B. Hacıhamdioğlu

发表

Risk assessment of obstructive sleep apnea syndrome in pediatric patients with vitamin D deficiency

Gamze Ozgurhan, Aysel Vehapoğlu, Oznur Vermezoglu, 2016, Medicine.

Association of neck circumference and pulmonary function in children.

E. Karabulut, M. Arslan, C. Haymana, 2017, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Wider neck circumference is related to severe asthma in children

F. Gok, M. Arslan, E. Yeşilkaya, 2015, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease.

J. Lupski, R. Gibbs, D. Muzny, 2019, The Journal of clinical endocrinology and metabolism.

The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders

M. Kır, K. Ceyhan, Z. Şıklar, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V281l mutation in patients with premature pubarche

A. Tukun, Z. Şıklar, G. Ocal, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Relationships Between Osteocalcin, Glucose Metabolism, and Adiponectin in Obese Children: Is there Crosstalk Between Bone Tissue and Glucose Metabolism?

Z. Şıklar, M. Berberoğlu, B. Hacıhamdioğlu, 2012, Journal of clinical research in pediatric endocrinology.

CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

B. I. Hutchins, S. Wray, A. Topaloğlu, 2017, The Journal of clinical endocrinology and metabolism.

Regulatory T Cells and Vitamin D Status in Children with Chronic Autoimmune Thyroiditis

Z. Şıklar, M. Berberoğlu, A. Ikinciogullari, 2016, Journal of clinical research in pediatric endocrinology.

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?

Z. Şıklar, M. Berberoğlu, S. Fitöz, 2012, European Journal of Pediatrics.

Risk assessment of obstructive sleep apnea syndrome in pediatric patients with vitamin D de ﬁ ciency A questionnaire-based study

Gamze Ozgurhan, Aysel Vehapoğlu, Oznur Vermezoglu, 2016 .

22q11 deletion syndrome: current perspective

B. Hacıhamdioğlu, D. Hacıhamdioğlu, K. Delil, 2015, The application of clinical genetics.

The endocrine spectrum of intracranial cysts in childhood and review of the literature

Z. Şıklar, G. Ocal, M. Berberoğlu, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Is Adrenocorticotropic Hormone Deficiency Really Rare in Patients with Idiopathic Growth Hormone Deficiency and Normal Thyroid Function Tests

Z. Şıklar, G. Ocal, M. Berberoğlu, 2010, Hormone Research in Paediatrics.

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

N. Akar, Z. Aycan, Kadir Sipahi, 2010, European Journal of Pediatrics.

MANNITOL INDUCED ACUTE KIDNEY INJURY DURING TREATMENT OF CEREBRAL EDEMA DUE TO DIABETIC KETOACIDOSIS IN AN ADOLESCENT

M. Kul, S. Süleymanoğlu, B. Hacıhamdioğlu, 2015 .

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

S. Ellard, S. Flanagan, Z. Şıklar, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

The Association between Serum 25-Hydroxy Vitamin D Level and Urine Cathelicidin in Children with a Urinary Tract Infection

D. Altun, M. Kul, S. Süleymanoğlu, 2016, Journal of clinical research in pediatric endocrinology.

Clinical and radiographic findings in two brothers affected with a novel mutation in matrix metalloproteinase 2 gene

S. Ozen, L. Bonafė, Y. Alanay, 2010, European Journal of Pediatrics.

Ori Gi Nal Ar Tic Le Ad Dress for Cor Res Pon Den Ce the Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-like Growth Factor-1 Levels

Z. Şıklar, M. Berberoğlu, B. Hacıhamdioğlu, 2022 .

Clinical review of 95 patients with 46,XX disorders of sex development based on the new Chicago classification.

Z. Aycan, A. Tukun, Z. Şıklar, 2015, Journal of pediatric and adolescent gynecology.

Worldwide view of nephropathic cystinosis: results from a survey from 30 countries

V. Tasic, J. Ehrich, J. Bacchetta, 2017, BMC Nephrology.

Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome

L. Metherell, L. Guasti, H. Storr, 2017, The Journal of clinical investigation.

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

Z. Şıklar, M. Berberoğlu, B. Hacıhamdioğlu, 2016, Journal of clinical research in pediatric endocrinology.

Genetic and Clinical Characteristics of Patients with Vitamin D Dependent Rickets Type 1A

B. Hacıhamdioğlu, F. Dursun, H. Kırmızıbekmez, 2018, Journal of clinical research in pediatric endocrinology.

Genetic and clinical characteristics of the patients with Vitamin D Dependent Rickets Type 1 A

B. Hacıhamdioğlu, F. Dursun, H. Kırmızıbekmez, 2018 .

Polyarteritis nodosa: a case report -

F. Gok, S. Kalman, B. Ünay, 2009 .

Recurrent Streptococcus pneumoniae meningitis in a child with traumatic anterior cranial base defect

T. Kendirli, B. Ünay, B. Hacıhamdioğlu, 2006, Pediatrics international : official journal of the Japan Pediatric Society.

Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development

H. Karabulut, Z. Aycan, Z. Şıklar, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Anaphylaxis to gonadorelin acetate in a girl with central precocious puberty

E. Yeşilkaya, O. Akın, S. T. Yavuz, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature

H. Karabulut, Z. Şıklar, M. Berberoğlu, 2016, Journal of clinical research in pediatric endocrinology.

Genoa Syndrome and Central Diabetes Insipidus: A Case Report

Z. Şıklar, M. Berberoğlu, S. Fitöz, 2010, Journal of clinical research in pediatric endocrinology.

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.

B. Hacıhamdioğlu, Bahar Çaran, E. Keskin, 2018, The Turkish journal of pediatrics.

Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome. (3),

L. Metherell, L. Guasti, H. Storr, 2017 .

SGPL 1 mutations cause primary adrenal insufficiency and steroid resistant nephrotic syndrome 1

L. Metherell, L. Guasti, H. Storr, 2016 .

Primary adrenal insufficiency in a child after busulfan and cyclophosphamide-based conditioning for hematopoietic stem cell transplantation

M. Ertem, Z. Şıklar, G. Ocal, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Preperitoneal fat tissue may be associated with arterial stiffness in obese adolescents.

Z. Şıklar, M. Berberoğlu, S. Fitöz, 2014, Ultrasound in medicine & biology.

Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents

N. Akar, Z. Şıklar, M. Berberoğlu, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Urinary Netrin-1: A New Biomarker for the Early Diagnosis of Renal Damage in Obese Children

D. Altun, S. Süleymanoğlu, B. Hacıhamdioğlu, 2016, Journal of clinical research in pediatric endocrinology.

Amiodarone-induced Thyrotoxicosis in Children and Adolescents is a Possible Outcome in Patients with Low Iodine Intake

Z. Şıklar, M. Berberoğlu, B. Hacıhamdioğlu, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Evaluation of Hypercoagulability in Obese Children With Thrombin Generation Test and Microparticle Release: Effect of Metabolic Parameters

N. Akar, Z. Şıklar, M. Berberoğlu, 2011, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Perinatal form hypophosphatasia caused by a novel large duplication of ALPL gene and one year follow-up under enzyme replacement therapy; a case report.

B. Hacıhamdioğlu, C. Pereira, E. Tepeli, 2018, Journal of Clinical Research in Pediatric Endocrinology.

Subcutaneous Granuloma Annulare in a Child: A Case Report

S. Kalman, B. Hacıhamdioğlu, A. Özcan, 2008, Clinical pediatrics.

Genetic and Clinical Characteristics of Patients with Vitamin D Dependent Rickets Type 1A

B. Hacıhamdioğlu, F. Dursun, H. Kırmızıbekmez, 2019, Journal of clinical research in pediatric endocrinology.

Pathophysiology of critical illness hyperglycemia in children

Z. Şıklar, M. Berberoğlu, T. Kendirli, 2013, Journal of pediatric endocrinology & metabolism : JPEM.

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

S. Amselem, M. Legendre, Z. Şıklar, 2010, Journal of clinical research in pediatric endocrinology.

The prevalence of metabolic syndrome and frequency of cardiovascular risk factors in obese children

A. Abacı, M. Taşçılar, B. Hacıhamdioğlu, 2010 .

Case Report: Two Patients with Partial DiGeorge Syndrome Presenting with Attention Disorder and Learning Difficulties

Z. Şıklar, M. Berberoğlu, A. Ikinciogullari, 2011, Journal of clinical research in pediatric endocrinology.

Synchronous Occurrence of Papillary Carcinoma in the Thyroid Gland and Thyroglossal Duct in an Adolescent with Congenital Hypothyroidism

M. Kır, Z. Şıklar, M. Berberoğlu, 2012, Journal of clinical research in pediatric endocrinology.

Brachydactyly mental retardation syndrome in differential diagnosis of pseudopseudohypoparathyroidism

M. Arslan, E. Yeşilkaya, B. Hacıhamdioğlu, 2013, Journal of pediatric endocrinology & metabolism : JPEM.

Homozygous Mutation in the Insulin Receptor Gene Associated with Mild Type A Insulin Resistance Syndrome: A Case Report

B. Hacıhamdioğlu, K. Delil, E. Baş, 2020, Journal of clinical research in pediatric endocrinology.

Abdominal obesity is an independent risk factor for increased carotid intima- media thickness in obese children.

M. Kocaoglu, B. Hacıhamdioğlu, Y. Yozgat, 2011, The Turkish journal of pediatrics.

Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant

S. Ellard, Z. Şıklar, M. Berberoğlu, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

The Application of Clinical Genetics Dovepress 22q11 Deletion Syndrome: Current Perspective

B. Hacıhamdioğlu, D. Hacıhamdioğlu, K. Delil, 2022 .

Association of wider neck circumference and asthma in obese children.

M. Arslan, E. Yeşilkaya, O. Akın, 2016, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Goldenhar syndrome with duodenal atresia: a new finding.

D. Gül, B. Hacıhamdioğlu, S. Vurucu, 2008, Clinical dysmorphology.