Search Results - Demir, Korean

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  1. 1
    Genetic Causes of Rickets

    Genetic Causes of Rickets by Acar, Sezer, Demir, Korcan, Shi, Yufei

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  2. 2
    Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal Insufficiency

    Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal Insufficiency by Seven Menevse, Tuba, Kendir Demirkol, Yasemin, Gurpinar Tosun, Busra, Bayramoglu, Elvan, Yildiz, Melek, Acar, Sezer, Erisen Karaca, Seda, Orbak, Zerrin, Onder, Asan, Sobu, Elif, Anık, Ahmet, Atay, Zeynep, Bugrul, Fuat, Derya Bulus, Ayse, Demir, Korcan, Dogan, Durmus, Cihan Emeksiz, Hamdi, Kirmizibekmez, Heves, Ozcan Murat, Nurhan, Yaman, Akan, Turan, Serap, Bereket, Abdullah, Guran, Tulay

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  3. 3
    A Mutation in INSR in a Child Presenting with Severe Acanthosis Nigricans

    A Mutation in INSR in a Child Presenting with Severe Acanthosis Nigricans by Tuhan, Hale, Ceylaner, Serdar, Nalbantoğlu, Özlem, Acar, Sezer, Abacı, Ayhan, Böber, Ece, Demir, Korcan

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  4. 4
    Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey

    Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey by Poyrazoğlu, Şükran, Akçay, Teoman, Arslanoğlu, İlknur, Atabek, Mehmet Emre, Atay, Zeynep, Berberoğlu, Merih, Bereket, Abdullah, Bideci, Aysun, Bircan, İffet, Böber, Ece, Can, Şule, Cesur, Yaşar, Darcan, Şükran, Demir, Korcan, Dündar, Bumin, Ersoy, Betül, Esen, İhsan, Güven, Ayla, Kara, Cengiz, Keskin, Mehmet, Kurtoğlu, Selim, Memioğlu, Nihal, Özbek, Mehmet Nuri, Özgen, Tolga, Sarı, Erkan, Şıklar, Zeynep, Şimşek, Enver, Turan, Serap, Yeşilkaya, Ediz, Yüksel, Bilgin, Darendeliler, Feyza

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  5. 5
    A Rare Karyotype of Turner Syndrome: 45.X/47.XXX/Nadir Gorulen Bir Turner Sendromu Karyotipi: 45,X/47,XXX

    A Rare Karyotype of Turner Syndrome: 45.X/47.XXX/Nadir Gorulen Bir Turner Sendromu Karyotipi: 45,X/47,XXX by Altincik, Ayca, Catli, Gonul, Demir, Korean, Abaci, Ayhan, Bora, Elcin, Ercal, Derya, Bober, Ece

    Published in Güncel pediatri
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  6. 6
    A Rare Karyotype of Turner Syndrome: 45.X/47.XXX/Nadir Gorulen Bir Turner Sendromu Karyotipi: 45,X/47,XXX

    A Rare Karyotype of Turner Syndrome: 45.X/47.XXX/Nadir Gorulen Bir Turner Sendromu Karyotipi: 45,X/47,XXX by Altincik, Ayca, Catli, Gonul, Demir, Korean, Abaci, Ayhan, Bora, Elcin, Ercal, Derya, Bober, Ece

    Published in Güncel pediatri
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