Zobrazeno 1 - 10
of 17 940
pro vyhledávání: '"17-hydroxyprogesterone"'
Autor:
Noori, Maedeh1 (AUTHOR), Talebpour, Zahra1,2 (AUTHOR) ztalebpour@alzahra.ac.ir
Publikováno v:
Scientific Reports. 7/13/2024, Vol. 14 Issue 1, p1-11. 11p.
Autor:
Maedeh Noori, Zahra Talebpour
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Quantifying small amounts of the 17-hydroxyprogesterone in various matrix is crucial for different purposes. In this study, a commercial polydimethylsiloxane stir bar was used to extract hormone from water and urine samples. Analysis was per
Externí odkaz:
https://doaj.org/article/0892e9f977da409a87467fe33064362a
Publikováno v:
Proceedings, Vol 38, Iss 3 (2024)
Introduction: Congenital adrenal hyperplasia (CAH) is an autosomal-recessive condition primarily caused by 21- hydroxylase deficiency. It is the most common cause of ambiguous genitalia in infants and children. It can be a fatal condition if left unt
Externí odkaz:
https://doaj.org/article/53ad5afdbca54a838ad46ff7b0a2af45
Autor:
Beata Woźniak, Dorota Leszczyńska, Alicja Szatko, Karolina Nowak, Radosław Samsel, Anna Siejka, Lucyna Papierska, Wojciech Zgliczyński, Henrik Falhammar, Piotr Glinicki
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
In adrenal steroidogenesis, 17-hydroxyprogesterone (17-OHP) is a substrate for 21-hydroxylase, one of the crucial enzymes of the cortisol and aldosterone biosynthesis pathway. Thus, measurement serum 17-OHP concentration is used when the diagnosis of
Externí odkaz:
https://doaj.org/article/2df03d3f3cea474d8972cdffaf47cd47
Publikováno v:
In American Journal of Obstetrics and Gynecology April 2024
Autor:
Dubinski, Ilja, Bechtold-Dalla Pozza, Susanne, Bidlingmaier, Martin, Hawley, James, Keevil, Brian, Kunz, Sonja, Nowotny, Hannah Franziska, Reisch, Nicole, Schiergens, Katharina, Tschaidse, Lea, Schmidt, Heinrich
Publikováno v:
Journal of Pediatric Endocrinology & Metabolism; May2024, Vol. 37 Issue 5, p419-424, 6p
Autor:
Caritis, Steve N., Costantine, Maged M., Clark, Shannon, Stika, Catherine S., Kiley, Jessica W., Metz, Torri D., Chauhan, Suneet P., Venkataramanan, Raman
Publikováno v:
In American Journal of Obstetrics & Gynecology MFM July 2023 5(7)
Autor:
Woźniak B; Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland., Leszczyńska D; Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland., Szatko A; Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.; EndoLab Laboratory, Centre of Postgraduate Medical Education, Warsaw, Poland., Nowak K; Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland., Samsel R; Department of Surgery, Clinic of Surgical Oncology and Neuroendocrine Tumors, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland., Siejka A; Clinical Biochemistry Department, The Children's Memorial Health Institute, Warsaw, Poland., Papierska L; Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland., Zgliczyński W; Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland., Falhammar H; Department of Endocrinology, Karolinska University Hospital, Stockholm, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden., Glinicki P; Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.; EndoLab Laboratory, Centre of Postgraduate Medical Education, Warsaw, Poland.
Publikováno v:
Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2024 Nov 21; Vol. 15, pp. 1499836. Date of Electronic Publication: 2024 Nov 21 (Print Publication: 2024).
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Endocrine Connections, Vol 12, Iss 12, Pp 1-9 (2023)
Congenital adrenal hyperplasia (CAH) occurs due to enzyme defects in adrenal steroidogenesis. The 21-hydroxylase deficiency accounts for 90–95% of cases, triggering accumulation of 17-hydroxyprogesterone (17-OHP). Early diagnosis through neonatal s
Externí odkaz:
https://doaj.org/article/f6faf3bfb1a74e8bb44b1fd7b6526f1f