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Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature review
ArticleAbstract: Aldosterone synthase deficiency (ASD) is a rare autosomal recessive disorder characterized by severePalabras claves:Aldosterone synthesis, CYP11B2 mutations, Hypoaldosteronism, next-generation sequencingAutores:Chen S., Gong F., Jiang J., Liu J., Lu L., Lu Z., Miao H., Pan H., Richard J. Auchus, Yu Z., Zhu H.Fuentes:scopusExhaled nitric oxide decreases during academic examination stress in asthma
ArticleAbstract: Rationale: Fractional exhaled nitric oxide (FENO) is known to vary with multiple endogenous and exogPalabras claves:Asthma, Depression, Exhaled nitric oxide, Psychological stress, Salivary cortisolAutores:Ana Francisca Trueba, Liu J., Richard J. Auchus, Ritz T., Rosenfield D.Fuentes:scopus