المؤلفون: Karakaya, Amine Aktar, Ünal, Edip, Beştaş, Aslı, Haspolat, Yusuf Kenan

مصطلحات موضوعية: Down sendromu, Hipotroidi, Tiroid, Down syndrome, Hypothyroidism, Thyroid

وصف الملف: application/pdf

العلاقة: Fırat Tıp Dergisi; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Karakaya, A. A., Ünal, E., Beştaş, A. ve Haspolat, Y. K. (2023). Down sendromlu hastalarda tiroid fonksiyonlarının değerlendirilmesi. Fırat Tıp Dergisi, 28(1), 17-21.; https://search.trdizin.gov.tr/tr/yayin/detay/1177389Test; https://hdl.handle.net/11468/12142Test; 28; 17; 21

الإتاحة: https://hdl.handle.net/11468/12142Test
https://search.trdizin.gov.tr/tr/yayin/detay/1177389Test

المؤلفون: Beştaş, Aslı, Ünal, Edip, Demiral, Meliha, Karakaya, Amine Aktar, Haspolat, Yusuf K.

مصطلحات موضوعية: Central precocious puberty, GnRH stimulation test, Puberty

وصف الملف: application/pdf

العلاقة: Indian Journal of Endocrinology and Metabolism; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Beştaş, A., Ünal, E., Karakaya, A. A., Demiral, M. ve Haspolat, Y. K. (2023). Evaluation of clinical and laboratory findings in the differential diagnosis of central precocious puberty and premature thelarche. Indian Journal of Endocrinology and Metabolism, 27(3), 237-241.; https://journals.lww.com/indjem/Fulltext/2023/05000/Evaluation_of_Clinical_and_Laboratory_Findings_in.9.aspxTest; https://hdl.handle.net/11468/12636Test; 27; 237; 241; 2-s2.0-85165708470; Q3

الإتاحة: https://doi.org/10.4103/ijem.ijem_245_22Test
https://hdl.handle.net/11468/12636Test
https://journals.lww.com/indjem/Fulltext/2023/05000/Evaluation_of_Clinical_and_Laboratory_Findings_in.9.aspxTest

المؤلفون: Karakaya, Amine Aktar, Unal, Edip, Bestas, Asli, Yildirim, Ruken

مصطلحات موضوعية: Early Puberty, Puberty, Gonadotropin-Releasing Hormone Analogue, Final Height

العلاقة: Guncel Pediatri-Journal of Current Pediatrics; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://doi.org/10.4274/jcp.2022.54280Test; https://hdl.handle.net/11468/19655Test; 20; 174; 180; WOS:000965716700009; 2-s2.0-85147361124; Q4; N/A

الإتاحة: https://doi.org/10.4274/jcp.2022.54280Test
https://hdl.handle.net/11468/19655Test

المؤلفون: Karakaya, Amine Aktar, Beştaş, Aslı, Taş, Funda Feryal, Haspolat, Yusuf Kenan

مصطلحات موضوعية: Amiodaron, Hipertiroidi, Steroid

وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document

العلاقة: XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrim İçi Kongresi; Konferans Öğesi - Ulusal - Kurum Öğretim Elemanı; Karakaya, A. A., Beştaş, A., Taş, F. F. ve Haspolat, Y. K. (2020, Ekim-Kasım). Amiodaron ilişkili hipertroidi gelişen hastada takip ve tedavi. XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrim İçi Kongresi.; https://hdl.handle.net/11468/8270Test

الإتاحة: https://hdl.handle.net/11468/8270Test

المؤلفون: Karakaya, Amine Aktar, Beştaş, Aslı, Taş, Funda Feryal, Haspolat, Yusuf Kenan

مصطلحات موضوعية: Antropometrik ölçüm, Marfan sendromu, Uzun boy

وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document

العلاقة: XXIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi; Konferans Öğesi - Ulusal - Kurum Öğretim Elemanı; Karakaya, A. A., Beştaş, A., Taş, F. F. ve Haspolat, Y. K. (2019, Nisan). Uzun boy nedeniyle başvuran hastada Marfan sendromu. XXIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi.; https://hdl.handle.net/11468/8278Test

الإتاحة: https://hdl.handle.net/11468/8278Test

المؤلفون: Karakaya, Amine Aktar, Ünal, Edip, Beştaş, Aslı, Haspolat, Yusuf Kenan

المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Karakaya, Amine Aktar, Ünal, Edip, Beştaş, Aslı, Haspolat, Yusuf Kenan

مصطلحات موضوعية: Thyroid, Hypothyroidism, Down sendromu, Down syndrome, Tiroid, Hipotroidi

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______3346::83dc8cf00671ad194b035ddf6e00336eTest
https://search.trdizin.gov.tr/tr/yayin/detay/1177389Test

المؤلفون: Cayir, Atilla, Karakaya, Amine Aktar, Unal, Edip, Bestas, Asli, Solmaz, Asli Ece, Haspolat, Yusuf Kenan

مصطلحات موضوعية: LHCGR, Leydig cell hypoplasia, Missense Mutation, Primary amenorrhea, Luteinizing-Hormone Receptor, Empty Follicle Syndrome, Leydig-Cell Hypoplasia, Inactivating Mutations, 46,Xy Disorders, Patient

العلاقة: European Journal Of Obstetrics & Gynecology And Reproductive Biology; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11454/76515Test; https://doi.org/10.1016/j.ejogrb.2022.03.033Test; 272; 193; 197

الإتاحة: https://doi.org/10.1016/j.ejogrb.2022.03.033Test
https://hdl.handle.net/11454/76515Test

المؤلفون: Karakaya, Amine Aktar, Cayir, Atilla, Unal, Edip, Bestas, Asli, Solmaz, Asli Ece, Haspolat, Yusuf Kenan

مصطلحات موضوعية: Leydig cell hypoplasia, LHCGR, Primary amenorrhea, Luteinizing-Hormone Receptor, Empty Follicle Syndrome, Leydig-Cell Hypoplasia, Inactivating Mutations, Missense Mutation, 46,Xy Disorders, Patient

العلاقة: European Journal Of Obstetrics & Gynecology And Reproductive Biology; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://doi.org/10.1016/j.ejogrb.2022.03.033Test; https://hdl.handle.net/11454/76515Test; 272; 193; 197; WOS:000794015200016; 2-s2.0-85127137696

الإتاحة: https://doi.org/10.1016/j.ejogrb.2022.03.033Test
https://hdl.handle.net/11454/76515Test

المؤلفون: Beştaş, Aslı, Bolu, Semih, Ünal, Edip, Karakaya, Amine Aktar, Eroz, Recep, Tekin, Mehmet, Haspolat, Yusuf Kenan

مصطلحات موضوعية: Primary amenorrea, Delayed puberty, Hypertension

وصف الملف: application/pdf

العلاقة: Endocrine; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Beştaş, A., Bolu, S., Ünal, E., Karakaya, A.A., Eroz, R., Tekin, M. ve diğerleri. (2022). A rare cause of delayed puberty and primary amenorrhea: 17 alpha-hydroxylase enzyme deficiency. Endocrine, 75(3), 927-933.; https://link.springer.com/article/10.1007/s12020-021-02914-8Test; https://hdl.handle.net/11468/11092Test; 75; 927; 933; WOS:000713575900001; 2-s2.0-85118334339; Q2; Q3

الإتاحة: https://doi.org/10.1007/s12020-021-02914-8Test
https://hdl.handle.net/11468/11092Test

المؤلفون: Ünal, Edip, Karakaya, Amine Aktar, Beştaş, Aslı, Yıldırım, Ruken, Taş, Funda Feryal, Onay, Hüseyin, Özkınay, Ferda, Haspolat, Yusuf Kenan

مصطلحات موضوعية: AMHR2, Persistent müllerian duct syndrome, Novel mutation, Undescended testes

وصف الملف: application/pdf

العلاقة: Journal of Endocrinological Investigation; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Ünal, E., Karakaya, A. A., Beştaş, A., Yıldırım, R., Taş, F. F., Onay, H. ve diğerleri. (2021). Identification of four novel variant in the AMHR2 gene in six unrelated Turkish families. Journal of Endocrinological Investigation, 44(6), 1301-1307.; https://hdl.handle.net/11468/8364Test; 44; 1301; 1307; WOS:000575724600003; 2-s2.0-85092179929; Q2

الإتاحة: https://doi.org/10.1007/s40618-020-01437-9Test
https://hdl.handle.net/11468/8364Test