Results 1 -
7
of
7
for
"Acyl-CoA" dehydrogenase 9 deficiency
- ... not show signs and symptoms of the condition. Acyl-CoA dehydrogenase 9 deficiency Deficiency of acyl-CoA dehydrogenase family member 9 ... deficiency due to ACAD9 deficiency Genetic Testing Registry: Acyl-CoA dehydrogenase 9 deficiency Isolated complex I deficiency National Organization for Rare ...
- ... control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency. Mol Genet Metab. 2007 Jan;90(1):64-9. doi: 10.1016/j.ymgme.2006.08.002. ...
- ... J. Follow-up of patients with short-chain acyl-CoA dehydrogenase and isobutyryl-CoA dehydrogenase deficiencies identified through newborn screening: one center's experience. Genet Med. 2012 Mar;14(3):342-7. doi: 10.1038/gim.2011.9. Epub 2012 Jan 5. Citation on PubMed van ...
- ... control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency. Mol Genet Metab. 2007 Jan;90(1):64-9. doi: 10.1016/j.ymgme.2006.08.002. ...
- ... mitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase. Mol ... deficiency: clinical, biochemical, and pathological studies on three subjects ...
- ... Organization for Rare Disorders (NORD) ClinicalTrials.gov ... and acute life-threatening events in patients with glutaric acidemia type II. Mol Genet Metab. 2008 Jan;93(1):36-9. doi: 10.1016/j.ymgme.2007.09.015. ...
- ... deficiency. Neuromuscul Disord. 2009 May;19(5):324-9. doi: ... dehydrogenase (VLCAD) deficiency in the United States. Mol Genet Metab. 2015 ...