Zobrazeno 1 - 10
of 1 077
pro vyhledávání: '"17-hydroxyprogesterone"'
Autor:
Alizadeh, Fahimeh1, Mahmoudinia, Malihe2, Mirteimoori, Masoumeh3 Mirteimourim@mums.ac.ir, pourali, Lila2, Niroumand, Shabnam3
Publikováno v:
BMC Pregnancy & Childbirth. 3/1/2022, Vol. 22 Issue 1, p1-7. 7p.
Autor:
Irene Fylaktou, Anny Mertzanian, Ioanna Farakla, Alexandros Gryparis, Ioannis Anargyros Vasilakis, Maria Binou, Evangelia Charmandari, Christina Kanaka-Gantenbein, Amalia Sertedaki
Publikováno v:
Current Issues in Molecular Biology, Vol 46, Iss 10, Pp 10696-10713 (2024)
21-hydroxylase deficiency (21-OHD) represents the most common form of congenital adrenal hyperplasia (CAH) due to CYP21A2 gene pathogenic variants. Τhe aim of this study was the identification of CYP21A2 variants in 500 subjects of Greek origin with
Externí odkaz:
https://doaj.org/article/e59b3635a8214b3b8999d8e6b684b49e
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
Autor:
Madendag, Ilknur Col1 ilknurmadendag@gmail.com, Sahin, Mefkure Eraslan1
Publikováno v:
Annals of Medical of Research. Apr2020, Vol. 27 Issue 4, p1126-1130. 5p.
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 12, Pp 01-02 (2024)
Congenital Adrenal Hyperplasia (CAH) is a group of autosomal recessive disorders that occur due to defects in steroid synthesis. It is characterised by a deficiency of adrenocortical hormones and an excess of steroid precursors. A deficiency of 21-hy
Externí odkaz:
https://doaj.org/article/01773319874b4f119657d133bf9b4fa6
Akademický článek
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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:
K. V. Ivashchenko, K. A. Komshilova, N. V. Molashenko, A. A. Lavreniuk, A. M. Lapshina, I. V. Kim, V. A. Ioutsi, M. A. Antsupova, M. V. Utkina, N. M. Platonova, E. A. Troshina, N. G. Mokrysheva
Publikováno v:
Ожирение и метаболизм, Vol 20, Iss 4, Pp 363-370 (2024)
Hyperandrogenism is the most prevalent cause of menstrual cycle abnormalities and infertility in women. Here, we present a case of a 32-year-old woman with a 7-year history of menstrual irregularity and infertility. Laboratory test results revealed e
Externí odkaz:
https://doaj.org/article/87861a79039b46e1aeee5377fbf9576e
Autor:
Tania M. Espinosa Reyes, Alba Katherine Pesántez Velepucha, Julio Oscar Cabrera Rego, Wendy Valdés Gómez, Emma Domínguez Alonso, Henrik Falhammar
Publikováno v:
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-9 (2023)
Abstract Background Hyperandrogenism and supraphysiologic glucocorticoid replacement may lead to subclinical atherosclerosis in people with congenital adrenal hyperplasia (CAH) and predispose the development of cardiovascular diseases from an early a
Externí odkaz:
https://doaj.org/article/6a1f921c0797415487e7b98063244a0f
Autor:
Mendoza-Rojas, Víctor Clemente1, Díaz-Martínez, Luis Alfonso1, Mantilla-Mora, Gerardo1, Contreras-García, Gustavo Adolfo1, Mora-Bautista, Víctor Manuel2 victormr@uis.edu.co, Martínez-Paredes, Jhon Freddy3, Calderón-Rojas, Alba Luz3, Gómez-Tarazona, Carlos Augusto3, Pinzón-Mantilla, Katherine4
Publikováno v:
Colombia Medica. 2017, Vol. 48 Issue 4, p161-166. 6p.