Results 1 -
10
of
10
for
Glutaric "aciduria," type 1
- ... I Glutaryl-CoA dehydrogenase deficiency Genetic Testing Registry: Glutaric aciduria, type 1 Glutaric acidemia type I Disease InfoSearch National Organization ...
- Newborn Screening Tests for Your Baby (March of Dimes Foundation)Newborn Screening/Specifics ... Newborn Screening ... March of Dimes Foundation
- ... II in human. Genomics. 1996 Apr 1;33(1):131-4. doi: 10.1006/geno.1996.0170. Citation on PubMed Whitfield J, Hurst D, Bennett MJ, Sherwood WG, Hogg R, Gonsoulin W. Fetal polycystic kidney disease associated with glutaric aciduria type II: an inborn error of energy metabolism. Am ...
- ... North Carolina. Mol Genet Metab. 2006 May;88(1):90-2. doi: ... patients with glutaric aciduria type I. Mol Genet Metab. 2000 Nov;71(3): ...
- Amino Acid Metabolism Disorders (National Library of Medicine)Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Your digestive system breaks ...
- ... adipicaciduria GA II Glutaric acidemia, type 2 Glutaric aciduria, type 2 MAD MADD Multiple acyl-CoA ... patients with glutaric acidemia type II. Mol Genet Metab. 2008 Jan;93(1):36-9. doi: 10.1016/j.ymgme.2007. ...
- Mitochondrial Diseases (National Library of Medicine)... The diseases range from mild to severe. Some types can be fatal. Genetic ... therapy, vitamins and supplements, special diets, and medicines.
- ... in the signs and symptoms of glutaric acidemia type II. More About This Health Condition ... deficiency. Hum Mutat. 2003 Jul;22(1):12-23. doi: 10.1002/humu.10226. Citation ...
- Genetic Brain Disorders (National Library of Medicine)A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
- ... by an infection, fasting, strenuous exercise, or other types of stress.HMG-CoA lyase deficiency is ... A lyase. J Biol Chem. 2003 Aug 1;278(31):29016-23. doi: 10.1074/jbc. ...