22q11 deletion syndrome: current perspective

Por Hacıhamdioğlu, Bülent, Hacıhamdioğlu, Duygu, Delil, Kenan
Publicado no Appl Clin Genet (2015)

P05 - Wider neck circumference may be related with symptom persistence in children with allergic rhinitis

Por Yavuz, Süleyman Tolga, Hacıhamdioğlu, Bülent, Arslan, Mutluay
Publicado em 2014

P46 - Neck circumference may be related with severe asthma in children

Por Yavuz, Süleyman Tolga, Hacıhamdioğlu, Bülent, Arslan, Mutluay
Publicado em 2014

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

Por Şıklar, Zeynep, Karataş, Deniz, Doğu, Figen, Hacıhamdioğlu, Bülent, İkincioğulları, Aydan, Berberoğlu, Merih
Publicado no J Clin Res Pediatr Endocrinol (2016)

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

Por Abseyi, Nilay, Şıklar, Zeynep, Berberoğlu, Merih, Hacıhamdioğlu, Bülent, Savaş Erdeve, Şenay, Öçal, Gönül
Publicado em 2012

Escherichia coli Meningitis after Rotavirus Gastroenteritis in an Infant

Por Ozgurhan, Gamze, Vermezoglu, Oznur, Ocal Topcu, Didem, Karbuz, Adem, Vehapoglu, Aysel, Hacihamdioglu, Bulent
Publicado no Case Rep Infect Dis (2016)

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

Por Övünç Hacıhamdioğlu, Duygu, Hacıhamdioğlu, Bülent, Altun, Demet, Müftüoğlu, Tuba, Karademir, Ferhan, Süleymanoğlu, Selami
Publicado no J Clin Res Pediatr Endocrinol (2016)

Risk assessment of obstructive sleep apnea syndrome in pediatric patients with vitamin D deficiency: A questionnaire-based study

Por Ozgurhan, Gamze, Vehapoglu, Aysel, Vermezoglu, Oznur, Temiz, Rabia Nur, Guney, Asuman, Hacihamdioglu, Bulent
Publicado no Medicine (Baltimore) (2016)

The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels

Por Şıklar, Zeynep, Kocaay, Pınar, Çamtosun, Emine, İsakoca, Mehmet, Hacıhamdioğlu, Bülent, Savaş Erdeve, Şenay, Berberoğlu, Merih
Publicado no J Clin Res Pediatr Endocrinol (2015)

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

Por Savaş-Erdeve, Şenay, Şıklar, Zeynep, Hacıhamdioğlu, Bülent, Kocaay, Pınar, Çamtosun, Emine, Öcal, Gönül, Berberoğlu, Merih
Publicado no J Clin Res Pediatr Endocrinol (2016)

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 Retar...

Por Şıklar, Zeynep, Berberoğlu, Merih, Legendre, Maria, Amselem, Serge, Evliyaoğlu, Olcay, Hacıhamdioğlu, Bülent, Erdeve, Şenay Savaş, Öçal, Gönül
Publicado em 2010

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

Por Hacıhamdioğlu, Bülent, Berberoğlu, Merih, Şıklar, Zeynep, Doğu, Figen, Bilir, Pelin, Erdeve, Şenay Savaş, İkincioğulları, Aydan, Öçal, Gönül
Publicado em 2011

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

Por Şıklar, Zeynep, Berberoğlu, Merih, Yağmurlu, Aydın, Hacıhamdioğlu, Bülent, Savaş Erdeve, Şenay, Fitöz, Suat, Kır, Metin, Öçal, Gönül
Publicado em 2012

Genoa Syndrome and Central Diabetes Insipidus: A Case Report

Por Hacıhamdioğlu, Bülent, Şıklar, Zeynep, Erdeve, Şenay Savaş, Berberoğlu, Merih, Deda, Gülhiz, Tıraş, Serap Teber, Fitöz, Suat, Öçal, Gönül
Publicado em 2010

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

Por Delil, Kenan, Karabulut, Halil Gürhan, Hacıhamdioğlu, Bülent, Şıklar, Zeynep, Berberoğlu, Merih, Öçal, Gönül, Tükün, Ajlan, Ruhi, Hatice Ilgın
Publicado no J Clin Res Pediatr Endocrinol (2016)

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

Por Övünç Hacıhamdioğlu, Duygu, Altun, Demet, Hacıhamdioğlu, Bülent, Çekmez, Ferhat, Aydemir, Gökhan, Kul, Mustafa, Müftüoğlu, Tuba, Süleymanoğlu, Selami, Karademir, Ferhan
Publicado no J Clin Res Pediatr Endocrinol (2016)

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

Por Prasad, Rathi, Hadjidemetriou, Irene, Maharaj, Avinaash, Meimaridou, Eirini, Buonocore, Federica, Saleem, Moin, Hurcombe, Jenny, Bierzynska, Agnieszka, Barbagelata, Eliana, Bergadá, Ignacio, Cassinelli, Hamilton, Das, Urmi, Krone, Ruth, Hacihamdioglu, Bulent, Sari, Erkan, Yesilkaya, Ediz, Storr, Helen L., Clemente, Maria, Fernandez-Cancio, Monica, Camats, Nuria, Ram, Nanik, Achermann, John C., Van Veldhoven, Paul P., Guasti, Leonardo, Braslavsky, Debora, Guran, Tulay, Metherell, Louise A.
Publicado no J Clin Invest (2017)