scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0022-3476(05)83142-7 |
P698 | PubMed publication ID | 8151478 |
P2093 | author name string | Radner H | |
Ebner F | |||
Hauer A | |||
Stöckler S | |||
Karpf EF | |||
P2860 | cites work | Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathy | Q38639290 |
Glutaric aciduria type I: clinical heterogeneity and neuroradiologic features | Q48198554 | ||
Glutaric aciduria: biochemical and morphologic considerations | Q48295638 | ||
Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers. II. Morphology and pathogenesis | Q48900127 | ||
Glutaric acidemia type II: clinical, biochemical, and morphologic considerations | Q70375661 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Glutaric aciduria | Q5572455 |
P304 | page(s) | 601-604 | |
P577 | publication date | 1994-04-01 | |
P1433 | published in | The Journal of Pediatrics | Q7743611 |
P1476 | title | Symmetric hypoplasia of the temporal cerebral lobes in an infant with glutaric aciduria type II (multiple acyl-coenzyme A dehydrogenase deficiency). | |
P478 | volume | 124 |
Q37468328 | Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD). |
Q48713528 | Pathology of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation |
Q74662226 | Proton NMR spectroscopic analysis of multiple acyl-CoA dehydrogenase deficiency--capacity of the choline oxidation pathway for methylation in vivo |