Publications & Works

Refereed Congress / Symposium Publications in Proceedings

Clinical Characteristics of Turkish Children and Adolescents with Type 2 Diabetes

10th International Meeting of Pediatric Endocrinology, Washington, Kiribati, 14 - 17 September 2020, vol.88, pp.1-628

Rare Causes of Osteogenesis Imperfecta are Commonin Consanguineous Pedigrees

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019

A rare cause of hypophosphatemia: Raine Syndrome

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019, vol.91

A Case Of Syndromic Hypopituitarism

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, 19 - 21 September 2019, vol.91, pp.1-682 identifier identifier identifier

Genotype and Phenotype Characterization ofTurkish Patients with Vitamin D Dependent RicketsType IA

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019, vol.91

Nationwide Hypophosphatemic Rickets Study

57.th Annual Meeting of the European Society for Paediatric Endocrinology(ESPE), ATİNA, Greece, 27 - 29 September 2018

Relation of serum IGF-1 and IGFBP3 levels with acute exacerbation in cystic fibrosis

28th International Congress of the European-Respiratory-Society (ERS), Paris, France, 15 - 19 September 2018, vol.52 identifier

Persistent Mullerian duct syndrome: Rare But Important Aetiology of an Inguinal Hernia and Cryptorchidism in Boys

HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, 27 - 29 September 2018, vol.90, pp.568

An 18 Month Old Boy with Hypoglycemic Convulsion and Obesity Due to POMC Deficiency

HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, 27 - 29 September 2018, vol.90, pp.514

Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene

HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, 27 - 29 September 2018, vol.90, pp.597

Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi

22. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Antalya, Turkey, 18 - 22 April 2018

Neuroendocrin Regulation of Energy Homeostasis and Hypothalamic Obesity in Children

3rd International Congress of the Turkish-Neuroendocrinology-Society, Malatya, Turkey, 29 June - 01 July 2018, vol.107, pp.2 identifier

17OH-pregnenolone seems a major drive of androgen excess in patient with 11 beta hydroxylase deficiency

10th Joint Meeting of Paediatric Endocrinology, Washington, Kiribati, 14 - 17 September 2017, vol.88, pp.54

17OH-PREGNENOLONE SEEMS A MAJOR DRIVE OF ANDROGEN EXCESS IN PATIENTS WITH 11ß-HYDROXYLASE DEFICIENCY

. 10th Individual Abstracts for International Meeting of Pediatric Endocrinology, 14 - 17 September 2017

Nonsense Mutation in SPARC Gene Causing Autosomal Recessive Ostegenesis Imperfecta

55th Annual Metting of the ESPE Paris, 10 - 12 September 2016, vol.86, pp.167

Frequency of Recessive Osteogenesis Imperfecta in a Turkish Cohort and Genetic Causes

55th Annual Meeting of the ESPE, Paris, 10 - 12 September 2016, vol.86, pp.175-176

Reconsideration of Mid Parental Height Calculation

55th Annual Meeting of the ESPE, 10 - 12 September 2016, vol.86, pp.451

Periferal Puberte Prekokslu 129 Çocukta Etiyolojik Dağılım Ve Klinik Özellikler

19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Turkey, 22 - 24 October 2015

Nonklasik Konjenital Adrenal Hiperplazi Hastalarının Genotip Ve Fenotip Özellikleri

19. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Turkey, 22 - 24 October 2015

Merkezi Yenidogan Tarama Programi ile Tani Almis Konjenital Hipotiroidili Vakalarimizin İzlemi

19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Turkey, 22 - 24 October 2015

Otozomal Resesif Osteogenezis İmperfekta Populasyonumuzdaki Sıklığı Ve Genetik Nedenleri

19. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Turkey, 22 - 24 October 2015

Friedreich s Ataxia Presenting with Diabetes Mellitusin an Adolescent

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 1 - 03 October 2015

Central or Primary Hypothyroidism How toDifferentiate in Patients with Low T4 but MildlyElevated TSH Levels

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 1 - 03 October 2015

Factors Effecting Response to Growth HormoneTreatment in Children with Turner Syndrome

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 1 - 03 October 2015

ANTLEY BİXLER SENDROMLU BİR OLGUMUZ

Cocuk Endokrinoloji Dernegi 7.Olgu Sunumlari Toplantisi, İzmir, Turkey, 18 - 20 May 2015

Identification of novel dentin matrix protein-1 (DMP1) mutations in two unrelated kindreds with autosomal recessive hypophosphatemia

29th Annual Meeting of the American-Society-for-Bone-and-Mineral-Research, Hawaii, United States Of America, 16 - 19 September 2007, vol.22 identifier

Detection of Y chromosomal material in patients with a 45,X karyotype by PCR method

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, vol.15, pp.125-126 identifier

Sağlıklı bebeklerde serum alkalen fosfataz değerleri

11. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Konya, Turkey, 14 - 17 September 2006, pp.118

Maternal and cord blood zinc (Zn), IGF-1, IGFBP3 levels in IUGR neonates

7th World Congress of Perinatal Medicine, Zagreb, Croatia, 21 - 24 September 2005, pp.225-228 identifier

Renal agenezi olan bir Beckwith-Wiedemann Olgusu

49. Milli Pediatri Kongresi, İstanbul, Turkey, 14 - 17 September 2005, pp.353