Amendt BA and Rhead WJ |
The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts. |
1986 |
J. Clin. Invest. |
pmid:3722376
|
Ikeda Y et al. |
Biosynthesis of electron transfer flavoprotein in a cell-free system and in cultured human fibroblasts. Defect in the alpha subunit synthesis is a primary lesion in glutaric aciduria type II. |
1986 |
J. Clin. Invest. |
pmid:3760196
|
Eastman MA et al. |
Conformation of the 18-23 loop region of bovine prothrombin in the absence and presence of a model Ca2+ ion. An energy minimization study. |
1986 |
Int. J. Pept. Protein Res. |
pmid:3733321
|
Srb V et al. |
Cytogenetic monitoring of a 24-hour effect of ethylmalonate platinum complex on human peripheral blood lymphocytes. |
1986 |
Neoplasma |
pmid:3785467
|
Gregersen N et al. |
Riboflavin responsive multiple acyl-CoA dehydrogenation deficiency. Assessment of 3 years of riboflavin treatment. |
1986 |
Acta Paediatr Scand |
pmid:3751563
|
Amendt BA et al. |
Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients. |
1987 |
J. Clin. Invest. |
pmid:3571488
|
Harpey JP et al. |
Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency. |
1987 |
J. Pediatr. |
pmid:3585604
|
O'Harte FP et al. |
Methylmalonic acid in the diagnosis of cobalt deficiency in barley-fed lambs. |
1989 |
Br. J. Nutr. |
pmid:2605162
|
Schiffer SP et al. |
Organic aciduria and butyryl CoA dehydrogenase deficiency in BALB/cByJ mice. |
1989 |
Biochem. Genet. |
pmid:2712823
|
Wood PA et al. |
Short-chain acyl-coenzyme A dehydrogenase deficiency in mice. |
1989 |
Pediatr. Res. |
pmid:2919115
|