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Publications by Signe Mosegaard
FLAD1 ‐associated Multiple Acyl‐CoA Dehydrogenase Deficiency Identified by Newborn Screening
Molecular genetics & genomic medicine
Genetics
Molecular Biology
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Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Evaluation of Genotype-Phenotype Correlation in Patients Detected by Newborn Screening
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Assessment of Parenting Stress Related to Treatment and Management of a Child With Medium Chain Acyl-CoA Dehydrogenase Deficiency Identified by Newborn Screening
ICAN: Infant, Child, & Adolescent Nutrition
Evaluation of Newborn Screening for Medium Chain Acyl-CoA Dehydrogenase Deficiency in 275 000 Babies
Archives of Disease in Childhood: Fetal and Neonatal Edition
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Cost-Effectiveness Analysis of Universal Newborn Screening for Medium Chain Acyl-CoA Dehydrogenase Deficiency in France
BMC Pediatrics
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Short Chain Acyl-CoA Dehydrogenase Deficiency
MEDIUM CHAIN ACYL-CoA DEHYDROGENASE (MCD) DEFICIENCY
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Screening for Medium Chain Acyl-CoA Dehydrogenase Deficiency Has Still Not Been Evaluated
BMJ
Medium-Chain Acyl-CoA Deficiency: Outlines From Newborn Screening,In SilicoPredictions, and Molecular Studies
The Scientific World Journal
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Screening for Medium Chain Acyl-CoA Dehydrogenase Deficiency Using Electrospray Ionisation Tandem Mass Spectrometry
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