenschaftliche Arbeiten

Prof. Dr. Gönül Çatlı

217 Publikationen. Neben jeder Publikation steht die Quelle der Angabe.

Zurück zum Profil

  1. Long-term clinical outcomes of primary adrenal insufficiency caused by homozygous CYP11A1 p.R451W variant

    European Journal of Endocrinology, 2026

    DOI 10.1093/ejendo/lvag110 PMID 42340003 Frei zugänglicher VolltextQuelle: OpenAlex

  2. Genotype-Phenotype Correlation Analysis and Identification of a Novel Variant in Children with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

    The Journal of Pediatric Research, 2026

    DOI 10.4274/jpr.galenos.2026.07448 Quelle: OpenAlex

  3. Is oxytocin related to psychiatric symptoms in adolescents with obesity?

    Journal of Pediatric Endocrinology and Metabolism, 2025

    DOI 10.1515/jpem-2024-0583 PMID 39953894 Frei zugänglicher VolltextQuelle: OpenAlex

  4. SUN-202 Nerve Conduction Studies May Predict the Natural Course of Mild Subclinical Hypothyroidism in Children

    Journal of the Endocrine Society, 2025

    DOI 10.1210/jendso/bvaf149.1828 Quelle: OpenAlex

  5. Could the Use of Pacifiers in Infancy Be Associated with Binge Eating Disorder and Obesity in Adolescents?

    Journal of College of Physicians And Surgeons Pakistan, 2025

    DOI 10.29271/jcpsp.2025.12.1574 PMID 41351092 Frei zugänglicher VolltextQuelle: OpenAlex

  6. Evaluation of Family Functioning and Eating Attitudes in Adolescents Diagnosed with Obesity with and without Binge Eating Disorder and Their Comparison with Healthy Adolescents

    Çocuk ve Gençlik Ruh Sağlığı Dergisi / Turkish Journal of Child and Adolescent Mental Health, 2024

    DOI 10.4274/tjcamh.galenos.2024.72687 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  7. Genetic Findings in Short Turkish Children Born to Consanguineous Parents

    Hormone Research in Paediatrics, 2024

    DOI 10.1159/000539696 PMID 38838658 3 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  8. Androgen receptor CAG repeat polymorphism might be a possible cause of familial constitutional delay of growth and puberty

    Journal of Endocrinological Investigation, 2024

    DOI 10.1007/s40618-024-02502-3 PMID 39570490 1 Zitation (Europe PMC) Quelle: OpenAlex

  9. 6687 New indication for monogenic diabetes genetic testing in children – implication for routine clinical practice

    British Society for Paediatric Endocrinology and Diabetes Meeting (BSPED), 2024

    DOI 10.1136/archdischild-2024-rcpch.361 Quelle: OpenAlex

  10. Does Voiding Cystouretrography Cause Thyroid Dysfunction in Pediatric Patients with Chronic Kidney Disease?

    Research Square, 2024

    DOI 10.21203/rs.3.rs-5296155/v1 Frei zugänglicher VolltextQuelle: OpenAlex

  11. Clinical features, diagnosis and treatment outcomes of Cushing's disease in children: A multicenter study

    Clinical Endocrinology, 2023

    DOI 10.1111/cen.14980 PMID 37814958 4 Zitationen (Europe PMC) Quelle: OpenAlex

  12. POU6F2 mutation in humans with pubertal failure alters GnRH transcript expression

    Frontiers in Endocrinology, 2023

    DOI 10.3389/fendo.2023.1203542 PMID 37600690 12 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  13. Resting Electroencephalography Differences Between Eyes-Closed and Eyes-Open Conditions in Children with Subclinical Hypothyroidism

    Turkish Archives of Pediatrics, 2023

    DOI 10.5152/turkarchpediatr.2022.22144 PMID 36598209 1 Zitation (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  14. Evaluation of the effects of insulin resistance on ECG parameters in obese children.

    PubMed, 2023

    DOI 10.26355/eurrev_202309_33797 PMID 37782187 2 Zitationen (Europe PMC) Quelle: OpenAlex

  15. Sensory and Sensorimotor Gating in Children with Subclinical Hypothyroidism

    The Anatolian Journal of General Medical Research, 2023

    DOI 10.4274/terh.galenos.2021.68815 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  16. Clinical Characteristics of Children with Combined Pituitary Hormone Deficiency and the Effects of Growth Hormone Treatment

    Klinische Pädiatrie, 2023

    DOI 10.1055/a-2186-9304 PMID 38049102 Quelle: OpenAlex

  17. Are serum MOTS-c levels and MOTS-c m.1382A>C polymorphism related to polycystic ovary syndrome?

    Archives of Endocrinology and Metabolism, 2023

    DOI 10.20945/2359-4292-2026-0031 PMID 41945630 Frei zugänglicher VolltextQuelle: OpenAlex

  18. Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor

    European Journal of Medical Genetics, 2022

    DOI 10.1016/j.ejmg.2022.104654 PMID 36343887 6 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  19. Atypical STAT5B deficiency, severe short stature and mild immunodeficiency associated with a novel homozygous STAT5B Variant

    Molecular and Cellular Endocrinology, 2022

    DOI 10.1016/j.mce.2022.111799 PMID 36265659 8 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  20. Are Thyroid Functions Affected in Multisystem Inflammatory Syndrome in Children?

    Journal of Clinical Research in Pediatric Endocrinology, 2022

    DOI 10.4274/jcrpe.galenos.2022.2022-4-7 PMID 35770945 6 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  21. The effect of breast milk nesfatin-1 and ghrelin levels on growth in infants with SGA

    The Turkish Journal of Pediatrics, 2022

    DOI 10.24953/turkjped.2021.1075 PMID 35611412 2 Zitationen (Europe PMC) Quelle: OpenAlex

  22. Asfotase Alfa Treatment in a 2-year-old Girl with Childhood Hypophosphatasia

    The Journal of Pediatric Research, 2022

    DOI 10.4274/jpr.galenos.2021.51333 Quelle: OpenAlex

  23. Elevated neurotensin levels among obese adolescents may be related to emotion dysregulation and impulsivity: a cross-sectional, case-control study

    The Turkish Journal of Pediatrics, 2022

    DOI 10.24953/turkjped.2021.1437 PMID 35611414 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  24. Leptin and leptin receptor gene polymorphisms in obese and healthy children

    Çukurova medical journal (Online)/Çukurova medical journal, 2022

    DOI 10.17826/cumj.977534 Quelle: OpenAlex

  25. A rare endocrinological complication of chronic kidney disease

    The Turkish Journal of Pediatrics, 2022

    DOI 10.24953/turkjped.2020.3601 PMID 35611427 Quelle: OpenAlex

  26. Evaluation of Thyroid Function Tests in Children With Covid-19

    Research Square, 2022

    DOI 10.21203/rs.3.rs-1433666/v1 Frei zugänglicher VolltextQuelle: OpenAlex

  27. MKRN3 Gene Mutation in a Case of Familial Central Precocious Puberty

    Güncel Pediatri, 2022

    DOI 10.4274/jcp.2022.02439 Frei zugänglicher VolltextQuelle: OpenAlex

  28. Virilizing Adrenocortical Carcinoma Oncocytic Variant in a Child with Heterosexual Precocious Puberty and a Literature Review

    The Journal of Pediatric Research, 2022

    DOI 10.4274/jpr.galenos.2022.05579 Quelle: OpenAlex

  29. A childhood primary hyperparathyroidism due to parathyroid adenoma: Atypical presenting with leg pain and normocalcemia

    Pediatric Academic Case Reports, 2022

    DOI 10.61107/pacr.2022.001 Quelle: OpenAlex

  30. Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency

    The Journal of Clinical Endocrinology & Metabolism, 2021

    DOI 10.1210/clinem/dgab225 PMID 33830237 28 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  31. Oxytocin receptor gene polymorphism and low serum oxytocin level are associated with hyperphagia and obesity in adolescents

    International Journal of Obesity, 2021

    DOI 10.1038/s41366-021-00876-5 PMID 34091593 13 Zitationen (Europe PMC) Quelle: OpenAlex

  32. Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics

    Diabetologia, 2021

    DOI 10.1007/s00125-021-05597-y PMID 34686905 20 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  33. Diagnostic Value of Bilateral Petrosal Sinus Sampling in Children with Cushing Disease: A Multi-center Study

    Journal of Clinical Research in Pediatric Endocrinology, 2021

    DOI 10.4274/jcrpe.galenos.2021.2021.0152 PMID 34538049 9 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  34. Early and late diagnoses of 17β‐Hydroxysteroid dehydrogenase type‐3 deficiency in two unrelated patients

    Andrologia, 2021

    DOI 10.1111/and.14017 PMID 33586216 4 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  35. The relationship of carotid intima-media thickness with anthropometric and metabolic parameters in patients with classic congenital adrenal hyperplasia

    TURKISH JOURNAL OF MEDICAL SCIENCES, 2021

    DOI 10.3906/sag-2001-57 PMID 33486914 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  36. Childhood-onset mild diabetes caused by a homozygous novel variant in the glucokinase gene

    HORMONES, 2021

    DOI 10.1007/s42000-021-00330-1 PMID 34697762 3 Zitationen (Europe PMC) Quelle: OpenAlex

  37. High serum neurotensin level in obese adolescents is not associated with metabolic parameters, hyperphagia or food preference

    Journal of Pediatric Endocrinology and Metabolism, 2021

    DOI 10.1515/jpem-2021-0031 PMID 34147046 1 Zitation (Europe PMC) Quelle: OpenAlex

  38. Monogenik Obezite Ön Tanısı ile İncelenen Hastaların Klinik, Laboratuvar ve Genetik Sonuçlarının Değerlendirilmesi

    Güncel Pediatri, 2021

    DOI 10.4274/jcp.2021.0008 Frei zugänglicher VolltextQuelle: OpenAlex

  39. Gecikmiş Puberte: Kızlarda Gecikmiş Puberte, Tanı ve Tedavisi

    2021

    Quelle: OpenAlex

  40. Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases

    The Journal of Clinical Endocrinology & Metabolism, 2020

    DOI 10.1210/clinem/dgaa022 PMID 31950145 20 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  41. The Spectrum From Classic to Non-Classic 11β-Hydroxylase Deficiency

    SSRN Electronic Journal, 2020

    DOI 10.2139/ssrn.3712924 Frei zugänglicher VolltextQuelle: OpenAlex

  42. Can ocular changes be detected early in children and adolescents with type 1 diabetes mellitus without retinopathy by using optical biometry and optical coherence tomography?

    International Ophthalmology, 2020

    DOI 10.1007/s10792-020-01430-4 PMID 32488589 6 Zitationen (Europe PMC) Quelle: OpenAlex

  43. Can we use copeptin as a biomarker for masked hypertension or metabolic syndrome in obese children and adolescents?

    Journal of Pediatric Endocrinology and Metabolism, 2020

    DOI 10.1515/jpem-2020-0240 PMID 33581704 7 Zitationen (Europe PMC) Quelle: OpenAlex

  44. Comparison of the effectiveness of simple carbohydrates on hypoglycemic episodes in children and adolescents with type 1 diabetes mellitus: A randomized study in a diabetes camp

    Pediatric Diabetes, 2020

    DOI 10.1111/pedi.13077 PMID 32662200 4 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  45. Does fludrocortisone treatment cause hypomagnesemia in children with primary adrenal insufficiency?

    TURKISH JOURNAL OF MEDICAL SCIENCES, 2020

    DOI 10.3906/sag-2008-167 PMID 33155789 Frei zugänglicher VolltextQuelle: OpenAlex

  46. Konjenital Hiperinsülinemik Hipoglisemi Tanılı Hastalarda Klinik ve Genetik Özellikler ile Tedavi Sonuçları: Tek Merkez Deneyimi

    Bursa Uludag University - AVESIS, 2020

    DOI 10.32941/pediatri.841408 Quelle: OpenAlex

  47. Clinical, Genetic Features and Treatment Results in Patients with Congenital Hyperinsulinemic Hypoglycemia: A Single Center Experience

    Güncel Pediatri, 2020

    DOI 10.4274/jcp.2020.0029 Quelle: OpenAlex

  48. Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

    Journal of Clinical Research in Pediatric Endocrinology, 2019

    DOI 10.4274/jcrpe.galenos.2019.2019.0098 PMID 31514490 11 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  49. Evaluation of Molecular Characteristics and Steroid Metabolomics in a Large Cohort of Children with 3β-Hydroxysteroid Dehydrogenase 2 Deficiency

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Quelle: OpenAlex

  50. Ambulatory blood pressure monitoring parameters in obese children and adolescents with masked hypertension

    Blood Pressure Monitoring, 2019

    DOI 10.1097/mbp.0000000000000402 PMID 31567187 12 Zitationen (Europe PMC) Quelle: OpenAlex