Gönül Öcal,

发表

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.

Disorders of Sexual Development: An Overview of 18 Years Experience in the Pediatric Endocrinology Department of Ankara University

T. Soygür, N. Akar, Z. Şıklar, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study

F. Baş, Z. Aycan, S. Çetinkaya, 2013, 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.

Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphism (-675 4G/SG) Associated with Obesity and Vascular Risk in Children

N. Akar, Z. Şıklar, M. Berberoğlu, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Factors Contributing to Sex Assignment and Reassignment Decisions in Turkish Children with 46,XY Disorders of Sex Development

M. Berberoğlu, M. Çakmak, Ö. Özcan, 2007, Journal of pediatric endocrinology & metabolism : JPEM.

The Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome: A Multicenter Study

F. Baş, F. Darendeliler, T. Isbir, 2012, Hormone Research in Paediatrics.

Osteopetrosis, Renal Tubular Acidosis Without Urinary Concentration Abnormality, Cerebral Calcification and Severe Mental Retardation in Three Turkish Brothers

Z. Aycan, E. Cetinkaya, P. Adiyaman, 2001, 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.

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.

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.

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

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

Risk Factors for Non-Alcoholic Fatty Liver Disease in Obese Children

Z. Şıklar, M. Berberoğlu, G. Öcal,, 2009, Hormone Research in Paediatrics.

A new deletion of the 5α‐reductase type 2 gene in a Turkish family with 5α‐reductase deficiency

S. Lumbroso, J. Lobaccaro, C. Sultan, 1995 .

Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome

M. Tekin, N. Akar, Z. Aycan, 2008, Pediatrics international : official journal of the Japan Pediatric Society.

Depression, Levels of Anxiety and Self-Concept in Girls with Turner's Syndrome

G. Öcal,, A. Ergür, B. Kılıç, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

Alterations in Serum Growth Hormone (GH)/GH Dependent Ternary Complex Components (IGF-I, IGFBP-3, ALS, IGF-I/IGFBP-3 Molar Ratio) and the Influence of these Alterations on Growth Pattern in Female Rhythmic Gymnasts

N. Akar, P. Adiyaman, G. Öcal,, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

Late effects of chemoradiotherapy in pediatric Hodgkin's disease.

A. Çavdar, G. Yavuz, S. Gözdaşoğlu, 1995, Journal of chemotherapy.

Vitamin D Deficiency in Turkish Mothers and Their Neonates and in Women of Reproductive Age

Z. Şıklar, M. Berberoğlu, B. Atasay, 2009, Journal of clinical research in pediatric endocrinology.

EVALUATION OF GLUCOSE HOMEOSTASIS IN TRANSFUSION-DEPENDENT THALASSEMIC PATIENTS

M. Ertem, Z. Şıklar, M. Berberoğlu, 2008, Pediatric hematology and oncology.

Polyglandular autoimmune syndrome accompanied by Munchausen syndrome

S. Akçurin, A. Kansu, M. Berberoğlu, 2000, Pediatrics international : official journal of the Japan Pediatric Society.

Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey

A. Elhan, Z. Aycan, F. Sadeghi, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

Functional relationships between three novel homozygous mutations in the ACTH receptor gene and familial glucocorticoid deficiency

C. Tsigos, A. Penhoat, D. Naville, 2002, Journal of Molecular Medicine.

Syndrome of Congenital Adrenocortical Unresponsiveness to ACTH. Report of Six Patients

N. Akar, Z. Aycan, A. Penhoat, 2001, Journal of pediatric endocrinology & metabolism : JPEM.