Results 71 to 80 of about 6,192 (214)
Novel Compound Heterozygous Variants in the COG5 Gene Causing Fetal Hydrops and Skeletal Dysplasia
Two affected fetuses in a COG5‐CDG family exhibited fetal hydrops and skeletal malformations, which were found to segregate with the paternal frameshift variant c.1972del and the maternal splice‐site variant c.2168_2168+4delinsCATAAAA in the COG5 gene.
Qi Yang +8 more
wiley +1 more source
Lactate-Protected Hypoglycemia (LPH)
Here, we provide an overview of the concept of a lactate-protected hypoglycemia (“LPH”), originally proposed as lowering glucose while simultaneously increasing lactate concentration as a method by which tumors might be targeted.
Matthew L. Goodwin +2 more
doaj +1 more source
Hyperlactatemia in critical illness and cardiac surgery [PDF]
We read with interest the article by Nichol and colleagues [1] in a recent issue of Critical Care. Their study of more than 7,000 medical and surgical patients supports the claim that an admission plasma lactate level in the upper normal range is associated with increased mortality.
O'Connor, Edna D., Fraser, John F.
openaire +4 more sources
ABSTRACT Background & Aims The efficacy of renal replacement therapy (RRT) in critically ill patients with cirrhosis remains dubious. We aimed to assess the impact of RRT on these patients' outcomes. Methods Multicenter retrospective cohort study including adult patients with cirrhosis admitted to intensive care units at University of Alberta Hospital (
Filipe S. Cardoso +5 more
wiley +1 more source
ABSTRACT Aims This study aimed to assess the nutritional status of COVID‐19 patients within the first 24 h of Intensive Care Unit (ICU) admission and to determine its association with the risk of mechanical ventilation and mortality. Methods This retrospective study analyzed electronic medical records from 342 COVID‐19 patients admitted to Hanoi ...
Hoai Thu Thi Nguyen +6 more
wiley +1 more source
Pancreatitis in cats ranges from mild forms with low mortality to severe cases with poor prognosis, and early identification of high-risk patients remains a challenge.
Yada Siriphanporn +5 more
doaj +1 more source
ABSTRACT Glycogen storage disease type Ia (GSD Ia) is a rare autosomal recessive inherited disorder of carbohydrate metabolism, caused by a deficiency in glucose 6‐phosphatase‐α (G6PC1). Patients primarily suffer from failure to thrive, hepatomegaly, and severe fasting intolerance, biochemically characterized by hypoketotic, hypoglycemia, and ...
Ruiqi Xiao +7 more
wiley +1 more source
Background/Objectives: Hyperlactatemia is a common predictive factor for poor post-cardiovascular surgery outcomes. However, it is not well understood whether the rapid postoperative lactate level elevation in a short period of time is associated with ...
Kenichiro Kikuchi +2 more
doaj +1 more source
Three dogs with severe neurological signs from acute metaldehyde intoxication were treated with emergent haemodialysis using a medium cut‐off (MCO) dialyser. Neurological signs resolved within a single 4‐h session without adverse effects. Dialytic clearance of metaldehyde was 12.5 times higher than intrinsic clearance, demonstrating the clinical ...
Maxime Rodary +5 more
wiley +1 more source
raw data for "Clinical impact of intraoperative hyperlactatemia during craniotomy"
raw data for tables 1-4 and figure 1 in PONE-D-19-23758 PLOS ONE article "Clinical impact of intraoperative hyperlactatemia during ...
Diana Romano (7474154)
core +1 more source

