Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mirta Beatriz, Miras"'
Autor:
Romina Celeste Geysels, Carlos Eduardo Bernal Barquero, Mariano Martín, Victoria Peyret, Martina Nocent, Gabriela Sobrero, Liliana Muñoz, Malvina Signorino, Graciela Testa, Ricardo Belisario Castro, Ana María Masini-Repiso, Mirta Beatriz Miras, Juan Pablo Nicola
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundCongenital iodide transport defect (ITD) is an uncommon cause of dyshormonogenic congenital hypothyroidism characterized by the absence of active iodide accumulation in the thyroid gland. ITD is an autosomal recessive disorder caused by los
Externí odkaz:
https://doaj.org/article/48789212a11540bc9e817a0526e34302
Autor:
Cintia Soledad, Tarifa, Liliana Karina, Silvano, Silvia Edith, Martin, Veronica, Campi, Maria Cecilia, Aguirre, Gabriela Maria, Sobrero, Mariana, Ochetti, Mirta Beatriz, Miras, Noemi Liliana, Muñoz
Publikováno v:
Pediatric endocrinology reviews : PER. 17(3)
Gonadotropin and steroid concentrations obtained in various laboratories cannot often be compared because of methodological differences.to determine reference intervals for FSH, LH, T, E2, F and DHEA-S according to age and sex during the first year o
Autor:
Liliana Noemi, Muñoz, Mariana, Ochetti, Gonzalo, Perez, Gabriela Maria, Sobrero, Liliana Karina, Silvano, Silvia Edith, Martin, Graciela María, Testa, Mirta Beatriz, Miras
Publikováno v:
Pediatric endocrinology reviews : PER. 12(4)
Determination of 17α-nyaroxyprogesterone (17OHP) is used for the diagnosis and monitoring of Congenital Adrenal Hyperplasia (CAH). Problems associated with the specificity of antibodies used in direct immunoassays can yield high false results.To ana
Autor:
Miartus, Mirta Beatriz Miras
Publikováno v:
Journal of Pediatric Endocrinology & Metabolism; Oct2009, Vol. 22 Issue 10, p877-879, 3p