Works matching AU Savaş-Erdeve, Şenay


Results: 38
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    Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 2, p. 180, doi. 10.4274/jcrpe.galenos.2020.2020.0216
    By:
    • Savaş-Erdeve, Şenay;
    • Aycan, Zehra;
    • Çetinkaya, Semra;
    • Öztürk, Ayşe Pınar;
    • Baş, Firdevs;
    • Poyrazoğlu, Şükran;
    • Darendeliler, Feyza;
    • Özsu, Elif;
    • Şıklar, Zeynep;
    • Demiral, Meliha;
    • Unal, Edip;
    • Özbek, Mehmet Nuri;
    • Gürbüz, Fatih;
    • Yüksel, Bilgin;
    • Evliyaoğlu, Olcay;
    • Akyürek, Nesibe;
    • Berberoğlu, Merih
    Publication type:
    Article
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    Antimüllerian Hormone Levels of Infants with Premature Thelarche.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2019, v. 11, n. 3, p. 287, doi. 10.4274/jcrpe.galenos.2019.2018.0293
    By:
    • Şahin, Nursel Muratoğlu;
    • Bayramoğlu, Elvan;
    • Özcan, Hatice Nursun;
    • Kurnaz, Erdal;
    • Keskin, Melikşah;
    • Savaş-Erdeve, Şenay;
    • Çetinkaya, Semra;
    • Aycan, Zehra
    Publication type:
    Article
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    A major health problem facing immigrant children: nutritional rickets.

    Published in:
    Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 2, p. 223, doi. 10.1515/jpem-2021-0420
    By:
    • Kurnaz, Erdal;
    • Çetinkaya, Semra;
    • Elmaoğulları, Selin;
    • Araslı Yılmaz, Aslıhan;
    • Muratoğlu Şahin, Nursel;
    • Keskin, Melikşah;
    • Savaş Erdeve, Şenay
    Publication type:
    Article
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    Mild phenotype in two siblings with a missense GHR variant.

    Published in:
    Journal of Pediatric Endocrinology & Metabolism, 2021, v. 34, n. 10, p. 1349, doi. 10.1515/jpem-2021-0044
    By:
    • Sarıkaya Özdemir, Behiye;
    • Çetinkaya, Semra;
    • Güleray Lafcı, Naz;
    • Şakar, Merve;
    • Karacan Küçükali, Gülin;
    • Elmaoğullari, Selin;
    • Savaş Erdeve, Şenay
    Publication type:
    Article
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    Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height.

    Published in:
    Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 7, p. 759, doi. 10.1515/jpem-2017-0088
    By:
    • Savaş-Erdeve, Şenay;
    • Çetinkaya, Semra;
    • Abalı, Zehra Yavaş;
    • Poyrazoğlu, Şükran;
    • Baş, Firdevs;
    • Berberoğlu, Merih;
    • Sıklar, Zeynep;
    • Korkmaz, Özlem;
    • Buluş, Derya;
    • Akbaş, Emine Demet;
    • GüranGüran, Tülay;
    • Böber, Ece;
    • Akın, Onur;
    • Yılmaz, Gülay Can;
    • Aycan, Zehra
    Publication type:
    Article
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    Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations.

    Published in:
    Human Mutation, 2019, v. 40, n. 11, p. 2033, doi. 10.1002/humu.23847
    By:
    • Cohen, Enzo;
    • Belkacem, Sabrina;
    • Fedala, Soumeya;
    • Collot, Nathalie;
    • Khallouf, Eliane;
    • Dastot, Florence;
    • Polak, Michel;
    • Duquesnoy, Philippe;
    • Brioude, Frederic;
    • Rose, Sophie;
    • Viot, Géraldine;
    • Soleyan, Aude;
    • Carel, Jean‐Claude;
    • Sobrier, Marie‐Laure;
    • Chanson, Philippe;
    • Gatelais, Frédérique;
    • Heinrichs, Claudine;
    • Kaffel, Noureddine;
    • Coutant, Regis;
    • Savaş Erdeve, Şenay
    Publication type:
    Article
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