المؤلفون: Busra Gurpinar Tosun (11192361), Yasemin Kendir Demirkol (11199483), Tuba Seven Menevse (11199485), Sare Betul Kaygusuz (10524369), Mehmet Nuri Ozbek (11199487), Selda Ayça Altıncık (10366688), Jamala Mamadova (8080172), Atilla Cayir (11199489), Esra Doger (11199490), Elvan Bayramoglu (11199493), Özlem Nalbantoğlu (764161), Gul Yesiltepe Yesiltepe Mutlu (11199496), AghaRza Aghayev (11199498), Serap Turan (8080163), Abdullah Bereket (5165096), Tulay Guran (10524386)

مصطلحات موضوعية: Endocrinology, Paediatrics, Aldosterone synthase deficiency, Hypoaldosteronism, CYP11B2, catch-up growth, Steroid Hormone Profiles

العلاقة: https://figshare.com/articles/figure/Supplemantal_Figure_1_LC-MS_MS_determination_of_DOC_corticosterone_and_aldosterone_over_time_in_three_ASD_patients_after_discontinuation_of_fludrocortisone_treatment_/15070548Test

الإتاحة: https://doi.org/10.6084/m9.figshare.15070548.v4Test

المؤلفون: Bon Chu Chung, Goncagül Haklar, Serap Turan, Cengiz Kara, Jamala Mamadova, Tulay Guran, Melek Yildiz, Ahmet Anık, Eda Celebi Bitkin, Jen-Chieh Lin, Zeynep Atay, Teoman Akcay, Gönül Çatlı, Birgül Kirel, Hasan Önal, Azad Akbarzade, Onder Sirikci, Abdullah Bereket, Mehmet Keskin, Karl-Heinz Storbeck, Ayla Guven, Gülay Can Yılmaz, Tugba Baris, Filiz Tutunculer, Lise Barnard

المساهمون: İstinye Üniversitesi, Hastane, Akcay, Teoman, Ondokuz Mayıs Üniversitesi

المصدر: The Journal of clinical endocrinology and metabolism. 105(3)

مصطلحات موضوعية: Male, Turkey, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Physiology, Puberty, Precocious, Biochemistry, Endocrinology, HSD3B2, Chlorocebus aethiops, Missense mutation, 3 beta HSD2 deficiency, Child, Children, Sanger sequencing, Hsd3b2, CAH, Cah, Homozygote, Polycystic ovary, Child, Preschool, COS Cells, symbols, Metabolome, Female, adrenal insufficiency, medicine.medical_specialty, Adolescent, medicine.drug_class, Pediatric endocrinology, Mutation, Missense, Context (language use), symbols.namesake, children, Internal medicine, medicine, Adrenal insufficiency, Animals, Humans, Genetic Testing, Genetic Association Studies, Adrenal Hyperplasia, Congenital, business.industry, Progesterone Reductase, Biochemistry (medical), Infant, medicine.disease, 3 Beta Hsd2 Deficiency, Cross-Sectional Studies, Mineralocorticoid, business, Adrenal Insufficiency

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecfb0ff143eb66a4edc2f84c869cebcbTest
https://pubmed.ncbi.nlm.nih.gov/31950145Test