B. Özcabı

发表

Evaluation of Thyroid Nodules in Children and Adolescents: Multicenter Study in Turkey

B. Kırel, M. Keskin, N. Akyürek, 2021, Güncel Pediatri.

Vitamin D Deficiency and Hashimoto’s Thyroiditis in Children and Adolescents: a Critical Vitamin D Level for This Association?

M. Acar, O. Ercan, O. Evliyaoğlu, 2015, Journal of clinical research in pediatric endocrinology.

Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey

S. Poyrazoglu, F. Baş, F. Darendeliler, 2018, Journal of clinical research in pediatric endocrinology.

The association between vitamin B12, folate, homocysteine levels, and carotid intima-media thickness in children with obesity: a cross-sectional study

Elif Söbü, B. Özcabı, G. D. Kaya Özçora, 2022, Journal of pediatric endocrinology & metabolism : JPEM.

Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome

B. Tüysüz, S. Poyrazoglu, F. Baş, 2021, Journal of clinical research in pediatric endocrinology.

A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek Population

O. Ercan, O. Evliyaoğlu, B. Özcabı, 2016, Journal of clinical research in pediatric endocrinology.

Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation

S. Ellard, E. De Franco, O. Ercan, 2017, Journal of clinical research in pediatric endocrinology.

Is Waist-height Ratio Associated with Thyroid Antibody Levels in Children with Obesity?

O. Ercan, O. Evliyaoğlu, B. Özcabı, 2020, Journal of clinical research in pediatric endocrinology.

Lipid accumulation product is a predictor of nonalcoholic fatty liver disease in childhood obesity

Ayla Güven, B. Özcabı, M. Akyol, 2018, Korean journal of pediatrics.

homozygous PTF 1 A enhancer mutations and one with DEND syndrome due to KCNJ 11 mutation Short Running Title : Neonatal diabetes due to PTF 1 A enhancer and KCNJ 11 Manuscript Type : Case Report

S. Ellard, E. D. Franco, O. Ercan, 2017 .

Primary Adrenal Insufficiency Caused by a Novel Mutation in DAX1 Gene

O. Ercan, O. Evliyaoğlu, B. Özcabı, 2013, Journal of clinical research in pediatric endocrinology.

Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2

O. Ercan, Aydilek Dağdeviren Çakır, B. Özcabı, 2020, Journal of clinical research in pediatric endocrinology.

Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene

B. Tüysüz, O. Ercan, O. Evliyaoğlu, 2015, Journal of clinical research in pediatric endocrinology.

Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience

A. Çayır, Z. Aycan, Elvan Bayramoğlu, 2018, Journal of clinical research in pediatric endocrinology.

Management of thyrotoxicosis in children and adolescence: a Turkish multi-center experience

A. Çayır, Z. Aycan, Elvan Bayramoğlu, 2018, Journal of Clinical Research in Pediatric Endocrinology.

A CASE OF SOTOS SYNDROME CAUSED BY A NOVEL VARIANT IN THE NSD1 GENE: A PROPOSED RATIONALE TO TREAT ACCOMPANYING PRECOCIOUS PUBERTY.

G. Yeşil, B. Özcabı, H. Kırmızıbekmez, 2020, Acta endocrinologica.

Unresolved tachycardia in a 14 year old with acute lymphoblastic leukemia patient

O. Evliyaoğlu, B. Özcabı, T. Celkan, 2013 .

The Relationship Between Obesity, Depressive Symptoms and Sleep Duration in Children and Adolescents

Ayla Güven, B. Özcabı, Fahri Çelebi, 2021 .

Effective sociodemographic and clinical factors in weight loss in childhood obesity.

A. Bozaykut, B. Özcabı, G. Mutlu, 2018, Turk pediatri arsivi.

Clinical and genetic characteristics of patients with corticosterone methyloxidase deficiency type 2: Novel mutations in CYP11B2 SHORT TITLE: Novel mutations in CYP11B2 gene

O. Ercan, B. Özcabı, S. Ceylaner, 2020 .

Management of Rapidly Progressive Precocious Puberty in a Patient with Mosaic Turner Syndrome.

B. Özcabı, T. Guran, F. Dursun, 2021, Acta endocrinologica.

Hypogonadism: Is It Always Hypogonadotropic in an Adolescent With a Cleft Palate? A Surprising Case of Klinefelter Syndrome

Ayla Güven, B. Özcabı, Meriç Vatansever, 2020, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Apparent diffusion coefficient measurement of ovarian stroma: A potential tool for the diagnosis of polycystic ovary syndrome.

D. Alis, I. Adaletli, F. Ustabaşıoğlu, 2017, Diagnostic and interventional imaging.

Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study

S. Poyrazoglu, F. Darendeliler, Z. Aycan, 2022 .