Associated Papers
Pathogenesis of Primary Aldosteronism: Impact on Clinical Outcome.
Santana LS et al.
Frontiers in Endocrinology, 2022
Progress on Genetic Basis of Primary Aldosteronism.
Karwacka I et al.
Biomedicines, 2021
Novel Mutations Detection with Next-Generation Sequencing and Its Association with Clinical Outcome in Unilateral Primary Aldosteronism.
Wu CH et al.
Biomedicines, 2021
34572353 (PubMed )
Supplement: biomedicines-09-01167-s001.zip › biomedicines-1321403-supplementary.pdf
Familial hyperaldosteronism type III a novel case and review of literature.
Pons Fernández N et al.
Reviews in Endocrine & Metabolic Disorders, 2019
[Genetic alterations in primary aldosteronism].
Zennaro MC et al.
Medecine Sciences : M/s, 2015
An update on novel mechanisms of primary aldosteronism.
Zennaro MC et al.
The Journal of Endocrinology, 2015
Progress in the identification of responsible genes and molecular mechanisms in primary aldosteronism.
McManus F et al.
Expert Review of Endocrinology & Metabolism, 2014
Discordant genotype-phenotype correlation in familial hyperaldosteronism type III with KCNJ5 gene mutation: a patient report and review of the literature.
Adachi M et al.
Hormone Research in Paediatrics, 2014
Genetics of mineralocorticoid excess: an update for clinicians.
Zennaro MC et al.
European Journal of Endocrinology, 2013
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