Bilimsel çalışmalar

Prof. Dr. Gönül Çatlı

217 yayın. Her yayının yanında bilginin kaynağı yazar.

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  1. The Effect of L-Thyroxine Treatment on Hypothyroid Symptom Scores and Lipid Profile in Children with Subclinical Hypothyroidism

    Journal of Clinical Research in Pediatric Endocrinology, 2014

    DOI 10.4274/jcrpe.1594 PMID 25541895 14 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  2. Effect of gonadotropin-releasing hormone agonist therapy on body mass index and growth in girls with idiopathic central precocious puberty

    Indian Journal of Endocrinology and Metabolism, 2014

    DOI 10.4103/2230-8210.131770 PMID 25729690 18 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  3. A novel missense mutation in HSD17B3 gene in a 46, XY adolescent presenting with primary amenorrhea and virilization at puberty

    Clinica Chimica Acta, 2014

    DOI 10.1016/j.cca.2014.07.025 PMID 25064799 8 atıf (Europe PMC) Kaynak: OpenAlex

  4. The effect of L-thyroxine treatment on left ventricular functions in children with subclinical hypothyroidism

    Archives of Disease in Childhood, 2014

    DOI 10.1136/archdischild-2014-306381 PMID 25210105 13 atıf (Europe PMC) Kaynak: OpenAlex

  5. Fasting and postprandial levels of a novel anorexigenic peptide nesfatin in childhood obesity

    Journal of Pediatric Endocrinology and Metabolism, 2014

    DOI 10.1515/jpem-2013-0475 PMID 24825087 10 atıf (Europe PMC) Kaynak: OpenAlex

  6. Cross-reactivity of adrenal steroids with aldosterone may prevent the accurate diagnosis of congenital adrenal hyperplasia

    Journal of Pediatric Endocrinology and Metabolism, 2014

    DOI 10.1515/jpem-2014-0170 PMID 25503463 13 atıf (Europe PMC) Kaynak: OpenAlex

  7. Decreased vitamin D levels in children with familial M editerranean fever

    International Journal of Rheumatic Diseases, 2014

    DOI 10.1111/1756-185x.12253 PMID 24410734 6 atıf (Europe PMC) Kaynak: OpenAlex

  8. A novel activating ABCC8 mutation underlying neonatal diabetes mellitus in an infant presenting with cerebral sinovenous thrombosis

    Journal of Pediatric Endocrinology and Metabolism, 2014

    DOI 10.1515/jpem-2013-0263 PMID 24468609 4 atıf (Europe PMC) Kaynak: OpenAlex

  9. Isolated hyperthyrotropinemia in childhood obesity and its relation with metabolic parameters

    Journal of Endocrinological Investigation, 2014

    DOI 10.1007/s40618-014-0100-y PMID 24920280 10 atıf (Europe PMC) Kaynak: OpenAlex

  10. A Case of Central Precocious Puberty Due to Concomitant Hypothalamic Hamartoma and Juvenile Pilocytic Astrocytoma

    Journal of Clinical Research in Pediatric Endocrinology, 2014

    DOI 10.4274/jcrpe.1306 PMID 25241615 Açık erişimli tam metinKaynak: OpenAlex

  11. Acceleration of Puberty During Growth Hormone Therapy in a Child with Septo-Optic Dysplasia

    Journal of Clinical Research in Pediatric Endocrinology, 2014

    DOI 10.4274/jcrpe.1187 PMID 24932606 3 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  12. X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism: Mutation of the DAX-1 gene in a patient

    Turkiye Klinikleri Journal of Pediatrics, 2014

    Kaynak: OpenAlex

  13. Maternal 6q24 Hipometilasyonuna Bağlı Gelişen Geçici Neonatal Diabetes Mellitus

    Turkiye Klinikleri Journal of Endocrinology, 2014

    Kaynak: OpenAlex

  14. A Rare Karyotype of Turner Syndrome: 45.X/47.XXX

    Güncel Pediatri, 2014

    DOI 10.4274/jcp.02996 Kaynak: OpenAlex

  15. Antineutrophil Cytoplasmic Antibody-Positive Glomerulonephritis Associated with Long-Term Propylthiouracil Treatment in Children

    The Journal of Pediatric Research, 2014

    DOI 10.4274/jpr.15807 Kaynak: OpenAlex

  16. Boy Kısalığı ile Başvuran Kleidokranial Displazi Tanısı Alan Bir Olgu

    The Journal of Pediatric Research, 2014

    DOI 10.4274/jpr.43153 Kaynak: OpenAlex

  17. A Rare Cause of Hypercalcemia in Childhood; Parathyroid Adenoma: Case Report and Review of the Literature

    Güncel Pediatri, 2014

    DOI 10.4274/jcp.30602 Açık erişimli tam metinKaynak: OpenAlex

  18. A Rare Case of Swyer Syndrome with Spontaneous Breast Development and Menstruation

    53rd ESPE Meeting, 2014

    Kaynak: OpenAlex

  19. Molecular Genetic Analysis of Maturity Onset Diabetes of the Young (Mody) Genes in Children by Using Targeted Next-Generation Sequencing

    ESPE 2014, 2014

    Kaynak: OpenAlex

  20. The Diverse Phenotype of Mutations in T 3 Receptor Alpha (TR[alpha])

    ESPE 2014, 2014

    Kaynak: OpenAlex

  21. A Pediatric Case of Cushing's Disease Presenting with Diabetic Ketoacidosis

    2014

    Kaynak: OpenAlex

  22. The Relation of Serum Leptin and Soluble Leptin Receptor Levels with Metabolic and Clinical Parameters in Obese and Healthy Children

    ESPE 2014, 2014

    Kaynak: OpenAlex

  23. The relation of serum nesfatin-1 level with metabolic and clinical parameters in obese and healthy children

    Pediatric Diabetes, 2013

    DOI 10.1111/pedi.12009 PMID 23346951 52 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  24. Low Omentin-1 Levels Are Related with Clinical and Metabolic Parameters in Obese Children

    Experimental and Clinical Endocrinology & Diabetes, 2013

    DOI 10.1055/s-0033-1355338 PMID 24085389 27 atıf (Europe PMC) Kaynak: OpenAlex

  25. A novel GATA6 mutation leading to congenital heart defects and permanent neonatal diabetes: A case report

    Diabetes & Metabolism, 2013

    DOI 10.1016/j.diabet.2013.01.005 PMID 23639568 21 atıf (Europe PMC) Kaynak: OpenAlex

  26. Low serum nesfatin-1 levels may be a contributing factor for monogenic obesity due to prohormone convertase 1 deficiency

    Medical Hypotheses, 2013

    DOI 10.1016/j.mehy.2013.05.013 PMID 23759355 6 atıf (Europe PMC) Kaynak: OpenAlex

  27. A case of infantile-onset Graves

    Türk Pediatri Arşivi, 2013

    DOI 10.4274/tpa.833 Kaynak: OpenAlex

  28. Adölesanda Fiziksel ve Seksüel Gelişme

    Turkiye Klinikleri Pediatric Sciences - Special Topics, 2013

    Kaynak: OpenAlex

  29. P01-025 – Decreased vitamin D levels in children with FMF

    Pediatric Rheumatology, 2013

    DOI 10.1186/1546-0096-11-s1-a29 Açık erişimli tam metinKaynak: OpenAlex

  30. Iconography : A novel GATA6 mutation leading to congenital heart defects and permanent neonatal diabetes: A case report

    2013

    Kaynak: OpenAlex

  31. Çocukluk çağında hiperkalseminin nadir bir nedeni paratiroid adenomu: Bir olgu sunumu ve literatürün gözden geçirilmesi

    2013

    Kaynak: OpenAlex

  32. A Case of Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, Autonomic Dysregulation, and Neural Crest Tumor: Rohhadnet Syndrome

    Endocrine Practice, 2012

    DOI 10.4158/ep12140.cr PMID 23186956 27 atıf (Europe PMC) Kaynak: OpenAlex

  33. Clinical and diagnostic characteristics of hyperprolactinemia in childhood and adolescence

    Journal of Pediatric Endocrinology and Metabolism, 2012

    DOI 10.1515/jpem-2012-0327 PMID 23327784 9 atıf (Europe PMC) Kaynak: OpenAlex

  34. Hyperprolactinemia in children: clinical features and long-term results

    Journal of Pediatric Endocrinology and Metabolism, 2012

    DOI 10.1515/jpem-2012-0130 PMID 23329759 15 atıf (Europe PMC) Kaynak: OpenAlex

  35. Clinical profile and etiologies of children with central diabetes insipidus: a single-center experience from Turkey

    Journal of Pediatric Endocrinology and Metabolism, 2012

    DOI 10.1515/jpem-2012-0006 PMID 22876545 14 atıf (Europe PMC) Kaynak: OpenAlex

  36. Evaluation of neutrophil gelatinase-associated lipocalin in normoalbuminuric normotensive type 1 diabetic adolescents

    Journal of Pediatric Endocrinology and Metabolism, 2012

    DOI 10.1515/jpem-2011-0487 PMID 22876548 14 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  37. Permanent neonatal diabetes caused by a novel mutation in the INS gene

    Diabetes Research and Clinical Practice, 2012

    DOI 10.1016/j.diabres.2012.10.009 PMID 23107109 1 atıf (Europe PMC) Kaynak: OpenAlex

  38. Bilateral pheochromocytoma as first manifestation of von Hippel-Lindau disease: a case report

    The Turkish Journal of Pediatrics, 2012

    DOI 10.24953/turkjpediatr.2012.1682 PMID 23427520 1 atıf (Europe PMC) Kaynak: OpenAlex

  39. Vitamin D Dependent Rickets Type I: Two Cases Report

    Turkiye Klinikleri Journal of Medical Sciences, 2012

    DOI 10.5336/medsci.2011-25349 Kaynak: OpenAlex

  40. Evaluation of Urine Collection Methods for the Diagnosis of Urinary Tract Infection in Children

    Medical Principles and Practice, 2010

    DOI 10.1159/000273068 PMID 20357500 41 atıf (Europe PMC) Kaynak: OpenAlex

  41. Uluslararası Yayınlar

    Kaynak: livhospital.com profil sayfası

  42. Abaci A, Catli G, Anik A, Bober E. Epidemiology, classification and management of undescended testes: does medication have value in its treatment? J Clin Res Pediatr Endocrinol. 2013;5(2):65-72.

    Kaynak: livhospital.com profil sayfası

  43. Catli G, Abaci A, Bober E, Buyukgebiz A. Clinical and Diagnostic Characteristics of Hyperprolactinemia in Childhood and Adolescense. J Pediatr Endocrinol Metab. 2013;26(1-2):1-11.

    Kaynak: livhospital.com profil sayfası

  44. Anık A, Catli G, Abacı A, Dizdarer C, Böber E. Acute Vitamin D Intoxication Possibly Due To Faulty Production of A Multivitamin Preparation. J Clin Res Pediatr Endocrinol. 2013;5(2):136-139.

    Kaynak: livhospital.com profil sayfası

  45. Anık A, Çatlı G, Abacı A, Böber E. 46,XX Male Disorder of Sexual Development: A Case Report. J Clin Res Pediatr Endocrinol. 2013;5(4):258-260

    Kaynak: livhospital.com profil sayfası

  46. Anık A, Catli G, Makay B, Abacı A, Küme T, Unsal E, Böber E. Decreased Vitamin D Levels in Children with Familial Mediterranean Fever. Int J Rheum Dis. 2014;17(3):321-326.

    Kaynak: livhospital.com profil sayfası

  47. Anik A, Catli G, Abaci A, Güleryüz H, Güdücü Ç, Öniz A, Can Ş, Dündar B, Böber E. Olfactory Dysfunction in Children With Kallmann Syndrome: Relation of Smell Tests with Brain Magnetic Resonance Imaging. Hormones 2014,xxx doi: 10.14310/horm.2002.1562

    Kaynak: livhospital.com profil sayfası

  48. Abaci A, Çatli G, Anik A, Küme T, Özlem, Bober E, Dündar BN. Significance of Serum Neurokinin B and Kisspeptin Levels in the Differential Diagnosis of Premature Thelarche and Central Precocious Puberty. Peptides, 2015;64:29-33.

    Kaynak: livhospital.com profil sayfası

  49. Manyas H, Eroğlu Filibeli B, Ayrancı İ, Güvenç MS, Dündar BN, Çatlı G. Early and late diagnoses of 17β-Hydroxysteroid dehydrogenase type-3 deficiency in two unrelated patients. Andrologia. 2021 Feb 14:e14017. doi: 10.1111/and.14017.

    Kaynak: livhospital.com profil sayfası

  50. Ulusoy E, Demir K, Altıncık SA, Çatlı G, Abacı A, Bekem Soylu Ö, Böber E. "Vitamin D Bağımlı Rikets Tip I: İki Olgu Sunumu". Turkiye Klinikleri J Med Sci 2012;32(6):1786-1790.

    Kaynak: livhospital.com profil sayfası