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Metabolic Ketosis

Known as: Metabolic Ketoacidoses, Metabolic ketoacidosis, Ketoacidosis, Metabolic 
National Institutes of Health

Papers overview

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2016
2016
We describe two half-siblings with monocarboxylate transporter 1 (MCT1, SLC16A1) deficiency, a defect on ketone body utilization… Expand
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2012
2012
Type B insulin resistance (IR) is a rare autoimmune disease characterized by the presence of autoantibodies directed against the… Expand
2011
2011
We report a case of starvation-induced metabolic ketoacidosis in a previously healthy 29-year-old, nulliparous woman at 32 weeks… Expand
2000
2000
Propionyl-CoA carboxylase (PCC) catalyzes the biotin-dependent carboxylation of propionyl-CoA to d-methylmalonyl-CoA in the… Expand
Review
1999
Review
1999
Biotin is the cofactor of the 4 biotin-dependent carboxylases (propionyl-CoA carboxylase, 3-methylcrotonyl-CoA carboxylase… Expand
1995
1995
We report the identification of acetone (0.45 mg/mL) and isopropanol (0.17 mg/mL) but without the presence of ethanol in a blood… Expand
1990
1990
Propionic acidemia is a rare hereditary disease which is an autosomal recessive disorder. Defect of propionyl CoA carboxylase… Expand
1989
1989
Highly Cited
1981
Highly Cited
1981
Multiple carboxylase deficiency is characterized by deficient activities of three biotin-dependent enzymes, propionyl coenzyme A… Expand
Highly Cited
1980
Highly Cited
1980
A variety of chemicals potentiate haloalkane-induced liver injury, but structure-activity relationships are not apparent. Recent… Expand