Propionyl-CoA Carboxylase Deficiency (Propionicacidemia): A Cause of Non-Ketotic Hyperglycinemia

Pediatric Research - United States
doi 10.1203/00006450-197108000-00102
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

721 EFFECT OF CHOLESTEROL IN PROPIONYL CoA CARBOXYLASE (PCC) DEFICIENCY

Pediatric Research
Child HealthPediatricsPerinatology
1981English

Propionyl Coenzyme a (Propionyl-CoA) Carboxylase in Haloferax Mediterranei: Indispensability for Propionyl-CoA Assimilation and Impacts on Global Metabolism

Applied and Environmental Microbiology
Applied MicrobiologyBiotechnologyEcologyFood Science
2014English

Urinary Acid Profiles in Asymptomatic and Symptomatic Siblings With Propionyl CoA Carboxylase Deficiency.

Journal of Clinical Biochemistry and Nutrition
MedicineNutritionClinical BiochemistryDietetics
1989English

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
1980English

A Novel Compound Heterozygous Variant Identified in GLDC Gene in a Chinese Family With Non-Ketotic Hyperglycinemia

BMC Medical Genetics
Genetics
2018English

A Block in Glycine Cleavage Reaction as a Common Mechanism in Ketotic and Nonketotic Hyperglycinemia

Pediatric Research
Child HealthPediatricsPerinatology
1974English

The Oxidation of Glycine and Propionic Acid in Propionic Acidemia With Ketotic Hyperglycinemia

Pediatric Research
Child HealthPediatricsPerinatology
1972English

Pyruvate Carboxylase Deficiency

2020English

Hyperosmolar Non-Ketotic Diabetes

Postgraduate Medical Journal
Medicine
1971English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy