Works by Acar, Sezer

Results: 51
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    Is oxytocin related to psychiatric symptoms in adolescents with obesity?

    Published in:
    Journal of Pediatric Endocrinology & Metabolism, 2025, v. 38, n. 4, p. 318, doi. 10.1515/jpem-2024-0583
    By:
    • Özyurt, Gonca;
    • Çatlı, Gönül;
    • Acar, Sezer;
    • Cingöz, Gülten;
    • Özsoylu, Dua;
    • Küme, Tuncay;
    • Kızıldağ, Sefa;
    • Dündar, Bumin Nuri;
    • Öztürk, Yusuf;
    • Karagöz Tanıgör, Ezgi;
    • Tufan, Ali Evren;
    • Abaci, Ayhan
    Publication type:
    Article
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    Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal Insufficiency.

    Published in:
    Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 5, p. e1924, doi. 10.1210/clinem/dgac016
    By:
    • Menevse, Tuba Seven;
    • Demirkol, Yasemin Kendir;
    • Tosun, Busra Gurpinar;
    • Bayramoglu, Elvan;
    • Yildiz, Melek;
    • Acar, Sezer;
    • Karaca, Seda Erisen;
    • Orbak, Zerrin;
    • Onder, Asan;
    • Sobu, Elif;
    • Anık, Ahmet;
    • Atay, Zeynep;
    • Bugrul, Fuat;
    • Bulus, Ayse Derya;
    • Demir, Korcan;
    • Dogan, Durmus;
    • Emeksiz, Hamdi Cihan;
    • Kirmizibekmez, Heves;
    • Murat, Nurhan Ozcan;
    • Yaman, Akan
    Publication type:
    Article
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    Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics.

    Published in:
    Diabetologia, 2022, v. 65, n. 2, p. 336, doi. 10.1007/s00125-021-05597-y
    By:
    • Patel, Kashyap A.;
    • Ozbek, Mehmet N.;
    • Yildiz, Melek;
    • Guran, Tulay;
    • Kocyigit, Cemil;
    • Acar, Sezer;
    • Siklar, Zeynep;
    • Atar, Muge;
    • Colclough, Kevin;
    • Houghton, Jayne;
    • Johnson, Matthew B.;
    • Ellard, Sian;
    • Flanagan, Sarah E.;
    • Cizmecioglu, Filiz;
    • Berberoglu, Merih;
    • Demir, Korcan;
    • Catli, Gonul;
    • Bas, Serpil;
    • Akcay, Teoman;
    • Demirbilek, Huseyin
    Publication type:
    Article
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    Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3.

    Published in:
    PLoS ONE, 2018, v. 13, n. 3, p. 1, doi. 10.1371/journal.pone.0193388
    By:
    • Acar, Sezer;
    • BinEssa, Huda A.;
    • Demir, Korcan;
    • Al-Rijjal, Roua A.;
    • Zou, Minjing;
    • Çatli, Gönül;
    • Anık, Ahmet;
    • Al-Enezi, Anwar F.;
    • Özışık, Seçil;
    • Al-Faham, Manar S. A.;
    • Abacı, Ayhan;
    • Dündar, Bumin;
    • Kattan, Walaa E.;
    • Alsagob, Maysoon;
    • Kavukçu, Salih;
    • Tamimi, Hamdi E.;
    • Meyer, Brian F.;
    • Böber, Ece;
    • Shi, Yufei
    Publication type:
    Article
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    Doğumsal Hipotiroidi ile Ebeveyn Yaşı İlişkisi.

    Published in:
    Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2019, v. 13, n. 6, p. 451, doi. 10.12956/tchd.572367
    By:
    • TUHAN, Hale;
    • ERKOYUN, Erdem;
    • ACAR, Sezer;
    • ABACI, Ayhan;
    • BÖBER, Ece;
    • DEMİR, Korcan
    Publication type:
    Article
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    A Case of Late-onset Hyperinsulinemic Hypoglycemia: HNF4A Mutation.

    Published in:
    Journal of Pediatric Research, 2020, v. 7, n. 2, p. 168, doi. 10.4274/jpr.galenos.2019.36034
    By:
    • Arslan, Gülçin;
    • Acar, Sezer;
    • Özdemir, Taha Reşid;
    • Nalbantoğlu, Özlem;
    • Kırbıyık, Özgür;
    • Köprülü, Özge;
    • Özkaya, Beyhan;
    • Özkan, Behzat
    Publication type:
    Article
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