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Publications by Maurice J Mahonev
Propionyl-CoA Carboxylase Deficiency (Propionicacidemia): A Cause of Non-Ketotic Hyperglycinemia
Pediatric Research
Child Health
Pediatrics
Perinatology
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721 EFFECT OF CHOLESTEROL IN PROPIONYL CoA CARBOXYLASE (PCC) DEFICIENCY
Pediatric Research
Child Health
Pediatrics
Perinatology
Propionyl Coenzyme a (Propionyl-CoA) Carboxylase in Haloferax Mediterranei: Indispensability for Propionyl-CoA Assimilation and Impacts on Global Metabolism
Applied and Environmental Microbiology
Applied Microbiology
Biotechnology
Ecology
Food Science
Urinary Acid Profiles in Asymptomatic and Symptomatic Siblings With Propionyl CoA Carboxylase Deficiency.
Journal of Clinical Biochemistry and Nutrition
Medicine
Nutrition
Clinical Biochemistry
Dietetics
Regulation of Acetyl-coA Carboxylase: Properties of coA Activation of Acetyl-coA Carboxylase.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Novel Compound Heterozygous Variant Identified in GLDC Gene in a Chinese Family With Non-Ketotic Hyperglycinemia
BMC Medical Genetics
Genetics
A Block in Glycine Cleavage Reaction as a Common Mechanism in Ketotic and Nonketotic Hyperglycinemia
Pediatric Research
Child Health
Pediatrics
Perinatology
The Oxidation of Glycine and Propionic Acid in Propionic Acidemia With Ketotic Hyperglycinemia
Pediatric Research
Child Health
Pediatrics
Perinatology
Pyruvate Carboxylase Deficiency
Hyperosmolar Non-Ketotic Diabetes
Postgraduate Medical Journal
Medicine
