Results 231 to 240 of about 2,405,617 (334)
Amyloid A in Serum and Ascitic Fluid as a Novel Diagnostic Marker of Spontaneous Bacterial Peritonitis. [PDF]
Badawi R +13 more
europepmc +1 more source
Differential diagnosis and therapy of ascites [PDF]
Schölmerich, J., Gerbes, Alexander L.
core
Severe Lactic Acidosis in Decompensated Cirrhosis Despite Nondiagnostic Imaging
ABSTRACT Lactic acidosis is a strong predictor of mortality in cirrhosis, reflecting both impaired hepatic clearance and systemic tissue hypoxia. We describe a 38‐year‐old man with decompensated alcohol‐associated cirrhosis who developed severe lactic acidosis despite stable hemodynamics and initially nondiagnostic vascular imaging.
Nakul Ganju +5 more
wiley +1 more source
Dissemination of bla NDM-5 Driven by Horizontal Transfer of IncFIA Plasmid Between Escherichia coli and Klebsiella pneumoniae Co-Isolated from a Patient's Ascitic Fluid. [PDF]
Yu J +7 more
europepmc +1 more source
K. Sreedharan, R. Philip, I. Singh
semanticscholar +1 more source
ABSTRACT Immune‐mediated hepatitis caused by immune checkpoint inhibitors (ICIs) is typically suspected based on aminotransferase elevation; however, biochemical signals may be blunted in advanced cirrhosis, potentially delaying recognition. A 71‐year‐old woman with cirrhosis due to metabolic dysfunction–associated steatohepatitis and Barcelona Clinic ...
Hidenobu Hara +17 more
wiley +1 more source
Endoscopic ultrasound‐guided paracentesis of ascitic fluid
R. Wardeh, J. Lee, M. Gu
semanticscholar +1 more source
ABSTRACT Rupture of renal artery aneurysm during pregnancy (PSRRAA) is a life‐threatening emergency that can lead to adverse outcomes for both the mother and the fetus. This paper reports a case of right renal artery aneurysm (RAA) rupture in a 32‐year‐old pregnant woman at 37 weeks of gestation, and discusses the clinical diagnosis and treatment of ...
SuFang Qiu +3 more
wiley +1 more source
Black ascitic fluid in a patient with history of alcohol abuse: report of an unusual case and literature review. [PDF]
Alanís Naranjo JM +1 more
europepmc +1 more source
Pediatric Wilson Disease in Sudan: A Rare Case, Sudan Conflict and Diagnostic Challenges
ABSTRACT Wilson disease is rarely reported among African children. Wilson disease is due to a mutation in ATP7B on an autosomal recessive pattern, which causes defective copper excretion and copper accumulation in tissues such as liver and brain.
Amjed Abdu Ali Mohammed +8 more
wiley +1 more source

