Bilimsel çalışmalar
Prof. Dr. Gönül Çatlı
217 yayın. Her yayının yanında bilginin kaynağı yazar.
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Relation of serum irisin level with metabolic and antropometric parameters in obese children
Journal of Diabetes and its Complications, 2016
DOI 10.1016/j.jdiacomp.2016.07.019 PMID 27539885 28 atıf (Europe PMC) Kaynak: OpenAlex
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Circulating betatrophin concentration is negatively correlated with insulin resistance in obese children and adolescents
Diabetes Research and Clinical Practice, 2016
DOI 10.1016/j.diabres.2016.02.008 PMID 27103367 22 atıf (Europe PMC) Kaynak: OpenAlex
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Relationship between oxidative stress and blood glucose fluctuations evaluated with daily glucose monitoring in children with type 1 diabetes mellitus
Journal of Pediatric Endocrinology and Metabolism, 2016
DOI 10.1515/jpem-2015-0212 PMID 26812775 9 atıf (Europe PMC) Kaynak: OpenAlex
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Association Between Vitamin D Receptor Polymorphism and Familial Mediterranean Fever Disease in Turkish Children
Biochemical Genetics, 2016
DOI 10.1007/s10528-015-9710-0 PMID 26742922 2 atıf (Europe PMC) Kaynak: OpenAlex
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A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty
Journal of Clinical Research in Pediatric Endocrinology, 2016
DOI 10.4274/jcrpe.2637 PMID 27087292 3 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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A novel mutation in steroidogenic factor (SF1/NR5A1) gene in a patient with 46 XY DSD without adrenal insufficiency
Andrologia, 2016
DOI 10.1111/and.12589 PMID 27135758 8 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Intratubular large cell hyalinizing Sertoli cell tumor of the testis presenting with prepubertal gynecomastia: a case report
Acta Clinica Belgica, 2016
DOI 10.1080/17843286.2016.1215869 PMID 27488929 6 atıf (Europe PMC) Kaynak: OpenAlex
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Effect of reward-based motivation on metabolic control in children and adolescents with type 1 diabetes mellitus
International Journal of Diabetes in Developing Countries, 2016
DOI 10.1007/s13410-016-0470-0 Kaynak: OpenAlex
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Subklinik Hipo- ve Hipertiroidiler, Tedavi Ne Zaman?
Turkiye Klinikleri Pediatric Sciences - Special Topics, 2016
Kaynak: OpenAlex
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Comparison of Two Different Stoss Therapy Doses in Children with Vitamin D Deficiency or Insufficiency without Rickets
55th Annual ESPE, 2016
Kaynak: OpenAlex
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The Relation of Glycaemic Variability Obtained by Continuous Subcutaneous Glucose Monitoring with IL-6 and Adiponectin Levels in Obese Children with Metabolic Syndrome and Insulin Resistance
55th Annual ESPE, 2016
Kaynak: OpenAlex
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The relationship between Subclinical Hypothyroidism and Iodine Deficiency, Serum Leptin Levels and Metabolic Syndrome in Obese Children
55th Annual ESPE, 2016
Kaynak: OpenAlex
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Spectrum of the Genetic Defects in Hypophosphatemic Rickets in A Group of Turkish Children
55th ESPE Meeting, 2016
Kaynak: OpenAlex
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Nerve Conduction Studies in Children with Subclinical Hypothyroidism
55th ESPE Meeting, 2016
Kaynak: OpenAlex
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Intratubular Large Cell Hyalinizing Sertoli Cell Tumor of the Testis Presenting with Prepubertal Gynecomastia: A Case Report
55th ESPE Meeting, 2016
Kaynak: OpenAlex
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Sulphonylurea Treatment in a Patient with Intermediate DEND Syndrome
55th ESPE Meeting, 2016
Kaynak: OpenAlex
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Adölesan sağlığında artış gösteren iki problem İnternet bağımlılığı Obezite Vaka kontrol çalışması
Çanakkale Onsekiz Mart University AVESIS, 2016
Kaynak: OpenAlex
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Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study
Journal of Clinical Research in Pediatric Endocrinology, 2015
DOI 10.4274/jcrpe.1771 PMID 25800473 44 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group
Journal of Clinical Research in Pediatric Endocrinology, 2015
DOI 10.4274/jcrpe.2023 PMID 26831551 7 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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The Growth Characteristics of Patients with Noonan Syndrome, and First 2 Years Results of GH Treatment: A Nationwide Multicentre Study
54th ESPE Meeting (ESPE 2015), 2015
Kaynak: OpenAlex
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Turner Sendromlu Türk Kızlarının Büyüme Eğrileri: FAVOR Turner Sendromu Çalışma Grubu
Çanakkale Onsekiz Mart University AVESIS, 2015
Kaynak: OpenAlex
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Turner Sendromlu Türk Kızlarının Büyüme Eğrileri:
Çanakkale Onsekiz Mart University AVESIS, 2015
Kaynak: OpenAlex
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Primary Adrenal Insufficiency in Children without Congenital Adrenal Hyperplasia: Molecular and Clinical Characterisation of a Nationwide Cohort
54th ESPE Meeting (ESPE 2015), 2015
Kaynak: OpenAlex
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Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort
The Journal of Clinical Endocrinology & Metabolism, 2015
DOI 10.1210/jc.2015-3250 PMID 26523528 130 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Maturity-onset diabetes of the young (MODY): an update
Journal of Pediatric Endocrinology and Metabolism, 2015
DOI 10.1515/jpem-2014-0384 PMID 25581748 123 atıf (Europe PMC) Kaynak: OpenAlex
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Gonadal malignancy risk and prophylactic gonadectomy in disorders of sexual development
Journal of Pediatric Endocrinology and Metabolism, 2015
DOI 10.1515/jpem-2014-0522 PMID 25879315 38 atıf (Europe PMC) Kaynak: OpenAlex
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Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing
Journal of Pediatric Endocrinology and Metabolism, 2015
DOI 10.1515/jpem-2014-0430 PMID 26226118 23 atıf (Europe PMC) Kaynak: OpenAlex
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Significance of serum neurokinin B and kisspeptin levels in the differential diagnosis of premature thelarche and idiopathic central precocious puberty
Peptides, 2015
DOI 10.1016/j.peptides.2014.12.011 PMID 25572302 23 atıf (Europe PMC) Kaynak: OpenAlex
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Levothyroxine replacement in primary congenital hypothyroidism: the higher the initial dose the higher the rate of overtreatment
Journal of Pediatric Endocrinology and Metabolism, 2015
DOI 10.1515/jpem-2015-0047 PMID 26244672 20 atıf (Europe PMC) Kaynak: OpenAlex
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Is Patch Testing with Food Additives Useful in Children with Atopic Eczema?
Pediatric Dermatology, 2015
DOI 10.1111/pde.12588 PMID 25873103 12 atıf (Europe PMC) Kaynak: OpenAlex
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Clinical and laboratory findings in the differential diagnosis of central precocious puberty and premature thelarche
Türk Pediatri Arşivi, 2015
DOI 10.5152/tpa.2015.2281 PMID 26078693 18 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Serum nesfatin-1 and leptin levels in non-obese girls with premature thelarche
Journal of Endocrinological Investigation, 2015
DOI 10.1007/s40618-015-0277-8 PMID 25833360 13 atıf (Europe PMC) Kaynak: OpenAlex
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An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation
Journal of Clinical Research in Pediatric Endocrinology, 2015
DOI 10.4274/jcrpe.1919 PMID 26316442 7 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Neonatal diabetes mellitus due to a novel mutation in the GATA6 gene accompanying renal dysfunction: A case report
American Journal of Medical Genetics Part A, 2015
DOI 10.1002/ajmg.a.36984 PMID 25708516 8 atıf (Europe PMC) Kaynak: OpenAlex
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An Unusual Presentation of Pediatric Cushing Disease: Diabetic Ketoacidosis
AACE Clinical Case Reports, 2015
DOI 10.4158/ep14284.cr Kaynak: OpenAlex
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The Role of Thyrotropin-Releasing Hormone Stimulation Test in Management of Hyperthyrotropinemia in Infants
Journal of Clinical Research in Pediatric Endocrinology, 2015
DOI 10.4274/jcrpe.1985 PMID 26831555 2 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Recovery of Central Fever after GH Therapy in a Patient with GH Deficiency Secondary to Posttraumatic Brain Injury
Journal of Clinical Research in Pediatric Endocrinology, 2015
DOI 10.4274/jcrpe.1639 PMID 25800481 Açık erişimli tam metinKaynak: OpenAlex
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Çocuk ve Ergenlerde Obezite: Tanım ve Epidemiyoloji
Turkiye Klinikleri Pediatric Sciences - Special Topics, 2015
Kaynak: OpenAlex
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Clinical and Biochemical Characteristics of a Female Patient with a Novel Homozygous STAT5B Mutation but Lack of Pulmonary Disease
54th Annual ESPE, 2015
Kaynak: OpenAlex
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Pituitary Stalk Interruption Syndrome Presenting with Normogonadotropic Amenorrhea and Hypoprolactinemia
54th ESPE Meeting (ESPE 2015), 2015
Kaynak: OpenAlex
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Elevated Serum Irisin Level is not Related to Metabolic and Anthropometric Parameters in Obese Children
54th Annual ESPE, 2015
Kaynak: OpenAlex
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Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor [alpha] Mutations
54th ESPE Meeting (ESPE 2015), 2015
Kaynak: OpenAlex
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A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty
54th Annual ESPE, 2015
Kaynak: OpenAlex
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A Novel Mutation in Steroidogenic Factor Gene in a Patient with 46, XY DSD without Adrenal Insufficiency
54th Annual ESPE, 2015
Kaynak: OpenAlex
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Turner Sendromlu Çocukların Başvuru Özellikleri ve Eşlik Eden Patolojiler: 842 Vakanın Ulusal Veritabanında Değerlendirme Sonuçları
AYBU AVESIS, 2014
Kaynak: OpenAlex
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Incidence of maternal vitamin D deficiency in a region of Ankara, Turkey: a preliminary study
TURKISH JOURNAL OF MEDICAL SCIENCES, 2014
DOI 10.3906/sag-1304-107 PMID 25551932 12 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Adipokines in Breast Milk: An Update
Journal of Clinical Research in Pediatric Endocrinology, 2014
DOI 10.4274/jcrpe.1531 PMID 25541889 50 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Subclinical hypothyroidism in childhood and adolescense
Journal of Pediatric Endocrinology and Metabolism, 2014
DOI 10.1515/jpem-2014-0089 PMID 25153584 22 atıf (Europe PMC) Kaynak: OpenAlex
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The relation of leptin and soluble leptin receptor levels with metabolic and clinical parameters in obese and healthy children
Peptides, 2014
DOI 10.1016/j.peptides.2014.03.015 PMID 24703965 22 atıf (Europe PMC) Kaynak: OpenAlex
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Psychomotor Retardation Caused by a Defective Thyroid Hormone Transporter: Report of Two Families with Different MCT8 Mutations
Hormone Research in Paediatrics, 2014
DOI 10.1159/000365191 PMID 25247785 18 atıf (Europe PMC) Kaynak: OpenAlex