Publications by authors named "Merih Berberoglu"

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Close relationship, similar phenotype of GATA4 and NR5A1 mutations: gonadal dysgenesis and puberty development.
Sema Nilay Abseyi, Zeynep Şıklar, Elif Özsu, Sirmen Kızılcan Çetin, Şafak Demirtaş

J Endocrinol Invest· December 2025

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Understanding rickets in osteopetrosis via a case: mechanisms and treatment implications.
Meliha Esra Bilici, Zeynep Şıklar, Elif Özsu, Serdar Ceylaner, Zehra Aycan

J Pediatr Endocrinol Metab· November 2025

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Assessing cortisol levels in non-classical congenital adrenal hyperplasia: focus on the V281L variant.
Meliha Esra Bilici, Zeynep Iklar, Elif Özsu, Zehra Aycan, Rukiye Uyanık

Ther Adv Endocrinol Metab· November 2025

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Pubertal characteristics, final height, and associated factors in patients with nonclassical congenital adrenal hyperplasia: a single center experience.
Sema Nilay Abseyi, Seda Erişen Karaca, Zeynep Şıklar, Gizem Şenyazar, Sirmen Kızılcan Çetin

J Pediatr Endocrinol Metab· November 2025

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The Impact of an Adolescent-Friendly Approach on Metabolic Control in Adolescents with Type 1 Diabetes in Türkiye.
Ayşegül Şahiner, Ayşe Gül Güven, Zeynep Şıklar, Merih Berberoğlu, Elif Özsu

J Clin Med· October 2025

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Molecular Characterization and Phenotype-Genotype Correlation of Childhood Thyroid Nodules and Cancers: A Study of 62 Patients.
Zehra Aycan, Sirmen Kızılcan Çetin, Hale Kıvrak, Burcu Çevik, Koray Ceyhan

Horm Res Paediatr· October 2025

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Clinical insights of the C.856 C>T variant: a case report and literature review on neonatal isolated ACTH deficiency.
Sirmen Kizilcan Cetin, Zeynep Siklar, Zehra Aycan, Elif Ozsu, Aysegul Ceran, Merih Berberoglu

J Pediatr Endocrinol Metab· September 2025

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Familial Clinical Heterogeneity of Medullary Thyroid Cancer with Germline S891A Protooncogene Mutation: 7-year Follow-up with Successful Sorafenib Treatment.
Sirmen Kızılcan Çetin, Zeynep Şıklar, Elif Özsu, Ayşegül Ceran, Koray Ceyhan

J Clin Res Pediatr Endocrinol· August 2025

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A Challenging Case of Ectopic Adrenocorticotropin Hormone Syndrome with Bronchial Carcinoid and Literature Review.
Sema Nilay Abseyi, Zeynep Şıklar, Elif Özsu, Ayten Kayı Cangır, Emel Cabi Ünal

J Clin Res Pediatr Endocrinol· August 2025

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Comparison of the clinical characteristics of children with Silver-Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study.
İlker Tolga Özgen, Tuğçe Kandemir, Melek Yıldız, Şükran Poyrazoğlu, Zeynep Şıklar

J Pediatr Endocrinol Metab· August 2025

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Effect of Obesity and Metabolic Syndrome on Pulmonary Functions and Exhaled Nitric Oxide in Adolescents.
Nermin Hetemli, Fazilcan Zirek, Rukiye Uyanık, Merih Berberoglu, Zeynep Siklar

Klin Padiatr· July 2025

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Long-Term Follow-up of a Case with TBX19 Mutation, a Rare Cause of Isolated ACTH Deficiency and Literature Review.
Aysegul Ceran, Zehra Aycan, Zeynep Siklar, Elif Ozsu, Sirmen Kizilcan Cetin, Merih Berberoglu

J Clin Res Pediatr Endocrinol· July 2025

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Insights Into Pediatric Non-congenital Adrenal Hyperplasia: A Review Based on 5 Different Rare Cases with Primary Adrenal Insufficiency.
Sirmen Kizilcan Cetin, Zeynep Siklar, Elif Ozsu, Zehra Aycan, Merih Berberoglu

Turk Arch Pediatr· May 2025

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Clinical characteristics, risk stratifications, and long-term follow-up of childhood differentiated thyroid cancer: a single-center experience.
Sirmen Kızılcan Çetin, Zehra Aycan, Zeynep Şıklar, Elif Özsu, Suat Fitöz

Ann Pediatr Endocrinol Metab· April 2025

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Evaluation of Growth Characteristics and Final Height of Cases Diagnosed with Noonan Syndrome on Growth Hormone Treatment.
Zeynep Şıklar, Merih Berberoğlu, Sirmen Kızılcan Çetin, Melek Yıldız, Serap Turan

J Clin Res Pediatr Endocrinol· March 2025

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Adrenal hypoandrogenism in adolescents with premature ovarian insufficiency.
Meliha Esra Bilici, Zeynep Şıklar, Semra Çetinkaya, Elif Özsu, Zehra Aycan

J Pediatr Endocrinol Metab· March 2025

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Assessment of the Admission and Follow-up Characteristics of Children Diagnosed with Secondary Osteoporosis.
Emine Kübra Şen, Merih Berberoğlu, Gizem Şenyazar, Sirmen Kızılcan Çetin, Ayşegül Ceran

J Clin Res Pediatr Endocrinol· December 2024

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Unraveling the Genetic Puzzle: Could Be a Candidate Gene for RASopathies? Case Presentation.
Sirmen Kizilcan Cetin, Zeynep Siklar, Zehra Aycan, Elif Ozsu, Serdar Ceylaner

J Clin Res Pediatr Endocrinol· October 2024

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Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study.
Zeynep Şıklar, Elif Özsu, Sirmen Kızılcan Çetin, Samim Özen, Filiz Çizmecioğlu-Jones

J Clin Res Pediatr Endocrinol· September 2024

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Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship.
Elif Özsu, Semra Çetinkaya, Semih Bolu, Nihal Hatipoğlu, Şenay Savaş Erdeve

J Clin Res Pediatr Endocrinol· September 2024

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17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.
Zeynep Siklar, Emine Camtosun, Semih Bolu, Melek Yildiz, Aysehan Akinci, Merih Berberoglu

Endocrine· September 2024

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Evaluation of quality of life in children with precocious puberty.
İlkay N Yılmazer, Sema Nilay Abseyi, Gizem Şenyazar, Merih Berberoğlu, Zeynep Şıklar

Clin Endocrinol (Oxf)· April 2024

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Exploring Multiple Endocrinological Issues and Dysautonomia in a Rare Case: Hypoparathyroidism in MIRAGE Syndrome.
Sirmen Kızılcan Çetin, Elif Özsu, Zeynep Şıklar, Hasan Fatih Çakmaklı, Gizem Şenyazar

J Clin Res Pediatr Endocrinol· March 2024

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Clinic Heterogeneity and Management of Pediatric Patients With Germline RET Proto-oncogene Mutation: Single-center Experience.
Zeynep Şıklar, Tuğba Kontbay, Handan Dincaslan, Emel Ünal, Merih Berberoglu

J Pediatr Hematol Oncol· October 2023

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Impact of the COVID-19 pandemic on diabetic ketoacidosis management in the pediatric intensive care unit.
Fevzi Kahveci, Buse Önen Ocak, Emrah Gün, Anar Gurbanov, Hacer Uçmak

Acute Crit Care· August 2023

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