Amanote Research
Register
Sign In
Glutaryl-CoA Dehydrogenase Deficiency
doi 10.32388/o0r47j
Full Text
Open PDF
Abstract
Available in
full text
Date
February 10, 2020
Authors
Unknown
Publisher
Qeios
Related search
Intraventricular Baclofen for Treatment of Severe Dystonia Associated With Glutaryl-CoA Dehydrogenase Deficiency (GA1): Report of Two Cases
Movement Disorders Clinical Practice
Neurology
Short Chain Acyl-CoA Dehydrogenase Deficiency
Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
Journal of Inherited Metabolic Disease
Genetics
MEDIUM CHAIN ACYL-CoA DEHYDROGENASE (MCD) DEFICIENCY
Pediatric Research
Child Health
Pediatrics
Perinatology
Hyperinsulinism Due to Short Chain 3-Hydroxylacyl-CoA Dehydrogenase Deficiency
Outcome of Medium Chain Acyl-CoA Dehydrogenase Deficiency After Diagnosis
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
FLAD1 ‐associated Multiple Acyl‐CoA Dehydrogenase Deficiency Identified by Newborn Screening
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Immunochemical and Molecular Analysis of Medium-Chain Acyl CoA Dehydrogenase Deficiency.
Journal of Clinical Biochemistry and Nutrition
Medicine
Nutrition
Clinical Biochemistry
Dietetics