Wissenschaftliche Arbeiten

Prof. Dr. Gönül Çatlı

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

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  1. Macular Variability in Children and Adolescents with Metabolic Syndrome: A Cross-sectional Study Examining the Associations with Anthropometric Measurements, Metabolic Parameters and Inflammatory Markers

    Journal of Clinical Research in Pediatric Endocrinology, 2019

    DOI 10.4274/jcrpe.galenos.2019.2019.0082 PMID 31434461 9 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  2. Impaired systolic and diastolic left ventricular function in children and adolescents with congenital adrenal hyperplasia receiving corticosteroid therapy

    Cardiology in the Young, 2019

    DOI 10.1017/s1047951118002330 PMID 30675832 7 Zitationen (Europe PMC) Quelle: OpenAlex

  3. Novel VDR Mutations in Patients with Vitamin D–Dependent Rickets Type 2a: A Mild Disease Phenotype Caused by A Novel Canonical Splice-Site Mutation

    Endocrine Practice, 2019

    DOI 10.4158/ep-2019-0295 PMID 31557081 5 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  4. Social cognition and emotion regulation may be impaired in adolescents with obesity independent of the presence of binge eating disorder: a two-center study

    Psychiatry and Clinical Psychopharmacology, 2019

    DOI 10.1080/24750573.2019.1693727 12 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  5. Auditory event-related potentials demonstrate early cognitive impairment in children with subclinical hypothyroidism

    Journal of Pediatric Endocrinology and Metabolism, 2019

    DOI 10.1515/jpem-2018-0463 PMID 31194683 5 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  6. Neonatal adrenal insufficiency: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report

    Türk Pediatri Arşivi, 2019

    DOI 10.5152/turkpediatriars.2018.01822 PMID 31236037 6 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  7. Evaluation of Turner Syndrome Knowledge among Physicians and Parents

    Journal of Clinical Research in Pediatric Endocrinology, 2019

    DOI 10.4274/jcrpe.galenos.2019.2019.0041 PMID 31486330 3 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

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

    58th Annual ESPE Meeting (ESPE 2019), 2019

    1 Zitation (OpenAlex) Quelle: OpenAlex

  9. Rare Cause of 46,XY Sexual Development Disorder: 17β-Hydroxysteroid Dehydrogenase Type 3 Deficiency

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Quelle: OpenAlex

  10. PTEN Hamartoma Tumor Syndrome (Overlap of Cowden syndrome and the Bannayan-Riley-Ruvalcaba Syndrome): Case Report

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Quelle: OpenAlex

  11. Pituitary Stalk Interruption Syndrome Diagnosed with Different Clinical Findings: Report of Two Cases

    The Anatolian Journal of General Medical Research, 2019

    DOI 10.5222/terh.2019.37801 Quelle: OpenAlex

  12. Three Cases with Familial Short Stature: Leri-Weill Syndrome

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Quelle: OpenAlex

  13. The Relationship Between Serum Neurotensin Levels and Metabolic Parameters and Eating Behavior in Obese Children

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Quelle: OpenAlex

  14. A Case of Late-Onset Monogenic Diabetes Due to a Homozygous Variant in the GCK Gene

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Quelle: OpenAlex

  15. Biotine interference in a patient with non-clinic high thyroid hormone levels

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Quelle: OpenAlex

  16. Two Siblings Case with Diagnosis of Autoimmune Polyglandular Syndrome Type 1

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Quelle: OpenAlex

  17. ABCC8 MODY in an Obese Adolescent Misdiagnosed with Type 2 Diabetes

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Quelle: OpenAlex

  18. Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3 beta-hydroxysteroid dehydrogenase 2 deficiency

    AYBU AVESIS, 2019

    Quelle: OpenAlex

  19. Nationwide Hypophosphatemic Rickets Study

    Trakya University's Institutional Open Access System (Trakya University), 2018

    Frei zugänglicher VolltextQuelle: OpenAlex

  20. Nationwide Hypophosphatemic Rickets Study

    Bursa Uludag University - AVESIS, 2018

    Quelle: OpenAlex

  21. Genotype–phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

    Journal of Endocrinological Investigation, 2018

    DOI 10.1007/s40618-018-0940-y PMID 30132287 21 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  22. Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3

    PLoS ONE, 2018

    DOI 10.1371/journal.pone.0193388 PMID 29505567 22 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  23. Targeted next generation sequencing in patients with maturity-onset diabetes of the young (MODY)

    Journal of Pediatric Endocrinology and Metabolism, 2018

    DOI 10.1515/jpem-2018-0184 PMID 30447144 25 Zitationen (Europe PMC) Quelle: OpenAlex

  24. A Novel Homozygous Selenocysteine Insertion Sequence Binding Protein 2 (SECISBP2, SBP2) Gene Mutation in a Turkish Boy

    Thyroid, 2018

    DOI 10.1089/thy.2018.0015 PMID 29882503 24 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  25. Increased concentrations of serum nesfatin-1 levels in childhood with idiopathic chronic malnutrition

    TURKISH JOURNAL OF MEDICAL SCIENCES, 2018

    DOI 10.3906/sag-1705-20 PMID 29714458 8 Zitationen (Europe PMC) Quelle: OpenAlex

  26. A Synopsis of Current Practice in the Diagnosis and Management of Patients with Turner Syndrome in Turkey: A Survey of 18 Pediatric Endocrinology Centers

    Journal of Clinical Research in Pediatric Endocrinology, 2018

    DOI 10.4274/jcrpe.0003 PMID 29699389 6 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  27. Brain injury markers: S100 calcium-binding protein B, neuron-specific enolase and glial fibrillary acidic protein in children with diabetic ketoacidosis

    Pediatric Diabetes, 2018

    DOI 10.1111/pedi.12667 PMID 29484801 1 Zitation (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  28. Does Obesity Affect the Ocular Choroid Tissue in Children and Adolescents?

    The Journal of Pediatric Research, 2018

    DOI 10.4274/jpr.48303 Quelle: OpenAlex

  29. Personality and subjective psychiatric symptoms of parents of obese youth: a controlled study

    Psychiatry and Clinical Psychopharmacology, 2018

    DOI 10.1080/24750573.2018.1510676 Frei zugänglicher VolltextQuelle: OpenAlex

  30. Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2, Ürokortin 3 ve Antimüllerian Hormon Düzeyleri

    DergiPark (Istanbul University), 2018

    Quelle: OpenAlex

  31. CAN Triponderal Mass Index be a New Indicator in the Predicting Cardiometabolic Risk in Obese Adolescents

    57th Annual ESPE, 2018

    Quelle: OpenAlex

  32. A Rare Cause of Hypercalcemia in Childhood: Hypercalcemia Associated with Parathormon-Related Peptid

    57th Annual ESPE, 2018

    Quelle: OpenAlex

  33. The Relationship between Anthropometric Measurements and Breast Milk Ghrelin and Nesfatin-1 Levels in Infants with Small for Gestational Age

    57th Annual ESPE, 2018

    Quelle: OpenAlex

  34. Comprehensive Genetic Testing Shows One in Five Children with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology

    Dspace Repository (Marmara Üniversitesi), 2018

    Frei zugänglicher VolltextQuelle: OpenAlex

  35. A 13 Year-Old Boy Diagnosed as Osteogenesis Omperfecta with Normal Bone Mineral Density

    57th Annual ESPE, 2018

    Quelle: OpenAlex

  36. SOCIAL COGNITION AND EMOTIONAL FUNCTIONING IN OBESE ADOLESCENTS WITH OR WITHOUT BINGE EATING DISORDER

    Bursa Uludag University - AVESIS, 2018

    Quelle: OpenAlex

  37. Comprehensive Genetic Testing Shows One in FiveChildren with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology.

    Kocaeli Üniversitesi - AVESİS, 2018

    Quelle: OpenAlex

  38. An Assessment of Retinal Nerve Fiber Layer Thickness in Non-Diabetic Obese Children and Adolescents

    Journal of Clinical Research in Pediatric Endocrinology, 2017

    DOI 10.4274/jcrpe.4810 PMID 28739552 14 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  39. The Relationship Between Glycemic Variability and Inflammatory Markers in Obese Children with Insulin Resistance and Metabolic Syndrome

    Journal of Clinical Research in Pediatric Endocrinology, 2017

    DOI 10.4274/jcrpe.4031 PMID 28163257 17 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  40. Can Stoss Therapy Be Used in Children with Vitamin D Deficiency or Insufficiency without Rickets?

    Journal of Clinical Research in Pediatric Endocrinology, 2017

    DOI 10.4274/jcrpe.3842 PMID 28077342 11 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  41. Changes in the Frequency of Diabetic Ketoacidosis in Type I Diabetes Mellitus Cases at Diagnosis: A Fifteen-Year Single Center Experience

    The Journal of Pediatric Research, 2017

    DOI 10.4274/jpr.16768 Quelle: OpenAlex

  42. Tip 1 Diyabetes Mellitus Olgularının Tanı Anındaki Demografik, Klinik ve Laboratuvar Özelliklerinin Değerlendirilmesi

    Turkish Journal of Pediatric Disease, 2017

    DOI 10.12956/tjpd.2017.317 Quelle: OpenAlex

  43. ACUTE KIDNEY INJURY ACCORDING TO PRIFLE CRITERIA IN CHILDREN WITH DIABETIC KETOACIDOSIS

    2017

    Quelle: OpenAlex

  44. PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: A MULTICENTER STUDY FROM TURKEY

    Bursa Uludag University - AVESIS, 2017

    Quelle: OpenAlex

  45. 5-alfa redüktaz tip 2 eksikliği tanılı olguların fenotipik, hormonal ve moleküler genetik özellikleri: Çok merkezli ulusal veriler

    Bursa Uludag University - AVESIS, 2017

    Quelle: OpenAlex

  46. The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

    Journal of Clinical Research in Pediatric Endocrinology, 2016

    DOI 10.4274/jcrpe.3013 PMID 27125300 20 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  47. Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

    American Journal of Medical Genetics Part A, 2016

    DOI 10.1002/ajmg.a.37498 PMID 26788866 8 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  48. Internet addiction, sleep and health-related life quality among obese individuals: a comparison study of the growing problems in adolescent health

    Eating and Weight Disorders - Studies on Anorexia Bulimia and Obesity, 2016

    DOI 10.1007/s40519-016-0327-z PMID 27757931 42 Zitationen (Europe PMC) Quelle: OpenAlex

  49. Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations

    The Journal of Clinical Endocrinology & Metabolism, 2016

    DOI 10.1210/jc.2016-1404 PMID 27144938 46 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  50. The Relationship between Serum Zonulin Level and Clinical and Laboratory Parameters of Childhood Obesity

    Journal of Clinical Research in Pediatric Endocrinology, 2016

    DOI 10.4274/jcrpe.3682 PMID 28008865 48 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex