Disease: Pseudohypoaldosteronism type 1- autosomal dominant
- A case of novel mutation of Cullin 3 gene in pseudohypoaldosteronism type II
- A Case of Pseudohypoaldosteronism Type (PHA2) Caused by a Novel Mutation of KLHL3
- A Case of Pseudohypoaldosteronism Type Ⅱ (PHA2) Caused by a Novel Mutation of <em>KLHL</em>3
- A case of secondary pseudohypoaldosteronism that presented as poor weight gain
- A case of severe systemic type 1 pseudohypoaldosteronism with 10 years of evolution
- A Case Report of Neonatal Vomiting due to Adrenal Hemorrhage, Abscess and Pseudohypoaldosteronism
- A Five-Month-Old Boy With Hypotonia, Electrolyte Derangements, and Failure to Thrive
- A late diagnosis of Pseudohypoaldosteronism type I in an infant with hypoplastic left heart syndrome presenting with failure to thrive
- A mild and transient form of autosomal recessive pseudohypoaldosteronism type 1 caused by a novel mutation in the <em>SCNN1A</em> gene
- A mild and transient form of autosomal recessive pseudohypoaldosteronism type 1 caused by a novel mutation in the SCNN1A gene
- A Neonate with Autosomal Dominant Pseudohypoaldosteronism Type 1 Due to a Novel Microdeletion of the <em>NR3C2</em> Gene at 4q31.23
- A Neonate with Autosomal Dominant Pseudohypoaldosteronism Type 1 Due to a Novel Microdeletion of the NR3C2 Gene at 4q31.23
- A Novel Homozygous KLHL3 Mutation as a Cause of Autosomal Recessive Pseudohypoaldosteronism Type II Diagnosed Late in Life
- A novel splice site CUL3 variant in a patient with neurodevelopmental delay
- A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of <em>WNK1</em>
- A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population
- Acid-Base Imbalance in Pseudohypoaldosteronism Type 1 in Comparison With Type IV Renal Tubular Acidosis
- Adult-onset transient pseudohypoaldosteronism secondary to obstructive nephropathy: a case report
- Aldosterone defects in infants and young children with hyperkalemia: A single center retrospective study
- An infant case of pseudohypoaldosteronism type1A caused by a novel NR3C2 variant
- An unusual case of Pseudohypoaldosteronism coexisting with cystic fibrosis
- Analysis of patients presenting with serum electrolyte imbalance in terms of the differential diagnosis of pseudohypoaldosteronism
- Are CUL3 variants an underreported cause of congenital heart disease?
- Association of Familial Hyperkalemia and Hypertension with Proximal Renal Tubular Acidosis and Epileptic Seizures
- Asymptomatic hyperkalemia as a form of presentation of pseudohypoaldosteronism
- Autosomal Dominant Pseudohypoaldosteronism Type 1 in a Newborn With Failure to Thrive
- Brugada syndrome uncovered in patient with pseudohypoaldosteronism due to hyperkalaemia
- Cardiac arrest in a newborn: A case of pseudohypoaldosteronism
- Case Report: A Novel Compound Heterozygote Mutation of the <em>SCNN1B</em> Gene Identified in a Chinese Familial Pseudohypoaldosteronism Disease Type I With Persistent Hyperkalemia
- Case Report: A Novel Compound Heterozygote Mutation of the SCNN1B Gene Identified in a Chinese Familial Pseudohypoaldosteronism Disease Type I With Persistent Hyperkalemia
- Case report: Early molecular confirmation and sodium polystyrene sulfonate management of systemic pseudohypoaldosteronism type I
- Case report: Life threatening hyponatremia in infants with urinary tract infections: two cases of type III pseudohypoaldosteronism and review of the literature
- Case Report: Newborns With Pseudohypoaldosteronism Secondary to Excessive Gastrointestinal Losses Through High Output Stoma
- Challenges of Diagnosing Pseudohypoaldosteronism (PHA) in an Infant
- Classification of pseudohypoaldosteronism type II as type IV renal tubular acidosis: results of a literature review
- Claudins in kidney health and disease
- Combined Kelch-like 3 and Cullin 3 Degradation is a Central Mechanism in Familial Hyperkalemic Hypertension in Mice
- Control of sodium and potassium homeostasis by renal distal convoluted tubules
- Cullin 3 and Blood Pressure Regulation: Insights From Familial Hyperkalemic Hypertension
- Cullin 3 Exon 9 Deletion in Familial Hyperkalemic Hypertension Impairs Cullin3-Ring-E3 Ligase (CRL3) Dynamic Regulation and Cycling
- Cullin 3 mutant causing familial hyperkalemic hypertension lacks normal activity in the kidney
- Diagnostic and management considerations in pseudohypoaldosteronism type 1b
- Difficulties in the diagnosis and management of eight infants with secondary pseudohypoaldosteronism
- Double synonymous mutations in exon 9 of the Cullin3 gene restore exon inclusion by abolishing hnRNPs inhibition
- Dysregulation of the WNK4-SPAK/OSR1 pathway has a minor effect on baseline NKCC2 phosphorylation
- Early-in-Life Serum Aldosterone Levels Could Predict Surgery in Patients with Obstructive Congenital Anomalies of the Kidney and Urinary Tract: A Pilot Study
- Eosinophilic cystitis-an obscure case of obstructive uropathy in infancy
- Errate: Salt-Losing Syndrome in a Girl with Type I and II Pseudohypoaldosteronism
- Familial hyperkalemic hypertension: hyperkalemia not hypertension defines dominant KLHL3 disease and may permit earlier recognition and tailored therapy
- Generation and analysis of pseudohypoaldosteronism type II knock-in mice caused by a nonsense KLHL3 mutation in the Kelch domain
- Gordon syndrome caused by a <em>CUL3</em> mutation in a patient with short stature in Korea: a case report
- Gordon's syndrome in pregnancy
- Hereditary causes of hypertension due to increased sodium transport
- Hormone resistance in children: what primary care physicians need to know
- How Much Is Too Much? Exploring Pseudohyperaldosteronism in Glycyrrhizic Acid Toxicity From Chronic Licorice Root Consumption
- Hypoaldosteronism
- Hypoaldosteronism
- Identification of a novel KLHL3-interacting motif in the C-terminal region of WNK4
- Importance of cascade family screening and precision medicine for patients with familial hyperkalaemia: a case report
- Insights into the diverse mechanisms and effects of variant CUL3-induced familial hyperkalemic hypertension
- Kelch-like protein 3 in human disease and therapy
- KLHL3-dependent WNK4 degradation affected by potassium through the neddylation and autophagy pathway
- Mechanistic insights into the primary and secondary alterations of renal ion and water transport in the distal nephron
- Mild Clinical Phenotype in an 8-Year-Old Boy with Pseudohypoaldosteronism Type 2E: A Diagnostic Challenge
- Monogenic forms of low-renin hypertension: clinical and molecular insights
- NCC regulation by WNK signal cascade
- Neonatal Pseudohypoaldosteronism Type-1 in Japan
- Neonatal systemic pseudohypoaldosteronism type I
- Novel <em>CUL3</em> Variant Causing Familial Hyperkalemic Hypertension Impairs Regulation and Function of Ubiquitin Ligase Activity
- Novel homozygous mutation in SCNN1A gene in an Iranian boy with PHA1B
- NR3C2 microdeletions-an underrecognized cause of pseudohypoaldosteronism type 1A: a case report and literature review
- Pseudo-hypoaldosteronism secondary to infantile urinary tract infections: role of ultrasound
- Pseudohypoaldosteronism and acquired renal aldosterone resistance with hyperkalemic type IV renal tubular acidosis in 2 cats
- Pseudohypoaldosteronism associated with hypertrophic cardiomyopathy, hypertension and thrombocytosis due to mutation in the ELAC2 gene: a case report
- Pseudohypoaldosteronism Type 1: The Presentation and Management of a Neonate With a Novel Mutation of the SCNN1B Gene Found in Two Hispanic Siblings
- Pseudohypoaldosteronism Type 1B and Cohen Syndrome: Novel Mutation, Unusual Combination, and Presentation
- Pseudohypoaldosteronism type 1b in fraternal twins of a Chinese family: report of two cases and literature review
- Pseudohypoaldosteronism type 2: CUL3 mutation confirmed 15 years following initial diagnosis
- Pseudohypoaldosteronism Type II or Gordon Syndrome: A Rare Syndrome of Hyperkalemia and Hypertension With Normal Renal Function
- Rare forms of genetic paediatric adrenal insufficiency: Excluding congenital adrenal hyperplasia
- Regulation of kidney on potassium balance and its clinical significance
- Role of epithelial sodium channel-related inflammation in human diseases
- Salt-Losing Syndrome in a Girl with Type I and II Pseudohypoaldosteronism
- Secondary pseudohypoaldosteronism: a 15-year experience and a literature review
- Sequence and structural variations determining the recruitment of WNK kinases to the KLHL3 E3 ligase
- Successful Management of Systemic Pseudohypoaldosteronism Type 1 in an Infant
- Systemic Pseudohypoaldosteronism Type 1 Due to a Novel Mutation in SCNN1B Gene: A Case Report
- The Epithelial Sodium Channel-An Underestimated Drug Target
- The Post-Translational Modification Networking in WNK-Centric Hypertension Regulation and Electrolyte Homeostasis
- The small molecule activator S3969 stimulates the epithelial sodium channel (ENaC) by interacting with a specific binding pocket in the channel's β-subunit
- The small molecule activator S3969 stimulates the epithelial sodium channel by interacting with a specific binding pocket in the channel's β-subunit
- Transient pseudohypoaldosteronism in infancy mainly manifested as poor appetite and vomiting: Two case reports and review of the literature
- TRANSIENT PSEUDOHYPOALDOSTERONISM SECONDARY TO URINARY TRACT INFECTION IN A MALE INFANT WITH UNILATERAL HYDRONEPHROSIS DUE TO PRIMARY OBSTRUCTIVE MEGAURETER: A CASE REPORT
- Transient secondary pseudo-hypoaldosteronism in infants with urinary tract infections: systematic literature review
- UBR5 is a novel regulator of WNK1 stability
- Unanticipated domain requirements for Drosophila Wnk kinase in vivo
- Unusual skin and eyelid changes in a neonate with pseudohypoaldosteronism
- When the Going Gets Tough: A Case Report and Review of Calcinosis Cutis in an Infant with Pseudo-Hypoaldosteronism
- WNK1 in the kidney
- WNK1/HSN2 mediates neurite outgrowth and differentiation via a OSR1/GSK3β-LHX8 pathway