Academic Members

Prof.
Gönül Çatlı

Çocuk Endokrinolojisi (Çocuk Sağlığı ve Hastalıkları)

After graduating from Ankara University Faculty of Medicine in 2004, Dr Gönül Çatlı completed her residency in pediatrics in Ankara Dr Sami Ulus Children’s Health and Diseases Training and Research Hospital in 2010, and her pediatric endocrinology fellowship in Dokuz Eylül University Faculty of Medicine in 2013. Between 2013 and 2015, she worked at Health Sciences University Tepecik Training and Research Hospital. During this period, she actively participated in the training of pediatrics residents. She worked as an instructor of pediatrics at İzmir Katip Celebi University between 2016 and 2021. She has been working at Liv Hospital Ulus and Vadistanbul since September 2021 and Istinye University School of Medicine since March 2022. She was successful in the "Turkish Society of Pediatric Endocrinology Board Exam". Since 2013, she has been an active member of the European Society of Pediatric Endocrinology (ESPE). Dr. Çatlı’s clinical interests are childhood obesity, diabetes mellitus, insulin pump therapy and pubertal disorders. She focused her scientific studies on the molecular and biochemical background of obesity and its metabolic complications.

Araştırma Alanları

Obesity
Diabetes
Pediatric Endocinology
Endocrine disrupters
menstrual irregularities
insulin pump theapy
adolescent health
Congenital Hypothyroidism

Çalışma Alanları

Sağlık Bilimleri Temel Alanı
Çocuk Endokrinolojisi (Çocuk Sağlığı ve Hastalıkları)

Does fludrocortisone treatment cause hypomagnesemia in children with primary adrenal insufficiency?, 2021
Childhood-onset mild diabetes caused by a homozygous novel variant in the glucokinase gene, 2021
Evaluation of Turner Syndrome Knowledge among Physicians and Parents, 2020
Can we use copeptin as a biomarker for masked hypertension or metabolic syndrome in obese children and adolescents?, 2020
Revisiting classical 3β-hydroxysteroid dehydrogenase 2 deficiency: lessons from 31 pediatric cases, 2020
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets, 2020
Konjenital Hiperinsülinemik Hipoglisemi Tanılı HastalardaKlinik ve Genetik Özellikler ile Tedavi Sonuçları: TekMerkez Deneyimi, 2020
NOVEL VDR MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATION, 2020
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, 2020
Social cognition and emotion regulation may be impaired in adolescents with obesity independent of the presence of binge eating disorder: a two-center study, 2019
Impaired systolic and diastolic left ventricular function in children and adolescents with congenital adrenal hyperplasia receiving corticosteroid therapy, 2019
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, 2019
NOVEL VDR MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE SITE MUTATION, 2019
Auditory event-related potentials demonstrate early cognitive impairment in children with subclinical hypothyroidism, 2019
Personality and subjective psychiatric symptoms of parents of obese youth: a controlled study, 2019
Evaluation of Turner Syndrome Knowledge among Physicians and Parents, 2019
Ambulatory blood pressure monitoring parameters in obese children and adolescents with masked hypertension, 2019
Relations of Macular Variability with Anthropometric Measurements, Metabolic Parameters and Inflammatory Markers in Children and Adolescents with Metabolic Syndrome: A Cross-Sectional Study, 2019
57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2018
Nationwide hypophosphatemic rickets study57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 2018
Comprehensive Genetic Testing Shows One in Five Children with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology, 2018
Personality and subjective psychiatric symptoms of parents of obese youth: a controlled study, 2018
CAN WE USE COPEPTIN AS A BIOMARKER FOR MASKED HYPERTENSION IN OBESE CHILDREN AND ADOLESCENTS?, 2018
The Relationship Between Anthropometric Measurements and Breast Milk Ghrelin and Nesfatin-1 Levels in Infants with Small for Gestational Age, 2018
Can Triponderal Mass Index Be a New Indicator in the Predicting Cardiometabolic Risk in Obese Adolescents?, 2018
A Rare Cause of Hypercalcemia in Childhood: Hypercalcemia Associated with Parathormon- Related Peptid, 2018
Polikistik Over Sendromlu Adölesanlarda Serum Ürokortin 2,Ürokortin 3 ve Antimüllerian Hormon Düzeyleri Serum Urocortin 2, Urocortin 3 and Antimullerian Hormone Levels in Adolescents with Polycystic Ovary Syndrome, 2018
Brain injury markers: S100 calcium-binding protein B, neuron-specific enolase and glial fibrillary acidic protein in children with diabetic ketoacidosis, 2018
Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3., 2018
A Synopsis of Current Practice in the Diagnosis and Management of Patients with Turner Syndrome in Turkey: A Survey of 18 Pediatric Endocrinology Centers, 2018
Targeted next generation sequencing in patients with maturity-onset diabetes of the young (MODY), 2018
A Novel Homozygous Selenocysteine Insertion Sequence Binding Protein 2 (SECISBP2, SBP2) Gene Mutation in a Turkish Boy, 2018
Increased concentrations of serum nesfatin-1 levels in childhood with idiopathic chronic malnutrition, 2018
An Assessment of Retinal Nerve Fiber Layer Thickness in Non-Diabetic Obese Children and Adolescents., 2018
The Relationship between Serum Zonulin Level and Clinical and Laboratory Parameters of Childhood Obesity, 2017
Tip 1 Diyabetes Mellitus Olgularının Tanı Anındaki Demografik,Klinik ve Laboratuvar Özelliklerinin Değerlendirilmesi, 2017
Effect of reward-based motivation on metabolic control in children and adolescents with type 1 diabetes mellitus, 2017
The Relationship Between Glycemic Variability and Inflammatory Markers in Obese Children with Insulin Resistance and Metabolic Syndrome, 2017
Can Stoss Therapy Be Used in Children with Vitamin D Deficiency or Insufficiency without Rickets?, 2017
The Relationship between Serum Zonulin Level and Clinical and Laboratory Parameters of Childhood Obesity, 2017
Changes in the Frequency of Diabetic Ketoacidosis in Type I Diabetes Mellitus Cases at Diagnosis: A Fifteen-Year Single Center Experience, 2017
Subklinik Hipo ve Hipertiroidiler Tedavi Ne Zaman, 2016
Levothyroxine replacement in primary congenital hypothyroidism the higher the initial dose the higher the rate of overtreatment, 2016
Rare Causes of Primary Adrenal Insufficiency Genetic and Clinical Characterization of a Large Nationwide Cohort, 2016
Circulating betatrophin concentration is negatively correlated with insulin resistance in obese children and adolescents, 2016
Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor Mutations, 2016
A novel mutation in steroidogenic factor SF1 NR5A1 gene in a patient with 46 XY DSD without adrenal insufficiency, 2016
Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome, 2016
Relationship between oxidative stress and blood glucose fluctuations evaluated with daily glucose monitoring in children with type 1 diabetes mellitus, 2016
Internet addiction sleep and health related life quality among obese individuals a comparison study of the growing problems in adolescent health, 2016
Association Between Vitamin D Receptor Polymorphism and Familial Mediterranean Fever Disease in Turkish Children, 2016
The Growth Characteristics of Patients with Noonan Syndrome Results of Three Years of Growth Hormone Treatment A Nationwide Multicenter Study, 2016
A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty, 2016
Intratubular large cell hyalinizing Sertoli cell tumor of the testis presenting with prepubertal gynecomastia a case report, 2016
Relation of serum irisin level with metabolic and antropometric parameters in obese children, 2016
Significance of serum neurokinin B and kisspeptin levels in the differential diagnosis of premature thelarche and idiopathic central precocious puberty, 2015
A novel missense mutation in HSD17B3 gene in a 46 XY adolescent presenting with primary amenorrhea and virilization at puberty, 2015
Maturity onset diabetes of the young MODY an update, 2015
The effect of L thyroxine treatment on left ventricular functions in children with subclinical hypothyroidism, 2015
Molecular diagnosis of maturity onset diabetes of the young MODY in Turkish children by using targeted next generation sequencing, 2015
Neonatal Diabetes Mellitus Due To A Novel Mutation In The GATA6 Gene Accompanying Renal Dysfunction A Case Report, 2015
Gonadal malignancy risk and prophylactic gonadectomy in disorders of sexual development, 2015
Serum nesfatin 1 and leptin levels in non obese girls with premature thelarche, 2015
Cross reactivity of adrenal steroids with aldosterone may prevent the accurate diagnosis of congenital adrenal hyperplasia, 2015
Effect of gonadotropin releasing hormone agonist therapy on body mass index and growth in girls with idiopathic central precocious puberty, 2015
An Unusual Presentation of Pediatric Cushing Disease Diabetic Ketoacidosis, 2015
Recovery of Central Fever after GH Therapy in a Patient with GH Deficiency Secondary to Posttraumatic Brain Injury, 2015
Clinical and laboratory findings in the differential diagnosis of central precocious puberty and premature thelarche, 2015
Turner Syndrome and Associated Problems in Turkish Children A Multicenter Study, 2015
Is Patch Testing with Food Additives Useful in Children with Atopic Eczema, 2015
An Unusual Presentation of 46 XY Pure Gonadal Dysgenesis Spontaneous Breast Development and Menstruation, 2015
The Role of Thyrotropin Releasing Hormone Stimulation Test in Management of Hyperthyrotropinemia in Infants, 2015
Çocuk ve Ergenlerde Obezite Tanım ve Epidemiyoloji, 2015
The relation of leptin and soluble leptin receptor levels with metabolic and clinical parameters in obese and healthy children, 2014
Subclinical hypothyroidism in childhood and adolescense, 2014
Fasting and postprandial levels of a novel anorexigenic peptide nesfatin in childhood obesity, 2014
Isolated hyperthyrotropinemia in childhood obesity and its relation with metabolic parameters, 2014
Adipokines in Breast Milk An Update, 2014
Incidence of maternal vitamin D deficiency in a region of Ankara Turkey a preliminary study, 2014
The Effect of L Thyroxine Treatment on Hypothyroid Symptom Scores and Lipid Profile in Children with Subclinical Hypothyroidism, 2014
Çocukluk Çağında Hiperkalseminin Nadir Bir Nedeni Paratiroid Adenomu Bir Olgu Sunumu ve Literatürün Gözden Geçirilmesi, 2014
Nadir Görülen Bir Turner Sendromu Karyotipi 45 X 47 XXX, 2014
Maternal 6q24 Hipometilasyonuna Bağlı Gelişen Geçici Neonatal Diabetes Mellitus Olgu Sunumu, 2014
Çocukluk Çağında Diyabetin Nadir Bir Nedeni Glukokinaz Mutasyonu MODY2, 2014
Boy Kısalığı İle Başvuran Kleidokranial Displazi Tanısı Alan Bir Olgu, 2014
X Linked Adrenal Hypoplasia Congenita and Hypogonadotropic Hypogonadism Mutation of the DAX 1 Gene in a Patient, 2014
Acceleration of Puberty During Growth Hormone Therapy in a Child with Septo Optic Dysplasia, 2014
Antineutrophil Cytoplasmic Antibody Positive Glomerulonephritis Associated with Long Term Propylthiouracil Treatment in Children, 2014
Olfactory Dysfunction in Children With Kallmann Syndrome Relationo Of Smell Tests with Brain Magnetic Resonance Imaging, 2014
Psychomotor Retardation Caused By A Defective Thyroid Hormone Transporter Report of Two Families With Different MCT8 Mutations, 2014
A Case of Central Precocious Puberty Due to Concomitant Hypothalamic Hamartoma and Juvenile Pilocytic Astrocytoma, 2014
A Novel Activating ABCC8 Mutation Underlying Neonatal Diabetes Mellitus in An Infant Presenting With Cerebral Sinovenous Thrombosis, 2014
Decreased Vitamin D Levels in Children with Familial Mediterranean Fever, 2014
Permanent neonatal diabetes caused by a novel mutation in the INS gene, 2013
Low serum nesfatin 1 levels may be a contributing factor for monogenic obesity due to prohormone convertase 1 deficiency, 2013
Clinical and diagnostic characteristics of hyperprolactinemia in childhood and adolescence, 2013
A novel GATA6 mutation leading to congenital heart defects and permanent neonatal diabetes A case report, 2013
Low Omentin 1 Levels Are Related with Clinical and Metabolic Parameters in Obese Children, 2013
The relation of serum nesfatin 1 level with metabolic and clinical parameters in obese and healthy children, 2013
Acute Vitamin D Intoxication Possibly Due to Faulty Production of a Multivitamin Preparation, 2013
A Case of Rapid Onset Obesity with Hypothalamic Dysfunction Hypoventilation Autonomic Dysregulation and Neural Crest Tumor Rohhadnet Syndrome, 2013
46 XX Male Disorder of Sexual Development A Case Report, 2013
Epidemiology Classification and Management of Undescended Testes Does Medication Have Value in its Treatment, 2013
Erken Başlangıçlı Graves Olgusu, 2013
Çocukluk Çağı Obezitesinde Serum Chemerin Düzeyinin Metabolik ve Antropometrik Parametrelerle Olan İlişkisi, 2013
Olgu Sunumu Tanınız Nedir Çocukluk çağında subklinik hipotiroidinin nadir bir nedeni Lingual tiroid, 2013
Adölesanda Fiziksel ve Seksüel Gelişme, 2013
Clinical profile and etiologies of children with central diabetes insipidus a single center experience from Turkey, 2012
Hyperprolactinemia in children clinical features and long term results, 2012
Evaluation of neutrophil gelatinase associated lipocalin in normoalbuminuric normotensive type 1 diabetic adolescents, 2012
Vitamin D Bağımlı Rikets Tip I İki Olgu Sunumu, 2012
Bilateral Pheochromocytoma as First Manifestation of Von Hippel Lindau Disease A Case Report, 2012
Evaluation of Urine Collection Methods for the Diagnosis of Urinary Tract Infection in Children, 2010

Evaluation of Clinical, Genetical, and Steroid Profile Features of Cases with 3Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency, 2017
Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3 beta-hydroxysteroid dehydrogenase 2 deficiency, 2019
Biotine interference in a patient with non-clinic high thyroid hormone levels, 2019
Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3β-hydroxysteroid dehydrogenase 2 deficiency, 2019
Social cognition and emotional functioning in adolescents with binge eating disorder with their relationship to clinical profile: apreliminary report,
Comprehensive Genetic Testing Shows One in FiveChildren with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology., 2018
Olgu Çocukluk Çağında İzole Hiperfosfatazemi, 2018
Characteristics in 5-Alpha Reductase Type 2 Deficiency: A Multicenter Study from Turkey., 2017
Acute kidney injury according to pRIFLE criterıa in Children with diabetıc ketoacidosis, 2017
Psodohipoparatiroidizm Tip 1A/1C ve Tip 1B: Üç olgu ile Psodohipoparatiroidizmde Klinik Spektrum,
Diyabetik Ketoasidoza Bağlı Santral Sinir Sistemi Hasarını Öngörmede Serum S100B, Nöron Spesifik Enolaz ve Gliyal Fibriller Asidik Proteinin Önemi-2,
Investigation of Androgen Receptor Gen MutationSpectrum in the Turkish Patients with Disorder of Sex Development, 2017
Clinical and Genetic Features of Our Patients with Hypophosphatemic Rickets, 2017
Genotypic and phenotypic features and treatment Results of a selenocysteine insertion sequence binding Protein 2 (SECIBP2) Mutatıon, 2017
Serum levels of S100B, neuron-specific enolase (NSE) and glial fıbrıllary acidic proteın (GFAP) in predicting the dıabetıc ketoacidosis-induced central nervous system damage, 2017
Diyabetik Ketoasidoz Tanısı Konan Çocuklarda Akut Böbrek Hasarının pRIFLE Kriterleri ile Değerlendirilmesi, 2017
The growing adolescent health problems Obesity and internet addiction, 2016
Kronik malnütrisyonda serum nesfatin 1 düzeyinin metabolik ve antropometrik parametreler ile olan ilişkisinin değerlendirilmesi,
Spectrum of the Genetic Defects in Hypophosphatemic Rickets in A Group of Turkish Children,
Comparison of Two Different Stoss TherapyDoses in Children with Vitamin D De ciency or Insuf ciency without Rickets,
Sulphonylurea Treatment in a Patient with Intermediate DEND Syndrome,
Intratubular Large Cell Hyalinizing Sertoli Cell Tumor of the Testis Presenting with Prepubertal Gynecomastia A Case Report,
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,
The relationship between Subclinical Hypothyroidism and Iodine De ciency Serum Leptin Metabolic Syndrome in Obese Children,
Nerve Conduction Studies in Children with Subclinical Hypothyroidism,
Turner sendromlu Türk kızlarının Büyüme Eğrileri FAVOR Turner Sendromu Çalışma Grubu, 2015
Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor a Mutations, 2015
Elevated Serum Irisin Level is not Related to Metabolic and Anthropometric Parameters in Obese Children, 2015
Clinical and Biochemical Characteristics of a Female Patient with a Novel Homozygous STAT5B Mutation but Lack of Pulmonary Disease, 2015
Effect of Reward based Motivation on Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus, 2015
Primary Adrenal Insufficiency in Children without Congenital Adrenal Hyperplasia Molecular and Clinical Characterisation of a Nationwide Cohort, 2015
Pituitary Stalk Interruption Syndrome Presenting with Normogonadotropic Amenorrhea and Hypoprolactinemia, 2015
The Growth Characteristics of Patients with Noonan Syndrome and First 2 Years Results of GH Treatment A Nationwide Multicentre Study, 2015
A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty, 2015
A Novel Mutation in Steroidogenic Factor Gene in a Patient with 46 XY DSD without Adrenal Insufficiency, 2015
İnsülin Direnci Olan Obez Çocuklarda İnflamasyon Belirteçlerinin ve Sürekli Ciltaltı Glukoz Monitorizasyonu İle Elde Edilen Glisemik Değişkenliğin Metabolik Sendrom ile İlişkisi, 2016
Vitamin D Eksikliği Olan Çocuklarda İki Farklı Stoss Tedavi Protokolünün Etkinlik ve Yan Etkiler Açısından Karşılaştırılması, 2016
Multiple Endokrin Neoplazi Tip 2A Ailesi Erken Profilaktik Tiroidektominin Önemi,
COL2A1 Geninde De Novo Mutasyona Bağlı Akondrogenezis tip 2 Hipokondrogenezis Olgusu,
Konjenital Diyabet ve Epifiziel Displazili Wolcott Rallison Sendromu Tanılı Bir Olgu,
Noonan Sendromu Tanısı ile İzlenen Olgularda Serebrovasküler Malformasyonlar,
Obez Çocuk ve Adolesanlarda Subklinik Hipotiroidinin Etyolojisinde İyot Eksikliği ve Leptinin Rolü,
Intermediate DEND Sendromu 17 Yaşında Neonatal Diyabet Tanısı Alan Bir Olguda Sülfonilüre Tedavisinin Sonuçları,
Subklinik Hipotiroidili Çocuklarda Nöromusküler Fonksiyonların Elektronöromiyografi ile Değerlendirilmesi,
Obez Çocuklarda Yüksek Saptanan İrisin Düzeyinin Antopometrik Ve Metabolik Parametrelerle Olan İlişkisi,
Pankreas Hipoplazili Neonatal Diyabet Olgusu PTF1A Mutasyonu,
Obez ve Sağlıklı Çocuklarda Serum Betatrofin Düzeyinin Metabolik ve Klinik Parametreler ile Olan İlişkisi,
Bilateral jinekomastinin nadir bir nedeni Sertoli hücre hiperplazisi,
Farklı klinik ve biyokimyasal özellikler ile prezente olan ve yeni tanımlanan homozigot mutasayona bağlı bir STAT5b eksikliği olgusu,
Yeni Bir Tiroid Hormon Direnci Nedeni Olan THRA Mutasyonlarına Bağlı Hipotiroidinin Genotipik Ve Fenotipik Özelliklerinin Değerlendirilmesi,
Levothyroxine Replacement in Primary Congenital Hypothyroidism The Higher the Initial Dose the Higher the Rate of Overtreatment, 2015
Çocukluk Çağı Obesite ve İnsülin Direncinde Tanısal Yaklaşım,
Diyabetik Ketoasidoz ile Başvuran Bir Cushing Hastalığı Olgusu,
Spontan Meme Gelişimi ve Menstruasyonu Olan Swyer Sendromlu Bir Olgu,
Multiple Endokrin Neoplazi Tip 2A Ailesi Erken Profilaktik Tiroidektominin Önemi,
COL2A1 Geninde De Novo Mutasyona Bağlı Akondrogenezis tip 2 Hipokondrogenezis Ogusu,
Konjenital Diyabet ve Epifiziel Displazili Wolcott Rallison Sendromu Tanılı Bir Olgu,
Psödohipoaldesteronizm ile Karışabilen Bir Konjenital Adrenal Hiperplazi Olgusu,
Hiperinsülinemik Hipoglisemi Tanılı Bir Olguda Lanreotid Somatulin Autogel ve Sürekli Cilt Altı Oktreotid İnfüzyonu Tedavisi,
RET Protoonkogeninde C634Y Mutasyonu Olan MEN2A Tanılı Bir Olguda Profilaktik Tiroidektomi,
Çocukluk Çağında Diyabetin Nadir Bir Nedeni Glukokinaz Mutasyonu MODY2,
Primer Amenore ve Virilizasyon Bulgulari ile Başvuran ve 17ß Hidroksisteroid Dehidrogenaz Geninde Yeni Bir Mutasyon Saptanan Olgu,
Tip 1 Diyabetli Çocuklarda Basit Karbonhidratların Kesme şeker Bal ve Meyve suyu Hipoglisemik Epizot Üzerine Etkinliğinin Değerlendirilmesi 2014 Diyabetli Çocuklar Yaz Kampı Çalışması,
Gençlikte Ortaya Çıkan Erişkin Tip Diyabet Mody Tanısı Ile Izlenen Çocuklarda Yeni Nesil Dizi Analizi Yöntemi Ile Tanımlanmış Genlerin Araştırılması,
Santral Erken Puberte Tanisinda Serum Nörokinin B Düzeyinin Önemi ve Serum Kisspeptin ve Leptin Düzeyleri ile ilişkisi,
46 XY Cinsiyet Gelişim Bozukluğu Olan Bir Olguda Adrenal Yetmezlik Olmaksızın SF1 NR5A1 Geninde Yeni Bir Mutasyon,
Üç Olguda Tiroid Hormonu Alfa Reseptörü Mutasyonu ile Ilişkili Tiroid Hormon Direnci,
Turner Sendromlu Çocukların Başvuru Özellikleri ve Eşlik Eden Patolojiler 842 Vakanın Ulusal Veritabanında Değerlendirme Sonuçları,
Obez Çocuk ve Adolesanlarda Subklinik Hipotiroidinin Metabolik Parametreler Üzerine Etkisi,
ABCC8 Geninde Yeni Bir Mutasyon Saptanan Hiperinsülinemik Hipoglisemili Bir Olguda Erken Spontan İyileşme,
Doğumsal Hiperinsülinizm Tanılı Iki Kardeşte Cerrahi Tedaviye Alternatif Olarak Lanreotid Somatuline Autogel Tedavisi,
Hipergonadotropik Hipogonadizmin Nadir Bir Nedeni 46 XX Sry Erkek Cinsiyet Gelişim Bozukluğu,
Tip 1 Diyabetli Hastalarda Ödüle Dayalı Motivasyonun Metabolik Kontrol Üzerine Etkisi,
Konjenital Primer Hipotiroidizimde Başlangıç Tedavisinde En Güvenilir Doz Nedir,
GATA6 Mutasyonuna Bağlı Gelişen Neonatal Diyabetli Bir Olguda Pankreas Agenezisi ve Proteinüri Birlikteliği,
Primer Amonere ile Başvuran Bir Olguda Komplete Androjen Duyarsızlık Sendromu,
Erken Meme Gelişimi ile Başvuran Kız Olguların Nihai Tanılarına Göre Klinik ve Laboratuvar Bulgularının Değerlendirilmesi,
Diyabetik Ketoasidoz ile Başvuran Tip 1 Diyabetes Mellituslu Çocukların Klinik ve Laboratuvar Özellikleri,
Tip 1 Diyabetes Mellituslu Hastalarımızın Demografik ve Klinik Özellikleri,
Prematür Telarş Olgularında Serum Nesfatin 1 Düzeyinin Klinik Önemi ve Serum Leptin Düzeyi ile İlişkisi,
Obez Çocuklarda Açlik ve Tokluk Serum Nesfatin Düzeylerinin Antropometrik ve Metabolik Parametreler ile Olan İlişkisi,
Tanı ve Tedavisinde Güçlük Yaşanan Bir Erken Puberte Olgusu,
Neonatal Diyabetli Bir Olguda Pankreas Agenezisi ve Konjenital Kalp Hastalığı GATA6 Geninde Yeni Bir Mutasyon,
Subklinik Hipotiroidili Çocuklarda L Tiroksin Tedavisinin Sol Ventrikül Fonksiyonlarina Etkisi,
Subklinik Hipotiroidili Çocuklarda L tiroksin Tedavisinin Lipoproteinler ve Klinik Bulgular Üzerine Etkisi,
Boy Kısalığı ile Başvuran Kleidokranial Displazili Bir Olgu,
Makrodonti ile Tanınabilen KBG Sendromlu Bir Olgunun Uzun Dönem Takip Sonuçları,
Kallmann Sendromu Tanili Olgularda Olfaktör Bulbus Volümleri ile Objektif ve Subjektif Koku Testinin Sonuçlari,
Santral Erken Pubertenin Çok Nadir Bir Nedeni Hipotalamik Hamartom ve Juvenil Pilositik Astrositom Birlikteliği,
Çocukluk Çağında Nadir Bir Tanı 46 XX Erkek Cinsel Gelişim Bozukluğu Bir Olgu Sunumu,
Ankaranın Keçiören İlçesinde Maternal Vitamin D Eksikliğinin İnsidansı,
Çocukluk Çağı Obezitesinde Serum Chemerin Düzeyinin Metabolik ve Antropometrik Parametreler ile Olan İlişkisi,
Leptin ve Soluble Leptin Reseptörünün Obez Çocuklarda Vücut Kitle İndeksi ve İnsülin Direnci ile İlişkisi,
Maternal 6q24 Hipometilasyonuna Bağlı Gelişen Geçici Neonatal Diabetes Mellitus Olgu Sunumu,
Mikrosefalik Primordial Dwarfizm MOPD Sendromunda Perisentrin PCNT Geninde Yeni Bir Mutasyon Olgu Sunumu,
Serebral Venöz Sinüs Trombozu ile Başvuran Neonatal Diabetes mellitus Bir Olgu ABCC8 Geninde Yeni Bir Mutasyon,
Çocukluk Çağında Hiperkalseminin Nadir Bir Nedeni Paratiroid Adenomu,
Hızlı Başlangıçlı Obezite Hipertansiyon Hipotalemik Disfonksiyon Otonomik Disregülasyon ROHHAD Sendromu,
Obez ve Sağlıklı Çocuklarda Serum Nesfatin 1 Düzeyinin Metabolik ve Klinik Parametreler ile Olan İlişkisi,
Yeni Tanımlanan INS Gen Mutasyonuna Bağlı Kalıcı Bir Neonatal Diyabet Olgusu,
Multivitamin Kullanımına İkincil Gelişen D Vitamini İntoksikasyonu 3 Olgu Sunumu,
Ailesel Akdeniz Ateşi Olan Çocuklarda D Vitamini Düzeyi,
X e Bağlı Konjenital Adrenal Hipoplazi ve Hipogonadotropik Hipogonadizm DAX1 Gen Mutasyonu Olan Bir Hasta,
İdiyopatik Santral Puberte Prekoks Tanısı Alan Çocuklarda GnRH Anolog Tedavisinin Vücut Kitle İndeksi Üzerine Etkisi,
Santral Diabetes İnsipiduslu Çocukların Klinik Laboratuvar ve Etyolojik Özellikleri,
Vitamin D Bağımlı Rikets Tip 1 İki Olgu Sunumu,
Pansitopeni ile Başvuran Bir Olguda Fanconi Aplastik Anemisi Seckel Sendromu Birlikteliği,
Molecular Genetic Analysis of Maturity Onset Diabetes of the Young Mody Genes in Children by Using Targeted Next Generation Sequencing, 2015
Rare Case of Swyer Syndrome with Spontaneous Breast Development and Menstruation,
Recovery of Central Fever After GH Therapy in a Patient with GH De ciency Secondary to Posttraumatic Brain Injury, 2014
A Novel GATA6 Mutation Leading to Congenital Heart Defects and Permanent Neonatal Diabetes A Case Report, 2013
Permanant Neonatal Diabetes Caused By A Novel Mutation in The INS Gene, 2013
Can neutrophil gelatinase associated lipocalin be an early marker of kidney injury in type 1 diabetics,
Investigating food additive hypersensitivity by using atopy patch test in children with atopic eczema,
Düşük Omentin 1 Düzeyinin Obez Çocuklarda Klinik ve Metabolik Önemi,
Anormal Tiroid Fonksiyon Testleri ve Ailevi Motor Mental Retardasyon,
Propitozis ile başvuran infantil graves olgusu, 2011
Neonatal Diyabet Tedavisinde Zorluk Çekilen Bir Vaka Tip 1 Diyabet Problem Olgular ve Çözüm Önerileri,
14 Yaşında Sulfonilüre Tedavisine Yanıt Veren Neonatal Diyabetli Bir Olgu,
46 XY Cinsel Farklılaşma Kusurunun Nadir Bir Nedeni Frasier Sendromu,
Tip 1 Diyabetli Çocuk ve Adolesanlarda Kan Şekeri Değişkenliğinin Klinik ve Laboratuvar Değerler ile İlişkisi,
Nadir Görülen Bir Turner Sendromu Karyotipi 45 X 47 XXX,
Ailesel Feokromasitoma Nedeniyle İzlenen ve Von Hippel Lindau Sendromu Tanısı Alan Bir Olgu,
Çocuklarda Hiperprolaktinemi Etyoloji Klinik Özellikleri ve Tedavi,
Akselere Pubertal Gelişim Gösteren Septo Optik Displazi Olgusu,
Tip 1 Diyabetli Çocuk ve Adolesanlarda Böbrek Hasarının Erken Bulgularının Araştırılması Notrofil jelatinaz İlişkili Lipokalin Bir Belirteç Olabilirmi,
İzmir Manisa Bölgesinde Tip 1 Diyabet 2008 ile 2010 Verilerinin Karşılaştırılması,
Çölyak Hastalığına İkincil Karaciğer Etkilenimi,
Çocukluk Çağında Akut Pankreatitin Nadir Bir Nedeni Akut Hepatit A,
The Relation of Serum Leptin and Soluble Leptin Receptor Levels with Metabolic and Clinical Parameters in Obese and Healthy Children, 2014
The Diverse Phenotype of Mutations in T Receptor Alpha TRa,
A Pediatric Case of Cushing s Disease Presenting with Diabetic Ketoacidosis,
The Effect of L Thyroxine Treatment on Left Ventricular Functions in Children with Subclinical Hypothyroidism, 2014
Clinical Features of Kallmann Syndrome and The Importance of Smell Test S and Brain Magnetic Resonance İmaging in Diagnosis Report of Five Adolescents, 2014
Long Term Follow up of A Case With A Clinically Recognisable Genetic Cause of Short Stature KBG Syndrome,
Acute Vitamin D İntoxication in Three Children Unproven Manufacturing Error of Unique Multivitamin Preparation, 2013
Decreased Vitamin D Levels in Children with Familial Mediterranean Fever, 2014
Low Omentin 1 Levels are Related with Clinical and Metabolic Parameters in Obese Children, 2013
A Case of Rapid Onset Obesity With Hypothalemic Dysfunction Hypoventilation Autonomic Dysregulation and Neural Crest Tumours Rohhadnet Syndrome, 2013
Hyperprolactinemia in Children Etiology Clinical Aspects and Treatment, 2012
Aetiologies and Clinical Characteristics of Childhood Central Diabetes İnsipidus, 2012
Bilateral Phaechromocytoma as First Manifestation of Von Hippel Lindau Disease A Case Report, 2012
The relation of serum nesfatin 1 Level with Metabolic and Clinical Parameters in Obese and Healthy Children, 2013
A case of Osteopetrosis Tarda in Childhood Presenting with Polyarthralgia and Rickets,
Abnormal thyroid function tests in two mentally and motor disabled brothers monocarboxylate transporter 8 deficiency,

Olgu Örnekleri İle Tanıdan Tedaviye Çocuk Hastalıkları, ISBN: 978-605-9415-29-3, 2017
Olgu Örnekleri ile Tanıdan Tedaviye Çocuk Hastalıkları, ISBN: 978-605-9415-29-3, 2017
Pediatrinin Esasları, ISBN: 978-605-4949-74-8, 2016
Temel Pediatrik Endokrinoloji, ISBN: 978-605-5013-44-08, 2015
Temel Pediatrik Endokrinoloji, ISBN: 978-605-5013-44-08, 2015
Çocuk Endokrinolojisinde Uzlaşı, ISBN: 978-605-335-094-1, 2014
Çocuk Endokrinolojisi, ISBN: 978-605-335-011-8, 2013