Prof.
Bülent Hacıhamdioğlu
Çocuk Endokrinolojisi (Çocuk Sağlığı ve Hastalıkları)
I was born in Balıkesir in 1977. I completed primary, secondary and high school education in Alanya. I graduated from Gulhane Military Medical Academy Faculty of Medicine in 2000. In 2007, I became a Child Health and Diseases Specialist and in 2011 I became a Child Endocrinology Specialist. I became Associate Professor in 2014. I worked as the administrative and educational officer of the Child Clinic in Süleymaniye Gynecology and Pediatrics Training and Research Hospital. I started to work as a lecturer at Istinye University in 2018 and was appointed as a professor at Istinye University in July 2019. I am married and have 3 children
Araştırma Alanları
- Çocuk Sağlığı ve Hastalıkları
- Çocuk Endokrinolojisi
Çalışma Alanları
- Sağlık Bilimleri Temel Alanı
- Çocuk Endokrinolojisi (Çocuk Sağlığı ve Hastalıkları)
- Homozygous mutation in the insulin receptor gene and mild form of insulin resistance syndrome a case report, 2020
- Exome sequencing of a primary ovarian insufficiency cohort reveals common molecular etiologies for a spectrum of disease, 2019
- Perinatal form hypophosphatasia caused by a novel large duplication of ALPL gene and one year follow-up under enzyme replacement therapy a case report., 2019
- Genetic and Clinical Characteristics of Patients with Vitamin D Dependent Rickets Type 1A, 2018
- Glycogen storage disease type 0 due to a novel frameshift mutation in glycogen synthase 2 (GYS2) gene in a child presenting with fasting hypoglycemia and postprandial hyperglycemia., 2018
- Perinatal form hypophosphatasia caused by a novel large duplication of ALPL gene and one year follow-up under enzyme replacement therapy a case report, 2018
- Abdominal obesity is an independent risk factor for increased carotid intima- media thickness in obese children, 2018
- 22q11 deletion syndrome: current perspective, 2018
- Escherichia coli Meningitis after Rotavirus Gastroenteritis in an Infant, 2018
- Worldwide view of nephropathic cystinosis: results from a survey from 30 countries, 2017
- Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome, 2017
- CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism, 2017
- Association of neck circumference and pulmonary function in children, 2017
- Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature, 2016
- Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height, 2016
- Regulatory T Cells and Vitamin D Status in Children with Chronic Autoimmune Thyroiditis, 2016
- Urinary Netrin-1: A New Biomarker for the Early Diagnosis of Renal Damage in Obese Children, 2016
- The Association between Serum 25-Hydroxy Vitamin D Level and Urine Cathelicidin in Children with a Urinary Tract Infection, 2016
- Association of wider neck circumference and asthma in obese children, 2016
- Risk assessment of obstructive sleep apnea syndrome in pediatric patients with vitamin D deficiency, 2016
- Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification, 2015
- Wider neck circumference is related to severe asthma in children, 2015
- Anaphylaxis to gonadorelin acetate in a girl with central precocious puberty, 2015
- Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development, 2015
- The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels, 2015
- Preperitoneal Fat Tissue May Be Associated with Arterial Stiffness in Obese Adolescents, 2014
- The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders, 2014
- Analysis Of Allergic Diseases In Obese Children, 2013
- Pathophysiology of critical illness hyperglycemia in children, 2013
- Brachydactyly mental retardation syndrome in differential diagnosis of pseudopseudohypoparathyroidism, 2013
- Evaluation of Hypercoagulability in Obese Children With Thrombin Generation Test and Microparticle Release: Effect of Metabolic Parameters, 2012
- Synchronous Occurrence of Papillary Carcinoma in the Thyroid Gland and Thyroglossal Duct in an Adolescent with Congenital Hypothyroidism, 2012
- The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does “disorders of sexual development (DSD)” classification based on new Chicago consensus cover all sex chromosome DSD?, 2012
- Relationships Between Osteocalcin, Glucose Metabolism and Adiponectin in Obese Children: Is there Crosstalk Between Bone Tissue and Glucose Metabolism?, 2012
- Is Adrenocorticotropic Hormone Deficiency Really Rare in Patients with Idiopathic Growth Hormone Deficiency and Normal Thyroid Function Tests?, 2011
- Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents, 2011
- Two Patients with Partial DiGeorge Syndrome Presenting with Attention Disorder and Learning Difficulties - Case Report, 2011
- Efficiency of Fluid Treatments with Different Sodium Concentration in Children with Type 1 Diabetic Ketoacidosis, 2011
- Primary adrenal insufficiency in a child after busulfan and cyclophosphamide-based conditioning for hematopoietic stem cell transplantation, 2011
- The endocrine spectrum of intracranial cysts in childhood and review of the literature, 2011
- Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V281l mutation in patients with premature pubarche, 2011
- Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell, 2011
- Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant, 2011
- Clinical and radiographic findings in two brothers affected with a novel mutation in matrix metalloproteinase 2 gene, 2010
- A novel mutation of 5α-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment, 2010
- Amiodarone-induced Thyrotoxicosis in Children and Adolescents is a Possible Outcome in Patients with Low Iodine Intake, 2010
- Two Siblings with Isolated GH Deficiency Due to Loss-of-Function Mutation in the GHRHR Gene: Successful Treatment with Growth Hormone Despite Late Admission and Severe Growth Retardation-Case Report, 2010
- Genoa syndrome and central diabetes ınsipidus: A case report, 2010
- Idiopathic infantile hypercalcemia and renal involvement, 2008
- Subcutaneous Granuloma Annulare in a Child: A Case Report, 2008
- Goldenhar syndrome with duodenal atresia: a new finding, 2008
- Recurrent Streptococcus pneumoniae meningitis in a child with traumatic anterior cranial base defect, 2006
- Prader Willi Sendromlu Hastalarda Büyüme Hormonu Tedavisinin Uyku Solunum Bozuklukları ve Karbonhidrat Metabolizması Üzerine Etkilerinin Retrospektif Olarak Değerlendirilmesi, 2019
- İdiyopatik Hipogonadotropik Hipogonadizm’de CCDC141 Mutasyonları, 2017
- Antenatal hidronefroz tanısı olan infantların doğum sonrası izlem sonuçları, 2017
- 22q11 Delesyon tanısı alan 5 olgunun klinik özellikleri, 2017
- Renal Functions in newborns with moderate or severe Hypoxic Ischemic Encephalopathy Treated with Therapeutic Hypothermia, 2018
- Sözel Sunum Dalında Birincilik Ödülü, 2011
- Sözel Sunum Dalında İkincilik Ödülü., 2012
- Sözel Sunum Dalında Birincilik Ödülü, 2017
- Sözel Sunum Dalında Birincilik Ödülü, 2012
