يعرض 1 - 20 نتائج من 320 نتيجة بحث عن '"POYRAZOĞLU, ŞÜKRAN"', وقت الاستعلام: 0.73s تنقيح النتائج
  1. 1
    Academic Journal
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    Academic Journal
  3. 3
    Academic Journal

    المصدر: Schröder, Mariska A M; Neacşu, Mihaela; Adriaansen, Bas P H; Sweep, Fred C G J; Ahmed, S Faisal; Ali, Salma R; Bachega, Tânia A S S; Baronio, Federico; Birkebæk, Niels Holtum; de Bruin, Christiaan; Bonfig, Walter; Bryce, Jillian; Clemente, Maria; Cools, Martine; Elsedfy, Heba; Globa, Evgenia; Guran, Tulay; Güven, Ayla; Amr, Nermine Hussein; Janus, Dominika; Lenherr-Taube, Nina; Markosyan, Renata; Miranda, Mirela; Poyrazoğlu, Şükran; Rees, Aled; Salerno, Mariacarolina; Stancampiano, Marianna Rita; Vieites, Ana; de Vries, Liat; Yavas Abali, Zehra; et al (2023). Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective ....

    مصطلحات موضوعية: Medical Clinic, 610 Medicine & health

    وصف الملف: application/pdf

    Relation: https://www.zora.uzh.ch/id/eprint/254821/1/lvad143.pdf; info:pmid/37837609; urn:issn:0804-4643

  4. 4
    Academic Journal
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    Academic Journal

    المساهمون: OMÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, orcid:0000-0001-7374-229X, Aydın, Murat

    وصف الملف: application/pdf

    Relation: Journal of Clinical Research in Pediatric Endocrinology; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; ÇAKIR A. D,BAŞ F,AKIN O,ŞIKLAR Z,ÖZCABI B,BERBEROĞLU M,KARDELEN A. D,BAYRAMOĞLU E,POYRAZOĞLU Ş,AYDIN M,ERGÜR A,GÖKŞEN D,BOLU S,AYCAN Z,TÜYSÜZ B,ERCAN O,EVLİYAOĞLU O (2021). Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome. Journal of Clinical Research in Pediatric Endocrinology, 13(3), 308 - 319. Doi:10.4274/jcrpe.galenos.2021.2020.0228; 1308-5727 / 1308-5735; https://doi.org/10.4274/jcrpe.galenos.2021.2020.0228; https://hdl.handle.net/20.500.12712/33046; 13; 308; 319

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  8. 8
    Academic Journal

    مصطلحات موضوعية: Hypophosphatemic rickets, PHEX, Treatment

    وصف الملف: application/pdf

    Relation: JCRPE Journal of Clinical Research in Pediatric Endocrinology; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Şıklar, Z., Turan, S., Bereket, A., Baş, F., Güran, T., Akberzade, A. ve diğerleri (2020). Nationwide Turkish cohort study of hypophosphatemic rickets. JCRPE Journal of Clinical Research in Pediatric Endocrinology, 12(2), 150-159.; http://cms.galenos.com.tr/Uploads/Article_30174/JCRPE-12-150-En.pdf; https://hdl.handle.net/11468/7222; 12; 150; 159; WOS:000538971700005; 2-s2.0-85085960835; https://search.trdizin.gov.tr/yayin/detay/378077; Q2; Q3

  9. 9
    Electronic Resource

    المصدر: Schröder, Mariska A M; Neacşu, Mihaela; Adriaansen, Bas P H; Sweep, Fred C G J; Ahmed, S Faisal; Ali, Salma R; Bachega, Tânia A S S; Baronio, Federico; Birkebæk, Niels Holtum; de Bruin, Christiaan; Bonfig, Walter; Bryce, Jillian; Clemente, Maria; Cools, Martine; Elsedfy, Heba; Globa, Evgenia; Guran, Tulay; Güven, Ayla; Amr, Nermine Hussein; Janus, Dominika; Lenherr-Taube, Nina; Markosyan, Renata; Miranda, Mirela; Poyrazoğlu, Şükran; Rees, Aled; Salerno, Mariacarolina; Stancampiano, Marianna Rita; Vieites, Ana; de Vries, Liat; Yavas Abali, Zehra; et al (2023). Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study. European Journal of Endocrinology, 189(4):460-468.

  10. 10
    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal
  15. 15
    Academic Journal

    المساهمون: 4254477

    Relation: Journal of clinical research in pediatric endocrinology; Yildiz M., Onal Z., Yesil G., Kabil T. G., Toksoy G., Poyrazoglu Ş., Bas F., Durmaz O., Darendeliler F., "A Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two Siblings.", Journal of clinical research in pediatric endocrinology, 2023; vv_1032021; av_33606810-a2fe-4856-b184-f33932f77332; http://hdl.handle.net/20.500.12627/189037; https://doi.org/10.4274/jcrpe.galenos.2023.2022-10-4

  16. 16
    Academic Journal

    المساهمون: 4259178

    Relation: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation; Guaragna-Filho G., Guerra-Junior G., Tadokoro-Cuccaro R., Hughes I. A., Barros B. A., Hiort O., Balsamo A., Guran T., Holterhus P. M., Hannema S., et al., "Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as Girls.", Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation, ss.1-10, 2023; av_28cd257a-306d-40cd-8daf-4d5d1e473857; vv_1032021; http://hdl.handle.net/20.500.12627/188947; https://doi.org/10.1159/000526997; 10

  17. 17
    Academic Journal

    المساهمون: 4079739

    Relation: Journal of clinical research in pediatric endocrinology; Saygili S., Kocaaga M., Kaya G., Sukur M., Bas F., Poyrazoglu Ş., Bundak R., Darendeliler F., "Increased Carotid Intima-media Thickness and Its Association with Carbohydrate Metabolism and Adipocytokines in Children Treated with Recombinant Growth Hormone.", Journal of clinical research in pediatric endocrinology, 2022; vv_1032021; av_24a0525a-92e5-44b6-b899-eb062eeb7530; http://hdl.handle.net/20.500.12627/187083; https://avesis.istanbul.edu.tr/api/publication/24a0525a-92e5-44b6-b899-eb062eeb7530/file; https://doi.org/10.4274/jcrpe.galenos.2022.2022-8-19

  18. 18
    Book

    المؤلفون: POYRAZOĞLU, ŞÜKRAN

    المساهمون: İstanbul Üniversitesi , İstanbul Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü, 3402773

    Relation: POYRAZOĞLU Ş., Kalsiyum, fosfor ve magnezyum bozuklukları, "Neonatoloji", Türkan Dağoğlu, Fahri Ovalı, Editör, Nobel Tıp Kitabevleri, ss.1145-1154, 2017; vv_1032021; av_542c8d18-84f1-4510-9010-f2da8c1e89e9; http://hdl.handle.net/20.500.12627/182787

  19. 19
    Book

    المساهمون: 3402746

    Relation: Öner H. A. , POYRAZOĞLU Ş., Psödohipoaldosteronizm, "Pediatrik Nefroendokrin", Feyza Darendeliler, Ahmet Nayır, Zeynep Nagehan Yürük Yıldırım, Editör, Ema Tıp Kitapevi, ss.367-379, 2021; av_7a71b82c-4c16-4e0c-a66f-04307697dee1; vv_1032021; http://hdl.handle.net/20.500.12627/183405

  20. 20
    Book

    المساهمون: 3402744

    Relation: TÜRKKAN Ö. N. , POYRAZOĞLU Ş., GENETİK SENDROMLAR, "Pediatrik Nefroendokrin", Feyza Darendeliler, Ahmet Nayır, Zeynep Nagehan Yürük Yıldırım, Editör, Ema Tıp Kitapevi, ss.411-469, 2021; av_52eb4558-06a4-470f-8b7b-d85685778678; vv_1032021; http://hdl.handle.net/20.500.12627/182771