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, Yıldırım, Ruken, Taş, Funda Feryal, Tekin, Suat, Ceylaner, Serdar, Haspolat, Yusuf Kenan

مصطلحات موضوعية: 17α-hydroxylase, CYP17A1 gene, Delayed puberty, Hypertension, Primary amenorrhea

وصف الملف: application/pdf

العلاقة: Gynecological Endocrinology; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Ünal, E., Yıldırım, R., Taş, F. F., Tekin, S., Ceylaner, S., Haspolat, Y. K. ve diğerleri. (2020). A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in CYP17A1 gene. Gynecological Endocrinology, 36(8), 739-742.; https://pubmed.ncbi.nlm.nih.gov/31885295Test/; https://hdl.handle.net/11468/8341Test; 36; 739; 742; WOS:000504809000001; 2-s2.0-85077858612; Q2; Q3

الإتاحة: https://doi.org/10.1080/09513590.2019.1707798Test
https://hdl.handle.net/11468/8341Test
https://pubmed.ncbi.nlm.nih.gov/31885295Test/

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

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

مصطلحات موضوعية: Male, Delayed puberty, Pediatrics, medicine.medical_specialty, Adolescent, Endocrinology, Diabetes and Metabolism, Mixed Function Oxygenases, Deletion, Endocrinology, Hypergonadotropic hypogonadism, Diabetes mellitus, medicine, Humans, Family, Congenital adrenal hyperplasia, Multiplex ligation-dependent probe amplification, Child, Amenorrhea, Puberty, Delayed, Chinese Patients, Adrenal Hyperplasia, Congenital, business.industry, Gender Identity, Steroid 17-alpha-Hydroxylase, 17,20-Lyase, 17-Hydroxylase/17,20-Lyase Deficiency, medicine.disease, Hypokalemia, Blood pressure, CYP17A1, Cyp17A1 Gene, Mutation, Primary amenorrea, Hypertension, Female, medicine.symptom, business, Mutations

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e70470305c1b015462d97933e714f119Test
https://hdl.handle.net/11468/11092Test

المؤلفون: Funda Feryal Taş, Serdar Ceylaner, Ruken Yıldırım, Suat Tekin, Yusuf Kenan Haspolat, Edip Unal

المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Ünal, Edip, Taş, Funda Feryal, Tekin, Suat, Haspolat, Yusuf Kenan

المصدر: Gynecological Endocrinology. 36:739-742

مصطلحات موضوعية: Delayed puberty, medicine.medical_specialty, Cytochrome, biology, Hydroxylase deficiency, Endocrinology, Diabetes and Metabolism, XY karyotype, Obstetrics and Gynecology, CYP17A1 gene, urologic and male genital diseases, medicine.disease, Endocrinology, CYP17A1, Internal medicine, Hypertension, Primary amenorrhea, medicine, biology.protein, Congenital adrenal hyperplasia, medicine.symptom, 17α-hydroxylase, Gene

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a0042650033b02bf90e69eedd624801Test
https://doi.org/10.1080/09513590.2019.1707798Test