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ArticlesPeer ReviewedFull Text
A rare endocrinological complication of chronic kidney disease
Author / Creator:Çamlar, Seçil Arslansoyu ; Filibeli, Berna ; Soyaltın, Eren ; Manyas, Hayrullah ; Çatlı, Gönül ; Alaygut, Demet ; Mutlubaş, Fatma ; Dündar, Bumin Nuri ; Demir, Belde Kasap
Publisher:Ankara: Akdema Informatics and Publishing
Journal title:Turkish journal of pediatrics, 2022-03, Vol.64 (2), p.375-380
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ArticlesPeer ReviewedFull Text
Virilizing Adrenocortical Carcinoma Oncocytic Variant in a Child with Heterosexual Precocious Puberty and a Literature Review
Author / Creator:Bulut, Seyran ; Catli, Gonul ; Filibeli, Berna Eroglu ; Manyas, Hayrullah ; Ayranci, Ilkay ; Meral, Rabia ; Kizmazoglu, Deniz ; Dundar, Bumin Nuri
Publisher:Galenos Yayinevi Tic. Ltd
Journal title:The journal of pediatric research, 2022-09, Vol.9 (3), p.307-313
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ArticlesPeer ReviewedFull Text
Can ocular changes be detected early in children and adolescents with type 1 diabetes mellitus without retinopathy by using optical biometry and optical coherence tomography?
Author / Creator:Öztürk, Hakan ; Özen, Bediz ; Manyas, Hayrullah ; Çatlı, Gönül ; Dündar, Bumin
Publisher:Dordrecht: Springer Netherlands
Journal title:International ophthalmology, 2020-10, Vol.40 (10), p.2503-2514
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ArticlesPeer ReviewedFull Text
Early and late diagnoses of 17β‐Hydroxysteroid dehydrogenase type‐3 deficiency in two unrelated patients
Author / Creator:Manyas, Hayrullah ; Eroğlu Filibeli, Berna ; Ayrancı, İlkay ; Güvenç, Merve S. ; Dündar, Bumin N. ; Çatlı, Gönül
Publisher:Germany: John Wiley & Sons, Inc
Journal title:Andrologia, 2021-07, Vol.53 (6), p.e14017-n/a
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ArticlesPeer ReviewedFull Text
Long-term Impact of Continuous Glucose Monitoring Assistance on Glycemic Control in Children and Adolescents with Type 1 Diabetes Following the 2023 Kahramanmaraş Earthquake
Author / Creator:Tarçın, Gürkan ; Ataş, Nurgül ; Yaşar, Mevra ; Şahin, Kadriye Cansu ; Trabzon, Gül ; Dündar, İsmail ; Çiçek, Dilek ; Balkı, Hanife Gül ; Manyas, Hayrullah ; Bitkay, Abdurrahman ; Celiloğlu, Can ; Özdemir Dilek, Semine ; Kılıç, Sümeyra ; Düzcan Kilimci, Duygu ; Ata, Aysun ; Çamtosun, Emine ; Mengen, Eda ; Karaoğlan, Murat ; Yüksel, Bilgin ; Uçaktürk, Seyit Ahmet
Publisher:Turkey
Journal title:Journal of clinical research in pediatric endocrinology, 2024-12
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ArticlesPeer ReviewedFull Text
MKRN3 Gene Mutation in a Case of Familial Central Precocious Puberty
Author / Creator:Eroğlu Filibeli, Berna ; Ayrancı, İlkay ; Manyas, Hayrullah ; Kırbıyık, Özgür ; Dündar, Bumin N. ; Çatlı, Gönül
Journal title:Güncel pediatri, 2022-04, Vol.20 (1), p.97-102
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ArticlesPeer ReviewedFull Text
MKRN3 Gene Mutation in a Case of Familial Central Precocious Puberty/ MKRN3 Gen Mutasyonu ile Iliskili Ailesel Santral Puberte Prekoks Olgusu
Author / Creator:Filibeli, Berna Eroglu ; Ayranci, Ilkay ; Manyas, Hayrullah ; Kirbiyik, Ozgur ; Dundar, Bumin N ; Catli, Gonul
Publisher:Galenos Yayinevi Tic. Ltd
Journal title:Güncel pediatri, 2022-04, Vol.20 (1), p.97
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ArticlesPeer ReviewedFull Text
Monogenik Obezite Ön Tanısı ile İncelenen Hastaların Klinik, Laboratuvar ve Genetik Sonuçlarının Değerlendirilmesi
Author / Creator:Ayrancı, İlkay ; Çatlı, Gönül ; Eroğlu Filibeli, Berna ; Yiğit, Elif ; Özyılmaz, Berk ; Manyas, Hayrullah ; Dündar, Bumin N
Journal title:Güncel pediatri, 2021-04, Vol.19 (1), p.52-59
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ArticlesPeer ReviewedFull Text
Evaluation of Clinical, Laboratory and Genetic Results of Patients Who Examined with a Pre-Diagnosis of Monogenic Obesity/Monogenik Obezite On Tanisi ile Incelenen Hastalarin Klinik, Laboratuvar ve Ge...
Author / Creator:Ayranci, Ilkay ; Catli, Gonul ; Filibeli, Berna Eroglu ; Yigit, Elif ; Ozyilmaz, Berk ; Manyas, Hayrullah ; Dundar, Bumin N
Publisher:Galenos Yayinevi Tic. Ltd
Journal title:Güncel pediatri, 2021-04, Vol.19 (1), p.52
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ReportsFull Text
Early and late diagnoses of 17β-Hydroxysteroid dehydrogenase type-3 deficiency in two unrelated patients
Author / Creator:Manyas, Hayrullah ; Eroğlu Filibeli, Berna ; Ayrancı, İlkay ; Güvenç, Merve S ; Dündar, Bumin N ; Çatlı, Gönül
Journal title:Andrologia, 2021, Vol.53 (6), p.e14017-e14017
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A rare endocrinological complication of chronic kidney disease

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Virilizing Adrenocortical Carcinoma Oncocytic Variant in a Child with Heterosexual Precocious Puberty and a Literature Review

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Can ocular changes be detected early in children and adolescents with type 1 diabetes mellitus without retinopathy by using optical biometry and optical coherence tomography?

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Early and late diagnoses of 17β‐Hydroxysteroid dehydrogenase type‐3 deficiency in two unrelated patients

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Long-term Impact of Continuous Glucose Monitoring Assistance on Glycemic Control in Children and Adolescents with Type 1 Diabetes Following the 2023 Kahramanmaraş Earthquake

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MKRN3 Gene Mutation in a Case of Familial Central Precocious Puberty

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MKRN3 Gene Mutation in a Case of Familial Central Precocious Puberty/ MKRN3 Gen Mutasyonu ile Iliskili Ailesel Santral Puberte Prekoks Olgusu

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Monogenik Obezite Ön Tanısı ile İncelenen Hastaların Klinik, Laboratuvar ve Genetik Sonuçlarının Değerlendirilmesi

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Evaluation of Clinical, Laboratory and Genetic Results of Patients Who Examined with a Pre-Diagnosis of Monogenic Obesity/Monogenik Obezite On Tanisi ile Incelenen Hastalarin Klinik, Laboratuvar ve Ge...

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Early and late diagnoses of 17β-Hydroxysteroid dehydrogenase type-3 deficiency in two unrelated patients

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