Prof. Dr.
Bülent Hacıhamdioğlu
Çocuk Endokrinolojisi (Çocuk Sağlığı ve Hastalıkları)
2000 yılında GATA Tıp fakültesinden mezun olan Hacıhamdioğlu, 2007 yılında GATA Tıp fakültesinde Çocuk sağlığı ve hastalıkları uzmanlığını tamamlamıştır. 2011 yılında Ankara üniversitesi çocuk endokrinolojisi yan dal uzmanlığını almıştır. Doçentliğini ise 2014 yılında ise çocuk endokrinolojisi dalında almaya hak kazanmıştır.
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
