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 202...
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.
Articles
A Novel Homozygous Selenocysteine Insertion Sequence Binding Protein 2 (SECISBP2, SBP2) Gene Mutation in a Turkish Boy , 2018
Impaired systolic and diastolic left ventricular function in children and adolescents with congenital adrenal hyperplasia receiving corticosteroid therapy , 2019
The Relationship between Serum Zonulin Level and Clinical and Laboratory Parameters of Childhood Obesity , 2017
Evaluation of Turner Syndrome Knowledge among Physicians and Parents , 2020
Does fludrocortisone treatment cause hypomagnesemia in children with primary adrenal insufficiency? , 2021
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
Can we use copeptin as a biomarker for masked hypertension or metabolic syndrome in obese children and adolescents? , 2020
Childhood-onset mild diabetes caused by a homozygous novel variant in the glucokinase gene , 2021
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets , 2020
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
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
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
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
Tip 1 Diyabetes Mellitus Olgularının Tanı Anındaki Demografik,Klinik ve Laboratuvar Özelliklerinin Değerlendirilmesi , 2017
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
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
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
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 profile and etiologies of children with central diabetes insipidus a single center experience from Turkey , 2012
Clinical and diagnostic characteristics of hyperprolactinemia in childhood and adolescence , 2013
The relation of leptin and soluble leptin receptor levels with metabolic and clinical parameters in obese and healthy children , 2014
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
Hyperprolactinemia in children clinical features and long term results , 2012
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
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
Cross reactivity of adrenal steroids with aldosterone may prevent the accurate diagnosis of congenital adrenal hyperplasia , 2015
Evaluation of neutrophil gelatinase associated lipocalin in normoalbuminuric normotensive type 1 diabetic adolescents , 2012
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
Evaluation of Neutrophil Gelatinase Associated Lipocalin in Normoalbuminuric Normotensive Type 1 Diabetic Adolescents , 2012
Adipokines in Breast Milk An Update , 2014
Adipokines in Breast Milk An Update , 2014
Cross Reactivity of Adrenal Steroids With Aldosterone May Prevent The Accurate Diagnosis of Congenital Adrenal Hyperplasia , 2014
Serum nesfatin 1 and leptin levels in non obese girls with premature thelarche , 2015
Gonadal malignancy risk and prophylactic gonadectomy in disorders of sexual development , 2015
Acute Vitamin D Intoxication Possibly Due to Faulty Production of a Multivitamin Preparation , 2013
Acute Vitamin D Intoxication Possibly Due to Faulty Production of a Multivitamin Preparation , 2013
Low serum nesfatin 1 levels may be a contributing factor for monogenic obesity due to prohormone convertase 1 deficiency , 2013
Incidence of maternal vitamin D deficiency in a region of Ankara Turkey a preliminary study , 2014
Incidence of Maternal Vitamin D Deficiency In a Region of Ankara Turkey A Preliminary Study , 2014
Isolated Hyperthyrotropinemia in Childhood Obesity and Its Relation with Metabolic Parameters , 2014
A Case of Rapid Onset Obesity with Hypothalamic Dysfunction Hypoventilation Autonomic Dysregulation and Neural Crest Tumor Rohhadnet Syndrome , 2013
A Case of Rapid Onset Obesity with Hypothalamic Dysfunction Hypoventilation Autonomic Dysregulation and Neural Crest Tumor Rohhadnet Syndrome , 2013
Fasting and Postprandial Levels of A Novel Anorexigenic Peptide Nesfatin in Childhood Obesity , 2014
Subclinical Hypothyroidism in Childhood and Adolescense , 2014
Hyperprolactinemia in Children Clinical Features and Long Term Results , 2012
The Relation of Serum Nesfatin 1 Level with Metabolic and Clinical Parameters in Obese and Healthy Children , 2013
Low Omentin 1 Levels Are Related with Clinical and Metabolic Parameters in Obese Children , 2013
A Novel GATA6 Mutation Leading To Congenital Heart Defects and Permanent Neonatal Diabetes A Case Report , 2013
The Relation of Leptin and Soluble Leptin Receptor Levels with Metabolic and Clinical Parameters in Obese and Healthy Children , 2014
Clinical and Diagnostic Characteristics of Hyperprolactinemia in Childhood and Adolescense , 2013
Clinical Profile and Etiologies of Children with Central Diabetes İnsipidus A Single Center Experience From Turkey , 2012
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
Epidemiology Classification and Management of Undescended Testes Does Medication Have Value in its Treatment , 2013
46 XX Male Disorder of Sexual Development A Case Report , 2013
Effect of gonadotropin releasing hormone agonist therapy on body mass index and growth in girls with idiopathic central precocious puberty , 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
An Unusual Presentation of Pediatric Cushing Disease Diabetic Ketoacidosis , 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
Recovery of Central Fever after GH Therapy in a Patient with GH Deficiency Secondary to Posttraumatic Brain Injury , 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
Santral Erken Puberte ve Prematür Telarş Ayırıcı Tanısında Klinik ve Laboratuvar Bulgular , 2015
Turner Syndrome and Associated Problems in Turkish Children A Multicenter Study , 2015
Significance of Serum Neurokinin B and Kisspeptin Levels in the Differential Diagnosis of Premature Thelarche and Central Precocious Puberty , 2015
The Effect of L Thyroxine Treatment on Hypothyroid Symptom Scores and Lipid Profile in Children with Subclinical Hypothyroidism , 2014
Is Patch Testing with Food Additives Useful in Children with Atopic Eczema , 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
Erken Başlangıçlı Graves Olgusu , 2013
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
An Unusual Presentation of 46 XY Pure Gonadal Dysgenesis Spontaneous Breast Development and Menstruation , 2015
The Effect of L thyroxine Treatment on Left Ventricular Functions in Children with Subclinical Hypothyroidism , 2015
The Role of Thyrotropin Releasing Hormone Stimulation Test in Management of Hyperthyrotropinemia in Infants , 2015
Çocuk ve Ergenlerde Obezite Tanım ve Epidemiyoloji , 2015
Çocukluk Çağı Obezitesinde Serum Chemerin Düzeyinin Metabolik ve Antropometrik Parametrelerle Olan İlişkisi , 2013
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
Olgu Sunumu Tanınız Nedir Çocukluk çağında subklinik hipotiroidinin nadir bir nedeni Lingual tiroid , 2013
Adölesanda Fiziksel ve Seksüel Gelişme , 2013
Vitamin D Bağımlı Rikets Tip I İki Olgu Sunumu , 2012
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
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
Reports
Evaluation of Clinical, Genetical, and Steroid Profile Features of Cases with 3Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency - GÜRAN TÜLAY,KARA CENGİZ,ATAY ZEYNEP,AKBARZADE AZAD,YILMAZ GÜLAY,ÇELEBİ BİTKİN EDA,AKÇAY TEOMAN,YILDIZ MELEK,GÜVEN AYLA,ÇATLI GÖNÜL,YEŞİL GÖZDE,BAS SERPİL,VATANSEVER PINAR,HAKLAR GONCAGÜL,ŞİRİKÇİ ÖNDER,TURAN SERAP,BEREKET ABDULLAH
Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3 beta-hydroxysteroid dehydrogenase 2 deficiency - GÜRAN TÜLAY,KARA CENGİZ,YILDIZ MELEK,Çelebi Bitkin Eda,HAKLAR GONCAGÜL,Lin JenChieh,Gilligan Lorna C,Barnard Lise,KESKİN MEHMET,ANIK AHMET,ÇATLI GÖNÜL,GÜVEN AYLA,Kirel Birgül,TÜTÜNCÜLER KÖKENLİ FİLİZ,ÖNAL HASAN,Turan Serap,Akçay Teoman,ATAY ZEYNEP,Baranowski Elizabeth S,Can Yılmaz Gülay,Mamadova Jamala,Akbarzade Azad,Sırıkcı Önder,Aghayev AghaRza,ALKAN AFRA,Shackleton Cedric H L,Storbeck Karl H,Barış Tuğba,Arlt Wiebke,Chung BonChu,BEREKET ABDULLAH
Biotine interference in a patient with non-clinic high thyroid hormone levels - AYRANCI İLKAY,FİLİBELİ BERNA EROĞLU,MANYAS HAYRULLAH,DÜNDAR BUMİN NURİ,ÇATLI GÖNÜL
Biotine interference in a patient with non-clinic high thyroid hormone levels - AYRANCI İLKAY,FİLİBELİ BERNA EROĞLU,MANYAS HAYRULLAH,DÜNDAR BUMİN NURİ,ÇATLI GÖNÜL
Biotine interference in a patient with non-clinic high thyroid hormone levels - AYRANCI İLKAY,FİLİBELİ BERNA EROĞLU,MANYAS HAYRULLAH,DÜNDAR BUMİN NURİ,ÇATLI GÖNÜL
Biotine interference in a patient with non-clinic high thyroid hormone levels - AYRANCI İLKAY,FİLİBELİ BERNA EROĞLU,MANYAS HAYRULLAH,DÜNDAR BUMİN NURİ,ÇATLI GÖNÜL
Biotine interference in a patient with non-clinic high thyroid hormone levels - AYRANCI İLKAY,FİLİBELİ BERNA EROĞLU,MANYAS HAYRULLAH,DÜNDAR BUMİN NURİ,ÇATLI GÖNÜL
Biotine interference in a patient with non-clinic high thyroid hormone levels - AYRANCI İLKAY,FİLİBELİ BERNA EROĞLU,MANYAS HAYRULLAH,DÜNDAR BUMİN NURİ,ÇATLI GÖNÜL
Biotine interference in a patient with non-clinic high thyroid hormone levels - AYRANCI İLKAY,FİLİBELİ BERNA EROĞLU,MANYAS HAYRULLAH,DÜNDAR BUMİN NURİ,ÇATLI GÖNÜL
Biotine interference in a patient with non-clinic high thyroid hormone levels - AYRANCI İLKAY,FİLİBELİ BERNA EROĞLU,MANYAS HAYRULLAH,DÜNDAR BUMİN NURİ,ÇATLI GÖNÜL
Biotine interference in a patient with non-clinic high thyroid hormone levels - AYRANCI İLKAY,FİLİBELİ BERNA EROĞLU,MANYAS HAYRULLAH,DÜNDAR BUMİN NURİ,ÇATLI GÖNÜL
Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3β-hydroxysteroid dehydrogenase 2 deficiency - GÜRAN TÜLAY,KARA CENGİZ,YILDIZ MELEK,BİTKİN EC,HAKLAR GONCAGÜL,Lin JC,Gilligan LC,Barnard L,KESKİN MEHMET,ANIK AHMET,ÇATLI GÖNÜL,GÜVEN AYLA,KIREL BİRGÜL,TÜTÜNCÜLER KÖKENLİ FİLİZ,ÖNAL HASAN,TURAN SERAP,AKÇAY T,ATAY ZEYNEP,Baranowski ES,Yılmaz GC,Mamadova J,Akbarzade Az,SIRIKCI Ö,Aghayev A,ALKAN AFRA,Shackleton CHL,Storbeck KH,Barış T,Arlt W,Chung BC,BEREKET ABDULLAH
Social cognition and emotional functioning in adolescents with binge eating disorder with their relationship to clinical profile: apreliminary report - Turan Serkan,ÖZYURT GONCA,ÖZTÜRK YEŞİM,ABACI AYHAN,ÇATLI GÖNÜL,AKAY AYNUR
A 13 Year-Old Boy Diagnosed As OsteogenesisImperfecta With Normal Bone Mineral Density - TINAZTEPE TUĞBA,FLİBELİ BERNA EROĞLU,ÇATLI GÖNÜL,DÜNDAR BUMİN NURİ
A Rare Cause of Hypercalcemia in Childhood: Hypercalcemia Associated with Parathormon- Related Peptid - ÇATLI GÖNÜL,FİLİBELİ BERNA EROĞLU,KASAP DEMİR BELDE,MUTLUBAŞ FATMA,DÜNDAR BUMİN NURİ
Can Triponderal Mass Index Be a New Indicator in the Predicting Cardiometabolic Risk in Obese Adolescents? - CİNGÖZ GÜLTEN,FİLİBELİ BERNA EROĞLU,DÜNDAR BUMİN NURİ,ÇATLI GÖNÜL
Can we use Copeptin as a biomarker for masked hypertention in obese children and adolescents? - ERTAN DUYGU,KASAP DEMİR BELDE,ALPARSLAN CANER,ERBAK HURİYE,ÇATLI GÖNÜL,MUTLUBAŞ FATMA,EĞLENOĞLU ALAYGUT DEMET,SOYALTIN EREN,ÇALAR SEÇİL ARSLANSOY,YAVAŞCAN ÖNDER
Comprehensive Genetic Testing Shows One in FiveChildren with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology. - kashyap patel,colclough kevin,özbek mehmet nuri,yıldız melek,GÜRAN TÜLAY,koçyiğit cemil,ACAR SEZER,ŞIKLAR ZEYNEP,ATAR MÜGE,jonson matt,Flanagan Sarah E,Ellard Sian,ÇİZMECİOĞLU FİLİZ MİNE,BERBEROĞLU MERİH,DEMİR KORCAN,ÇATLI GÖNÜL,BAŞ SERPİL,akçay teoman,DEMİRBİLEK HÜSEYİN,weedon michael,Hattersley Andrew T
The Relationship Between Anthropometric Measurements and Breast Milk Ghrelin and Nesfatin-1 Levels in Infants with Small for Gestational Age - FİLİBELİ BERNA EROĞLU,KARABULUT MELİKE,AKSUN SALİHA,ÇATLI GÖNÜL,DÜNDAR BUMİN NURİ
Düşük Doğum Ağırlıklı Doğan Bebeklerin Anne Sütü Ghrelin ve Nesfatin-1 Düzeylerinin Bebeğin Antropometrik Ölçümleri ile İlişkisi - FİLİBELİ BERNA EROĞLU,Karabulut Melike,AKSUN SALİHA,ÇATLI GÖNÜL,DÜNDAR BUMİN NURİ
A Rare Cause of Hypercalcemia in Childhood: Hypercalcemia Associated with Parathormon- Related Peptid - ÇATLI GÖNÜL,FİLİBELİ BERNA EROĞLU,KASAP DEMİR BELDE,MUTLUBAŞ FATMA,DÜNDAR BUMİN NURİ
Can we use Copeptin as a biomarker for masked hypertention in obese children and adolescents - ERTAN DUYGU,KASAP DEMİR BELDE,ALPARSLAN CANER,ERBAK HURİYE,ÇATLI GÖNÜL,MUTLUBAŞ FATMA,EĞLENOĞLU ALAYGUT DEMET,SOYALTIN EREN,ÇAMLAR SEÇİL ARSLANSOY,YAVAŞCAN ÖNDER
Characteristics in 5-Alpha Reductase Type 2 Deficiency: A Multicenter Study from Turkey. - ABACI AYHAN,ÇATLI GÖNÜL,Kırbıyık Özgür,ŞAHİN NURSEL MURATOĞLU,ABALI ZEHRA YAVAŞ,ÜNAL EDİP,ŞIKLAR ZEYNEP,MENGEN EDA,ÖZEN SAMİM,GÜRAN TÜLAY,KARA CENGİZ,YILDIZ MELEK,EREN ERDAL,NALBANTOPĞLU ÖZLEM,GÜVEN AYLA,ÇAYIR ATİLLA,AKBAŞ EMİNE DEMET,KOR YILMAZ,ÇÜREK YUSUF,AYCAN ZEHRA,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BERBEROĞLU MERİH
Acute kidney injury according to pRIFLE criterıa in Children with diabetıc ketoacidosis - ANIK AHMET,ACAR SEZER,İLGÜN DENİZ,KOÇYİĞİT CEMİL,PAKETÇİ AHU,ÇATLI GÖNÜL,DÜNDAR BUMİN NURİ,ABACI AYHAN,ÜNÜVAR TOLGA
Psodohipoparatiroidizm Tip 1A/1C ve Tip 1B: Üç olgu ile Psodohipoparatiroidizmde Klinik Spektrum - CİNGÖZ GÜLTEN,SAT BERNA,ÇATLI GÖNÜL,DÜNDAR BUMİN NURİ,DURMAZ ERDEM
Diyabetik Ketoasidoza Bağlı Santral Sinir Sistemi Hasarını Öngörmede Serum S100B, Nöron Spesifik Enolaz ve Gliyal Fibriller Asidik Proteinin Önemi-2 - ÇATLI GÖNÜL,ANIK AHMET,ACAR SEZER,KÜME TUNCAY,Karabulut Melike,GÜRSOY ÇALAN ÖZLEM,DÜNDAR BUMİN NURİ,ABACI AYHAN
Investigation of Androgen Receptor Gen MutationSpectrum in the Turkish Patients with Disorder of Sex Development - ONAY HÜSEYİN,ÖZEN SAMİM,Türk Tuba Sözen,DARCAN ŞÜKRAN,ATİK TAHİR,ANIK AHMET,ERCAN OYA,EVLİYAOĞLU SAADET OLCAY,ÇATLI GÖNÜL,Hazan Filiz,ABACI AYHAN
Clinical and Genetic Features of Our Patients with Hypophosphatemic Rickets - ACAR SEZER,Al Rijal Roua A,Meyer Brian,Shi Yufei,DEMİR KORCAN,BÖBER ECE,Kattan Walaa E,ÇATLI GÖNÜL,Binessa Huda,ABACI AYHAN,DÜNDAR BUMİN NURİ,Zou Minjing,KAVUKÇU SALİH
Genotypic and phenotypic features and treatment Results of a selenocysteine insertion sequence binding Protein 2 (SECIBP2) Mutatıon - ÇATLI GÖNÜL,KIRBIYIK ÖZGÜR,GENÇPINAR PINAR,ÖZDEMİR TAHA REŞİT,ONAT MERVE,DÜNDAR BUMİN NURİ
Serum levels of S100B, neuron-specific enolase (NSE) and glial fıbrıllary acidic proteın (GFAP) in predicting the dıabetıc ketoacidosis-induced central nervous system damage - ÇATLI GÖNÜL,ANIK AHMET,ACAR SEZER,KÜME TUNCAY,GÜRSOY ÇALAN ÖZLEM,DÜNDAR BUMİN NURİ,ABACI AYHAN
The growing adolescent health problems Obesity and internet addiction - ELİAÇIK KAYI,KOÇYİĞİT CEMİL,KANIK ALİ,SELKIE ELLEN,ÇATLI GÖNÜL,OLGAÇ DÜNDAR NİHAL,DÜNDAR BUMİN NURİ
Kronik malnütrisyonda serum nesfatin 1 düzeyinin metabolik ve antropometrik parametreler ile olan ilişkisinin değerlendirilmesi - ACAR SEZER,ÇATLI GÖNÜL,KÜME TUNCAY,ÜNVER TUHAN HALE,GÜRSOY ÇALAN ÖZLEM,DEMİR KORCAN,BÖBER ECE,ABACI AYHAN
Spectrum of the Genetic Defects in Hypophosphatemic Rickets in A Group of Turkish Children - ACAR SEZER,Al Rijjal Roua A,DEMİR KORCAN,Kattan Walaa E,ÇATLI GÖNÜL,BinEssa Huda,ABACI AYHAN,DÜNDAR BUMİN NURİ,Zou Minjing,KAVUKÇU SALİH,Meyer Brian,BÖBER ECE,Sh Yufei
Comparison of Two Different Stoss TherapyDoses in Children with Vitamin D De ciency or Insuf ciency without Rickets - KOÇYİĞİT CEMİL,ÇATLI GÖNÜL,İNCE GÜLBERAT,CAN ŞULE PENBE,DÜNDAR BUMİN NURİ
Sulphonylurea Treatment in a Patient with Intermediate DEND Syndrome - ÇATLI GÖNÜL,KOÇYİĞİT CEMİL,GENÇPINAR PINAR,CAN PENBE ŞULE,OLGAÇ DÜNDAR NİHAL,DÜNDAR BUMİN NURİ
Intratubular Large Cell Hyalinizing Sertoli Cell Tumor of the Testis Presenting with Prepubertal Gynecomastia A Case Report - ÜNVER TUHAN HALE,ABACI AYHAN,SARSIK KUMBARACI BANU,ÖZTÜRK TÜLAY,OLGUNER MUSTAFA,ÇATLI GÖNÜL,ANIK AHMET,OLGUN HATİCE NUR,BÖBER ECE
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 - KAYA ABDURRAHMAN,KOÇYİĞİT CEMİL,ÇATLI GÖNÜL,CAN PENBE ŞULE,SÜTÇÜ RECEP,DÜNDAR BUMİN NURİ
The relationship between Subclinical Hypothyroidism and Iodine De ciency Serum Leptin Metabolic Syndrome in Obese Children - DÜNDAR BUMİN NURİ,TANRISEVER ÖZGÜR,ÇATLI GÖNÜL,KOÇYİĞİT CEMİL,CAN ŞULE PENBE,PİRGON MUSTAFA ÖZGÜR
Nerve Conduction Studies in Children with Subclinical Hypothyroidism - ÇATLI GÖNÜL,YİŞ ULUÇ,ÜNVER TUHAN HALE,AYANOĞLU MÜGE,HIZ AYŞE SEMRA,BÖBER ECE,ABACI AYHAN
Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor a Mutations - DEMİR KORCAN,GUHT ANJA VAN,BÜYÜKİNAM MUAMMER,ÇATLI GÖNÜL,YAVUZ AYHAN,BAŞ VEYSEL NİJAT,DÜNDAR BUMİN NURİ,ÖZKAN BEHZAT,MEİMA MARCEL E,W EDWARD VİSSER,PEETERS ROBİN P,VİSSER THEO J
Elevated Serum Irisin Level is not Related to Metabolic and Anthropometric Parameters in Obese Children - ABACI AYHAN,ÇATLI GÖNÜL,ÜNVER TUHAN HALE,ANIK AHMET,KÜME TUNCAY,ÇALAN ÖZLEM GÜRSOY,BÖBER ECE
Clinical and Biochemical Characteristics of a Female Patient with a Novel Homozygous STAT5B Mutation but Lack of Pulmonary Disease - ÇATLI GÖNÜL,HWA VİVİAN,LOSEQOOT MONİQUE,ÖZYILMAZ BERK,EDEER NESLİHAN,DÜNDAR BUMİN NURİ,WİT JAN MARTİN
Effect of Reward based Motivation on Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus - KOÇYİĞİT CEMİL,ÇATLI GÖNÜL,CAN ŞULE PENBE,DÜNDAR BUMİN NURİ
Primary Adrenal Insufficiency in Children without Congenital Adrenal Hyperplasia Molecular and Clinical Characterisation of a Nationwide Cohort - GÜRAN TÜLAY,BUONOCORE FEDERİCA,SAKA NURCİN,ÖZBEK MEHMET NURİ,AYCAN ZEHRA,BEREKET ABDULLAH,BAŞ FİRDEVS,DARCAN ŞÜKRAN,BİDECİ AYSUN,TURAN SERAP,GÜVEN AYLA,TARIM ÖMER FARUK,AĞLADIOĞLU SEBAHAT YILMAZ,ZEYNEP ATAY,ÖZEN SAMİM,DEMİR KORCAN,AKINCI AYŞEHAN,AYDIN BANU KÜÇÜKEMRE,BÜYÜKİNAM MUAMMER,YÜKSEL BİLGİN,YILDIZ METİN,AKÇAY TEOMAN,KARA CENGİZ,ÖZGEN İLKER TOLGA,ÇATLI GÖNÜL,IŞIK EMREGÜL,BOLU SEMİH,ÖZHAN BAYRAM,GÜRBÜZ FATİH,UÇAR AHMET,DEMİRBİLEK HÜSEYİN,ABALI ZEHRA YAVAŞ,DOGER ESRA,EREN ERDAL,BERBEROĞLU MERİH,HACİHAMDİOĞLU BÜLENT,ACHERMAN JOHN C
Pituitary Stalk Interruption Syndrome Presenting with Normogonadotropic Amenorrhea and Hypoprolactinemia - ÇATLI GÖNÜL,KOÇYİĞİT CEMİL,CAN ŞULE PENBE,DÜNDAR BUMİN NURİ
The Growth Characteristics of Patients with Noonan Syndrome and First 2 Years Results of GH Treatment A Nationwide Multicentre Study - ŞIKLAR ZEYNEP,BERBEROĞLU MERİH,GENENS MİKAYİR,POYRAZOĞLU ŞÜKRAN,BAŞ FİRDEVS,DARENDELİLER FATMA FEYZA,BUNDAK RÜVEYDA,AYCAN ZEHRA,ERDEVE ŞENAY SAVAŞ,ÇETİNKAYA SEMRA,ABALI SAYGIN,ATAY ZEYNEP,TURAN SERAP,KARA CENGİZ,YILMAZ GÜLAY CAN,AKYÜREK NESİBE,ABACI AYHAN,SARI ERKAN,YEŞİLKAYA EDİZ,BOLU SEMİH,KORKMAZ HÜSEYİN ANIL,ŞİMŞEK ENVER,ÇATLI GÖNÜL,ÇAYIR ATİLLA,EVLİYAOĞLU SAADET OLCAY,İŞGÜVEN ŞÜKRİYE PINAR
A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty - KOÇYİĞİT CEMİL,ÇATLI GÖNÜL,SARITAŞ SERDAR,ONAY HÜSEYİN,DÜNDAR BUMİN NURİ
A Novel Mutation in Steroidogenic Factor Gene in a Patient with 46 XY DSD without Adrenal Insufficiency - ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,ÜNVER TUHAN HALE,ONAY HÜSEYİN,AYKUT AYCA,BÖBER ECE
İnsülin Direnci Olan Obez Çocuklarda İnflamasyon Belirteçlerinin ve Sürekli Ciltaltı Glukoz Monitorizasyonu İle Elde Edilen Glisemik Değişkenliğin Metabolik Sendrom ile İlişkisi - KAYA ABDURRAHMAN,KOÇYİĞİT CEMİL,ÇATLI GÖNÜL,CAN ŞULE PENBE,SÜTÇÜ RECEP,DÜNDAR BUMİN NURİ
Vitamin D Eksikliği Olan Çocuklarda İki Farklı Stoss Tedavi Protokolünün Etkinlik ve Yan Etkiler Açısından Karşılaştırılması - KOÇYİĞİT CEMİL,ÇATLI GÖNÜL,İNCE GÜLBERAT,CAN PENBE ŞULE,DÜNDAR BUMİN NURİ
Multiple Endokrin Neoplazi Tip 2A Ailesi Erken Profilaktik Tiroidektominin Önemi - ÇATLI GÖNÜL,KOÇYİĞİT CEMİL,CAN PENBE ŞULE,DÜNDAR BUMİN NURİ
COL2A1 Geninde De Novo Mutasyona Bağlı Akondrogenezis tip 2 Hipokondrogenezis Olgusu - ÇATLI GÖNÜL,ABACI AYHAN,ANIK AHMET,Shaheen RANAD,ÜNVER TUHAN HALE,ERÇAL MURAT DERYA,BÖBER ECE,Hashem MAİS O,IBRAHİM NİEMA A,Alkuraya FOWZAN SAMİ
Konjenital Diyabet ve Epifiziel Displazili Wolcott Rallison Sendromu Tanılı Bir Olgu - ÖZYILMAZ BERK,AKBAY SİNEM,KIRBIYIK ÖZGÜR,ÖZER ÖZGE,ÇATLI GÖNÜL,CAN ŞULE,DÜNDAR BUMİN NURİ
Obez Çocuk ve Adolesanlarda Subklinik Hipotiroidinin Etyolojisinde İyot Eksikliği ve Leptinin Rolü - ÖZGÜR TANRIVERDİ,ÇATLI GÖNÜL,KOÇYİĞİT CEMİL,CAN PENBE ŞULE,PİRGON MUSTAFA ÖZGÜR,DÜNDAR BUMİN NURİ
Intermediate DEND Sendromu 17 Yaşında Neonatal Diyabet Tanısı Alan Bir Olguda Sülfonilüre Tedavisinin Sonuçları - ÇATLI GÖNÜL,KOÇYİĞİT CEMİL,GENÇPINAR PINAR,DÜNDAR NİHAL OLGAÇ,CAN PENBE ŞULE,DÜNDAR BUMİN NURİ
Obez ve Sağlıklı Çocuklarda Serum Betatrofin Düzeyinin Metabolik ve Klinik Parametreler ile Olan İlişkisi - ÜNVER TUHAN HALE,ABACI AYHAN,ANIK AHMET,ÇATLI GÖNÜL,KÜME TUNCAY,ÇALAN ÖZLEM GÜRSOY,BÖBER ECE
Bilateral jinekomastinin nadir bir nedeni Sertoli hücre hiperplazisi - ÜNVER TUHAN HALE,ABACI AYHAN,ÇATLI GÖNÜL,ANIK AHMET,ÖZTÜRK TÜLAY,OLGUN HATİCE NUR,BÖBER ECE
Farklı klinik ve biyokimyasal özellikler ile prezente olan ve yeni tanımlanan homozigot mutasayona bağlı bir STAT5b eksikliği olgusu - ÇATLI GÖNÜL,Losekoot Monique,WİT JAN MARTİN,HWA VİVİAN,EDEER NESLİHAN,DÜNDAR BUMİN NURİ
Yeni Bir Tiroid Hormon Direnci Nedeni Olan THRA Mutasyonlarına Bağlı Hipotiroidinin Genotipik Ve Fenotipik Özelliklerinin Değerlendirilmesi - DEMİR KORCAN,GUHT ANJA VAN,BÜYÜKİNAM MUAMMER,ÇATLI GÖNÜL,AYHAN YAVUZ,NİJAT BAŞ VEYSEL,DÜNDAR BUMİN NURİ,ÖZKAN BEHZAT,MARCEL E MAİMA,VİSSER EDWARD,PEETERS ROBİN P,VİSSER THEO J
Pituitary Stalk Interruption Syndrome Presenting with Normogonadotropic Amenorrhea and Hypoprolactinemia - ÇATLI GÖNÜL,KOÇYİĞİT CEMİL,CAN ŞULE PENBE,DÜNDAR BUMİN NURİ
Levothyroxine Replacement in Primary Congenital Hypothyroidism The Higher the Initial Dose the Higher the Rate of Overtreatment - ÜNVER TUHAN HALE,ABACI AYHAN,ÇİÇEK GİZEM,ANIK AHMET,ÇATLI GÖNÜL,DEMİR KORCAN,BÖBER ECE
Diyabetik Ketoasidoz ile Başvuran Bir Cushing Hastalığı Olgusu - ÇATLI GÖNÜL,TANRISEVER ÖZGÜR,CAN ŞULE,DÜNDAR BUMİN NURİ
Spontan Meme Gelişimi ve Menstruasyonu Olan Swyer Sendromlu Bir Olgu - CAN ŞULE,ALPARSLAN CANER,AKBAY SİNEM,ÇATLI GÖNÜL,DÜNDAR BUMİN NURİ
Multiple Endokrin Neoplazi Tip 2A Ailesi Erken Profilaktik Tiroidektominin Önemi - ÇATLI GÖNÜL,KOÇYİĞİT CEMİL,CAN ŞULE PENBE,DÜNDAR BUMİN NURİ
COL2A1 Geninde De Novo Mutasyona Bağlı Akondrogenezis tip 2 Hipokondrogenezis Ogusu - ÇATLI GÖNÜL,ABACI AYHAN,ANIK AHMET,SHAHEEN RANAD,TUHAN HALE ÜNVER,ERÇAL MURAT DERYA,BÖBER ECE,HASHEM MAİS O,NİEMA A IBRAHİM,ALKURYA FOWZAN SAMİ
Konjenital Diyabet ve Epifiziel Displazili Wolcott Rallison Sendromu Tanılı Bir Olgu - ÖZYILMAZ BERK,AKBAY SİNEM,ÖZGÜR KIRBIYIK,ÖZER ÖZGE,ÇATLI GÖNÜL,CAN ŞULE,DÜNDAR BUMİN NURİ
Psödohipoaldesteronizm ile Karışabilen Bir Konjenital Adrenal Hiperplazi Olgusu - TUHAN HALE,ÇATLI GÖNÜL,ANIK AHMET,ABACI AYHAN,BÖBER ECE
Hiperinsülinemik Hipoglisemi Tanılı Bir Olguda Lanreotid Somatulin Autogel ve Sürekli Cilt Altı Oktreotid İnfüzyonu Tedavisi - ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,BÖBER ECE,TUHAN HALE ÜNVER
RET Protoonkogeninde C634Y Mutasyonu Olan MEN2A Tanılı Bir Olguda Profilaktik Tiroidektomi - AYDOĞAN CEYDA,ANIK AHMET,TUHAN HALE ÜNVER,ÇATLI GÖNÜL,ABACI AYHAN,BÖBER ECE
Çocukluk Çağında Diyabetin Nadir Bir Nedeni Glukokinaz Mutasyonu MODY2 - TUHAN HALE ÜNVER,ANIK AHMET,ÇATLI GÖNÜL,KIZILDAĞ SEFA,ABACI AYHAN,BÖBER ECE
Primer Amenore ve Virilizasyon Bulgulari ile Başvuran ve 17ß Hidroksisteroid Dehidrogenaz Geninde Yeni Bir Mutasyon Saptanan Olgu - TUHAN HALE,ANIK AHMET,ÇATLI GÖNÜL,CEYLANER SERDAR,DÜNDAR BUMİN NURİ,BÖBER ECE,ABACI AYHAN
Tip 1 Diyabetli Çocuklarda Basit Karbonhidratların Kesme şeker Bal ve Meyve suyu Hipoglisemik Epizot Üzerine Etkinliğinin Değerlendirilmesi 2014 Diyabetli Çocuklar Yaz Kampı Çalışması - ÇATLI GÖNÜL,ABACI AYHAN,ANIK AHMET,KOÇYİĞİT CEMİL,TUHAN HALE,ŞİMŞEK ERDEM,YILDIZ MELEK,BÖBER ECE,DÜNDAR BUMİN NURİ
Gençlikte Ortaya Çıkan Erişkin Tip Diyabet Mody Tanısı Ile Izlenen Çocuklarda Yeni Nesil Dizi Analizi Yöntemi Ile Tanımlanmış Genlerin Araştırılması - ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,KORKMAZ HÜSEYİN ANIL,DEMİR KORCAN,ALTINCIK AYÇA,SARI ERKAN,YEŞİLKAYA EDİZ,TUHAN HALE,ÖZKAN BEHZAT,KIZILDAĞ SEFA,BÖBER ECE
Santral Erken Puberte Tanisinda Serum Nörokinin B Düzeyinin Önemi ve Serum Kisspeptin ve Leptin Düzeyleri ile ilişkisi - ÇATLI GÖNÜL,ANIK AHMET,KÜME TUNCAY,GÜRSOY ÇALAN ÖZLEM,DÜNDAR BUMİN NURİ,BÖBER ECE,ABACI AYHAN
46 XY Cinsiyet Gelişim Bozukluğu Olan Bir Olguda Adrenal Yetmezlik Olmaksızın SF1 NR5A1 Geninde Yeni Bir Mutasyon - ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,TUHAN HALE,ONAY HÜSEYİN,AYKUT AYÇA,BÖBER ECE
Obez Çocuk ve Adolesanlarda Subklinik Hipotiroidinin Metabolik Parametreler Üzerine Etkisi - TANRISEVER ÖZGÜR,ÇATLI GÖNÜL,PİRGON MUSTAFA ÖZGÜR,DÜNDAR BUMİN NURİ
ABCC8 Geninde Yeni Bir Mutasyon Saptanan Hiperinsülinemik Hipoglisemili Bir Olguda Erken Spontan İyileşme - ANIK AHMET,ÜNÜVAR TOLGA,ÇATLI GÖNÜL,ABACI AYHAN,BÖBER ECE
Doğumsal Hiperinsülinizm Tanılı Iki Kardeşte Cerrahi Tedaviye Alternatif Olarak Lanreotid Somatuline Autogel Tedavisi - ÇATLI GÖNÜL,ŞULE CAN,KOÇYİĞİT CEMİL,DÜNDAR BUMİN NURİ
Hipergonadotropik Hipogonadizmin Nadir Bir Nedeni 46 XX Sry Erkek Cinsiyet Gelişim Bozukluğu - KOÇYİĞİT CEMİL,ÇATLI GÖNÜL,CAN ŞULE,DÜNDAR BUMİN NURİ
Tip 1 Diyabetli Hastalarda Ödüle Dayalı Motivasyonun Metabolik Kontrol Üzerine Etkisi - KOÇYİĞİT CEMİL,ÇATLI GÖNÜL,YILDIRIMER ÜLKÜ,CAN ŞULE,DÜNDAR BUMİN NURİ
Konjenital Primer Hipotiroidizimde Başlangıç Tedavisinde En Güvenilir Doz Nedir - TUHAN HALE,ANIK AHMET,ÇATLI GÖNÜL,ÇİÇEK GİZEM,ABACI AYHAN,BÖBER ECE
GATA6 Mutasyonuna Bağlı Gelişen Neonatal Diyabetli Bir Olguda Pankreas Agenezisi ve Proteinüri Birlikteliği - TUHAN HALE,ÇATLI GÖNÜL,ANIK AHMET,ABACI AYHAN,ÖZMEN DERYA,TÜRKMEN MEHMET ATİLLA,BÖBER ECE
Primer Amonere ile Başvuran Bir Olguda Komplete Androjen Duyarsızlık Sendromu - ANIK AHMET,TUHAN HALE ÜNVER,ÇATLI GÖNÜL,BAYRAM YUNUS SEZER,ABACI AYHAN,BÖBER ECE
Erken Meme Gelişimi ile Başvuran Kız Olguların Nihai Tanılarına Göre Klinik ve Laboratuvar Bulgularının Değerlendirilmesi - ÇATLI GÖNÜL,EDEM PINAR,ANIK AHMET,ABACI AYHAN,BÖBER ECE
Diyabetik Ketoasidoz ile Başvuran Tip 1 Diyabetes Mellituslu Çocukların Klinik ve Laboratuvar Özellikleri - ABACI AYHAN,GÖREN YILDIZ,ÇATLI GÖNÜL,ANIK AHMET,TUHAN HALE,BÖBER ECE
Tip 1 Diyabetes Mellituslu Hastalarımızın Demografik ve Klinik Özellikleri - GÖREN YILDIZ,ANIK AHMET,ÇATLI GÖNÜL,TUHAN HALE,ABACI AYHAN,BÖBER ECE
Prematür Telarş Olgularında Serum Nesfatin 1 Düzeyinin Klinik Önemi ve Serum Leptin Düzeyi ile İlişkisi - ÇATLI GÖNÜL,ANIK AHMET,KÜME TUNCAY,GÜRSOY ÇALAN ÖZLEM,DÜNDAR BUMİN NURİ,BÖBER ECE,ABACI AYHAN
Obez Çocuklarda Açlik ve Tokluk Serum Nesfatin Düzeylerinin Antropometrik ve Metabolik Parametreler ile Olan İlişkisi - ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,KÜME TUNCAY,BÖBER ECE
Tanı ve Tedavisinde Güçlük Yaşanan Bir Erken Puberte Olgusu - ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,BÖBER ECE
Neonatal Diyabetli Bir Olguda Pankreas Agenezisi ve Konjenital Kalp Hastalığı GATA6 Geninde Yeni Bir Mutasyon - ÇATLI GÖNÜL,ABACI AYHAN,SARAH E FLANAGAN,ELISA DE FRANCO,SIAN ELLARD,ANDREW HATTERSLEY,HANDAN GÜLERYÜZ,BÖBER ECE
Subklinik Hipotiroidili Çocuklarda L Tiroksin Tedavisinin Sol Ventrikül Fonksiyonlarina Etkisi - ÇATLI GÖNÜL,KIR MUSTAFA,ANIK AHMET,YILMAZ NUH,BÖBER ECE,ABACI AYHAN
Subklinik Hipotiroidili Çocuklarda L tiroksin Tedavisinin Lipoproteinler ve Klinik Bulgular Üzerine Etkisi - ÇATLI GÖNÜL,ANIK AHMET,TUHAN HALE,BÖBER ECE,ABACI AYHAN
Boy Kısalığı ile Başvuran Kleidokranial Displazili Bir Olgu - TUHAN HALE,ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,GÜLERYÜZ HANDAN,BÖBER ECE
Makrodonti ile Tanınabilen KBG Sendromlu Bir Olgunun Uzun Dönem Takip Sonuçları - DEMİR KORCAN,TEKİN MUSTAFA,ÇATLI GÖNÜL,ALTINCIK AYÇA,ABACI AYHAN,BÖBER ECE
Kallmann Sendromu Tanili Olgularda Olfaktör Bulbus Volümleri ile Objektif ve Subjektif Koku Testinin Sonuçlari - ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,GÜLERYÜZ HANDAN,GÜDÜCÜ ÇAĞDAŞ,ÖNİZ ADİLE,CAN ŞULE,DÜNDAR BUMİN NURİ,BÖBER ECE
Santral Erken Pubertenin Çok Nadir Bir Nedeni Hipotalamik Hamartom ve Juvenil Pilositik Astrositom Birlikteliği - ÇATLI GÖNÜL,ABACI AYHAN,ANIK AHMET,GÜLERYÜZ HANDAN,ÖZER ERDENER,ÖCAL İRFAN,YÜCEER NURULLAH,MUTAFOĞLU KAMER
Çocukluk Çağında Nadir Bir Tanı 46 XX Erkek Cinsel Gelişim Bozukluğu Bir Olgu Sunumu - ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,BÖBER ECE
Obez ve Sağlıklı Çocuklarda Serum Nesfatin 1 Düzeyinin Metabolik ve Klinik Parametreler ile Olan İlişkisi - ABACI AYHAN,ÇATLI GÖNÜL,ANIK AHMET,KÜME TUNCAY,BÖBER ECE
Yeni Tanımlanan INS Gen Mutasyonuna Bağlı Kalıcı Bir Neonatal Diyabet Olgusu - ÇATLI GÖNÜL,ABACI AYHAN,ANIK AHMET,BÖBER ECE
Multivitamin Kullanımına İkincil Gelişen D Vitamini İntoksikasyonu 3 Olgu Sunumu - ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,KÜME TUNCAY,DİZDARER CEYHUN,BÖBER ECE
Ailesel Akdeniz Ateşi Olan Çocuklarda D Vitamini Düzeyi - ANIK AHMET,MAKAY BALAHAN,ÇATLI GÖNÜL,ABACI AYHAN,KÜME TUNCAY,ÜNSAL ŞEVKET ERBİL,BÖBER ECE
X e Bağlı Konjenital Adrenal Hipoplazi ve Hipogonadotropik Hipogonadizm DAX1 Gen Mutasyonu Olan Bir Hasta - ÇATLI GÖNÜL,ANIK AHMET,ABACI AYHAN,BÖBER ECE
İdiyopatik Santral Puberte Prekoks Tanısı Alan Çocuklarda GnRH Anolog Tedavisinin Vücut Kitle İndeksi Üzerine Etkisi - ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,BÖBER ECE
Santral Diabetes İnsipiduslu Çocukların Klinik Laboratuvar ve Etyolojik Özellikleri - ÇATLI GÖNÜL,ABACI AYHAN,DEMİR KORCAN,ULUSOY EMEL,ALTINCIK AYÇA,BÜYÜKGEBİZ ATİLLA,BÖBER ECE
Vitamin D Bağımlı Rikets Tip 1 İki Olgu Sunumu - ULUSOY EMEL,DEMİR KORCAN,ALTINCIK AYÇA,ÇATLI GÖNÜL,ABACI AYHAN,BEKEM SOYLU ÖZLEM,BÖBER ECE
Pansitopeni ile Başvuran Bir Olguda Fanconi Aplastik Anemisi Seckel Sendromu Birlikteliği - ÇATLI GÖNÜL,AKELMA AHMET ZÜLFİKAR,ÖZ FATMA NUR,TÜKÜN FATMA AJLAN,YARALI NEŞE,TUNÇ BAHATTİN
Molecular Genetic Analysis of Maturity Onset Diabetes of the Young Mody Genes in Children by Using Targeted Next Generation Sequencing - ANIK AHMET,ÇATLI GÖNÜL,TUHAN HALE UNVER,ABACI AYHAN,KORKMAZ HÜSEYİN ANIL,ÖZKAN BEHZAT,SARI ERKAN,YEŞİLKAYA EDİZ,ALTINCIK AYÇA,KIZILDAĞ SEFA,BÖBER ECE
Rare Case of Swyer Syndrome with Spontaneous Breast Development and Menstruation - DÜNDAR BUMİN NURİ,PENBE ŞULE CAN,ALPARSLAN CANER,AKBAY SİNEM,ÇATLI GÖNÜL,KELEKÇİ SEFA
Recovery of Central Fever After GH Therapy in a Patient with GH De ciency Secondary to Posttraumatic Brain Injury - TUHAN HALE ÜNVER,ANIK AHMET,ÇATLI GÖNÜL,ABACI AYHAN,BÖBER ECE
A Novel GATA6 Mutation Leading to Congenital Heart Defects and Permanent Neonatal Diabetes A Case Report - ÇATLI GÖNÜL,ABACI AYHAN,FLANAGAN SARAH E,FRANCO ED,ELLARD SİAN,HATTERSLEY A,GÜLERYÜZ HANDAN,BÖBER ECE
Permanant Neonatal Diabetes Caused By A Novel Mutation in The INS Gene - ÇATLI GÖNÜL,ABACI AYHAN,FLANAGAN SE,ANIK AHMET,ELLARD SİAN,BÖBER ECE
Can neutrophil gelatinase associated lipocalin be an early marker of kidney injury in type 1 diabetics - DEMİR KORCAN,ABACI AYHAN,KÜME TUNCAY,ALTINCIK SELDA AYÇA,ÇATLI GÖNÜL,BÖBER ECE
Investigating food additive hypersensitivity by using atopy patch test in children with atopic eczema - DUMAN HANDAN,ÇATLI GÖNÜL,BOSTANCI İLKNUR,MISIRLIOĞLU EMİNE DİBEK,ÖZMEN SERAP,ERTAN ÜLKER
