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MEDIUM CHAIN ACYL-CoA DEHYDROGENASE (MCD) DEFICIENCY
Pediatric Research
Child Health
Pediatrics
Perinatology
Very Long-Chain Acyl-CoA Synthetase 3: Overexpression and Growth Dependence in Lung Cancer
PLoS ONE
Multidisciplinary
Mitochondrial Fatty Acid Biosynthesis and Muscle Fibre Plasticity in Very Long-Chain Acyl-CoA Dehydrogenase-Deficient Mice
FEBS Letters
Genetics
Cell Biology
Molecular Biology
Biochemistry
Structural Biology
Biophysics
Recurrent ACADVL Molecular Findings in Individuals With a Positive Newborn Screen for Very Long Chain Acyl-coA Dehydrogenase (VLCAD) Deficiency in the United States
Molecular Genetics and Metabolism
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Outcome of Medium Chain Acyl-CoA Dehydrogenase Deficiency After Diagnosis
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Immunochemical and Molecular Analysis of Medium-Chain Acyl CoA Dehydrogenase Deficiency.
Journal of Clinical Biochemistry and Nutrition
Medicine
Nutrition
Clinical Biochemistry
Dietetics
Deficiency of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase: A Cause of Lethal Myopathy and Cardiomyopathy in Early Childhood
Pediatric Research
Child Health
Pediatrics
Perinatology
Carnitine Supplementation Induces Acylcarnitine Production in Tissues of Very Long-Chain Acyl-CoA Dehydrogenase-Deficient Mice, Without Replenishing Low Free Carnitine
Pediatric Research
Child Health
Pediatrics
Perinatology
Diagnosis of Medium Chain Acyl-Coa Dehydrogenase (MCAD) Deficiency in an Asymptomatic Neonate
Annals of Clinical Biochemistry
Medicine
Clinical Biochemistry
Hyperinsulinism Due to Short Chain 3-Hydroxylacyl-CoA Dehydrogenase Deficiency
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