Aim. Aim of the study was to investigate the need to perform the adrenocorticotropic hormone (ACTH) stimulation test by recognizing the importance of a second look at basal serum 17-alpha hydroxyprogesterone (17-OHP) levels and calculating new serum 17-OHP cut-off level
52nd Conference of the European-Society-of-Human-Genetics (ESHG) -- JUN 15-18, 2019 -- Gothenburg, S...
Objective: The purpose of this study was to evaluate the usefulness of 17 hydroxyprogesterone (17OHP...
Background: Undiagnosed congenital adrenal hyperplasia (CAH) can cause adrenal incidentalomas, but t...
OBJETIVOS: avaliar se os níveis de 17-hidroxiprogesterona podem predizer o resultado do teste de est...
Congenital adrenal hyperplasia (CAH), the inherited inability to synthesize cortisol, leading to exc...
Heterozygote carriers of 21-hydroxylase deficiency (21-OHD) cannot be detected by measurements of ba...
The phenotypic manifestation of congenital adrenal hyperplasia (CAH) is variable, and this largely d...
Congenital adrenal hyperplasia (CAH) comprises a group of rare autosomal recessively inherited disor...
Background: Basal levels of androgens, in particular 17-hydroxyprogesterone (17OHP), are widely deba...
BACKGROUND: Congenital adrenal hyperplasia is a group of disorders caused by defects in the adrenal ...
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders affecting cortisol ...
[[abstract]]A rapid, simple, and specific method was developed for the diagnosis of congenital adren...
[[abstract]]Congenital adrenal hyperplasia (CAH), a disorder caused by a deficiency of the 21-hydrox...
Item does not contain fulltextCongenital adrenal hyperplasia (CAH) is a group of autosomal recessive...
A forma não-clássica da hiperplasia adrenal congênita (HAC) por deficiência da 21-hidroxilase (D21OH...
52nd Conference of the European-Society-of-Human-Genetics (ESHG) -- JUN 15-18, 2019 -- Gothenburg, S...
Objective: The purpose of this study was to evaluate the usefulness of 17 hydroxyprogesterone (17OHP...
Background: Undiagnosed congenital adrenal hyperplasia (CAH) can cause adrenal incidentalomas, but t...
OBJETIVOS: avaliar se os níveis de 17-hidroxiprogesterona podem predizer o resultado do teste de est...
Congenital adrenal hyperplasia (CAH), the inherited inability to synthesize cortisol, leading to exc...
Heterozygote carriers of 21-hydroxylase deficiency (21-OHD) cannot be detected by measurements of ba...
The phenotypic manifestation of congenital adrenal hyperplasia (CAH) is variable, and this largely d...
Congenital adrenal hyperplasia (CAH) comprises a group of rare autosomal recessively inherited disor...
Background: Basal levels of androgens, in particular 17-hydroxyprogesterone (17OHP), are widely deba...
BACKGROUND: Congenital adrenal hyperplasia is a group of disorders caused by defects in the adrenal ...
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders affecting cortisol ...
[[abstract]]A rapid, simple, and specific method was developed for the diagnosis of congenital adren...
[[abstract]]Congenital adrenal hyperplasia (CAH), a disorder caused by a deficiency of the 21-hydrox...
Item does not contain fulltextCongenital adrenal hyperplasia (CAH) is a group of autosomal recessive...
A forma não-clássica da hiperplasia adrenal congênita (HAC) por deficiência da 21-hidroxilase (D21OH...
52nd Conference of the European-Society-of-Human-Genetics (ESHG) -- JUN 15-18, 2019 -- Gothenburg, S...
Objective: The purpose of this study was to evaluate the usefulness of 17 hydroxyprogesterone (17OHP...
Background: Undiagnosed congenital adrenal hyperplasia (CAH) can cause adrenal incidentalomas, but t...