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

por Evliyaoğlu, Olcay
Publicado 2016

Children with chronic disease and COVID-19

por Evliyaoğlu, Olcay
Publicado 2020

Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene

por Şahin, Sezgin, Hiort, Olaf, Thiele, Susanne, Evliyaoğlu, Olcay, Tüysüz, Beyhan
Publicado 2017

COVID-19 in children

por Evliyaoğlu, Olcay, Kılınç, Ayşe Ayzıt, Önal, Pınar, Aygün, Fatih, Çokuğraş, Haluk
Publicado 2020

Primary Adrenal Insufficiency Caused by a Novel Mutation in DAX1 Gene

por Evliyaoğlu, Olcay, Dokurel, İpek, Bucak, Feride, Özcabı, Bahar, Ercan, Oya, Ceylaner, Serdar
Publicado 2013

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

por Erdeve, Şenay Savaş, Berberoğlu, Merih, Şıklar, Zeynep, Evliyaoğlu, Olcay, Hiort, Olaf, Öcal, Gönül
Publicado 2010

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

por Ergür, Ayça Törel, Evliyaoğlu, Olcay, Şıklar, Zeynep, Bilir, Pelin, Öcal, Gönül, Berberoğlu, Merih
Publicado 2011

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

por Dağdeviren Çakır, Aydilek, Turan, Hande, Aykut, Ayça, Durmaz, Asude, Ercan, Oya, Evliyaoğlu, Olcay
Publicado 2018

An Unusual Presentation of Carney Complex

por Dağdeviren Çakır, Aydilek, Turan, Hande, Celkan, Tiraje, Çomunoğlu, Nil, Ercan, Oya, Evliyaoğlu, Olcay
Publicado 2020

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

por Evliyaoğlu, Olcay, Acar, Manolya, Özcabı, Bahar, Erginöz, Ethem, Bucak, Feride, Ercan, Oya, Kucur, Mine
Publicado 2015

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

por Dağdeviren Çakır, Aydilek, Turan, Hande, Kuruğoğlu, Sebuh, Özcan, Rahsan, Öztürk, Tülin, Ercan, Oya, Evliyaoğlu, Olcay
Publicado 2023

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

por Özcabi, Bahar, Tarçın, Gürkan, Şengenç, Esma, Tahmiscioğlu Bucak, Feride, Ercan, Oya, Bolayırlı, İbrahim Murat, Evliyaoğlu, Olcay
Publicado 2021

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 2010

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

por Özcabı, Bahar, Tahmiscioğlu Bucak, Feride, Ceylaner, Serdar, Özcan, Rahşan, Büyükünal, Cenk, Ercan, Oya, Tüysüz, Beyhan, Evliyaoğlu, Olcay
Publicado 2015

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

por Özcabı, Bahar, Tahmiscioğlu Bucak, Feride, Jaferova, Sevinç, Oruç, Çiğdem, Adrovic, Amra, Ceylaner, Serdar, Ercan, Oya, Evliyaoğlu, Olcay
Publicado 2016

Clinical indicators that influence a clinician’s decision to start L-thyroxine treatment in prematurity with transient hypothyroxinemia

por Yilmaz, Aslan, Ozer, Yavuz, Kaya, Nesrin, Cakir, Aydilek Dagdeviren, Culpan, Hazal Cansu, Perk, Yildiz, Vural, Mehmet, Evliyaoglu, Olcay
Publicado 2023

Correction: Clinical indicators that influence a clinician’s decision to start L-thyroxine treatment in prematurity with transient hypothyroxinemia

por Yilmaz, Aslan, Ozer, Yavuz, Kaya, Nesrin, Cakir, Aydilek Dagdeviren, Culpan, Hazal Cansu, Perk, Yildiz, Vural, Mehmet, Evliyaoglu, Olcay
Publicado 2023

Differentiated Thyroid Cancer in Children and Adolescents: Clinicopathological Characteristics of 32 Patients Followed up in our Pediatric Endocrinology Unit

por Cakir, Aydilek Dagdeviren, Bucak, Feride Tahmiscioglu, Tarcin, Gurkan, Turan, Hande, Ozcan, Rahsan, Evliyaoglu, Olcay, Kabasakal, Levent, Ercan, Oya
Publicado 2023

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

por Evliyaoğlu, Olcay, Ercan, Oya, Ataloğlu, Emel, Zübarioğlu, Ümit, Özcabı, Bahar, Dağdeviren, Aydilek, Erdoğan, Hande, De Franco, Elisa, Ellard, Sian
Publicado 2018

The factors associated with transient hypothyroxinemia of prematurity

por Yilmaz, Aslan, Ozer, Yavuz, Kaya, Nesrin, Turan, Hande, Acar, Hazal Cansu, Ercan, Oya, Perk, Yildiz, Evliyaoglu, Olcay, Vural, Mehmet
Publicado 2021