O. Evliyaoğlu

发表

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

F. Baş, F. Darendeliler, F. Demirel, 2016, American journal of medical genetics. Part A.

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

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

Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

S. Poyrazoglu, F. Baş, F. Darendeliler, 2015, Journal of clinical research in pediatric endocrinology.

The factors associated with transient hypothyroxinemia of prematurity

O. Ercan, O. Evliyaoğlu, M. Vural, 2021, BMC Pediatrics.

Incidence of Iodine Deficiency in Patients Presenting with Goitre - Discrepancy Between Clinical and Ultrasonographic Evaluation of the Thyroid: Comparison of Patients With and Without Autoimmune Thyroiditis - Clinical, Hormonal and Urinary Iodine Excretion Studies

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

A rare intrauterine onset growth retardation syndrome caused by mosaic 19p13.3 microduplication: evaluation of GH/IGF- 1 axis and GH therapy response.

B. Tüysüz, O. Evliyaoğlu, B. Karaman, 2021, The Turkish journal of pediatrics.

Evaluation of Adenovirus-36 (Ad-36) antibody seropositivity and adipokine levels in obese children.

Pelin Yüksel, Z. Taner, H. Dinc, 2017, Microbial pathogenesis.

Incidence of iodine deficiency in Turkish patients with congenital hypothyroidism

C. Kara, O. Evliyaoğlu, S. Atavci, 2008, Pediatrics international : official journal of the Japan Pediatric Society.

The clinical and radiological assessment of cyclic intravenous pamidronate administration in children with osteogenesis imperfecta.

Z. Aycan, G. Ocal, M. Berberoğlu, 2004, The Turkish journal of pediatrics.

Evaluation of Thyroid Functions with Respect to Iodine Status and TRH Test in Chronic Autoimmune Thyroiditis

Z. Şıklar, M. Berberoğlu, O. Evliyaoğlu, 2011, Journal of clinical research in pediatric endocrinology.

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

F. Baş, F. Darendeliler, F. Demirel, 2015, Journal of clinical research in pediatric endocrinology.

Factors influencing blood pressure and microalbuminuria in children with type 1 diabetes mellitus: salt or sugar?

O. Ercan, O. Evliyaoğlu, D. Konukoğlu, 2020, Pediatric Nephrology.

Evaluation of the left ventricular systolic function and myocardial deformation by real-time three-dimensional (four-dimensional) and speckle-tracking echocardiography in children with type 1 diabetes mellitus

O. Evliyaoğlu, A. Eroğlu, H. C. Acar, 2022, Cardiology in the Young.

Relationship Between Plasma Leptin, Insulin and Tumor Necrosis Factor Alpha in Obese Children

H. Çaksen, N. Akar, Z. Aycan, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

Final height of patients with classical congenital adrenal hyperplasia.

Z. Aycan, G. Ocal, M. Berberoğlu, 2009, The Turkish journal of pediatrics.

Evaluation of insulin resistance in Turkish girls with premature pubarche using the homeostasis assessment (HOMA) model.

Z. Aycan, G. Ocal, M. Berberoğlu, 2007, The Turkish journal of pediatrics.

Experience with Long-term Glucocorticoid Treatment in Congenital Adrenal Hyperplasia: Growth Pattern Compared with Genetic Height Potential

Z. Aycan, G. Ocal, M. Berberoğlu, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

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.

Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children

E. Eren, Z. Şıklar, M. Berberoğlu, 2021, Journal of clinical research in pediatric endocrinology.

Exaggerated TSH Responses to TRH in Patients with Goiter and ‘Normal’ Basal TSH Levels

Z. Aycan, M. Berberoğlu, O. Evliyaoğlu, 2005, Hormone Research in Paediatrics.

Two Novel Variants and One Previously Reported Variant in the Insulin Receptor Gene in Two Cases with Severe Insulin Resistance Syndrome

T. Kutlu, O. Ercan, O. Evliyaoğlu, 2020, Molecular Syndromology.

Loss-of-Function Mutations in SEMA3F and gePLXNA3 Encoding Semaphorin-3F and its Receptor Plexin-A3 Respectively Cause Idiopathic Hypogonadotropic Hypogonadism

F. Darendeliler, A. Topaloğlu, L. D. Kotan, 2022 .

Management of Gonads in Adults with Androgen Insensitivity: An International Survey

L. Looijenga, K. Kluivers, S. Ahmed, 2018, Hormone Research in Paediatrics.

Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia

A. Öztürk, S. Poyrazoglu, F. Baş, 2020, Journal of clinical research in pediatric endocrinology.

What is already known on this topic ?

T. Celkan, N. Çomunoğlu, O. Ercan, 2003 .

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.

Spondyloepimetaphyseal dysplasia Pakistani type: Expansion of the phenotype

B. Tüysüz, M. Günel, K. Bilguvar, 2013, American journal of medical genetics. Part A.

Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results

Z. Aycan, A. Kansu, A. Ensari, 2010, Journal of clinical research in pediatric endocrinology.

Iodine status of Turkish pregnant women and their offspring: A national cross-sectional survey.

M. Unal, D. Aliefendioğlu, Abdulkadir Celik, 2020, Journal of Trace Elements in Medicine and Biology.

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.

Serum IGF-1 and IGFBP-3 Levels in Healthy Children Between 0 and 6 Years of Age

F. Darendeliler, N. Mungan, A. Bideci, 2011, 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.

Is Waist-Height Ratio Associated with Thyroid Antibody Levels in Children with Obesity? Ozcabi B et al. Thyroid Antibodies and Central Adiposity

O. Ercan, O. Evliyaoğlu, B. Ozcabi, 2020 .

Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

F. Darendeliler, A. Topaloğlu, L. D. Kotan, 2021, Genetics in Medicine.

Recommendations for Clinical Decision-making in Children with Type 1 Diabetes and Celiac Disease: Type 1 Diabetes and Celiac Disease Joint Working Group Report

F. Baş, F. Darendeliler, Z. Aycan, 2021, Journal of clinical research in pediatric endocrinology.

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

A. Elhan, S. Poyrazoglu, F. Baş, 2016, Journal of clinical research in pediatric endocrinology.

General health status and intelligence scores of children of mothers with acromegaly do not differ from those of healthy mothers

B. Poyraz, P. Kadıoğlu, O. Evliyaoğlu, 2016, Pituitary.

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 .

Proteinuria in a patient with Graves’ disease: Answers

O. Ercan, O. Evliyaoğlu, Aydilek Dağdeviren Çakır, 2019, Pediatric Nephrology.

Proteinuria in a patient with Graves’ disease: Questions

O. Ercan, O. Evliyaoğlu, Aydilek Dağdeviren Çakır, 2019, Pediatric Nephrology.

Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation

O. Ercan, O. Evliyaoğlu, Aydilek Dağdeviren Çakır, 2017, Journal of clinical research in pediatric endocrinology.

A Novel Mutation of AMHR2 In Two Siblings with Persistent Müllerian Duct Syndrome

N. Çomunoğlu, H. Onay, O. Ercan, 2018, Sexual Development.

Gonadectomy In Conditions Affecting Sex Development - A Registry-Based Cohort Study.

K. Lachlan, S. Poyrazoglu, F. Darendeliler, 2021, European journal of endocrinology.

Plasma testosterone response at 1st and 4th day after short- and long-term hCG stimulation test.

Z. Aycan, G. Ocal, M. Berberoğlu, 2004, The Turkish journal of pediatrics.

Monitoring Serum Testosterone Levels on Androgen Therapy with Long-Acting Testosterone Esters in the Prepubertal and Pubertal Age Groups

Z. Aycan, M. Berberoğlu, O. Evliyaoğlu, 2005 .

Disorders of gonadal development: a broad clinical, cytogenetic and histopathologic spectrum.

Z. Aycan, M. Salih, Z. Şıklar, 2007, Pediatric endocrinology reviews : PER.

Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study

F. Baş, F. Darendeliler, Z. Aycan, 2015, Endocrine.

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.

Childhood asymmetric labium majus enlargement: is a conservative approach available?

T. Soyer, O. Evliyaoğlu, M. Çakmak, 2009, Journal of pediatric and adolescent gynecology.

Risk factors of hypothyroxinemia in premature infants

O. Evliyaoğlu, M. Vural, A. Yilmaz, 2021 .

Neonatal effects of thyroid diseases in pregnancy and approach to the infant with increased TSH: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report

S. Kurtoğlu, Z. Şıklar, A. Taştekin, 2018, Turk pediatri arsivi.

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

O. Evliyaoğlu, 2016, 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.

Left Ventricular Systolic Dysfunction Related to Adrenal Insufficiency in a Case due to Autoimmune Polyendocrine Syndrome Type 1 with a Novel Variant

O. Ercan, O. Evliyaoğlu, Aydilek Dağdeviren Çakır, 2022, Molecular Syndromology.

Side Effects of Metoclopramide: Does It Deserve to Prescribe For Nausea, Vomiting?

O. Evliyaoğlu, Erennur Tufan, E. Misirlioglu, 2010 .

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

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

Transsphenoidal surgery for pituitary adenomas in pediatric patients: a multicentric retrospective study

N. Tanriover, D. Locatelli, P. Castelnuovo, 2019, Child's Nervous System.

Neurosurgical treatment of Cushing disease in pediatric patients: case series and review of literature

N. Kocer, C. Islak, O. Ercan, 2018, Child's Nervous System.

Adherence to growth hormone therapy: results of a multicenter study.

F. Baş, F. Darendeliler, Z. Aycan, 2014, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

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.

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

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

Different clinical entities of the same mutation: a case report of three sisters with Wolfram syndrome and efficacy of dipeptidyl peptidase-4 inhibitor therapy

O. Ercan, O. Evliyaoğlu, Aydilek Dağdeviren Çakır, 2021, Journal of pediatric endocrinology & metabolism : JPEM.

Wolff-Chaikoff effect in a newborn: is it an overlooked problem?

O. Evliyaoğlu, M. Albayrak, M. Çakmak, 2006, Journal of Pediatric Surgery.

Successful treatment of insulin allergy in a 1-year-old infant with neonatal diabetes by lispro and glargine insulin.

C. Kara, O. Evliyaoğlu, A. Kutlu, 2005, Diabetes care.

Elevated Urinary VEGF-A, Transferrin, and Angiotensinogen Levels in Normoalbuminuric Children and Adolescents with Type 1 Diabetes: Can They Be Early Markers of Diabetic Kidney Disease?

O. Ercan, O. Evliyaoğlu, D. Konukoğlu, 2021, Hormone Research in Paediatrics.

Children with chronic disease and COVID-19

O. Evliyaoğlu, 2020, Turk pediatri arsivi.

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.

What is already known on this topic ?

T. Celkan, N. Çomunoğlu, O. Ercan, 2020 .

Long−Term Follow−Up of a Pseudohypoparathyroidism Type 1A Patient with Missense Mutation (Pro115Ser) in Exon 5

O. Hiort, Z. Şıklar, M. Berberoğlu, 2010, Journal of clinical research in pediatric endocrinology.

Clinical, biochemical, and radiological follow-up results of children and adolescents with Hashimoto’s thyroiditis: a single-center experience

O. Evliyaoğlu, I. Erbas, I. Erbaş, 2021, Journal of Pediatric Endocrinology & Metabolism (JPEM).

Latent Autoimmune Diabetes Mellitus in Children (LADC) with Autoimmune Thyroiditis and Celiac Disease

Z. Aycan, A. Ensari, Z. Şıklar, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

A Novel Mutation of AMHR2 In Two Siblings with Persistent Müllerian Duct Syndrome

N. Çomunoğlu, H. Onay, O. Ercan, 2018, Sexual Development.

The frequency of celiac disease in children with autoimmune thyroiditis.

T. Erkan, O. Ercan, O. Evliyaoğlu, 2018, Acta gastro-enterologica Belgica.

Thyroid Nodules in Children and Adolescents: A Single Institution’s Experience

S. Kuruğoğlu, O. Ercan, O. Evliyaoğlu, 2023, Turkish archives of pediatrics.

Effects on Bone Mineral Density of Gonadotropin Releasing Hormone Analogs Used in the Treatment of Central Precocious Puberty

Z. Aycan, Ö. Ünal, G. Ocal, 2003, Journal of pediatric endocrinology & metabolism : JPEM.

Ovarian reserve in children with juvenile idiopathic arthritis using biologic disease-modifying anti-rheumatic drugs

Elvan Bayramoğlu, O. Kasapcopur, O. Evliyaoğlu, 2023, Clinical Rheumatology.

High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients.

B. Keskinkılıc, Ş. Savaş-Erdeve, S. Çetinkaya, 2024, Journal of endocrinological investigation.