glutaric acid has been researched along with Embryopathies in 6 studies
glutaric acid: RN given refers to parent cpd
glutaric acid : An alpha,omega-dicarboxylic acid that is a linear five-carbon dicarboxylic acid.
Excerpt | Relevance | Reference |
---|---|---|
"When pregnancy is terminated because of enlarged hyperechoic kidneys in the fetus, autopsy is crucial for establishing the correct diagnosis." | 1.30 | Recurrent fetal polycystic kidneys associated with glutaric aciduria type II. ( Graem, N; Kjaergaard, S; Larsen, T; Skovby, F, 1998) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (16.67) | 18.7374 |
1990's | 3 (50.00) | 18.2507 |
2000's | 2 (33.33) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Hasegawa, Y | 1 |
Iga, M | 1 |
Kimura, M | 1 |
Shigematsu, Y | 1 |
Yamaguchi, S | 1 |
Hockey, A | 1 |
Knowles, S | 1 |
Davies, D | 1 |
Carey, W | 1 |
Hurst, J | 1 |
Goldblatt, J | 1 |
Kjaergaard, S | 1 |
Graem, N | 1 |
Larsen, T | 1 |
Skovby, F | 1 |
Vianey-Saban, C | 1 |
Bouvier, R | 1 |
Cochat, P | 1 |
Buenerd, A | 1 |
Divry, P | 1 |
Dumoulin, R | 1 |
Cordier, MP | 1 |
Medlock, MD | 1 |
Rhead, WJ | 1 |
Pollack, L | 1 |
Meredith, JT | 1 |
Pearl, G | 1 |
Reece, C | 1 |
Henderson, HE | 1 |
Balla, R | 1 |
de Jong, G | 1 |
Piek, CJ | 1 |
Mienie, LJ | 1 |
Erasmus, E | 1 |
6 other studies available for glutaric acid and Embryopathies
Article | Year |
---|---|
Prenatal diagnosis for organic acid disorders using two mass spectrometric methods, gas chromatography mass spectrometry and tandem mass spectrometry.
Topics: Amniotic Fluid; Carboxylic Acids; Carnitine; Female; Fetal Diseases; Gas Chromatography-Mass Spectro | 2005 |
Glutaric aciduria type II, an unusual cause of prenatal polycystic kidneys: report of prenatal diagnosis and confirmation of autosomal recessive inheritance.
Topics: Amino Acid Metabolism, Inborn Errors; Amniocentesis; Female; Fetal Diseases; Genes, Recessive; Gluta | 1993 |
Recurrent fetal polycystic kidneys associated with glutaric aciduria type II.
Topics: Acyl-CoA Dehydrogenases; Adult; Female; Fetal Diseases; Glutarates; Humans; Polycystic Kidney Diseas | 1998 |
Antenatal expression of multiple acyl-CoA dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Cells, Cultured; Electron-Transferring Flavoprotein | 2000 |
A case of glutaric acidemia type II (severe multiple acyl-CoA dehydrogenation disorder) with subsequent prenatal exclusion in a sibling.
Topics: Acidosis; Cerebral Hemorrhage; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Fetal Di | 1991 |
Postnatal and antenatal laboratory diagnosis of glutaric aciduria II in a South African family.
Topics: Female; Fetal Diseases; Glutarates; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Pregna | 1987 |