Results 61 to 70 of about 8,134 (194)
ABSTRACT Endoscopic submucosal dissection (ESD) is widely used for early esophageal cancer, even in patients with liver cirrhosis (LC). Corticosteroids, administered orally or by local injection, are often used to prevent post‐ESD esophageal stricture. However, their safety in patients with decompensated LC and refractory ascites remains unclear. A man
Yuki Tamura +9 more
wiley +1 more source
European ADPKD Forum multidisciplinary position statement on autosomal dominant polycystic kidney disease care [PDF]
Autosomal dominant polycystic kidney disease (ADPKD) is a chronic, progressive condition characterised by the development and growth of cysts in the kidneys and other organs and by additional systemic manifestations.
Alastair Kent +22 more
core +6 more sources
Long-Term Effects of High-Dose Tolvaptan for Autosomal Dominant Polycystic Kidney Disease Patients
Tolvaptan, a vasopressin V2 receptor antagonist, was initially approved in Japan for treatment of autosomal dominant polycystic kidney disease (ADPKD).
Shinya Nakatani +8 more
doaj +1 more source
Rare but relevant: MDMA and hyponatraemia
Abstract Conventionally used for its stimulant, empathogenic and entactogenic effects, 3,4‐methylenedioxymethamphetamine (MDMA, ecstasy) is one of the most commonly used psychoactive drugs, specifically among young adults and in nightlife and recreational party contexts.
Maria Rita Garcia +2 more
wiley +1 more source
In the randomized placebo-controlled Tolvaptan Efficacy and Safety in Management of Autosomal Dominant Polycystic Kidney Disease and its Outcomes (TEMPO) 3:4 trial, tolvaptan slowed kidney growth and renal function decline in subjects with autosomal ...
Olivier Devuyst +4 more
doaj +1 more source
Hyponatremia revisited: Translating physiology to practice [PDF]
The complexity of hyponatremia as a clinical problem is likely caused by the opposite scenarios that accompany this electrolyte disorder regarding pathophysiology (depletional versus dilutional hyponatremia, high versus low vasopressin levels) and ...
Adrogue HJ +62 more
core +2 more sources
Background Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disease characterized by the presence of renal cysts. Over time the expanding cysts lead to progressive renal failure.
Angela Maria Pellegrino +3 more
doaj +1 more source
A Case of Paroxysmal Sympathetic Hyperactivity due to Cardiogenic Shock
Paroxysmal sympathetic hyperactivity (PSH) following cardiogenic shock without structural brain injury. A patient with cardiogenic shock requiring mechanical circulatory support developed recurrent episodes of hyperthermia, tachycardia, tachypnea, diaphoresis, and hypertonia during recovery.
Takahito Katsuyama +8 more
wiley +1 more source

