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Publications by Meghan E. Strenk
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
Related publications
Essential Fatty Acid Deficiency in Very Long-Chain Acyl-Coa Dehydrogenase Deficient Patients
International Journal of Food and Nutritional Science
Proposal for an Individualized Dietary Strategy in Patients With Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
Journal of Inherited Metabolic Disease
Genetics
Proposal for an Individualized Dietary Strategy in Patients With Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
Journal of Inherited Metabolic Disease
Genetics
Short Chain Acyl-CoA Dehydrogenase Deficiency
Long-Term Correction of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency in Mice Using AAV9 Gene Therapy
Molecular Therapy
Molecular Medicine
Molecular Biology
Pharmacology
Medicine
Genetics
Drug Discovery
Tissue Carnitine Homeostasis in Very-Long-Chain Acyl-CoA Dehydrogenase–Deficient Mice
Pediatric Research
Child Health
Pediatrics
Perinatology
MEDIUM CHAIN ACYL-CoA DEHYDROGENASE (MCD) DEFICIENCY
Pediatric Research
Child Health
Pediatrics
Perinatology
Evaluation of Newborn Screening for Medium Chain Acyl-CoA Dehydrogenase Deficiency in 275 000 Babies
Archives of Disease in Childhood: Fetal and Neonatal Edition
Pediatrics
Gynecology
Perinatology
Obstetrics
Medicine
Child Health
Very Long-/ and Long Chain-3-Hydroxy Acyl CoA Dehydrogenase Deficiency Correlates With Deregulation of the Mitochondrial Fusion/Fission Machinery
Scientific Reports
Multidisciplinary
