Diagnosis of Medium Chain Acyl-Coa Dehydrogenase (MCAD) Deficiency in an Asymptomatic Neonate

Annals of Clinical Biochemistry - United Kingdom
doi 10.1177/000456329002700314
Full Text
Abstract

Available in full text

Date
Authors
Publisher

SAGE Publications

Related search

Outcome of Medium Chain Acyl-CoA Dehydrogenase Deficiency After Diagnosis

Archives of Disease in Childhood
Child HealthPediatricsPerinatology
1999English

MEDIUM CHAIN ACYL-CoA DEHYDROGENASE (MCD) DEFICIENCY

Pediatric Research
Child HealthPediatricsPerinatology
1984English

Short Chain Acyl-CoA Dehydrogenase Deficiency

2020English

Immunochemical and Molecular Analysis of Medium-Chain Acyl CoA Dehydrogenase Deficiency.

Journal of Clinical Biochemistry and Nutrition
MedicineNutritionClinical BiochemistryDietetics
1990English

Screening for Medium Chain Acyl-CoA Dehydrogenase Deficiency Has Still Not Been Evaluated

BMJ
2001English

Evaluation of Newborn Screening for Medium Chain Acyl-CoA Dehydrogenase Deficiency in 275 000 Babies

Archives of Disease in Childhood: Fetal and Neonatal Edition
PediatricsGynecologyPerinatologyObstetricsMedicineChild Health
2001English

Screening for Medium Chain Acyl-CoA Dehydrogenase Deficiency Using Electrospray Ionisation Tandem Mass Spectrometry

Archives of Disease in Childhood
Child HealthPediatricsPerinatology
1998English

Cost-Effectiveness Analysis of Universal Newborn Screening for Medium Chain Acyl-CoA Dehydrogenase Deficiency in France

BMC Pediatrics
Child HealthPediatricsPerinatology
2012English

Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Sudden and Unexpected Death of a 45 Year Old Woman

Genetics in Medicine
MedicineGenetics
1999English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy