• <em>Cryptococcus neoforman</em>s rapidly invades the murine brain by sequential breaching of airway and endothelial tissues barriers, followed by engulfment by microglia
• A frameshift mutation in the <em>SCNN1B</em> gene in a family with Liddle syndrome: A case report and systematic review
• A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review
• An Unexpected Cause of Chest Pain While Self-Pleasuring: A Ripping Doom Excitement
• Analysis of clinical factors associated with Kampo formula-induced pseudoaldosteronism based on self-reported information from the Japanese Adverse Drug Event Report database
• Case report: Severe respiratory failure caused by licorice
• Defining predictors of responsiveness to advanced therapies in Crohn's disease and ulcerative colitis: protocol for the IBD-RESPONSE and nested CD-metaRESPONSE prospective, multicentre, observational cohort study in precision medicine
• Dexamethasone Suppression Test
• Dexamethasone Suppression Test
• Difficult Diagnosis and Management of Concealed Cushing
• Dramatic recovery of left ventricular dysfunction in a patient with pseudoaldosteronism, hypokalaemia, and rhabdomyolysis: a case report
• Guanylyl cyclase C ameliorates visceral pain: an unsuspected link
• Hereditary causes of hypertension due to increased sodium transport
• Identification of a novel frameshift mutation in the SCNN1B causing Liddle syndrome
• Investigation of hospital discharge cases and SARS-CoV-2 introduction into Lothian care homes
• Kampo Medicine for Neurological Diseases
• Liddle syndrome
• Liddle Syndrome (Pseudohyperaldosteronism)
• Liddle syndrome presenting with normal aldosterone levels: A case report
• Mechanosensing Piezo channels in gastrointestinal disorders
• Mitral valve orifice area predicts outcome after biventricular repair in patients with hypoplastic left ventricles
• Monogenic Etiology of Hypertension
• Monogenic Hypertension Linked to the Renin-Angiotensin-Aldosterone System
• Neonatal presentation of a patient with Liddle syndrome, South Africa
• Pathophysiologic approach in genetic hypokalemia: An update
• Pendrin abundance, subcellular distribution, and function are unaffected by either αENaC gene ablation or by increasing ENaC channel activity
• Recording Sodium Self-Inhibition of Epithelial Sodium Channels Using Automated Electrophysiology in <em>Xenopus</em> Oocytes
• Regulation of kidney on potassium balance and its clinical significance
• Reverse Phenotypes of Patients with Genetically Confirmed Liddle Syndrome
• Reverse Phenotypes of Patients with Genetically Confirmed Liddle's Syndrome
• Safety of triazole antifungals: a pharmacovigilance study from 2004 to 2021 based on FAERS
• Severe osteoporosis in a young man with bilateral Cushing's syndrome: a case report
• The Differential Diagnosis between Cushing's Disease and Pseudocushing Syndrome in a Pre-agonic Patient
• The Epithelial Sodium Channel-An Underestimated Drug Target
• Therapeutic management of congenital forms of endocrine hypertension
• Torsade de Pointes Caused by a Compound Licorice Tablet
• Torsade de pointes during an oral surgery caused by a combination of herbal medicine-induced pseudoaldosteronism and trigeminocardiac reflex