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Mostrando ítems 11-20 de 20
Erratum : Clinical, Biochemical, and Genetic Characteristics of "Nonclassic" Apparent Mineralocorticoid Excess Syndrome (Journal of Clinical Endocrinology and Metabolism (2019) 104: 2 (595–603) DOI: 10.1210/jc.2018-01197)
(2019-05-01)
In the above-named article by Tapia-Castillo A, Baudrand R, Vaidya A, Campino C, Allende F, Valdivia C, Vecchiola A, Lagos CF, Fuentes CA, Solari S, Martinez-Aguayo A, Garcia H, Carvajal CA, and Fardella CE (J Clin Endocrinol ...
Regulación de la enzima 11 beta hidroxiesteroide deshidrogenasa tipo 2 [11ß-HSD2] por miRNA y su asociación con hipertensión arterial
(Universidad del Desarrollo. Facultad de Medicina, 2018)
Classical apparent mineralocorticoid excess (AME) is a rare recessive disorder, caused by 11β-HSD2 deficiency. AME manifests as low-renin pediatric hypertension, hypokalemia and high cortisol/cortisone (F/E) ratio. The ...
Serum cortisol and cortisone as potential biomarkers of partial 11 beta-hydroxysteroid dehydrogenase type 2 deficiency
(2018)
BACKGROUND Pathogenic variations in HSD11B2 gene triggers the apparent mineralo-corticoid excess syndrome (AME). There is scarce information regarding the phenotypes of subjects carrying heterozygous pathogenic variants ...
Cortisol/cortisone ratio and matrix metalloproteinase-9 activity are associated with pediatric primary hypertension
(Lippincott Williams & Wilkins, 2016)
Objective: To identify novel biomarkers associated with pediatric primary hypertension.
Methods: We recruited 350 participants (4-16 years). Anthropometric parameters and aldosterone, plasma renin activity, cortisol, ...
Serum Cortisol and Cortisone as Potential Biomarkers of Partial 11β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
(2018)
Background: Pathogenic variations in HSD11B2 gene triggers the apparent mineralocorticoid excess syndrome (AME). There is scarce information regarding the phenotypes of subjects carrying heterozygous pathogenic variants ...
Serum cortisol and cortisone as potential biomarkers of partial 11β-hydroxysteroid dehydrogenase type 2 deficiency
(2018-07-16)
BACKGROUND Pathogenic variations in HSD11B2 gene triggers the apparent mineralocorticoid excess syndrome (AME). There is scarce information regarding the phenotypes of subjects carrying heterozygous pathogenic variants in ...
Cortisol/cortisone ratio and matrix metalloproteinase-9 activity are associated with pediatric primary hypertension
(2016-09-01)
Objective: To identify novel biomarkers associated with pediatric primary hypertension. Methods: We recruited 350 participants (4-16 years). Anthropometric parameters and aldosterone, plasma renin activity, cortisol, ...
Adipokines: Novel Players In Resistant Hypertension
(Blackwell Publishing Inc., 2014)