Disease: Hyperaldosteronism familial type 2
- <em>CACNA1D</em> Gene Polymorphisms Associate With Increased Blood Pressure and Salt Sensitivity of Blood Pressure in White Individuals
- A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis
- Bartter Syndrome-Related Variants Distribution: Brazilian Data and Its Comparison with Worldwide Cohorts
- Ca(V)3.2 (CACNA1H) in Primary Aldosteronism
- Ca<sub>V</sub>3.2 (CACNA1H) in Primary Aldosteronism
- Case report: Two novel compound heterozygous variant of SLC12A3 gene in a gitelman syndrome family and literature review
- Characteristics and Outcomes in Primary Aldosteronism Patients Harboring Glucocorticoid-Remediable Aldosteronism
- Classic and current concepts in adrenal steroidogenesis: a reappraisal
- Clinical Findings and Genetic Analysis of Nine Mexican Families with Bartter Syndrome
- Enhanced Ca<sup>2+</sup> signaling, mild primary aldosteronism, and hypertension in a familial hyperaldosteronism mouse model (<em>Cacna1h</em><sup><em>M1560V/+</em></sup> )
- Familial hyperaldosteronism type 1 and pregnancy: successful treatment with low dose dexamethasone
- Functional characterization of SLC12A1 gene variants in 3 patients with Bartter syndrome type
- Functional characterization of SLC12A1 gene variants in 3 patients with Bartter syndrome type Ⅰ
- Genetic testing for primary aldosteronism in SPAIN: Results from the SPAIN-ALDO Registry and review of the literature
- Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3
- Gitelman syndrome with a novel frameshift variant in SLC12A3 gene accompanied by chronic kidney disease and type 2 diabetes mellitus
- Hypocalcemia as the Initial Presentation of Type 2 Bartter Syndrome: A Family Report
- Immunohistochemical Analysis of CYP11B2, CYP11B1 and β-catenin Helps Subtyping and Relates With Clinical Characteristics of Unilateral Primary Aldosteronism
- Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions
- Management and Outcomes of Primary Aldosteronism in Pregnancy: A Systematic Review
- Monogenic forms of low-renin hypertension: clinical and molecular insights
- Multiple Endocrine Neoplasia Type 1
- Paradoxes in magnesium transport in type 1 Bartter's syndrome and Gitelman's syndrome: a modeling analysis
- Recurrent transient severe hypocalcaemia in two siblings with type 1 Bartter syndrome
- Sex-specific Association of Primary Aldosteronism With Visceral Adiposity
- The mineralocorticoid receptor gene (NR3C2) is linked to and associated with polycystic ovarian syndrome in Italian families