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E W Naylor Selected Research

acylcarnitine

6/2001Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.

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E W Naylor Research Topics

Disease

2Hypothyroidism
11/2013 - 01/2003
1Autoimmune Thyroiditis (Lymphomatous Thyroiditis)
11/2013
1Phenylketonurias (Phenylketonuria)
06/2009
1Propionic Acidemia
11/2001
1Medium chain acyl CoA dehydrogenase deficiency
06/2001
1Protein Deficiency
01/2001
1Glutaric Acidemia I
01/2001
1isovaleric Acidemia
01/2001

Drug/Important Bio-Agent (IBA)

1ThyroglobulinFDA Link
11/2013
1AntibodiesIBA
11/2013
1sapropterin (tetrahydrobiopterin)FDA Link
06/2009
1Phenylalanine (L-Phenylalanine)FDA Link
06/2009
1Phenylalanine Hydroxylase (Phenylalanine 4 Monooxygenase)IBA
06/2009
1Thyrotropin (Thyroid-Stimulating Hormone)FDA Link
01/2003
1propionylcarnitineIBA
11/2001
1Acyl-CoA Dehydrogenase (Medium-Chain Acyl-Coenzyme A Dehydrogenase)IBA
06/2001
1acylcarnitineIBA
06/2001
1TransferasesIBA
01/2001
1Long-Chain Acyl-CoA Dehydrogenase (Long-Chain-Acyl-Coenzyme A Dehydrogenase)IBA
01/2001
1Coenzyme A (CoA)IBA
01/2001
1Oxidoreductases (Dehydrogenase)IBA
01/2001
1Carnitine (L-Carnitine)FDA LinkGeneric
01/2001