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Sandra C van Calcar Selected Research

2-Methylbutyryl-CoA Dehydrogenase Deficiency

2/20072-methylbutyryl-CoA dehydrogenase deficiency in Hmong infants identified by expanded newborn screen.
7/2003Prospective diagnosis of 2-methylbutyryl-CoA dehydrogenase deficiency in the Hmong population by newborn screening using tandem mass spectrometry.

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Sandra C van Calcar Research Topics

Disease

7Phenylketonurias (Phenylketonuria)
01/2017 - 02/2008
2Body Weight (Weight, Body)
12/2009 - 02/2008
22-Methylbutyryl-CoA Dehydrogenase Deficiency
02/2007 - 07/2003
1VLCAD deficiency
01/2016
1Inborn Genetic Diseases (Disease, Hereditary)
02/2008
1isovaleric Acidemia
02/2007

Drug/Important Bio-Agent (IBA)

7Phenylalanine (L-Phenylalanine)FDA Link
01/2017 - 02/2008
6Amino AcidsFDA Link
01/2017 - 02/2008
5caseinomacropeptideIBA
01/2017 - 02/2008
5Proteins (Proteins, Gene)FDA Link
08/2012 - 02/2008
2Phenylalanine Hydroxylase (Phenylalanine 4 Monooxygenase)IBA
12/2009 - 02/2008
2Isoleucine (L-Isoleucine)FDA Link
02/2007 - 07/2003
1Long-Chain Acyl-CoA Dehydrogenase (Long-Chain-Acyl-Coenzyme A Dehydrogenase)IBA
01/2016
1Whey ProteinsIBA
08/2012
1GhrelinIBA
08/2010
1MicronutrientsIBA
12/2009
1Leucine (L-Leucine)FDA Link
02/2007
12-methylacyl-CoA dehydrogenaseIBA
07/2003