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
- 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
- Analysis Of Allergic Diseases In Obese Children, 2013
- 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
- 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
