A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the SAMD9 Gene
Mengen, Eda, Küçükçongar Yavaş, Aynur, Uçaktürk, S. Ahmet
Published in Journal of clinical research in pediatric endocrinology (01.06.2020)
Published in Journal of clinical research in pediatric endocrinology (01.06.2020)
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CCDC141 Mutation Identified in Anosmic Hypogonadotropic Hypogonadism (Kallmann Syndrome) Alters GnRH Neuronal Migration
Hutchins, B. Ian, Kotan, L. Damla, Taylor-Burds, Carol, Ozkan, Yusuf, Cheng, Paul J, Gurbuz, Fatih, Tiong, Jean D. R, Mengen, Eda, Yuksel, Bilgin, Topaloglu, A. Kemal, Wray, Susan
Published in Endocrinology (Philadelphia) (01.05.2016)
Published in Endocrinology (Philadelphia) (01.05.2016)
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A duplication upstream of SOX9 associated with SRY negative 46,XX ovotesticular disorder of sex development: A case report
Mengen, Eda, Kayhan, Gülsüm, Kocaay, Pınar, Uçaktürk, Seyit Ahmet
Published in Journal of clinical research in pediatric endocrinology (01.09.2020)
Published in Journal of clinical research in pediatric endocrinology (01.09.2020)
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Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism
Kotan, Leman Damla, Ternier, Gaetan, Cakir, Aydilek Dagdeviren, Emeksiz, Hamdi Cihan, Turan, Ihsan, Delpouve, Gaspard, De Kardelen, Asli rya, Ozcabi, Bahar, Isik, Emregul, Mengen, Eda, De Cakir, Esra niz P., Yuksel, Aysegul, Agladioglu, Sebahat Yilmaz, Dilek, Semine Ozdemir, Evliyaoglu, Olcay, Darendeliler, Feyza, Gurbuz, Fatih, Akkus, Gamze, Yuksel, Bilgin, Giacobini, Paolo, Topaloglu, A. Kemal
Published in Genetics in medicine (01.06.2021)
Published in Genetics in medicine (01.06.2021)
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Emotion dysregulation and pediatric obesity: investigating the role of Internet addiction and eating behaviors on this relationship in an adolescent sample
Yilmaz Kafali, Helin, Uçaktürk, Seyit Ahmet, Mengen, Eda, Akpinar, Serap, Erguven Demirtas, Merve, Uneri, Ozden Sukran
Published in Eating and weight disorders (01.08.2021)
Published in Eating and weight disorders (01.08.2021)
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17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
Siklar, Zeynep, Camtosun, Emine, Bolu, Semih, Yildiz, Melek, Akinci, Aysehan, Bas, Firdevs, Dündar, İsmail, Bestas, Asli, Ünal, Edip, Kocaay, Pinar, Guran, Tulay, Buyukyilmaz, Gonul, Ugurlu, Aylin Kilinc, Tosun, Buşra Gurpinar, Turan, Ihsan, Kurnaz, Erdal, Yuksel, Bilgin, Turkkahraman, Doga, Cayir, Atilla, Celmeli, Gamze, Gonc, E. Nazli, Eklioğlu, Beray Selver, Cetinkaya, Semra, Yilmaz, Seniha Kiremitci, Atabek, Mehmet Emre, Buyukinan, Muammer, Arslan, Emrullah, Mengen, Eda, Cakir, Esra Deniz Papatya, Karaoglan, Murat, Hatipoglu, Nihal, Orbak, Zerrin, Ucar, Ahmet, Akyurek, Nesibe, Akbas, Emine Demet, Isik, Emregül, Kaygusuz, Sare Betul, Sutcu, Zumrut Kocabey, Seymen, Gulcan, Berberoglu, Merih
Published in Endocrine (2024)
Published in Endocrine (2024)
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Mutations within The Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency
Bulut, Fatma Derya, Özdemir Dilek, Semine, Kotan, Damla, Mengen, Eda, Gürbüz, Fatih, Yüksel, Bilgin
Published in Journal of clinical research in pediatric endocrinology (01.09.2020)
Published in Journal of clinical research in pediatric endocrinology (01.09.2020)
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The Significance of Thiol/Disulfide Homeostasis and Ischemia-modified Albumin Levels in Assessing Oxidative Stress in Obese Children and Adolescents
Mengen, Eda, Uçaktürk, Seyit Ahmet, Kocaay, Pınar, Kaymaz, Özlem, Neşelioğlu, Salim, Erel, Özcan
Published in Journal of clinical research in pediatric endocrinology (01.03.2020)
Published in Journal of clinical research in pediatric endocrinology (01.03.2020)
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Subclinical Myocardial Dysfunction Demonstrated by Speckle Tracking Echocardiography in Children with Euthyroid Hashimoto’s Thyroiditis
Azak, Emine, Uçaktürk, Seyit Ahmet, Çetin, İbrahim İlker, Gürsu, Hazım Alper, Mengen, Eda, Pamuk, Utku
Published in Journal of clinical research in pediatric endocrinology (01.12.2019)
Published in Journal of clinical research in pediatric endocrinology (01.12.2019)
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Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship
Özsu, Elif, Çetinkaya, Semra, Bolu, Semih, Hatipoğlu, Nihal, Savaş Erdeve, Şenay, Evliyaoğlu, Olcay, Baş, Firdevs, Çayır, Atilla, Dündar, İsmail, Akbaş, Emine Demet, Uçaktürk, Seyid Ahmet, Berberoğlu, Merih, Şıklar, Zeynep, Özalkak, Şervan, Muratoğlu Şahin, Nursel, Keskin, Melikşah, Şiraz, Ülkü Gül, Turan, Hande, Öztürk, Ayşe Pınar, Mengen, Eda, Sağsak, Elif, Dursun, Fatma, Akyürek, Nesibe, Odabaşı Güneş, Sevinç, Aycan, Zehra
Published in Journal of clinical research in pediatric endocrinology (01.09.2024)
Published in Journal of clinical research in pediatric endocrinology (01.09.2024)
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Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey
Eren, Erdal, Törel Ergür, Ayça, İşgüven, Şükriye Pınar, Çelebi Bitkin, Eda, Berberoğlu, Merih, Şıklar, Zeynep, Baş, Firdevs, Yel, Servet, Baş, Serpil, Söbü, Elif, Bereket, Abdullah, Turan, Serap, Sağlam, Halil, Atay, Zeynep, Ercan, Oya, Güran, Tülay, Atabek, Mehmet Emre, Korkmaz, Hüseyin Anıl, Kılınç Uğurlu, Aylin, Akıncı, Ayşehan, Döğer, Esra, Şimşek, Enver, Akbaş, Emine Demet, Abacı, Ayhan, Gül, Ülkü, Acar, Sezer, Mengen Uçaktürk, Eda, Yıldız, Melek, Ünal, Edip, Tarım, Ömer
Published in Journal of clinical research in pediatric endocrinology (01.06.2019)
Published in Journal of clinical research in pediatric endocrinology (01.06.2019)
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Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated families
Demirbilek, Huseyin, Ozbek, M. Nuri, Demir, Korcan, Kotan, L. Damla, Cesur, Yasar, Dogan, Murat, Temiz, Fatih, Mengen, Eda, Gurbuz, Fatih, Yuksel, Bilgin, Topaloglu, A. Kemal
Published in Clinical endocrinology (Oxford) (01.03.2015)
Published in Clinical endocrinology (Oxford) (01.03.2015)
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A Rare Side Effect of Diazoxide Therapy: Pulmonary Hipertension
Gürsu, Alper Hazim, Azak, Emine, Mengen, Eda, Ünal, Sevim, Çetin, İbrahim İlker
Published in Izmir Dr. Behçet Uz Çocuk Hastanesi dergisi (01.01.2020)
Published in Izmir Dr. Behçet Uz Çocuk Hastanesi dergisi (01.01.2020)
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Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations
Akkuş, Gamze, Kotan, Leman Damla, Durmaz, Erdem, Mengen, Eda, Turan, İhsan, Ulubay, Ayça, Gürbüz, Fatih, Yüksel, Bilgin, Tetiker, Tamer, Topaloğlu, A Kemal
Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
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Kronik karaciğer hastalığı olan çocukların D vitamini düzeyleri
Gürbüz, Fatih, Ağın, Mehmet, Mengen, Eda, Elçi, Hüseyin, Ünal, İlker, Tümgör, Gökhan, Yüksel, Bilgin
Published in Cukurova Medical Journal (31.12.2018)
Published in Cukurova Medical Journal (31.12.2018)
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Comparison Of Calcitonin And Pamidronate Treatments In Children With Osteogenesis Imperfecta
Gürbüz,Fatih, Topaloğlu,Ali Kemal, Yüksel,Bilgin, Mengen,Eda, Özgür,Özden
Published in Cukurova Medical Journal (01.04.2013)
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Published in Cukurova Medical Journal (01.04.2013)
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