Prof. Dr. Gönül Çatlı

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 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

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 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 Texte intégral en libre accèsSource : OpenAlex

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 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

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

Turkiye Klinikleri Journal of Pediatrics, 2014

Source : OpenAlex

Maternal 6q24 Hipometilasyonuna Bağlı Gelişen Geçici Neonatal Diabetes Mellitus

Turkiye Klinikleri Journal of Endocrinology, 2014

Source : OpenAlex

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

Güncel Pediatri, 2014

DOI 10.4274/jcp.02996 Source : OpenAlex

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

The Journal of Pediatric Research, 2014

DOI 10.4274/jpr.15807 Source : OpenAlex

Boy Kısalığı ile Başvuran Kleidokranial Displazi Tanısı Alan Bir Olgu

The Journal of Pediatric Research, 2014

DOI 10.4274/jpr.43153 Source : OpenAlex

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

Güncel Pediatri, 2014

DOI 10.4274/jcp.30602 Texte intégral en libre accèsSource : OpenAlex

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

53rd ESPE Meeting, 2014

Source : OpenAlex

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

ESPE 2014, 2014

Source : OpenAlex

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

ESPE 2014, 2014

Source : OpenAlex

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

2014

Source : OpenAlex

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

ESPE 2014, 2014

Source : OpenAlex

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 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

A case of infantile-onset Graves

Türk Pediatri Arşivi, 2013

DOI 10.4274/tpa.833 Source : OpenAlex

Adölesanda Fiziksel ve Seksüel Gelişme

Turkiye Klinikleri Pediatric Sciences - Special Topics, 2013

Source : OpenAlex

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

Pediatric Rheumatology, 2013

DOI 10.1186/1546-0096-11-s1-a29 Texte intégral en libre accèsSource : OpenAlex

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

2013

Source : OpenAlex

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

2013

Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

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 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

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 citation (Europe PMC) Source : OpenAlex

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 citation (Europe PMC) Source : OpenAlex

Vitamin D Dependent Rickets Type I: Two Cases Report

Turkiye Klinikleri Journal of Medical Sciences, 2012

DOI 10.5336/medsci.2011-25349 Source : OpenAlex

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 citations (Europe PMC) Source : OpenAlex

Uluslararası Yayınlar

Source : page de profil sur livhospital.com

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.

Source : page de profil sur livhospital.com

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.

Source : page de profil sur livhospital.com

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.

Source : page de profil sur livhospital.com

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

Source : page de profil sur livhospital.com

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.

Source : page de profil sur livhospital.com

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

Source : page de profil sur livhospital.com

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.

Source : page de profil sur livhospital.com

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.

Source : page de profil sur livhospital.com

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.

Source : page de profil sur livhospital.com